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1 Ministry of Public Health, Islamic Republic of Afghanistan General Directorate of Preventive Medicine Communicable Diseases Control Directorate National Malaria and Leishmaniasis Control Programme National Strategy for Community-based Management of Malaria (CBMM) in Afghanistan (2016-2020) 2016

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Page 1: Development of the National Strategy for Community-based ...old.moph.gov.af/Content/Media/Documents/CBMM... · Communicable Diseases Control Directorate National Malaria and Leishmaniasis

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Ministry of Public Health, Islamic Republic of Afghanistan

General Directorate of Preventive Medicine

Communicable Diseases Control Directorate

National Malaria and Leishmaniasis Control Programme

National Strategy for Community-based Management of

Malaria (CBMM) in Afghanistan (2016-2020)

2016

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Table of contents

ACKNOWLDGEMENTS……………………………………………………………………….… 3

ACROYNYMS…………………………………………………………...………………………… 4

1 BACKGROUND…………………...…………………………………………………………… 6

2 SITUATION ANALYSIS ………………………………………………………………...……. 8

2.1 Health Care system…………………………………………….………………………………. 8

2.2 Challenges………………………………………………………………………..………........... 14

2.3 Malaria Stratification…………………………………………………......…………………… 15

2.4 Ongoing community-based initiatives in Afghanistan…………………….………………… 16

2.5 Pilot community-based management of malaria in Badkhshan, Kunduz, and Takhar

Province………………………………………………………………………………………… 16

3 GOAL………………………………………………………...………………………...………... 17

4 STRATEGIC DIRECTION ………………………………………………………………….. 17

5 STRATEGIC BJECTIVES…….……………………………………………………………… 17

6 STRATEGIC COMPONENTS …..………………………………………………………..….. 17

6.1 Case Management…………………………………………………………………………….... 17

6.2 Capacity Building…………………………………………………………………………...….. 18

6.3 Advocacy, community sensitization and Education…………………….…………………… 20

6.4 Risk Management Strategy…………………………………………………………………… 21

7 INSTITUTIONAL FRAMEWORK …………………………………………………….…… 22

8. MECHANISMS FOR COORDINATION……………………………………………………. 22

8.1 The National Vector Born Disease Control Task Force (VBDCTF)……………………...… 22

8.2 The Provincial Vector Born Disease Control Task Force (VBDCTF)…………….………... 23

9 IMPLEMENTATION PLAN…………………………………………………………………. 24

10 MONITORING AND EVALUATION……………………………………………………… 25

10.1 Integrated supervision ……………………………………………………………………..… 25

10.2 Quality control at point of care …………………………………………………………...…. 25

ANNEX 1 - Stratification of districts of Afghanistan based on reported malaria incidence rate

(2009 data)……………………………………………………………………………....... 31

ANNEX 2 - Current contents of CHW kit (2009)……………………………….……………...... 38

ANNEX 3 - Tally Sheets for CBMM developed in the pilot RDT and ACT

Community-based project ……………………………………………………………….. 41

ANNEX 4 - Supervision Check List on ACTs and RDTs for Community Health Supervisors. 42

ANNEX 5 Timetable of activities………………………………………………………………….. 43

ANNEX 6 Budget components and financial gaps (USD)…………………………………….…. 45

ANNEX 7: CBMM Curriculum…………………………………………………………………... 47

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ACKNOWLEDGMENT: The Ministry of Public Health would like to acknowledge the contribution made by all stakeholders

working in the first revision of National Community Based Management of Malaria Strategy (CBMM

2016 – 2020) which will ensure universal coverage of Malaria confirmation at country level.

The malaria experts from CBHC directorate, WHO, UNDP, BRAC, HN-TPO, and other partners

deserve special mention for their invaluable technical guidance and ensuring that

Afghanistan’s CBMM strategy is comprehensive, effective and will have a significant impact in terms

of control and elimination of malaria in the country.

Finally, it is important to note that this Strategy should be regarded as a working document. All

comments, feedback and additional case materials will be considered in future reviews in order to

make it more relevant.

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ACRONYMS

ACTs Artemisinin Combination Therapy

BHCs Basic Health Centres

BRAC Bangladesh Rural Accreditation Committee

CBHC Community Based Health Centre

CDC Communicable Disease Control

CIMCI Community Integrated Management of Childhood Illness

CHS Community Health Supervisor

CHWs Community Health Workers

CQ Chloroquine

EMRO East Mediterranean Regional Office

EPHS Essential Package of Hospital Services

GF R8 Global Fund Round 8

GFATM Global Fund fight against AIDS, TB and Malaria

HMIS Health Management Information System

HN-TPO Health Net- Trans cultural Psycho-social organisation

HPRO Health Protection Research Organisation

IEC Information, Education and Communication

IM Intramuscular

IMCI Integrated Management of Childhood Illness

LLIN Long Lasting Insecticidal Nets

MoPH Ministry of Public Health

NGOs Non- Governmental Organisation

NMCLP National Malaria and Leishmaniasis Programme

NMSP National Malaria Strategic Plan

ORS Oral Rehydration Salts

PHC Primary Healthcare

PHD Provincial Health Directorate

PR Principal Recipient

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RDT Rapid Diagnostic Test

HSC Health Sub centres

TB Tuberculosis

TDR Tropical Disease Research

UN United Nations

UNDP United Nations Development Program

UNICEF United Nations Childrens Fund

USAID US Agency for International Development

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1. BACKGROUND

It is estimated that the number of cases of malaria rose from 233 million in 2000 to 244

million in 2005 but decreased to 225 million in 2009. The number of deaths due to malaria is

estimated to have decreased from 985000 in 2000 to 781000 in 2009.

Malaria is an endemic disease and a public health problem in Afghanistan. It causes a great

burden on the health and economic development of individuals, families and communities

living in endemic areas. The total number of reported malaria cases were 319742 in 2013,

295050 in 2014 and 366526 in 2015. Majority of these cases were clinically diagnosed:

85.5%, 71.6 % and 71.8 % respectively (HMIS 2015). The Government of Afghanistan

remains committed to the control of this disease. For this purpose the Government developed

the National Malaria Strategy Plan 2013-2017 with a vision of a malaria free Afghanistan.

The main quality-of-care challenge posed by the recent decline in malaria is now in

identifying those cases of fever which are in fact caused by malaria amongst the clinical

malaria cases and treating the correct species of infection according to NTG. Most fever in

Afghanistan is not caused by malaria. Most malaria, in turn, is not caused by P. falciparum,

but by P. vivax. since treatment for these two species differs, identification of the species is

important for treatment outcomes. In summary, the context for deployment of RDTs should

be in improving the treatment of fever at community level and ensuring that those with

malaria are a) parasitologically confirmed cases and b) treated appropriately. Appropriate

treatment, in this context, means that those with parasites are treated with an effective

antimalarial, and those without malaria parasites are appropriately treated with non-

antimalarial drugs.

The need to identify the presence or absence of malaria parasites (at species level) in

providing treatment lends itself to mixture of diagnostic methods each of which is appropriate

to the setting. The choice is between microscopy and RDTs. Microscopy is the preferred

method in clinic settings with a relatively high throughput of patients, but is also difficult and

expensive to maintain because of the need to monitor quality of the microscopists and

relatively high fixed costs (such as microscopes and salaries). RDTs may also play a role at

clinic level (BHC, SHC and MHT), in areas where microcopy is hard to maintain.

RDTs can also be deployed at community level, through CHWs, which may improve access

to effective treatments for both malarial and non-malarial causes of fever at community level.

Programs to increase access to RDTs also encounter challenges, such as maintenance and

monitoring of quality, supply and storage of the RDTs and in training of CHWs. Despite

these challenges, there is hope that RDTs have a role to play in improving diagnosis of

malaria and non-malarial causes of fever and through accurate diagnosis, to improve the

targeting of effective treatments.

Accurate diagnosis of malaria (using RDTs and micrsocopy) is also providing more accurate

and higher resolution surveillance data in most settings where they have been deployed. Until

now, most data has been based on clinical malaria cases (i.e. where there has been no parasite

based diagnosis), which results in a persistent over estimate of malaria burden – for example

in Herat province, in 2015, around 13225 clinical cases were reported through the HMIS

system. In clinics which have microscopy (in the most endemic districts of Herat) slide

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positivity rate was 0.85 %. If this figure is applied to the number of clinical cases identified,

the estimated confirmed malaria cases among reported clinical cases will be around 2-5 cases.

This improved accuracy in surveillance can result in the directing of resources more

effectively and in earlier detection of outbreaks and epidemics. It has additional advantages in

enhancing the type of intensive surveillance that will be required if Afghanistan officially

declares the goal of elimination.

The National Strategy for Community-based Management of Malaria (CBMM) in

Afghanistan outlines the basic approach to increase access to diagnostic testing of malaria

and effective treatment at the community level in all malaria endemic areas of Afghanistan.

It aims at mobilising commitment and resources from the Government of Afghanistan, the

implementing agencies and the community themselves, providing a common strategy for

concerted action. The development of this Strategy builds on the key policy elements of the

National Malaria Strategy (NMSP) of Afghanistan (2013-2017), the Basic Package of Health

Services (BPHS) for Afghanistan (2010/1389), and the Community-Based Health Care

Policy and Strategy (2015-2020). Currently Afghanistan enjoys a strong partnership amongst

Government, UN agencies, funding agencies, and national and international NGOs, which

creates an enabling environment for successful malaria control.

The CBMM Strategy aim to progressively expand access to highly effective antimalarial

treatment with Artesunate + SP (Sulfadoxine-Pyrimethamine) for the treatment of parasite

confirmed falciparum malaria and with chloroquine for treatment of parasite confirmed vivax

malaria, guided by the use of combination RDTs at peripheral clinics (BHC, SHC and MHT)

and at community level.

First time the CBMM strategy was developed in 2011 which was Implemented phase wise in

stratum one and two provinces. The implementaton of CBMM will be expanded to the entire

country in updated strategy.

2. SITUATION ANALYSIS:

Health Care System

As a result of improvements in health services, Afghans’ health status has improved

substantially since the rebuilding began. The infant mortality ratio (IMR) has declined from

165 in 2003 to 66 deaths per 1,000 live births in 2015; during the same period, under-five

mortality has dropped from 257 to 84 per 1,000 live births. The decline in MMR also has

been dramatic, falling from 1,600 to 396 per 100,000 live births and life expectancy at birth

has increased to 59 years for men and 61 years for women.

The national health policy of Afghanistan aims at providing a standardized package of basic

services in all primary health care facilities, as described in the Basic Package of Health

Services (BPHS). The Basic Package of Health Services includes six standard types of

health facilities, ranging from community outreach provided by CHWs at Health Posts,

through outpatient care at Health Sub Centers and Basic Health Centers and provided by

Mobile Health Teams, to inpatient services at Comprehensive Health Centers and district

hospitals. The section below summarizes the services provided by each type of facility.

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Health Posts: At the community level, basic health services are delivered by CHWs from

their own homes, which function as community health posts. A health post, ideally staffed by

one female and one male CHW, cover a catchments area of 1,000– 1,500 people, which is

equivalent to 100–150 families. The CHWs offer basic curative services, including

differential diagnosis and treatment of fever as well as a wide array of communicable

diseases.

