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KEDARURATAN BEDAH ANAK

[PPT]PowerPoint Presentation - FK UWKS 2012 C | born to be a ... · Web viewNecrotizing enterocolitis (NEC) 3. Perforasi gaster spontaneus kongenital 4. Kelainan saluran nafas bagian

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Page 1: [PPT]PowerPoint Presentation - FK UWKS 2012 C | born to be a ... · Web viewNecrotizing enterocolitis (NEC) 3. Perforasi gaster spontaneus kongenital 4. Kelainan saluran nafas bagian

KEDARURATAN BEDAH ANAK

Page 2: [PPT]PowerPoint Presentation - FK UWKS 2012 C | born to be a ... · Web viewNecrotizing enterocolitis (NEC) 3. Perforasi gaster spontaneus kongenital 4. Kelainan saluran nafas bagian
Page 3: [PPT]PowerPoint Presentation - FK UWKS 2012 C | born to be a ... · Web viewNecrotizing enterocolitis (NEC) 3. Perforasi gaster spontaneus kongenital 4. Kelainan saluran nafas bagian

KEDARURATAN PADA NEONATUS :

A. Kelainan Saluran Pernafasan kongenital

1. Obstruksi jalan nafas

2. Displacement Lung volume

3. Pulmonal parenchymal insufficiency

B. Kelainan Pencernaan kongenital

1. Obstruksi usus

2. Malrotasi

3. Perforrasi usus

C. Defect dinding abdomen

1. Omphalocele pecah

2. Gastroschisis

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Kelainan Saluran Pernafasan KongenitalA. Jenis Kelainan :

1. Saluran pernafasan bagian atas :

- Mikrognatia: Pierre Robin Syndrome

- Makroglosia

- Choanal Atresia

- Laryngeal/Tracheal stenosis

- Tumor larynx dan leher

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2. Kelainan Intratoraks :

- Atelektasis pulmonum

- Pnemotoraks

- Pnemomediastinum

- Kiste dan tumor paru-paru

- Congenital lobar emphysema

- Hernia diaphragmatika

- Eventerasi diaphragma

- Atresia esophagus dengan fistule trachea

- Trecheo dan bronchomalacia

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This drawing on the x-ray depicts the material in the chest, including stomach, large and small intestine, and the spleen. Note how little space remains for the heart and lungs. An NG tube is very helpful in these babies to decrease stomach and bowel distention.

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Operative photograph showing that upon opening the chest, a very large right upper lobe was encountered and was allowed to herniate out through the incision, thus

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B. TANDA DAN GEJALA :

1. Resletlessnes

2. Tachypnea

3. Retaction

4. Cyanosis

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C. DIAGNOSIS ;

1. Anamnesis :

a. Riwayat kehamilan:

- ibu hamil dengan hidramnion

- pre eklampsia, eklampsia

- selama hamil ibu pernah sakit

- riwayat trauma

- paritas kehamilan

- penggunaan obat-obatan, alkohol, merokok

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b. Riwayat kelahiran :

- kesulitan melahirkan

- bayi lahir melalui sectio cesaria

- trauma melahirkan

- penyukit pada saat melahirkan

c. Gejala dan tanda awal :

- tangis bayi saat lahir, sianosis, sesak nafas,

- apnea, nilai APGAR yang rendah dll

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2. Pemeriksaan fisik :

- Inspeksi torak: simetris, asimetris dll

- Gerakan pernafasan: simetris

- Retraksi dinding toraks

- Perkusi dinding toraks

- Auskultasi : ada kelainan suara nafas dll

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D. PENUNJANG DIAGNOSIS :

1. Pemeriksaan radiologis :

a. Foto polos toraks

b. Foto kontras saluran nafas

2. Pemeriksaan Laboratorium :

a. Laboratorium rutin : DL

b. Laboratorium khusus : AGD

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ATRESIA ESOPHAGUS

(panah merah)

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Atresia esophagus: NGT dalam segmen proksimal esophagus

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Atresia Esophagus : aspirasi pnemonia

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Foto polos Toraks: Hernia Difragmatika kiri

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AP chest films from the day of admission demonstrate hyperinflation of the right upper lobe.

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E. SIKAP DAN TINDAKAN :

1. Resusitasi jalan nafas dan pernafasan

2. Resusitasi jantung

3. Resusitasi cairan

4. Persiapan rujukan

5. Persiapan tindakan pembedahan

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A clinical photograph shows the hyperexpanded right chest.

