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QT Prolongation Considerations for IM Hospitalists Lenny Noronha, MD UNM Hospital Medicine Best Practices 2/8/12

QT Prolongation Considerations for IM Hospitalists

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QT Prolongation Considerations for IM Hospitalists. Lenny Noronha, MD UNM Hospital Medicine Best Practices 2/8/12. Outline. Review cardiac cycle, pathophysiology Discuss risk factors for Prolonged QT, TdP Analyze medication classes prescribed by Hospitalists - PowerPoint PPT Presentation

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Page 1: QT Prolongation Considerations for IM Hospitalists

QT Prolongation Considerations for IM Hospitalists

Lenny Noronha, MDUNM Hospital Medicine Best Practices

2/8/12

Page 2: QT Prolongation Considerations for IM Hospitalists

Outline

• Review cardiac cycle, pathophysiology

• Discuss risk factors for Prolonged QT, TdP

• Analyze medication classes prescribed by Hospitalists

• Propose “Best Practices”, discuss

Page 3: QT Prolongation Considerations for IM Hospitalists

Special thanks to:

• Carlos Macias, MD• Brook Parrish, MD• Davin Quinn, MD• Nicole Klein, MD• Vincent Zummo, PA• Katya Calvo, MD• Shmuel Inbar, MD

Page 4: QT Prolongation Considerations for IM Hospitalists

Case 44yf adm to Red Med team for GI sx, AMS

Adm to Pres 1 wk prior, ureter stented, on cipro 500 po bid.

1. AMS: “MRI pending”. Attributed to K 2.8 and ketones in urine.2. UTI: Order cultures, start zosyn3. “Prolonged QTc” Will repeat EKG after electrolytes replaced.4. Lip lac may need to be sutured.5. Pain control: tylenol and oxycodone6. Hospital issues

Page 5: QT Prolongation Considerations for IM Hospitalists

Case cont’d

Pt seen by neuro before IM eval. “Feeling funny…my heart fluttering like a butterfly”

QTc 600 documented.

Impression:• LOC c tongue abrasion, split lip, most likely secondary to

seizure• Low potassium• Prolonged QT

Page 6: QT Prolongation Considerations for IM Hospitalists

Initial ED EKG, K 2.8, QTc 602

Page 7: QT Prolongation Considerations for IM Hospitalists

HD 2, K 3.6, QTc 511

Page 8: QT Prolongation Considerations for IM Hospitalists

Subsequent courseHD 2 EEG normal.Cardiology consult HD 3 after several runs of nonsustained polymorphic

VT (8-9 beats).QTc range 528 – 699 during admission, despite electrolyte replacementOutpt EKG from 1yr prior: NSR, QTc 467

ID, Pulm consults for complex infectionStarted on Bb, titrated to tolerance

Family all had EKG’s. Daughter’s QTc 462.Pt dc’d c LifeVest, had ICD placed after 14 d course abx, ureteral

stone/stent removed

Page 9: QT Prolongation Considerations for IM Hospitalists

ZOLL LifeVest Wearable Defibrillator

http://lifevest.zoll.com/medical-professionals/

Page 10: QT Prolongation Considerations for IM Hospitalists

What is normal, prolonged?

“Prevention of Torsade de Pointes in Hospital Settings”, Barbara Drew, et al, JACC Scientific statement, 2010; 55, 9:934-947

“The QT interval: Too long, too short or just right”, Sami Viskin, Heart Rhythm, May 2009,: 6, 5: 711-715

Page 11: QT Prolongation Considerations for IM Hospitalists

Antiarrhythmic Overview

Carlos Macias, MDJan 31st 2012

Fellows Conference

Next 9 slides adapted from:

Page 12: QT Prolongation Considerations for IM Hospitalists

Part 1. Basic principals

• Cardiac action potential– Electrical impulse of the heart is the summation of

thousand of tiny electrical currents generated by thousands of individual cardiac cells.

– Electrical activity of an individual cardiac cell is described by the cardiac action potential.