Under CBMM all health posts will be provided RDT for confirmation of clinical malaria

cases and ACT for treatment of confirmed P. faliciparum cases. This will ensure the universal

coverage of parasitological diagnosis and proper treatment of malaria in the country.

Health Sub Centers: The extremely challenging geography, especially in some parts of the

country, the scattered pockets of population, the absence of basic infrastructure such as roads

and bridges, ethnic and security issues, etc. all pose difficult questions regarding the

establishment of BPHS health facilities based on the number of people covered. A HSC is

intended to cover a population of about 3,000-7,000, often residing in remote underserved

areas. The HSC is staffed by two technical staff (a male nurse and a community midwife), as

well as a cleaner/guard. The HSC provides most of the BPHS services that are available in

BHCs. HSCs will refer severe and complicated cases to higher level facilities. The HSCs are

not equipped with adequate malaria diagnostic facilities, therefore; HSCs will also be

supplied RDT and required anti-malarial for treatment of confirmed malaria cases.

Mobile Health Teams: Given all the challenges coupled with the scarcity of trained health

workers (particularly females), it may not be feasible to establish staffed fixed centers in

some remote areas, where the population is scattered and live in small communities. The

principal idea of mobile health services is to establish a limited number of mobile health

teams in each province by dividing the province into clusters of districts. The MHT ideally

has the following staff, male health provider (doctor or nurse), female health provider

(community midwife or nurse), vaccinator and driver. The MHTs are unable to offer

microscopic confirmation of malaria and they will also be supported through CBMM to

ensure parasitological diagnosis by RDT and proper treatment.

Basic Health Center: The BHC is a small facility offering primary outpatient care,

immunizations and Maternal and Newborn care. The services of the BHC cover a population

of about 15,000–30,000, depending on the local geographic conditions and the population

density (can be less than 15,000 where the population is very isolated). The minimal staffing

requirements for a BHC are a nurse, a community midwife, and two vaccinators. Mainly

BHC offer clinical malaria diagnostic services but some health facilities are equipped with

supplies and equipment for malaria microscopy, under some grants of MoPH.

To ensure parasitological diagnosis of malaria in remaining BHCs without lab will also be

supplied with RDTs.

Comprehensive Health Centers: The CHC covers a catchment area of about 30,000–60,000

people and offer a wider range of services than does the BHC. The facility usually has limited

beds inpatient care, and a laboratory equipped with microscopes. The staff of a CHC

comprises of doctors (male and female), nurses (male and female), midwives, one (male or

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female) psychosocial counsellor and pharmacy and laboratory technicians. Irregular

attendance by the laboratory technicians due to trainings, illness, commitment to other

programme related activities, results weakened laboratory diagnostic services. Furthermore,

high patient burden and long waiting lists may also limit access to malaria microscopy at

CHCs level.

District Hospitals: Each district hospital covers a population of about 100,000–300,000.

The district hospital is staffed with a number of doctors, including female

obstetricians/gynecologists; a surgeon, an anesthetist, a pediatrician, a doctor who serves as a

focal point for mental health: psychosocial counsellors/supervisors; midwives; laboratory and

X-ray technicians; a pharmacist; a dentist and dental technician; and two physiotherapists

(male and female). HMIS data shows some proportion of malaria cases are diagnosed

clinically despite the District Hospitals are equipped with microscopy due to high patient

burdens and long waiting lists in the outpatient departments.

Review of National Policies

Community-based health care

The Community-based Health Care in Afghanistan is fully described in the Community-

Based Health Care Policy and Strategy which is recently updated for 2015-2020.

Community-based health care (CBHC) is the basic strategy of the BPHS, providing the

context for the comprehensive interaction between the health system and the communities it

serves. Its success depends upon community participation and partnership between the

community and the health staff.

The implementation of CBHC activities recognizes first that families and communities have

always looked after their own health. Religion and cultural norms and beliefs play an

important part in health practices, and families are making decisions to maintain health or

care for illness every day. In addition, community members understand and have better

information on local needs, priorities, and dynamics in addition to the available local

resources to promote health within their own community. The partnership of health services

with communities therefore has two key aspects:

• To welcome and accept the guidance and collaboration of communities in the

implementation of health programs and the acceptable provision of health services, and

encourage them to identify and solve their own problems.

• To persuade families and communities to make appropriate use of formal health services,

and where necessary to change behavior and life styles

The main purpose of the CBHC program is to increase community awareness about

importance of promotive and preventive measures and to reduce treat common causes of

mortality and morbidity, particularly among children and mothers, who, in Afghanistan are

the most vulnerable of any community

The community based health care strategy 2015 -2020 focuses on below objectives:

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COMMUNITY DEVELOPMENT Health facility

Community

Female & male CHWs

CHS

School

Family Health Action Groups

Other influential

people

Facility Shura-e-Sehi

Family Health action group

Figure 3: Community-Based Health Care System, Afghanistan

Private Provider

1. To scale up CBHC services and initiatives to 90% of uncovered and underserved areas in

rural setting and 60% of poor urban and nomad population by 2020

2. To improve the quality of community based primary health care services at household

level

3. To empower communities to identify their own health needs and take initiatives to solve

identified health problems

4. To enhance the governance of CBHC programs at all levels of health system

The Afghan CBHC system is shown in the figure below, which emphasizes the dynamic

nature of the system. Key stakeholders include:

1. Community health workers

2. Community health supervisors

3. Health shura (Shura-e-Sehie)

4. Family health action groups

Community health workers (CHWs)

CHWs are important members of the health system working as they do with the community.

A CHW has to be from the same area he/she is serving so that she/he is familiar with the

culture and language of the community; the community they serve should also select them.

A CHW provides basic health services from his/her home, which is recognized as a health

post. Usually, both a female and a male community health worker staff a health post. In the

case of the unavailability of both a male and a female CHW, just one CHW may work at the

health post but this not an ideal situation. A health post is responsible for a catchment area for

1,000 to 1,500 people, equivalent to between 100 - 150 families. The coverage of a health

post can be changed according to a geographical area.At present in 2015 there are over

28,000 CHWs serving rural populations in Afghanistan.

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CHWs are trained for between four- six months to deliver basic health services. The main

responsibilities of community health workers are as follows:

• Health education, the promotion of health and changing the health habits of the community

• Referral of patients to health facilities when needed

• Provision of first aid

• Treatment of common and simple illnesses e.g. ARI. Diarrhea and malaria based on the C-

IMCI treatment protocol

• Mother and child health

• Community mobilization for health actions

• Follow-up of TB-DOTs

• Participation in national immunization days and other relevant campaigns

• Community based rehabilitation awareness.

Community health supervisors

CHWs are supervised and monitored by a community health supervisor from the nearest

health facility. A community health supervisor is member of the health facility. S/he is the

main link between the facility and the communities in the catchment area of the facility. S/he

supervises all the CHWs in the catchment area of the health facility, and guides them on the

delivery of the basic health services. Community health supervisors conduct monthly

supervisory meetings with CHWs and ensure the regular replacement of materials in the

CHW kits. In addition, a community health supervisor collects and processes all monthly

reports from CHWs and helps them in their practical work.

Health shura

There are two types of health shura in the CBHC program:

1. A health shura at the health post level

2. A health shura at the health facility level.

The health shura at the health post level supports health related activities in the community

and selects, helps and monitors the CHWs. The health shura at the health facility level works

with CHWs and BPHS staff to adapt health related services to community needs and ensure

improved quality of services and the satisfaction of patients and clients who have used a

health facility.

Family Health Action Group (FHA Group)

An FHA Group is a support group for female CHWs whose aim is to improve the life style of

mothers and appropriate use of health services by mothers and children.

Female CHWs select a group of 10-15 women as activists/volunteers with young children,

respected within their community, and improve their knowledge about health related actions.

Malaria treatment guidelines and management of fever

The MOPH of Afghanistan has updated the national malaria treatment guidelines and adopted

Artesunate + Sulfadoxine/Pyrimethamine as first line treatment of uncomplicated

P.falciparum malaria and Chloroquine+Primaquine for P.Vavix malaria, but the pregnant

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women in first trimester with confirmed plasmodium falciparum will be treated with quinine

and P. vivax with chloroquine without Primaquine in all trimesters. The adoption of ACTs as

antimalarial treatment policy was endorsed in the EMRO region in 20031. Afghanistan’s

treatment policy was last updated in 2014. Chloroquine + primaquine is the standard

treatment of P. vivax malaria at the health facility livel, but Primaquine is not recommended

to be used at community level, therefore, confirmed P.vivax malaria will be treated with

Chloroquine only at community level. Artemether /artesunate/IM is the recommended pre-

referral treatment for severe falciparum malaria at health facilities level (HSC, BHC and

CHC) as first dose, then patient should be referred, If referral is not possible, treatment with

IM artemether/ artesunate should continue until the patient is able to receive the medication

orally.

In order to properly implement the CBMM strategy, aiming at providing universal access to

parasitological confirmation of malaria, specific algorithms for diagnosis and management of

clinical malaria cases (fever without any obvious cause) will be used.

The CBMM will be fully integrated with the Community IMCI, promoting its

implementation for the management of referrals and treatment of malaria at community level.

The introduction of RDT will enable early identification of the non-malaria fevers, which,

due to the relatively low prevalence of malaria in most parts of Afghanistan.

Algorithm for Diagnosis of Malaria at Health Post Level

Registration of the patient

Use RDT

RDT

positive

(Pf/PAN)

RDT

negative

Patient

Stable.

Treat the

patient

Patient with

danger sign

Refer to health

facility

Children less

than 5 month.

Refer to health

facility

Pregnant

women (1st

trimester)

Refer to health

facility

Treat the patient as usual

according to CHWs

guideline

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Figure 4. Algorithm for diagnosis of malaria at health posts level

Malaria Stratification

Considering the major determinants of malaria transmission (altitude, agricultural practices

and incidence), Afghanistan was initially stratified by provinces into three (3) Strata; Stratum

1 (high-risk), Stratum 2 (moderate risk) and Stratum 3 (low-risk or risk-free).

Further analysis revealed that transmission was variable within provinces so the national

program refined the stratification to the district level into four (4) Strata (high-risk, moderate-

risk, low-risk and very low-risk/risk-free). The criteria used for the district re-stratification

included incidence and slide positivity rate during 2009-2010 and the environmental risk

mapping of 2006. All districts can be categorized into district level stratification as following:

Stratum 1 (high risk districts); includes 63 districts with estimated population of

2,944,800 people, that have active transmission of malaria and accounts for 83% of

nationally confirmed reported cases.

Stratum 2 (medium risk districts); are 138 districts with estimated population of

12,133,500 people living in these areas. Malaria is controlled in mentioned districts,

but the areas are receptive to reintroduction of the disease.

If Pf

positive

treat

with

ACT

If both Pf

& PAN

positive

treat with

ACT

If only PAN

positive

treat with

Chloroquine

Pregnant women

(2nd

& 3rd

trimester) If only

PAN positive treat

with Chloroquine

Pregnant women (2nd

& 3rd

trimester) If

only Pf or both Pf &

PAN positive treat

with ACT

Patient comes back with

symptoms after treatment

Refer the patient to the

nearest health facility

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Stratum 3 (low risk districts); are 96 districts with estimated population of

5,023,200 people. The risk of malaria transmission is low in these districts, but are at

risk of epidemics / outbreaks of the disease

Stratum 4 (Very low or Malaria free districts); includes 103 districts with

estimated population of 4,168,400 people. The transmission of malaria is very low or

there is no malaria transmission at all in these districts.