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Presently, children are not rushed to the operating room. As pulmonary hypertension is the major concern, and operative intervention can trigger this, aggressive attempts are made to stabilize the child for 5 to 7 days prior to operative correction. Interventions such as high-frequency ventilation and nitric oxide therapy are used. If the child cannot be stabilized, she can be placed on an ECMO (extra corporeal membrane oxygenation) circuit – essentially an artificial lung – for up to three weeks while the lung matures. In this case, the child stabilized on high-frequency ventilation and nitric oxide and was operated on six days after birth. Pre-operative positioning is shown here.

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KELAINAN SALURAN PENCERNAAN KONGENITAL

I. Obstruksi saluran pencernaan

II. Malrotasi saluran pencernaan

III. Perforasi saluran pencernaan

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Skema saluran pencernaan

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I. Obstruksi saluran pencernaan :A. Jenis kelainan :

1. Atresia esophagus

2. Pilorostenosis

3. Atresia duodenum

4. Atresia jejunum

5. Atresia ileum

6. Mekonium ileus

7. Mekonium plug syndrome

8. Penyakit Hirsachsprung’s

9. Anorectal malformation

10. Atresia kolon

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This drawing on the x-ray depicts the material in the chest, including stomach, large and small intestine, and the spleen. Note how little space remains for the heart and lungs. An NG tube is very helpful in these babies to decrease stomach and bowel distention.

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Operative photograph shows the massive fluid filled stomach (on the left) and duodenal bulb (on the right)

which was found to contain over 400 cc of fluid.

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Operative photograph showing dilation of the proximal jejunum with a blind end.

Operative Finding :

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B. Gejala Utama :

1. Muntah – muntah

2. Hipersalivasi

3. Distensi abdomen

4. Retensi mekonium

5. Gangguan defekasi

Page 36: [PPT]PowerPoint Presentation - FK UWKS 2012 C | born to be a ... · Web viewNecrotizing enterocolitis (NEC) 3. Perforasi gaster spontaneus kongenital 4. Kelainan saluran nafas bagian
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C. Penunjang Diagnosis :

1. Pemeriksaan radiologis :

a. Foto polos abdomen

b. Foto kontras saluran cerna

2. Pemeriksaan laboratorium :

a. Pemeriksaan lab. rutin : Dl,UL

b. Pemeriksaan Lab. Khusus

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ATRESIA ESOPHAGUS

(panah merah)

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Atresia esophagus: NGT dalam segmen proksimal esophagus

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Atresia Esophagus : aspirasi pnemonia

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Obstruksi usus ok P.Hirschsprung’s dilatasi usus halus dan kolon tanpa udara dalam rektum

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Obstruksi usus ok Intussusepsi

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Obstruksi usus halus

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Barium enema mekonium ileus, terlihat mikrokolon

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D. Sikap dan Tindakan :1. Bayi dipuasakan

2. Pasang pipa nasogastrik

3. Pasang infus sesuai kebutuhan

4. Berikan antibiotika sesuai indikasi

5. Letakkan bayi dalam penghangat

6. Siapkan bayi untuk dilakukan pembedahan

7. Segera rujuk bayi ke RS yang mampu menangani kasusnya

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II. MALROTASI SALURAN PENCERNAAN :A. Gambaran umum :

1. Diagnosis sulit ditegakkan

2. Gejala awal tampak sebagai tanda obstruksi

3. Setiap obstruksi usus setinggi duodenum dapat dicurigai sebagai adanya malrotasi usus

4. Obstruksi usus tinggi tinggi parsial selalu disebabkan oleh malrotasi

5. Malrotasi berbahaya dan menjadi emergensi jika mengalami volvulus

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Skema malrotasi usus

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Skema saluran pencernaan

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Malrotasi

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Volvulus

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Volvulus usus

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Volvulus

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B. PENUNJANG DIAGNOSIS :

Radiologi :

a. Foto polos abdomen :

hilangnya gambaran udara dalam duodenum

b. Foto dengan kontras enema barium :

terlihat gambaran posisi sekum di daerah plexura hepatis

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C. SIKAP DAN TINDAKAN :

1. Bayi dipuasakan dan dipasang infus

2. Pasang pipa nasogastrik

3. Berikan antibiotika sesuai indikasi

4. Persiapkan bayi untuk tindakan pembedahan

5. Segera rujuk bayi ke RS. yang mampu melakukan tindakan pembedahan

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Close-up operative photograph shows the entire midgut being twisted around a single narrow mesentery.

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Operative photograph shows the midgut to be dusky but not necrotic.

Operative Finding :

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Operative photograph showing the midgut to be dusky in color.