Page 13: QT Prolongation Considerations for IM Hospitalists
Page 14: QT Prolongation Considerations for IM Hospitalists

Part 1. Basic principals• Depolarization– Phase 0– Rapid sodium channels in the cell membrane are stimulated

to open.– Allows positively charged Na ions to rush into the cell.– Voltage spike – positively directed change the

transmembrane potential– Na channels are voltage dependent.– The speed of the slope determined how fast the next cell

will be stimulated to depolarize.– Anything that causes the causes the slope to change will

affect conduction velocity.

Page 15: QT Prolongation Considerations for IM Hospitalists

Part 1. Basic principals

• Repolarization corresponds to phases 1-3• Accounts for most of the action potential• Time from the end of phase 0 to late in phase

3 is considered refractory period. • Duration of the action potential determines

the refractory period.– Anything that increases duration of the action

potential also changes the refractory period.

Page 16: QT Prolongation Considerations for IM Hospitalists

Part 1. Basic principals

• Repolarization begins rapidly– Phase 1– Interrupted by plateau (Phase 2) “slow” Ca channels– Most important ionic shift during repol is the

outflow of positive K ions.– At least six different K “currents” have been

identified.– At the end of repolarization the transmembrane

voltage returns to baseline.

Page 17: QT Prolongation Considerations for IM Hospitalists

Part 1. Basic principals

Page 18: QT Prolongation Considerations for IM Hospitalists

Part 1. Basic principalsMechanism of cardiac tachyarrhythmias

Most tachyarrhythmias are thought to be due to one of the following mechanisms:

– Automaticity– Reentry– Channelopathy (congenital LQTS)– Triggered activity (dig tox arryth, CCB-sens VT, TdP)

Page 20: QT Prolongation Considerations for IM Hospitalists

Basic principalsTriggered mechanism

Ectopy triggered if threshold exceeded

Page 21: QT Prolongation Considerations for IM Hospitalists

Drug-Induced Prolongation of the QT Interval,Dan M. Roden, M.D., N Engl J Med 2004; 350:1013-1022

Current concepts in the mechanisms and management of drug-induced QT prolongation and torsade de pointes, Gupta, American Heart Journal, Jue 2007; 153: 891-899

Page 22: QT Prolongation Considerations for IM Hospitalists

Notes on TdP

• Usually self-limited

• Typical symptoms: palpitations, syncope, “seizure-like activity”

• Immediate tx: Mg Sulfate 2g IV bolus, followed by 2-4g IV infusion over 2 hours

Page 23: QT Prolongation Considerations for IM Hospitalists

Drugs and the QT Interval — Caveat DoctorBarbara A. Liu, M.D., and David N. Juurlink, M.D., Ph.D.N Engl J Med 2004; 351:1053-1056

1. Patient Factors

2. Direct drug effects

3. Indirect drug effects

Page 24: QT Prolongation Considerations for IM Hospitalists

Patient Factors

• Female gender• Age > 65• Electrolyte loss (i.e. Diuretics, Diarrhea)• Cardiac disease• Liver or Renal disease, Hypothyroidism• Congenital LQTS (1:2500 gen population)– h/o unexplained syncope, FH sudden death < 40

Page 25: QT Prolongation Considerations for IM Hospitalists

Direct Drug EffectsMost meds that prolong QT thought to block IKR

Psychiatric• Antipsychotics• TCA’s• Lithium• Citalopram

Cardiac• Quinidine, procainamide• Flecainide• Amiodarone, Sotalol

Antimicrobials• Macrolides• Quinolones•Azoles•Pentamidine•Amantadine

Other• Methadone•Hydroxyzine•Loratidine•Tacrolimus•Cocaine

Page 26: QT Prolongation Considerations for IM Hospitalists

Indirect Drug EffectsCommon C P450 3A4 Inhibitors

Cardiovasc• Diltiazem• Verapamil

Psych• Fluoxetine• Midazolam

Antimicrobials• Macrolides!• Ketoconazole• INH• HIV meds- Amprenavir, Delavirdine- Nelfinavir, Ritonavir

Endocrine•Ethinylestradiol•Gestodene•Mifepristone•Raloxifene•Tamoxifen

Others• Grapefruit juice•Resveratrol•Irinotecan

FYI :This is the mechanism for patients with liver disease

Page 27: QT Prolongation Considerations for IM Hospitalists

“Cardiac side effects of psychiatric drugs” Mackin, Human Psychopharmacology 2008; 23: 3-14.