Ongoing Community-Based Initiatives in Afghanistan

Based on BPHS and CBHC, the diagnosis of malaria by CHW is based on clinical diagnose

(fever without other obvious causes) and treatment with Chloroquine. The Basic Package of

Heath Services (BPHS) for Afghanistan does not yet include RDTs and ACTs in the CHW

kits which are distributed regularly.

The Key quantitative and other outputs of the CBHC strategy include:

• An increase in the number of CHWs from 18,939 to 28,250(based on information taken

from the HMIS)

• 4,447 FHA groups established (CHWs HR database and NGO reports)

CBHCC department has supported the recruitment of 219 more community health

supervisors

• The department has revised the CHW training curriculum which has been used for training

of 13,559 CHWs in 29 provinces

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• CBHCC department created position of provincial CBHC officers, and hired qualified staff

for mentioned position in 26 provinces since 2012.

Pilot Community-Based Management of Malaria in Badkhshan, Kunduz, and Takhar

Provinces

A community-based deployment of ACTs and RDTs was initiated in the Northern provinces

of Badkhshan, Kunduz, and Takhar involving community health workers at health post level.

In these provinces the pilot project was implemented by Merlin and CAF (Care for Afghan

Families), and involved 300 CHWs working in 150 health posts in 18 Districts. A total of 33

CHS have been trained to supervise the CHWs in these project areas (5 in Badkhshan, 14 in

Kunduz and 14 in Takhar).

One pilot project, was conducted with WHO TDR funding in 2007-8, evaluated the use of

RDTs by six CHWs in Nangahar and Kunduz, A second pilot project was implemented in

2011to assess the use of RDTs by community health workers using a randomised trial design.

in Kunduz and Nangahar Provinces.

Considering the results of mentioned piloted projects, the CBMM was developed (CBMM

strategy 2011-2015) and implemented into stratum 1&2 provinces of the country. Based on

revised strategy, the implementation of CBMM will be expanded to entire country.

3. GOAL

To contribute to the improvement of the health status in Afghanistan through the

Reduction of morbidity and mortality associated with malaria.

4. STRATEGIC OBJECTIVES:

To expand malaria confirmation at the community level to 100% in all malaria strata

by 2020

To reduce clinically diagnosed malaria cases to zero at community level by 2020

To ensure 100% of malaria cases are properly treated based on parasitological

confirmation at community level by 2020

5. STRATEGIC DIRECTION:

1. Ensure parasitological diagnosis and proper treatment of malaria at community level

2. Enhance community awareness on malaria prevention and control, with main focus on

accurate diagnosis and proper treatment,

Strategic direction #1: Ensure parasitological diagnosis and proper treatment of malaria at

community level

With the divergence in treatments between vivax and falciparum malaria and relative high

cost of ACT compared to chloroquine there is a need for greater emphasis on diagnosis at all

levels of the health system; if falciparum malaria is mistakenly treated as vivax treatment

failure is assured, and if vivax is treated as falciparum valuable drugs are needlessly wasted.

Malaria confirmation by RDT and treatment according to NTG should be ensured at

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community and lower health facility level. This improves efficiency and coverage and makes

better use of limited human and financial resources.

Pf/Pv RDTs should be used at the community level to distinguish Plasmodium falciparum

and Plasmodium vivax from other causes of fever. RDTs have been tested in Afghanistan and

the decision to implement this as diagnostic tool where microscopy is not available. Because

symptoms of malaria are non-specific, 70-99% of febrile illnesses submitted to microscopic

diagnosis are negative (i.e. slide positivity rates are 1-30% or less). Microscopy & RDT

diagnosis are needed to reduce wastage of anti-malarial drugs and to improve management of

patients who do not have malaria.

ACT has been incorporated into the BPHS as an essential drug and should be used for

treatment of confirmed falciparum cases. Vivax malaria should continue to be treated with

chloroquine.

Sustained high-quality diagnosis and treatment of malaria (and other diseases) can only be

achieved through regular trainings, technical monitoring and quality control of microscopy &

RDT by Quality Assurance Centres (QAC) of PHD/PMLCPs under direct supervision and

coordination through a national quality assurance unit of MoPH/NMLCP.

Interventions/activities:

1 Expansion of malaria confirmation

1.1 training for Community Health Workers and health staff of lower health facility

where microscopies are not available (BHC, SHC, MHT)

1.1.1 refresher training on malaria RDT for Community Health Workers (CHWs),

Community Health Supervisors (CHSs) and lower HFs

1.1.2 initial training on malaria RTD for newly recruited related health staff at community

and HF level

1.2 improvement of malaria diagnostic services

1.2.1 provision of malaria RDTs under CBMM strategy for HPs and health facilities

1.2.2 consumable and maintenance of malaria diagnostic services

2 Standardize malaria treatment at all health facilities

2.1 provision of update NTG for the health facilities

2.2 provision of anti-malarial drugs (ACT for HF and Community and primaquine for HFs)

3 M&E and Quality Assurance

3.1 regular monitoring of malaria case management at community and lower HFs

3.2 regular analysis and CBMM reported data

3.3 collection of the samples of tested RDTs from community and HFs for QA in PCR

Strategic direction #2: Enhance community awareness on malaria prevention and

control, with main focus on accurate diagnosis and proper treatment,

To assess the role of communication for behaviour change process, it is necessary to

understand if the lack of malaria treatment and prevention behaviour is due to a lack of

awareness that malaria is an important disease, negative attitudes towards the disease or lack

of skills or “know how” to make a change. Therefore, it is imperative to have a firm

understanding of the competitive behaviours among the target audience, whether in relation

to malaria treatment or prevention. This will allow for the most appropriate and effective

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communication intervention to be adopted. Target groups must be understood in terms of

their reasons for their actions or barriers to change. This approach aims to engage in four key

tactics, which will create competitive advantages: increasing benefits of the desired target

behaviour, decreasing the barriers and costs related to the desired behaviour, decreasing the

value of the competing behaviour and increasing the cost of the competing behaviour.

Intensification of information, education and communication efforts is needed to improve

people’s knowledge and enable them to adopt a behaviour that obviates risks of malaria

infection. The lack of essential knowledge has an adverse effect on people’s behaviour in

taking appropriate protective measures and seeking medical care once malaria is suspected.

Health education messages should emphasize the malaria risk in different geographical

localities. Messages disseminated through health forums should address clearly how the

disease is acquired and what are its manifestations to enable people to protect themselves and

seek medical care once symptoms are suspected. Messages should address measures of

prevention against malaria with special emphasis on accurate diagnosis and proper treatment.

Health care facilities should consider health education activities of relevance to malaria as

part of the routine services provided to the population. This may be through community

health workers offering counselling sessions on recognition of malaria symptoms, diagnosis,

treatment and prevention using LLINs.

Strategic Interventions/activities:

1. Enhance community awareness on malaria prevention and timely diagnosis &

treatment

1.1 Conducts community health forums for raising awareness on malaria symptoms,

transmission route and prevention

1.2 Malaria health sessions at community level by community health workers

1.3 Updating IEC materials

1.4 Distribute malaria IEC materials (poster, brochure, leaflet etc) through targeted HFs

and community

2. Assess the improvement of community behaviour on malaria prevention and

treatment

2.1 assessment of community behaviour on malaria case management

Procurement, storage and distribution

Procurement management of the GF grant related supply including CMM related shall be as

per UNDP rules and regulation and the procedures of the GF policies. The annual

procurement plan for CBMM supplies will be provided by national program with clear

specification and distribution areas.

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Stocks will be kept at the Provincial level and delivery of RDTs and ACTs at Provincial level

will be under the responsibility of the Implementing Agencies. In principle the ACTs and

RDTs should be delivered to the BPHS implementers, in order to avoid the creation of

parallel programs. NMCLP Provincial units should be informed of the transfer of diagnostic

tests and ACTs from Implementing Agency to the BPHS implementers.

Clear guidelines are needed on management of storage and distribution to maintain the RDTs

under cool conditions. The Guidelines on Transport, Storing and Handling Malaria

Diagnostic Tests in Health Facilities and at Central and Peripheral Storage Facilities,

developed by the USAID/Deliver Project will be adapted, translated in Dari & Pashto and

duplicated for use in training and programme support activities.

Supply to BHCs and HSCs will be based on a "pull system", with demand generated by the

BHCs and HSCs. The HPs will be receive the additional supplies ACTs and RDTs+ancillary

items (not yet included in the CHW kits) through the CHCs and/or BHCs which are currently

supplying the CHW kits. Delivery of ACTs and RDTs will be managed by the BPHS

implementers, without creating new parallel systems.

Stock management

The stock management of ACT and RDTs will be the responsibility of the BPHS

implementers, after receiving specific briefing on stock management, temperature monitoring

and reporting. Quarterly reports on status of stocks will be provided by the BPHS

implementers to NMLCP in order to guide possible re-deployment on of stocks (a loan-basis)

according to needs. The NMLCP will keep a limited stock of ACT and RDTs for emergency

and response at central .

Challenges

Performance incentive balance for field workers (CHS and CHW)

Health services are supported by a multitude of Partners, creating occasional

difficulties for coordinated approaches

Logistic barriers including limited road access to many parts of the country

Lack of clarity over the integration of a historically vertical programme into the

BPHS

Low salaries/ incentives for Government staff forcing competent staff to

supplement their income through private practice or seek employment in the

private, NGO or UN sectors where income is higher

Limited mobility of women (as professional staff, health workers, household

decision-makers, and patients)

Ongoing insecurity in some areas of the country

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6. INSTITUTIONAL FRAMEWORK

The Provincial Manager, responsible for the malaria team (often including one epidemiology

officer, two vector control officers, two technicians), has the main role of coordinating,

monitoring and supervising all malaria control activities in the province, and the malaria-

related activities implemented as part of the BPHS. The provincial malaria control program

is administratively under Provincial Health Directorate (PHD) and technically is responsible

and should report regularly to NMLCP.

The Provincial Project Manager/Focal Point of the Implementing Agency, in close liaison

with Provincial Health Director, is responsible for implementation of specific malaria

activities based on action plan and set targets. He/she manages the funds and logistics, and

generates specific reports to NMLCP and PR (UNDP). In those provinces where LLIN

distribution is planned, a LLIN officer is assigned in the implementing agency to manage

LLIN distribution and all related activities, including proper reporting.

The Community-Based Health Care (CBHC) focal point is assigned in 29 provinces who is

responsible for coordinating all activities managed at community level. In certain Provinces

this function is performed by the PHC unit, and in other a PHD Coordinating Committee is in

place to coordinate all programmes and implementing agencies (NGOs).

Implementation of the activities by Implementing Agencies (NGOs) is monitored by the

Provincial teams (PMLCP), while the central level is responsible for planning, budgeting,

training of trainers, data analysis and interpretation, including data from the HMIS relevant to

the project, and processing the reports prepared by Provincial managers.

7. MECHANISM FOR COORDINATION

In order to bring together the many players which are supporting the Ministry of Public

Health in the process of rehabilitating the health services, Task Forces are formed in the

health sector to provide a forum for discussion, planning and policy making. These task

forces play an important role in coordination and have representation from MoPH, WHO,

UNICEF, BPHS implementers, NGOs, and other sectors, including multiple stakeholders and

funding agencies.