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III. PERFORASI SALURAN CERNA :

A. Gejala :1. Distensi abdomen yang terjadi dengan cepat dan tiba-tiba

2. Bayi terlihat mengalami gangguan pernafasan

3. Liver dullnes hilang pada pemeriksaan abdomen

4. Pada perkusi abdomen tympani

5. Dengan pemeriksaan foto polos abdomen terlihat gambaran udara bebas dalam rongga peritoneum

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B. Penyebab perforasi saluran cerna :

1. Obstruksi saluran cerna

2. Necrotizing enterocolitis (NEC)

3. Perforasi gaster spontaneus kongenital

4. Kelainan saluran nafas bagian atas kongenital

C. Sikap dan tindakan :1. Resusitasi pernafasan dan cairan

2. Pasang pipa nasogastrik

3. Berikan antibiotik sesuai indikasi

4. Funktie steril rongga peritoneum untuk dekompresi

5. Segera rujuk bayi ke RS. yang mampu untuk pembedahan

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Necrotizing enterocolitis (NEC)

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NEC

Perforasi

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Operative photograph shows the bowel to be white and necrotic throughout its entire length from the duodenum

to the colon

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Meconium ileus is most often seen in the first few days of life in neonates with cystic fibrosis, but can rarely occur in infants with a normal pancreas. In cystic fibrosis, the abnormal pancreatic secretions lead to inspissated meconium that produces intestinal obstruction. The dilated coils of ileum are opened here to reveal the inspissated green meconium (which may also be tarry or gritty), while the unopened colon at the upper left and the appendix at the lower left beyond the ileocecal valve are not dilated, and little or no meconium is passed per rectum.

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Meconium peritonitis shown here as a greenish exudate overlying the serosal surfaces of the peritoneal cavity can complicate meconium ileus in utero, particularly in fetuses with cystic fibrosis. The bowel ruptures and leaks meconium, which produces a chemical peritonitis. Calcifications in the spilled meconium may be seen radiographically. Another complication of meconium ileus is volvulus.

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DEFEK DINDING ABDOMEN A. Jenis kelainan :

1. Omphalocele pecah

2. Gastroschisis

B. Problemnya :

1. Hipotermi

2. Hipovolume

3. Infeksi

4. Gangren saluran cerna

5. Kelainan penyerta organ lain

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Omphalocele

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Omphalocele

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Omphalocele utuh (tidak pecah)

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Gastroschisis

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Gastroschisis

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Gastroschisis

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Bagian usus yang nekrosis pada gastroschisis

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Pemasangan mesh pada gastroschisis

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Omphalocele dengan mesh yang telah diserap

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Hernia ventralis abdomen pasca repair omphalocele

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Omphalocele tidak pecah dengan granulasi dan epitelisasi

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Extrophia vesica urinaria (Exstrophia vesicae)

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Extrophia Vesicae

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Extrophia vesicae

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C. Sikap dan tindakan :

1. Cegah pasien mengalami hipotermi dengan menempatkan bayi pada penghangat

2. Berikan infus sesuai kebutuhan untuk mencegah hipovolume

3. Antibiotika intravena sesuai indikasi untuk mencegah infeksi

4. Organ abdomen yang diluar rongga dibungkus dengan baham steril

5. Segera rujuk pasien ke RS

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Kontra insisi pada kulit dinding abdomen untuk menutup defek pada gastroschisis dan omphalocele pecah

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Pasca repair extrophia vesicae

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KEDARURATAN PADA ANAK-ANAK :I. Usia dibawah usia 1 tahun :

1. Hernia inguinalis strangulasi

2. Intussusepsi ( Invaginasi)

3. Obstruksi usus ok. Berbagai penyebab

4. Trauma

II. Pada anak usia 1 – 6 tahun :

1. Hernia inguinalis strangulasi

2. Apendisitis akut

3. Obstruksi usus ok. Bolus askariasis

4. Trauma

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A clinical photograph demonstrates the currant jelly stools.

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Operative photograph shows the intussusception with the dusky terminal ileum (on the patient's left) protruding into the cecum (on

the patient's right). Note that the appendix is intussuscepted with the ileum.

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Operative photograph shows dilatation of almost the entire small bowel except for the decompressed terminal ileum in

the left lower corner of the photograph.

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Operative photograph is a close-up view of the area of caliber change and reveals a Meckel diverticulum with an

omphalomesenteric duct remnant. This remnant had been attached to the under surface of the umbilicus, serving as a fulcrum for a

small bowel volvulus.

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