Clinical Features Associated with risk of TdP

Page 28: QT Prolongation Considerations for IM Hospitalists

Literature: Antibiotics

Page 29: QT Prolongation Considerations for IM Hospitalists

“Oral Erythromycin and the Risk of Sudden Death from Cardiac Causes”, Ray, NEJM 2004

Response to case reports of TdP assoc c IV erythromycin

Retrospective review of TN Medicaid cohort investigated from sudden death ‘88-’93.

Compared matched population “person years” of current and former users of oral erythromycin to patients using amoxicillin at time of investigation

Page 30: QT Prolongation Considerations for IM Hospitalists

“Oral Erythromycin and the Risk of Sudden Death from Cardiac Causes”, Ray, NEJM 2004

Led to numerous letters, review articles, and…

Page 31: QT Prolongation Considerations for IM Hospitalists

2006 ACC/AHA/ESC GuidelineRecommend removing of offending agent in patients

with drug-induced LQTS

2010 ACC/AHA Scientific Statement, “Prevention of Torsades de Pointes in Hospital SettingsRecommend continuous cardiac monitoring for drugs at risk to cause TdP. If QTc becomes > 500ms or increases > 60ms, seek alternative therapies, assess for drug interactions. Patients should not be transported from the unit for procedures.

Page 32: QT Prolongation Considerations for IM Hospitalists

Literature: Antipsychotics

1980’s: Dose-dependent risk of QTP, TdP, sudden death noted with antipsychotics, especially droperidol, haldol and thioridizine

1990: UK Committee on Safety of Medicines recc gradual dose increase, EKG before and periodically in patients receiving high doses

Page 33: QT Prolongation Considerations for IM Hospitalists

Literature Review cont’d

2007: FDA label warning for QTP/TdP from Haldol IV in response to adverse events reports. Recc: continuous tele monitoring

Page 34: QT Prolongation Considerations for IM Hospitalists

2010 Systematic Review (Meyer-Massetti)

Methods:Cases of QTP/TdP from Pubmed, Embase, Scopus databases (1823-2009; FDA MedWatch reports (‘97-’08)

Results:70 cases, 2 deaths.42 of 54 cases of TdP preceded by QTP68 had identified RFTdP cases had cumulative dose 5-645 mgDeaths had cumulative doses of 530, 634 mg

Page 35: QT Prolongation Considerations for IM Hospitalists

2010 Systematic Review (Meyer-Massetti)

Discussion - APA 2004 recc: Haldol dosinginitial IV dosing 1-2mg q 2-4hGeriatric: 0.25-0.5mg q4, titrate as needed

Key Conclusion/UCSF policy:- IV haldol can be given in cumulative doses

< 2mg without tele/serial EKG in patients without risk factors

- Cardiac monitoring if doses greater than 2mg anticipated or risk factors for TdP

Page 36: QT Prolongation Considerations for IM Hospitalists

3/17/09

Recommendation 1 (Disclosure): Clinicians should inform patients of arrhythmia risk when they prescribe methadone. Recommendation 2 (Clinical History): Clinicians should ask patients about any history of structural heart disease, arrhythmia, and syncope. Recommendation 3 (Screening): Obtain a pretreatment electrocardiogram for all patients to measure the QTc interval and a follow-up electrocardiogram within 30 days and annually. Additional electrocardiography is recommended if the methadone dosage exceeds 100 mg/d or if patients have unexplained syncope or seizures. Recommendation 4 (Risk Stratification): If the QTc interval is greater than 450 ms but less than 500 ms, discuss the potential risks and benefits with patients and monitor them more frequently. If the QTc interval exceeds 500 ms, consider discontinuing or reducing the methadone dose; eliminating contributing factors, such as drugs that promote hypokalemia; or using an alternative therapy. Recommendation 5 (Drug Interactions): Clinicians should be aware of interactions between methadone and other drugs that possess QT interval–prolonging properties or slow the elimination of methadone.