The NMLCP has a task force to coordinate malaria control and elimination activities which is

called Vector Born Disease Control Task Force (VBDCTF). VBDCTF has the following

main term of references which is operational at both National and Provincial Levels:

8.1 The National Vector Born Disease Control Task Force (VBDCTF)

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1. Vector Born Disease Task Force will use its available means to promote, design, monitor

and implement malaria and leishmaniasis Program within the framework of relevant

policy documents (i.e. EPHS, BPHS, NMSP, NLSP and other relevant policies)

2. VBDTF recognises that the MoPH is the leading Health agency in Malaria, Leismaniasis

and other Vector Born Diseases and has authority over policy and implementation issues;

the task force members shall coordinate closely with the relevant MoPH departments

3. VBDTF represents the main technical and policy forums for Malaria, Leishmaniasis and

other vector born diseases in Afghanistan, Where possible, Change in malaria control and

elimination policy will be approved by consensus with the VBDTF acting as the first part

of call for proposal which effect malaria and leishmaniasis control policies and practice

4. VBDTF will aim to oversee the achievement of the relevant Millennium Development

Goals and other nationally approved development targets

5. VBDTF will act to promote malaria, leishmaniasis and other vector born disease

programs at all levels

6. VBDTF will act to maximise the effectiveness of activities through proper coordination

amongst the implementing partners, stakeholder and donors

7. VBDTF will advocate for funding of projects which aim to prevent and control these

diseases

8. VBDTF will ensure evidence based programming through reviewing scientific , technical

and policy documents

9. VBDTF will actively promote gender equity in the health sector, particularly concerning

the role of women

Permanent Members of VBDCTF:

MoPH: Manager Program support coordinator, NMLCP technical advisor, other

NMLCP staff as an appropriate.

WHO: Medical Officer and National Officer, WHO Afghanistan, and other WHO

staff as appropriate

UNDP (the PR for GF NFM)

NGOs: Health Net-TPO, BRAC, HPRO

Other BPHS implementer who are SR for malaria grant, as appropriate

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Non-permanent Members of VBDCTF:

The VBDCTF may invite either permanently, or on ad hoc basis other partners or

organisations, such as funding agencies, media, members of other task-force of MoPH, as

may be necessary to reach the objectives of the task force.

Mode of Action:

The VBDCTF will meet on the second Wednesday of each month at 10AM. In case of any

urgent issue, NMLCP manger may convene the task force before the mentioned date.

The meetings are called and organised by the Manager NMLCP (or his representative).

Decisions will be made by consensus and transparently. In the event that consensus cannot be

reached then the permanent members should vote and approve the proper and final decision.

Minutes of the meetings are public documents; they shall be communicated IN DRAFT form

to permanent members. Once finalised and approved; minutes shall be communicated to all

members, who are free to distribute them as they see fit.

8.2 The Provincial Vector Born Disease Control Task Force (VBDCTF)

The same structure established at central level is also present at Provincial level under the

coordination of the Provincial Public Health Directorate. At Provincial level the following

members contribute to the work of the Task Force:

PHD: Provincial Public Health Director, Provincial Malaria & Leishmaniasis

Control Program Manager, Provincial CDC Manager, PHA, Provincial TB

Manager, Provincial HMIS Manager, BPHS Implementer.

NGOs: implementing partner

WHO provincial sub-office, if available

UNDP

8. IMPLEMENTATION PLAN

Priorities areas and phased implementation

The Community-Based Management of Malaria (CBMM) strategy will be implemented in

the entire country.

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The CBMM was initially piloted in 150 Health Posts (involving 300 CHWs and 33 CHS), in

the 18 districts of Badakhshan , Kunduz and Takhar which helped to consolidate the lessons

learnt and guided the implementation of the community-based management of malaria to all

Health Posts and low level health facilities (BHC, SHC, MHT), where microscopy are not

available. Moreover, consolidated experience in the use of RDTs in BHC and HSC will be

important to ensure supervision and support to CHW from the same catchment areas involved

in these activities.

Following the pilot phase, CBMM was implemented in the malaria high risk (stratum 1&2)

districts under Phase II of R8 GF malaria grant. The focus on districts with higher malaria

burden (Stratum 1&2) also enabled further improvement of the malaria stratification in the

country. Since most of the reported malaria cases are only clinical malaria cases (not

confirmed by microscopy), this strategy prioritizes the introduction of malaria diagnosis by

RDTs for areas where the majority of cases are reported based on clinical diagnosis alone.

CBMM implementation will be expanded to all four strata with support of GF NFM.

9. MONITORING AND EVALUATION

The relevant data collection forms which will be used at BHC, HSC and HP levels will be

developed by NMLCP in collaboration with HMIS Department to include ACT treatment and

testing by RDTs. As much as possible existing data flow and reporting system will be used

to monitor the implementation of the programme. Key indicators (outcome and impact)

specific for surveys will be implemented to monitor the effectiveness of the programme.

In line with the national malaria control strategic plan (2013-2017) the programme

implementation will be monitored on the basis of the data and indicators listed in Table 6,

below.

10.1 Integrated supervision

A specific checklist has been developed, combined with malaria monitoring checklist, to

monitor the CBMM implementation at HF and community level in the country. The

activities of CHWs, including CBMM implementation at community level, will be supervised

by CHS, while the supervisors of the implementing agencies will receive a specific training

on monitoring the quality of malaria case management and supervise the CBMM activities at

the health facility (BHC, SHC, MHT) and community level.

Besides, the national and provincial malaria control programs are also responsible for regular

monitoring of the CBMM activities at HF and community levels to ensure the quality

implementation of the CBMM in the country.

10.2 Quality control at point of care

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The main activities to control the quality of RDTs and ACTs deployment at point of care

should be part of the supervision visits by CHS and programme supervisors and focus on: 1)

conditions of storage; 2) checking temperature monitoring charts; 3) direct observation of

health workers in performing the test, interpreting the results, dispensing the treatment and

recording the data on case, results and treatment.

Monitoring of the daily max temperature of the warehouses in areas exposed to high

temperature will be done before and during the implementation phase. The temperature

monitoring charts with minimum-maximum thermometer should be available in all health

facilities and warehouses in all places where the daily temperature is expected to exceed

30 °C.

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Table 6 - Key indicators to monitor inputs, process, outcome of CBMM programm

No Indicator Formula Source of

data

Targets Level Frequency Remarks

16 17 18 19 20

1

Number of RDT received in

the country by implementing

agencies

Number of RDTs received in the

country per year by funding and

implementing agencies

Program records

National

yearly

2

Number of RDT delivered to

BPHS implementers at

provincial level

Number of RDTs delivered at

provincial level

to BPHS implementers

Program records

Provincial/

National

Every 6 months

3

Proportion of targeted BHCs

and HSCs reporting no RDT

stock outs

Numerator: Number of targeted

BHCs and HSCs reporting no

RDT stock outs per month

Denominator: Number of

targeted BHCs and HSCs

submitting monthly stock reports

on RDT

Malaria

Information

System. PMLCP/BPH

S

Provincial/

National

Quarterly

4

Proportion of targeted HPs

reporting no RDT stock outs

Numerator: Number of targeted

HPs reporting no RDT stockouts

on tally sheets

Denominator: Number of

targeted HPs submitting tally

sheets with RDT stocks

Malaria

Information

System. PMLCP/BPH

S

Provincial/

National

Quarterly

5 Number of ACT received in

the country by implementing

agencies

Number of ACTs received in the

country per year by funding and

implementing agencies Program records

National

yearly

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6

Number of ACT delivered to

BPHS implementers at

provincial level

Number of ACTs delivered at

provincial level

to BPHS implementers (every 6

months)

Program

records

Provincial/

National

Every 6

months

7

Proportion of targeted BHCs

and HSCs reporting no ACT

stock outs

Numerator: Number of targeted

BHCs and HSCs reporting no

ACT stockouts per month

Denominator: Number of

targeted BHCs and HSCs

submitting monthly stock reports

on ACT

Malaria Information

System.

/HMIS

Provincial/

National

Quarterly

8

Proportion of targeted HPs

reporting no ACT stockouts

Numerator: Number of targeted

HPs reporting no ACT stockouts

on tally sheets

Denominator: Number of

targeted HPs submitting tally

sheets with ACT stocks

Malaria

Information System.

PMLCP/BPH

S

Provincial/

National

Quarterly

9

Proportion of malaria cases

confirmed by RDT in targeted

BHCs and HSCs

Numerator: Number of reported

malaria cases confirmed by RDT

in targeted BHCs and HSCs

Denominator: All reported

malaria cases from targeted BHCs

and HSCs

Malaria

Information

System. PMLCP/BPH

S

40

%

50

% 60%

70

%

80

%

Provincial/

National

Quarterly

10

Proportion of malaria cases

confirmed by RDT in targeted

Health Posts

Numerator: Number of reported

malaria cases confirmed by RDT

in targeted BHCs, HSCs and

Health Posts

Denominator: All reported

malaria cases from targeted

BHCs, HSCs and Health Posts

Malaria

Information

System. PMLCP/BPH

S

40

%

50

% 60%

70

%

80

%

Provincial/

National

Quarterly

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11

Proportion of reported

falciparum cases confirmed

by RDT treated with ACTs in

targeted BHCs and HSCs

Numerator: Number of reported

falciparum cases confirmed by

RDT treated with ACTs in

targeted BHCs and HSCs

Denominator: All reported

falciparum cases confirmed by

RDT from targeted BHCs and

HSCs

Malaria

Information System.

PMLCP/BPH

S

60 65 70

80

90

Provincial/

National

Quarterly

12

Proportion of reported

falciparum cases confirmed

by RDT treated with ACTs in

targeted Health Posts

Numerator: Number of reported

falciparum cases confirmed by

RDT treated with ACTs in

targeted BHCs, HSCs and Health

Posts

Denominator: All reported

falciparum cases confirmed by

RDT from targeted BHCs, HSCs

and Health Posts

Malaria

Information System.

PMLCP/BPH

S

50 55 60

65

70

Provincial/

National

Quarterly

13

Proportion of reported non-

falciparum cases confirmed

by RDT treated with

chloroquine + primaquine in

targeted BHCs and HSCs

Numerator: Number of reported

non-falciparum cases confirmed

by RDT treated with chloroquine

+ primaquine in targeted BHCs

and HSCs

Denominator: All reported non-

falciparum cases confirmed by

RDT from targeted BHCs and

HSCs

Malaria

Information

System.

PMLCP/BPHS

60 65 70

80

90

Provincial/National

Quarterly

14

Proportion of reported non-

falciparum cases confirmed

by RDT treated with

chloroquine in targeted Health

Posts

Numerator: Number of reportd

non-falciparum cases confirmed

by RDT treated with chloroquine

in targeted Health Posts

Denominator: All reported non-

falciparum cases confirmed by

RDT from targeted HPs

Malaria

Information

System. PMLCP/BPH

S

50 55 60

65

70

Provincial/

National

Quarterly

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The HMIS data flow in relation to malaria reporting at Provincial and Central levels is

shown in the Figure 6 below.

Figure 6. Reporting data flow (HMIS and other reporting systems relevant to CBMM)

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ANNEX 1 - Stratification of districts of Afghanistan based on reported malaria

incidence rate (2009 data)

Stratum 1 = Districts with reported malaria cases exceeded the median of reported annual malaria

incidence rate per district, i.e. >10/1000; Stratum 2 = Districts with reported annual malaria incidence

rate between 1 and 10/1000; and Stratum 3 = Districts with reported annual malaria incidence rate of 0-

1/1000 cases.

Pop = district population data provided by Central Statistics office (2009); IR = reported annual

malaria incidence rate, based on HIMS reports of 2009

Province

Name

Stratum 1 Stratum 2 Stratum 3

District

Name Pop IR District Name Pop IR District Name Pop IR

Badakhshan Baharak 26200 14.5 Arghanjwa 14700 9.6 Eshkashem 12600 1.0

Badakhshan Darayim 56000 35.4 Keren -O- Menjan 8700 1.3

Badakhshan Darwaz 24100 24.6 Khash 34600 6.3

Badakhshan Darwazi Bala 21100 12.7 Kofab 20400 6.4

Badakhshan Fayzabad 59800 85.1 Sheikai 24000 8.9

Badakhshan Jurm 34100 19.1 Shighnan 25300 2.3

Badakhshan Khwahan 15100 47.7 Wakhan 13600 1.2

Badakhshan Kishim 73500 131.8 Yamgan (Girwan) 23400 8.8

Badakhshan Kohistan 15100 22.4 Zebak 7100 1.8

Badakhshan Raghastan 36000 11.9

Badakhshan

Shar -i-

Buzurg 47600 40.5

Badakhshan Shuhada 31400 11.5

Badakhshan

Tagab

(Kishmi

Bala) 25500 70.0

Badakhshan Tashkan 27200 46.3

Badakhshan Urgo 71300 28.2

Badakhshan Wardug 19900 14.5

Badakhshan Yaftali Sufla 48100 56.4

Badakhshan Yawan 29500 21.8

Badghis Ab Kamari 66900 2.7 Dahana-I- Ghuri 53500 0.2

Badghis Ghormach 50100 5.8 Dih Salah 29100 0.8

Badghis Jawand 71800 3.1 Dushi 60800 0.2

Badghis Muqur 21600 7.5 Nahreen 62800 0.2

Badghis Murghab 88400 2.7

Badghis Qadis 82800 2.4

Badghis Qala-I- Naw 59800 4.3

Baghlan Andarab 23200 4.4

Baghlan Baghlani Jadid 154900 7.3

Baghlan Burka 47900 4.4

Baghlan Khenjan 27700 2.1

Baghlan Pul -i- Hisar 25200 2.9

Baghlan Puli Khumri 188000 1.4

Baghlan Tala Wa Barfak 27500 4.7

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Province

Name

Stratum 1 Stratum 2 Stratum 3

District

Name Pop IR District Name Pop IR District Name Pop IR

Balkh Khulm 63500 36.6 Chahar Bolak 73600 3.0 Balkh 108400 0.2

Balkh Sholgara 103300 18.3 Chimtal 83500 7.3 Chahar Kint 40500 0.5

Balkh Dawlatabad 95000 1.7 Dihdadi 61300 0.4

Balkh Kaldar 18200 4.3 Marmul 10300 0.0

Balkh Kishindih 44300 4.6 Nahri Shahi 40900 0.8

Balkh Mazari Sharif 326100 1.3

Balkh Shortepa 36000 9.8

Balkh Zari 39900 5.5

Bamyan Kahmard 33100 23.2 Shibar 26800 1.0 Bamyan 75500 0.3

Bamyan Shayghan 21800 19.6 Yakawlang 79500 5.0 Panjab 62000 0.2

Bamyan Waras 99300 0.1

Daykundi Gitti 30500 13.9 Mir amor 57000 8.2

Daykundi Gizab 61400 29.7 Sangi Takht 46100 1.3

Daykundi Gujran 31900 33.0

Daykundi Ishtarlee 43400 12.5

Daykundi Khadir 42400 16.7

Daykundi Nili 37100 16.9

Daykundi Shahristan 60500 15.9

Farah Lash -i- Juwayn 25500 15.9 Bakwa 32300 2.2 AnarDara 25300 0.9

Farah Gulestan 39400 4.6 Bala Buluk 65000 0.6

Farah Khaki Safed 27600 2.2 Farah 100600 0.3

Farah Pur Chaman 48600 9.3 Pusht Rod 37000 0.0

Farah Qala-I-Kah 28000 0.3

Farah Shib Koh 21300 0.1

Faryab Balcheraqh 47500 13.2 Almar 63900 1.9 Andkhoy 35300 0.1

Faryab Dawlatabad 44100 15.2 Garziwan 69000 5.0

Khani Chahar

Bagh 21100 0.0

Faryab

Khwaja Sabz

Posh 46200 51.0 Kohistan 49600 9.5 Qaramqol 17900 0.3

Faryab Maymana 71500 13.4 Qaysar 129600 7.4 Qurghan 42900 0.2

Faryab Pashtun Kot 171700 21.1

Faryab Shirin Tagab 74100 29.3

Ghazni Ab Band 25000 24.9

Bahrami Shahid

(Jaghatu) 28900 1.2 Jaghuri 160600 0.2

Ghazni Ajristan 26200 48.3 Dih Yak 44500 1.9 Malestan 74600 0.0

Ghazni Andar 113500 11.3 Ghazni 146200 4.6 Nawur 86000 0.8

Ghazni Gellan 52700 20.3 Giro 33200 6.3

Wali

Muhammadi

Shahid 18300 0.7

Ghazni Muqur 45700 33.9 Khwaja Umary 17300 6.2

Ghazni Nawa 27100 80.4 Qarabagh 129900 5.4

Ghazni Rashidan 16300 13.2 Waghaz 35100 5.4

Ghazni ZanaKhan 11500 1.6

Ghor Saghar 31600 34.3 Chaghcharan 123100 2.6 Dawlat Yar 29800 0.2

Ghor Charsada 24900 1.2 Duleena 32800 0.3

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Province

Name

Stratum 1 Stratum 2 Stratum 3

District

Name Pop IR District Name Pop IR District Name Pop IR

Ghor Pasaband 86300 2.7

Lal-o-Sar-i-I

Jangal 101900 0.0

Ghor Shahrak 54400 5.4

Ghor Teyora 83200 5.6

Ghor Tolak 46900 3.9

Hilmand Lashkar Gah 92700 31.4 Bughran 74200 5.4 Dishu 18600 0.0

Hilmand NawZad 46300 14.4 Garm seir 80000 8.3

Hilmand Washeir 14200 46.5 Kajaki 65000 3.0

Hilmand Musa Qala 53800 5.7

Hilmand Nad Ali 107500 3.8

Hilmand Nahr -i- Sarraj 106500 2.3

Hilmand

Nawa-I- Barak Zayi 84600 6.5

Hilmand

Reg -i- khan

sheen 24000 2.7

Hilmand Sangin Qalah 54400 9.4

Hirat Chishti Sharif 21600 15.4 Adraskan 48900 6.9 Guzara 133600 0.4

Hirat Farsi 27900 21.0 Ghoryan 79600 8.5 Hirat 386600 0.1

Hirat Kushki Kuhna 41600 23.8 Gulran 85700 7.0 Injil 222500 0.3

Hirat Karukh 57900 6.2 Kohsan 49500 0.8

Hirat Kushk 112700 8.2 Obeh 68800 0.2

Hirat Zinda Jan 52000 5.5

Pashtun

Zarghun 91200 0.2

Hirat Shindand 162600 0.9

Jawzjan Khamyab 12700 13.4 Aqcha 53900 4.2

Jawzjan Mangajak 39000 27.4 Darzab 44700 3.9

Jawzjan Qarqin 22200 27.6 Fayzabad 37900 5.9

Jawzjan Qush Tepa 21400 34.1 Khanaqa 35800 10.0

Jawzjan Khwaja Du Koh 24500 7.2

Jawzjan Mardyan 35100 4.6

Jawzjan Shibirghan 149500 6.7

Kabul Kalakan 27600 14.6 Bagrami 50500 1.0 Estalif 30600 0.0

Kabul Surobi 50500 20.3 Chahar Asyab 33300 9.0 Kabul 2831400 0.7

Kabul Dih Sabz 49100 5.7

Kabul Farza 19600 2.8

Kabul Guldara 20900 8.8

Kabul Khaki Jabbar 13000 4.5

Kabul Mir Bacha Kot 47600 1.5

Kabul Musayi 21300 4.9

Kabul Paghman 110000 1.2

Kabul Qarabagh 69500 7.7

Kabul Shakardara 74900 2.9

Kandahar Arghandab 56400 16.6 Kandahar 481100 8.5 Shorabak 10400 0.4

Kandahar Arghistan 31300 48.3 Nesh 12200 5.4

Kandahar Daman 31500 42.1 Panjwayi 79200 2.4

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Province

Name

Stratum 1 Stratum 2 Stratum 3

District

Name Pop IR District Name Pop IR District Name Pop IR

Kandahar Khak Reiz 20800 10.5 Spin Boldak 103000 5.4

Kandahar Maroof 30000 10.5 Zhari 78100 1.3

Kandahar Maywand 53400 14.9

Kandahar Shah Wali Kot 39400 37.0

Kapisa

Hisa-i-

Duwumi

Kohistan 40900 17.6 Koh Band 21400 1.2 Alasay 34400 0.6

Kapisa Mahmudi Raqi 58400 10.8 Kohistan 61900 6.9

Kapisa Tagab 73600 12.0 Nijrab 102300 2.0

Khost Bak 20100 60.9

Mando Zayi

(Ismayel Khel) 51300 4.2

Khost Gurbuz 23800 16.8 Musa Khel 37300 7.3

Khost Jaji Maydan 21900 86.3

Khost Khost(Matun) 124900 14.8

Khost Nadir Shah Kot 29000 21.7

Khost Qalandari 9300 33.8

Khost Sabari 64500 14.6

Khost Shemal 12400 12.6

Khost Spera 22200 17.1

Khost Tani 54200 14.4

Khost Terezayi 40700 11.9

Kunar Asadabad 30000 92.1

Kunar Bar Kunar 20000 143.1

Kunar Chapa Dara 28200 86.4

Kunar Chawki 32500 150.2

Kunar Dangam 15400 138.6

Kunar Dara-I-Pech 49800 71.9

Kunar Ghaziabad 17000 83.1

Kunar Khas Kunar 31800 141.4

Kunar Marawara 18600 39.3

Kunar

Narang

(Tara-gn-o-

Badil) 27500 149.1

Kunar Nari 25100 87.1

Kunar Noor Gul 28800 120.4

Kunar Sar kani 24800 158.9

Kunar Shigal O Sheltan 26600 138.3

Kunar Wata Pur 24900 101.4

Kunduz Aliabad 42900 20.3 Kunduz 277900 9.4

Kunduz Archi 76900 28.8

Kunduz Chahar Dara 66800 10.5

Kunduz

Hazrat Imam

Sahib 210500 21.5

Kunduz Khanabad 145200 30.9

Kunduz Qalay-I- Zal 62700 13.9

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Province

Name

Stratum 1 Stratum 2 Stratum 3

District

Name Pop IR District Name Pop IR District Name Pop IR

Laghman Alingar 88000 64.9

Laghman Alishing 64900 35.7