Especially in doses over 100 mg/d

Page 37: QT Prolongation Considerations for IM Hospitalists

Suggested “Best Practices”

1. Awareness of “Patient Factors” for prolonged QT– Age > 65– Female– ANY cardiac disease– Hypokalemia– Hypomagnesemia– Hypocalcemia– CKD, Chronic liver disease, hypothyroidism– FH Sudden death/prolonged QT

Page 38: QT Prolongation Considerations for IM Hospitalists

Suggested “Best Practices”

2. Awareness of chronic outpatient medications most likely to prolong QT interval- Methadone- Erythromycin (i.e. gastroparesis)

- Amiodarone- Atypical antipsychotics- Tricyclic antidepressants

Page 39: QT Prolongation Considerations for IM Hospitalists

Suggested “Best Practices”

3. Obtain EKG or tele strip measurement of QTc in patients with Patient Factors/above meds before starting AND after doses of:

- Antipsychotics- Macrolides- Quinolones- Pentamidine (i.e. PJP)- CYP 3A4 inhibitors

Page 40: QT Prolongation Considerations for IM Hospitalists

Suggested “Best Practices”

Do NOT add meds than can prolong QT in patients with QTc > 500

Discontinue meds that can prolong QT if QTc increases > 60msec after addition

Page 41: QT Prolongation Considerations for IM Hospitalists

Suggested “Best Practices”

4. Patient Educationwww.qtdrugs.orgwww.azcert.com

Page 42: QT Prolongation Considerations for IM Hospitalists

Suggested “Best Practices”

5. Document QTc in progress note if EKG ordered to measure

6. Add diagnosis to Powerchart problem list and Discharge Summary

426.82 – Long QT syndrome (I45.81 in ICD-10)794.31 – Nonspec Abnormal EKG (R94.31)

Page 43: QT Prolongation Considerations for IM Hospitalists

Suggested “Best Practices”

For delirious patient with QTc > 500, consider:• Trazadone• Depakote• Seroquel, Abilify (less QT effect)

• Telephone consultation with PES attending

Page 44: QT Prolongation Considerations for IM Hospitalists

Questions?

Page 45: QT Prolongation Considerations for IM Hospitalists

What is normal QT?

Page 46: QT Prolongation Considerations for IM Hospitalists
Page 47: QT Prolongation Considerations for IM Hospitalists
Page 48: QT Prolongation Considerations for IM Hospitalists

References“Antiarrhthmic Overview”, Macias, Carlos, Fellow Conference 1/31/12

“Drugs and the QT Interval — Caveat Doctor”, Barbara A. Liu, M.D., and David N. Juurlink, M.D., Ph.D.N Engl J Med 2004; 351:1053-1056

“Oral Erythromycin and the Risk of Sudden Death from Cardiac Causes”, Wayne A. Ray, Ph.D., Katherine T. Murray, M.D., Sarah Meredith, M.B., B.S., Sukumar Suguna Narasimhulu, M.B., B.S., M.P.H., Kathi Hall, M.S., and C. Michael Stein, M.B., Ch.B.N Engl J Med 2004; 351:1089-1096

“Current concepts in the mechanisms and management of drug-induced QT prolongation and torsade de pointes”, Gupta, American Heart Journal, Jue 2007; 153: 891-899

“Drug-Induced Prolongation of the QT Interval”, Dan M. Roden, M.D., N Engl J Med 2004; 350:1013-1022

“Cardiac side effects of psychiatric drugs” Mackin, Human Psychopharmacology 2008; 23: 3-14.

“Consensus statement on high-dose antipsychotic medication” Royal College of Psychiatrists, October 2005

“Prevention of Torsade de Pointes in Hospital Settings”, Barbara Drew, et al, JACC Scientific statement, 2010; 55, 9:934-947

“The QT interval: Too long, too short or just right”, Sami Viskin, Heart Rhythm, May 2009,: 6, 5: 711-715