Laghman Dawlat Shah 30200 53.0

Laghman Mihtarlam 124500 47.2

Laghman Qarghayi 89200 45.6

Logar Azra 18500 28.9 Baraki Barak 79600 2.4

Logar Kharwar 23900 17.2 Charkh 40400 2.5

Logar Khushi 21900 2.8

Logar Muhammad Agha 68700 9.0

Logar Puli Alam 96000 2.5

Nangarhar Achin 91200 74.9

Nangarhar Bati Kot 68900 134.7

Nangarhar Bihsud 103400 43.2

Nangarhar Chaparhar 54800 98.3

Nangarhar Dara-I-Nur 36700 36.6

Nangarhar Dih Bala 36700 274.4

Nangarhar Dur Baba 21200 131.9

Nangarhar Goshta 24800 137.8

Nangarhar Hisarak 28000 29.1

Nangarhar Jalalabad 183000 37.4

Nangarhar Kama 69900 67.8

Nangarhar Khogyani 118600 96.4

Nangarhar Kot 47400 179.5

Nangarhar Kuz Kunar 50100 69.2

Nangarhar LalPur 18600 335.2

Nangarhar

Muhmand

Dara 40900 205.2

Nangarhar Nazyan 13300 176.1

Nangarhar

Pachir Wa

Agam 38700 62.6

Nangarhar Rodat 62900 40.3

Nangarhar Sherzad 60300 48.9

Nangarhar Shinwar 54500 72.1

Nangarhar Surkh Rod 109600 13.9

Nimroz KhashRod 23100 1.3

Asl-i-Chakhansur 21600 0.3

Nimroz Zaranj 50700 4.0 Chahar Burjak 24100 0.0

Nimroz Kang 20400 0.8

Nuristan Barg -i- Matal 14200 49.2

Nuristan DuAb 7100 70.6

Nuristan Kamdesh 23100 30.4

Nuristan Mandol 18000 21.1

Nuristan NoorGram 29400 24.6

Nuristan Paroon 12300 33.2

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Province

Name

Stratum 1 Stratum 2 Stratum 3

District

Name Pop IR District Name Pop IR District Name Pop IR

Nuristan Wama 10000 63.2

Nuristan Waygal 17800 77.9

Paktika Dila 22900 32.0 Barmal 31600 3.2

Paktika Gomal 7000 295.6

Paktika Jani Khel 21800 26.7

Paktika Mata Khan 22700 30.7

Paktika Nika 11300 112.7

Paktika Omna 11000 86.2

Paktika Sar Hawza 21100 34.6

Paktika Sarobi 11400 54.0

Paktika Sharan 45500 109.2

Paktika Urgoon 50300 58.3

Paktika Waza Khwa 21100 55.0

Paktika Yahya Khel 15800 22.4

Paktika Yosuf Khel 12300 47.7

Paktika

Zarghun

Shahr 27200 15.4

Paktika Ziruk 17500 14.3

Paktya Ahmadabad 25300 11.0 Chamkanay 45500 7.6 Sayid Karam 58400 1.0

Paktya

Dand Wa

Patan 24200 84.8 Wuza Zadran 32300 9.3

Paktya Gardez 75300 12.2 Zurmat 97800 9.7

Paktya Jaji 57300 20.4

Paktya JaniKhel 31800 24.7

Paktya

Lija Ahmad

Khel 20800 26.0

Paktya Shwak 5100 67.5

Panjsher Rukha 20900 13.0 Bazarak 17100 4.0 Paryan 13400 0.7

Panjsher Shutul 9900 14.2 Dara 22700 2.3

Panjsher Uanaba 16300 39.8

Hisa-I-Awal

Panjsher 36400 2.1

Parwan Bagram 94300 5.3 Ghorband 88100 0.2

Parwan Chaharikar 158800 1.4 Shekh Ali 22400 0.7

Parwan Jabalussaraj 58100 1.9 Surkhi Parsa 37200 0.2

Parwan Kohi Safi 28200 6.8

Parwan Salang 23700 3.3

Parwan Sayd Khel 41500 5.1

Parwan Shinwari 37400 2.9

Samangan Dara-I-Suf Bala 58800 1.1 Aybak 93200 0.8

Samangan Feroz Nakhchir 11900 7.3

Dara-I-Suf

Payin 65000 0.2

Samangan Hazrat -i- Sultan 37700 4.5

Khuram Wa Sarbagh 36300 0.9

Samangan Ruyi Du Ab 41500 0.1

Sari Pul Balkhab 45800 10.1 Gosfandi 51600 4.4

Sari Pul Sozma Qala 45000 19.2 Kohistanat 72800 8.4

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Province

Name

Stratum 1 Stratum 2 Stratum 3

District

Name Pop IR District Name Pop IR District Name Pop IR

Sari Pul Sangcharak 91700 1.6

Sari Pul Sari Pul 140300 8.4

Sari Pul Sayyad 49700 3.0

Takhar Baharak 28100 21.2

Takhar Bangi 31900 34.0

Takhar ChahAb 70800 31.2

Takhar Chal 25700 25.6

Takhar Darqad 24500 34.4

Takhar Dashti Qala 29100 27.0

Takhar Eshkamish 53700 16.8

Takhar Farkhar 42500 27.8

Takhar HazarSumuch 12500 30.2

Takhar Kalafgan 32000 35.6

Takhar

Khwaja

Bahawuddin 21200 21.0

Takhar Khwaja Ghar 60800 21.2

Takhar Namak Ab 11100 98.7

Takhar Rustaq 149000 45.6

Takhar Taluqan 203300 16.5

Takhar Warsaj 34500 19.3

Takhar Yangi Qala 40200 34.0

Uruzgan Chorah 46500 5.5

Uruzgan Dihrawud 55400 9.0

Uruzgan Khas Uruzgan 51400 1.4

Uruzgan Shahidi Hassas 53700 3.6

Uruzgan Tirin Kot 93200 7.1

Wardak

Chaki

Wardak 76800 12.3 Day Mirdad 28200 5.0

Hisa-I- Awali

Bihsud 33700 0.2

Wardak Jaghatu 41600 1.5 Jalrez 48200 0.6

Wardak Maydan Shahr 36600 1.0 Markazi Bihsud 108600 0.2

Wardak Saydabad 105700 2.3 Nirkh 51800 0.7

Zabul Arghandab 29700 15.4 Daichopan 35800 6.0

Zabul Atghar 7900 57.3 Mizan 12500 2.2

Zabul Qalat 31900 37.4

Zabul Shahjoy 53200 47.2

Zabul Shamulzayi 23500 49.2

Zabul Shinkay 21400 11.6

Zabul

Tarnak -O-

Jaldak 15600 16.2

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ANNEX 2 - Current contents of CHW kit (2009)

No Description Strength Unit Quantity New quantity Remarks

I. Monthly-based Expendable items

1 Sol Gentian Violet 1% 05ml/10ml Bottle 1 15-Feb

2 Tab Cotrimoxazole 085mg Tab 105 055

0 Packet ORS Packet 20 05 (during the

summer Jawza-

Sunbullah)

0 Coated tablet Ferrous sulfate

+folic acid

(05mg iron

+400 ug folic)

Coated

Tablet

255 055

0 Tab Chloroquine 250mg 205mg Tab 05 155 (during the

summer Jawza-

Sunbullah)

0 Tab Paracetamol 500mg 055mg Tab 105 055

7 Tetracycline Eye ointment Ointment 0 15

8 Tab Mebendazole 155mg Tab 05 155

9 Tab contraceptive ( Ethinyl

estradaiol+levonorgestrol)

Sachet 12 10

15 Tab.

Pyrimethamine+Sulfadoxine

Fansidar))

25mg+500mg Tab 12 18 all months

and 30(during

the summer

Jawza-

Sunbullah)

11 Condom Piece 155 255

12 Retinol (Vitamin A) 05555 iu Cap 05

10 Multi vitamin coated tab 055

10 Chlorine 055ml Bottle 0

10 Depo Medroxy Progesterone

Acetate(DMPA)

105mg Bottle 0

10 Zinc tab 25mg Tab 055

17 plastic bags Small size Small size

bags

105g For

distribution

of medicine

18 Referral card Sheets 155

II. Quarterly -based Expandable items

19 Chlorhexidine solution 5% 055ml Bottle 1

25 Gauze bandage hydrophyl

7.0*15

roll 10 05

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No Description Strength Unit Quantity New quantity Remarks

21 Leucoplast(2.5*5) roll 1 0

22 Cotton 200gr roll 1

20 Gauze Pad Sterile 10*10cm Piece 0-Oct 05

20 Triangular bandage

(handkerchief )

Piece 2 Considering

Infection

prevention

20 Art paper Piece 2

20 Collared pencils or markers Dozen 1

27 Towel medium size 05*25cm Piece 1

28 Soap Bar Piece 0

29 Permanent Marker Piece 2

05 Pen Piece 0

01 Simple Plastic File Piece 1

02 Pencil Piece 1

00 Note book 155 Pages Copies 1

00 Pictorial Tally sheet Copies 1 Once every six

month.

00 sterile Gloves piece 155

00 Pencil sharpner Piece 1

07 Clean delivery kit set 5 0

III. Non-Expendable items

Note: these items can be resupplied based on assessments or demand by CHWs when old or dysfunctional.

08 Dressing forceps metallic 10.0

cm

Piece 1

09 Scissors Piece 1

05 Sterilizer small size Piece 1

01 Kidney Dish Medium Piece 1

02 Metal square tray medium Piece 1

00 Pot medium size Piece 1

00 Soap dish Piece 1

00 Table spoon Piece 1

00 Measurements glass with ml

scale ( metallic)

Piece 1

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37

No Description Strength Unit Quantity New quantity Remarks

07 Bag ( locally made cloth bag ) Piece 1

08 Ruler metallic 30cm Piece 1

09 CHW manual Set 1

05 Flip chart ( Paper material) Set 1

01 Educational posters Set 1 Quality

assurance

process

suggest list

of IEC

materials to

be supplied

to HP

02 Metallic box (medium size ) Piece 1

00 Thermometer (Digital) Piece 1

00 Tape for measuring arm

circumference

Piece 1

00 Stop watch/Timer Piece 1

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ANNEX 3 - Tally Sheets for CBMM developed in the pilot RDT and ACT

community-based project

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ANNEX 4 - Supervision Check List on ACTs and RDTs for Community Health

Supervisors

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ANNEX 5 Timetable of activities

The quarterly plan of implementation of the activities outlined in the CBMM Strategy is provided in

the Table below.

Year 1 Year 2 Year 3 Year 4 Year 5

Q

1

Q

2

Q

3

Q

4

Q

1

Q

2

Q

3

Q

4

Q

1

Q

2

Q

3

Q

4

Q

1

Q

2

Q

3

Q

4

Q

1

Q

2

Q

3

Q

4

Programme

planning and

management

Writing TORs

for malaria

CBMM coordinator

X

Appoint malaria

CBMM

Coordinator

X

Development of

Guidelines

Case

management of fever

X

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Year 1 Year 2 Year 3 Year 4 Year 5

Q

1

Q

2

Q

3

Q

4

Q

1

Q

2

Q

3

Q

4

Q

1

Q

2

Q

3

Q

4

Q

1

Q

2

Q

3

Q

4

Q

1

Q

2

Q

3

Q

4

Fever

management

algorithms

X

RDT quality

assurance at point of care

X

RDT transport

and storage methods

X

Develop IEC

materials X

RDT

procurement

and logistics

RDT, gloves,

sharp boxes

procurement

X X X X X

Receive RDTs

(staggered delivery)

X X X X X X X X X X

Distribution of

RDT and other

supplies to the field

X X X X X X X X X X

ACT

procurement

and logistics

ACT

procurement X X X X X

Receive ACTs

(staggered delivery)

X X X X X X X X X X

Distribution of

ACTs to the field

X X X X X X X X X X

RDT Quality

Assurance

Write SOPs and

Job Aids for RDTs

X

RDT Post-

shipment lot-

testing (as

appropriate)

X X X X X

Training

Develop

training tools

for RDTs and ACTs

X

Develop

training tools for supervisors

X

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Year 1 Year 2 Year 3 Year 4 Year 5

Q

1

Q

2

Q

3

Q

4

Q

1

Q

2

Q

3

Q

4

Q

1

Q

2

Q

3

Q

4

Q

1

Q

2

Q

3

Q

4

Q

1

Q

2

Q

3

Q

4

Conduct

Training of

Trainers courses

X X X X X

Training of

health workers and supervisors

X X X X X X X X X X

Communication

Community

sensitization X X X X X X X X X X X X X X X X X X

Supervision

Regular

supervision X X X X X X X X X X X X X X X X X X

Monitoring and

evaluation

Review record

forms and

procedures

X

Monitoring

outcome indicators

X X X X X X X X X X X X X X X X X X

Operational

Research

Introduction of

RDTs in DH and CBC

X X X X

Evaluating

incentive

schemes for

CHWs

X X X X

Malaria

treatment

seeking behaviour

X X X X

ANNEX 6 Budget components and financial gaps (USD)

The annual budget (in USD) for the main activities outlined in the CBMM Strategy are presented in the

Table below. Funding for commodities which are already supplied by BPSH are not included, i.e. for

the procurement and distribution of chloroquine, primaquine and antibiotics for the management of

non-malaria fevers of bacterial origin. The funding gap has been calculated only for years 1 and 2, in

view of the firm commitment from the GFR8.

Activity Year 1 Year 2 Year 3 Year 4 Year 5

Development of

Guidelines

Guidelines for

RDT transport and storage

10,000

Fever

management algorithm

5,000

Supervision 5,000

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Activity Year 1 Year 2 Year 3 Year 4 Year 5

checklists and

temp. charts

RDT procurement

and supply

management

RDT, gloves,

sharp boxes procurement

111,350 171,982 284,228 389,978 389,978

Distribution of

RDT and other

supplies to the

field (10%)

11,135 17,198 28,423 38,998 38,998

ACT procurement

and supply

management

ACT procurement 11,329 17,497 28,918 39,677 39,677

Distribution of

ACTs to the field (10%)

1,133 1,750 2,892 3,968 3,968

RDT Quality

Assurance

Post-shipment lot-

testing of RDTs (as appropriate)

100 100

Training

Instructions and

training manual for supervisors

5'000

Training of

trainers 4,620 36,805 42,644 26,991 26,991

Training of health

workers 4,896 42,982 42,670 32,559 31,452

Training of

supervisors 574 4,563 5,286 3,346 3,346

Communication

Community

sensitization

(health forum)

3,000 129,300 129,300 221,680 221,680

Supervision

Regular

supervision 4,920 38,880 12,660 29,880 44,220

Monitoring and

evaluation

Develop record

forms, survey

procedures

10,000

Health facility

survey for

outcome indicators

5,000 5,000 5,000 5,000 5,000

OR: introduction

of RDTs in DH and CBC

20,000

OR: evaluating

incentive schemes 25,000

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Activity Year 1 Year 2 Year 3 Year 4 Year 5

for CHWs

OR: malaria

treatment seeking

behaviour

20'000

TOTAL

FUNDS

REQUIRED

188,057 486,056 607,021 792,077 805,310

BUDGET

AVAILABLE

(R8 GF malaria)*

392,573 656,528 551,610 565,313 579,701

FINANCIAL

GAP -204,516 -170,472 55,411 226,764 225,609

* calculated from approved funding Global Fund R8 malaria grant

The total core budget required to implement the 5 years strategy is USD 2,878,521. Considering the

total funding available to implement the GF R8 grant, amounting to USD 2,745,725 the funding gap

amounts to USD 132,796 for the 5 years implementation of the CBMM Strategy.

ANNEX 7: CBMM training Curriculum Contents

1. Background

2. Introduction of CBMM

What is CBMM

What CBMM offers

Why CBMM

CBMM providers

Components of CBMM

Why CHW training on CBMM

3. Necessity of the curriculum

4. Contents of the curriculum

Chapter one:

General information about malaria

What is malaria

Signs & symptoms of malaria

Causative agents of malaria

Vector of malaria

Mode of transmission of malaria

Diagnosis of malaria

Prevention of malaria

Chapter two:

Introduction of RDT

What is RDT

Advantage and disadvantage of RDT

Procedure of RDT use

Storage of RDT

Chapter three:

Practical use of RDT

Technique of blood collection from patient’s finger

Use of RDT for malaria diagnosis

Interpretation of the result of RDT

Chapter four:

Treatment of malaria

Introduction of ACT

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Treatment of malaria by using ACT

flow chart of Malaria treatment

Chapter five:

Sessions of the training

Objective of the session

Methods of lesson

Topic of the session

Materials

Annex

1. Annex a - Instructions for the training

2. Annex b – Training schedule

3. Annex c- Pre-test

4. Annex d- Post-test

5. Annex e- pictorial instruction for RDT use

6. Annex f- Malaria Treatment Dosage Chart

7. Annex g- RDT follow up tally sheet

8. Annex h- RDT monthly Aggregated report

9. Annex i- ACT use tally sheet

10. Annex j- Monthly report on ACT use

11. Annex k - Referral form

Background

Malaria is an endemic disease and a major public health problem in many Provinces of Afghanistan. It

causes a great burden on the health and economic development of individuals, families and

communities living in endemic areas. The total number of reported malaria cases were 427,743 1n

2006, 390729 in 2009 and 390121 in 2010. Majority of these cases were clinically diagnosed: 79.77%,

83.40% and 80.04% respectively(HMIS 2010). The Government of Afghanistan remains committed to

the control of this disease. For this purpose the Government developed the National Malaria Strategy

Plan 2008-2013 with a vision of a malaria free Afghanistan. Two priority targets mentioned in NMSP

2008-2013 include:

By the end of 2013, 60% of targeted Health Posts will be able to diagnose malaria by RDTs

By the end of 2009, in order to strengthen malaria control at the community level, the

NMLCP and all PMLCPs will have a Community-Based Component including Home

Management of Malaria (CBMM)

Introduction of CBMM-

What is CBMM (Community Based Management of Malaria)

It is a care delivery strategy at community level to diagnose and provide effective treatment for

uncomplicated plasmodium falciparum malaria which will reduce the burden of morbidity and

mortality due to malaria in endemic areas.

What CBMM offers?

At present at health post level CHWs have Sulfadoxine Pyrimethamine and Chloroquine in their kit to

treat malaria. CHWs are treating malaria without any confirmed diagnosis. CBMM approach will

include RDTs and ACTs in their kits along with SP and Chloroquine. RDTs will be used for rapid

diagnosis of malaria and ACTs will be used to treat confirm uncomplicated falciparum malaria cases.

Why CBMM?

The Government of Afghanistan is committed to provide health care services to the entire nation to

improve the health condition of the people. But unfortunately in some geographical areas communities

are remotely located from the health facilities limiting access to health services. During 2010, 31,2267

malaria cases were clinically diagnosed throughout Afghanistan from which 137,670 cases i.e. 40.08%

were clinically diagnosed at health post level. Therefore CBMM will play a pivotal role in confirming

malaria diagnosis at health post level up to households. This will limit the excess use of Chloroquine &

SP as well as prevent resistance (plasmodium falciparum) to Sulfadoxine Pyrimethamine. In addition to

the treatment, CHWs will be able to differentiate the severe cases and refer to health facilities for

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proper management. This strategy will assist weak health care systems, where women and children

cannot reach health facilities and where self-treatment is common and often misguided.

CBMM providers:

Community Health Workers will provide specific health care services (diagnosis using RDT

and treatment via ACT) at health post level.

Community Health Supervisors will monitor and supervise activities of the CHWs

Component of CBMM

Diagnosis of malaria by using RDT test

Treatment of uncomplicated Plasmodium falciparum malaria by ACT

Why CHWs training on CBMM?

A health post operates as a basic health service is delivered by the CHW. This grassroots level health

service delivery point is ideally staffed by one male and one female CHW. CHWs provide care to an

average of 27% of the total number of outpatients visiting the health facilities (2008). The numbers of

outpatients have increased with the expansion of health posts as a result of which over the past two

years, the numbers seen per health post have increased by 50%. Unlike health facilities, there is no

decline in visits during the winter months, 40% - 45% of childhood illnesses are managed by CHWs.

(CBHC Policy and Strategy, Page 9), highlighting the importance trained CHWs contributes towards

malaria diagnosis and treatment at community level.

Why this curriculum?

This curriculum is developed for training CHWs & CHS on CBMM. As mentioned above the

Government of Afghanistan is committed to control malaria in Afghanistan. Introduction of RDTs for

early diagnosis of malaria and establishment of CBMM at community level are key interventions that

will reduce morbidity and mortality of malaria. This curriculum will help to enhance their knowledge

about malaria as well as it will build their confidence to introduce RDT for early diagnosis and ACT

for treatment of falciparum malaria at community level.

Chapter one:

General information about malaria & approach to a malaria clinicalpatient

What is malaria-

Malaria is a vector borne parasitic febrile communicable disease.

Symptoms of malaria

The main symptom is fever

Fever may result in chills

Fever appears at the same time of the day

Fever disappears with sweating

After the disappearance of fever individual feels well/ healthy

Other signs and symptoms of malaria are:

Headache

Joint and body pain

Shivering

Vomiting

Diarrhoea (especially in children)

Causative agent of malaria:

Malaria is caused by a parasite called Plasmodium. There are four main types of Plasmodium.

These are-

Plasmodium falciparum (Pf)

Plasmodium vivax (Pv)

Plasmodium malariae (Pm)

Plasmodium ovale (Po)

In Afghanistan Pv is more prevalent than Pf

Vector of malaria:

Female anopheles mosquito is the vector of malaria

Mode of transmission:

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Female anopheles bites a malarial patient and gets Plasmodium with blood

This infected mosquito bites a healthy individual and introduces Plasmodium into the blood.

Malaria undergoes a sexual cycle inside the infected individuals

After a period of time the healthy individual suffers from malaria

Figure: Mode of transmission of malaria

Diagnosis of malaria: malaria can be diagnosed

Clinically

By microscopic examination of blood of the clinicalperson

By using RDT (Rapid Diagnostic Test)

Prevention of malaria:

There are three main ways in which we try to reduce the spread of malaria:

Treat people who are sick with malaria quickly so that the microorganisms cannot be sucked

up by a mosquito,

Reduce the numbers of mosquitoes by controlling their breeding sites, and

Preventing mosquito bites by using bed nets with insecticide.

The most effective method is the use of long lasting insecticidal nets.

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Approach to the patient:

Step 1. Register the patient. If the CHW is illiterate the family member or patient or patient’s family

member will help to register the patient.

Step 2. Please follow the procedures

1. ASK about : ( ask the patient or guardian in case of children)

The chief complaints: fever, headache, earache, throat pain, chilling, vomiting, cough,

breathing difficulties, burning micturition.

Present illness: explanation of the above symptoms eg patient complains of fever and CHW

must enquire after the fever history

Past history of the complaints: History of body feeling hot within 2-3 days, duration of the

symptoms

History of past illness: history of past episode of fever, malaria etc

2. LOOK:

Observe the appearance- ill looking/ unconsciousness/ drowsiness/ stable

3. FEEL:

Use the back of your palm to check if the patient’s forehead feels hot

4. Inspect the patient for : (more emphasise in case of children)

Ear discharge ( ask about ear pain)

Infection of the skin

Fast breathing / breathing difficulties

Sore throat ( ask about throat pain)

5. TEST

Measure body temperature with thermometer from armpit (≥37.5°C/99.5° F or above) if the

patient has fever

Use RDT (if needed)

Action to be taken By CHW:

1. If the patient’s symptoms are similar to that of malaria and his/her condition is stable without

any danger sign, use RDT. Treat the patient with ACT or Chloroquine if the result is positive

for the malaria test. Give the first dose instantly.

2. Refer the patient with danger signs to the nearest health facility.

The danger signs are:

He/she is uunable/unwilling to drink or feed (breastfeeding for children)

He/she vomits everything

History of convulsions

Presence of Lethargy / drowsiness / unconsciousness

she is severely anaemic

3. Refer the patient of less than 5 months age with RDT positive result to the nearest health

facility.

4. Refer the pregnant women (1st trimester) with RDT positive result to the nearest health facility.

N.B. Please follow the malaria flow chart and treatment guideline.

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Chapter Two

Introduction of RDT

What is RDT (Rapid Diagnostic Test)

RDT is a malaria diagnostic device that detects malaria specific protein (antigens) which is produced

by malaria parasites.

It has

• Space A for buffer

• Space S for blood sample

• Window C for control

• Window test for Pf or PAN (Plasmodium another- P. vivax, or P. malaria or P. ovale) result

Advantages of RDT:

No need for laboratory facilities

Easy to carry

Simplicity and rapidity of the tests.

No need for electricity or laboratory equipment.

Minimal requirement for training (basic skills acquired in 1 day).

Acceptable levels of sensitivity and specificity, and

Disadvantages of RDT:

More expensive than microscopy.

Prolonged positive result after effective treatment.

Storage conditions of RDTs

Procedure of RDT use:

1-Prepare the materials needed

• RDT

• new, unopened lancet

• Alcohol swab

• disposable gloves

• timer or watch

• Safety box

• Pencil or marker for labeling the RDT

• Record book and pen for results

Take time to explain briefly to the patient what you are going to do

2- Check

- Expiration date of the RDT

- Colour of desiccant

DO NOT use expired damaged RDT or if there is a sign of exposure to humidity!

3- Wear disposable gloves.

Doing the test (1)

1) Open the RDT packet and take out device just before use

2) Label RDT with patient’s name or ID before doing the test

3) Clean the patient’s finger with an alcohol swab and let it dry before doing a finger prick

4) Discard used lancet immediately in the safety box

5) Touch the surface of the blood with the collecting tube/device to get 5L of blood

DO NOT collect too much blood as this may affect the test result

6) Slowly deliver the blood from the collecting tube onto the sample wall (S)

7) Discard the used blood collecting tube immediately in the sharp box

8) Invert the buffer bottle vertically and slowly dispense the required number of

drops into the buffer well (A)

9) Wait for the prescribed time (e.g.15-20 minutes) before reading the results

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Storage of RDT:

• Keep RDTs in the coolest part of the room, but never freeze them. They do not need

refrigeration

• Protect RDTs from excessive heat (Keep it within 40-30

0 C)

• Store away from direct sunlight

• Do not store close to a wall or ceiling, as both absorb heat during the day

• Store a minimum of 30 cm away from walls and ceiling

• Do not store directly on the ground

• To reduce damage from moisture, water, and pests, store on a shelving unit or shelf, if

possible

Chapter Three:

Practical use of RDT

Technique of the blood collection:

Take alcohol swab and clean the patient’s finger

Let it dry before the pricking

Open the lancet

Prick the finger with lancet

Discard the lancet in to the sharp box

Swab the first drop of blood

Press the pricked finger for second drop of blood

Touch the surface of the blood with the collecting tube to get 5L of blood

Slowly deliver the blood from the collecting tube on to the sample wall (S)

Discard the used blood collecting tube immediately in the safety box

Practical use of RDT:

Participants will follow the instruction of RDT use (mentioned above)

They will follow the given Pictorial procedure of RDT use

They will apply on patients

Otherwise they will form groups and do the practical on each other.

Interpretation of the result:

• Invalid result (the test device is invalid):

a. No line in the control window or

b. No line in the control & test window

• Valid result( the test device is valid):

a. Red line only in the control window or

b. Red line in the control & test window

• Negative result

a. Red line in the control window and

b. No line in the test window

• Positive result

a. Red line in the control window and

b. Red line in the test window

Interpretation of positive result:

Picture of RDTs with result mentioned above

Picture of RDTs with result mentioned above

Picture of RDTs with result mentioned above

Picture of RDTs with result mentioned above

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a. Red line in control window & in Pf line of test window – Pf malaria case

b. Red line in control window & in PAN line of test window – Pv malaria case

c. Red line in control window , in Pf line & PAN line of test window – mix infection

After doing the test

1) Discard used gloves, swab, and desiccant in a non-sharp waste container

2) Keep used RDTs in the box. Return used RDTs for replacement with new RDTs

3) Record results in the register.

Chapter Four:

Treatment of malaria

What is ACT:

ACT - it is artemisinin combination therapy. It includes Artesunate 50/100mg + SP (sulfadoxine500

mg +Pyrimathamine 25 mg).

Treatment of P. falciparum malaria:

Artesunate(50 mg or 100 mg ) and SP( sulfadoxine500 mg +Pyrimathamine 25 mg) the recommended

drugs for effective malaria treatment in Afghanistan

Dosage Chart

First Day Second day Third day

Remarks

Age SP Artesunate Artesunate Artesunate

5-11 months

Half tablet Half tablet

Of 50 mg

Half tablet Half tablet

Child

blister 1-6 years

One tablet One tablet

Of 50 mg

One tablet One tablet

7-13 years

Two tablets Two tablets

Of 50 mg

Two tablets Two tablets

Above 13 years

Three tablets Two tablets

Of 100 mg

Two tablets Two tablets Adult

blister

Important;

Day1 dose should be administrated as a Direct Observation therapy(DOT)

Remind the patient to complete the treatment.

Advice the patient to sleep under a long lasting insecticidal net to prevent Malaria attack

Note

The dose chart is only applicable for:

Blister 1: adult blister

Artesunate 100 and sulfadoxin +Pyrimthamine 500mg+25mg TABLET

Blister 2 Children Blister

Artesunate 50 mg and Sulfadoxin + Pyrimethamine 500 mg + 25 mg TABLET

Treatment of P. vivax malaria:

Chloroquine (150mg base tablet)

Age

(years)

Weight

(kg)

DAY 1

(no. of tablets)

DAY 2

(no. of tablets)

DAY 3

(no. of tablets)

<1 <10 ½ ½ ½

1-<3 10-<14 1 1 ½

3 –< 5 14-19 1 ½ 1 ½ ½

5-11 20-35 2 ½ 2 ½ 1

11-12 36-50 3 3 2

14+ 50+ 4 4 2

(Source: Revised National Treatment Guideline, April, 2010)

Treatment of mix infection: Treat as Pf malaria.

Picture of RDTs with result mentioned above

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Malaria Flow Chart At Health Post Level

Registration of the patient

Use RDT

RDT

positive

(Pf/PAN)

RDT

negative

Patient

Stable.

Treat the

patient

Patient with

danger sign

Refer to health

facility

Children less

than 5 month.

Refer to health

facility

Pregnant

women (1st

trimester)

Refer to health

facility

If Pf

positive

treat

with

ACT

If both Pf

& PAN

positive

treat with

ACT

If only

PAN

positive

treat with

Chloroquin

-e

Pregnant women

(2nd

& 3rd

trimester) If only

PAN positive treat

with Chloroquine

Pregnant women (2nd

& 3rd

trimester) If

only Pf or both Pf &

PAN positive treat

with ACT

Patient comes back with

symptoms after treatment

Refer the patient to the

nearest health facility

Treat the patient as

usual according to

CHWs guideline

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Chapter five:

Session 1: WELCOME and INTRODUCTION

During this session, the participants will:

Register

Introduce each other

Share their expectations of the training

Introduce with the rules & norms of the training

Undertake a pre-test

Introduce about goal & objectives of the training

Know about the general information of malaria

Objective:

At the end of the session the participants will be able to

Define malaria

Describe signs & symptoms of malaria

Identify the causative agent of malaria

Name the vector of malaria

Describe the mode of transmission of malaria

List the main malaria prevention methods.

Method:

Question and answer

Pictorial presentation

Lecture with discussion

Topics:

General Information about malaria

What is malaria

Signs & Symptoms of malaria

Causative agent of malaria

Vector of malaria

Mode of transmission of malaria

Prevention of malaria

Materials:

Note books

Pen, Pencil

Posters/ Pictures

Flip Chart

Session 2: Introduction of Rapid Diagnostic Test

Objective:

At the end of the session the participants will able to

Know what is RDT

Describe advantages & disadvantages of RDT

Use RDT to diagnose malaria

Store RDT at health post level

Methods:

Demonstration of RDT

Question and answer

Topics:

What is RDT

Advantage and disadvantage of RDT

Procedure of RDT use

Storage of RDT

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Materials:

RDT Kits

Pictorial instruction about RDT use

Safety box

Register form

Session3: Practical use of RDT

Objective:

At the end of the session the participants will able to

• Collect patient’s blood for RDT

• Use RDT for diagnosis of malaria

• Interpret the result of RDT

Method:

Practical group work

Practical use of RDT

Topic:

Technique of blood collection from patient’s finger

Use of RDT for malaria diagnosis

Interpretation of the result of RDT

Material:

RDT

Lancet

Alcohol swab

Buffer

Dropper

Pictorial instruction about RDT use

Timer/ Watch

Session 4: Management of malaria

Objective:

At the end of the session the participants will able to

Define ACT

Treat the falciparum malaria cases by using ACT

Methods:

Lecture with discussion

Demonstration of ACT

Role play

Topics:

Introduction of ACT

Treatment of malaria by using ACT

Materials:

ACT (Dosage forms)

Pictorial demonstration of ACT, Dosage & treatment

Session 5: Reporting on RDT, ACT & malaria cases

Objective:

At the end of the session the participants will able to

Report on used RDT, positive & negative RDT

Report on ACT use

Report on malaria cases

Methods:

Demonstration of reporting formats

Small group discussion

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Topics:

Reporting system about RDT

Reporting system about ACT use

Reporting system about malaria cases

Materials:

Different kinds of reporting formats

Session 6: Reporting on RDT, ACT & malaria cases

Methods:

Question and answer

Discussion

Topics:

Review of the previous lessons

Post test

End evaluation of course

Materials:

Post test sheet

Course evaluation sheet