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Case Presentation
• B/O Shivamma
• 6 days /Female
• Holalkere,Chitradurga
• Was referred to our hospital from Basaveshwara
Medical college,Chitradurga with provisional
diagnosis of Malnourishment with Intestinal
obstruction.
• Chief complaints:Vomiting from D5 of life
• Baby had 8-10 episodes of vomiting which was
not associated with feeding,non projectile,bilious
in nature.
• No h/o constipation,delayed passage of
meconium or abdominal distension.
• No h/o poor feeding ,lethargy,convulsion,hurried
breathing,dcereased urine output.
Birth history:
• G2P2L1.
• Married life-4 ½ years,NCM,Elder sibling 3 yr
old male ,apparently healthy.
• Concieved spontaneously.Had regular ANC in
C’durga Govt hospital.Taken iron and folic acid
suuplements.Immunised with 2 doses of TT.
• Antenatal USG- was not reviewed at
admission
• No h/o maternal GDM,PE or Hypothyroidism.
• Baby born via naturalis at 6:15 am on
03/08/16 in C’durga govt hospital.
• B. wt-2.85kg.
• Cried immediately after birth,was breast fed
within one hour of birth.
• Baby passed meconium and urine within 24
hours .
• Baby has passed stool around 2-3 times/day.
• No episode of vomiting noted upto D5 of life.
On Examination:
• PR-148/min Good volume and regular,
RR-52/min , CRT<3 sec .Temp- 99 F.
• Icterus upto Zone 3.
• No pallor, cyanosis or edema.
• Cry reflex and activity-Good.
• Anthropometry:Wt-2.7kg, Length-49cm,OFC-
34cm.
• Head to toe examination-No dysphormic
features.
Systemic examination:
Per Abdomen Examination:
• RTA-3ml of bilious aspirate.
• Soft ,mildly distended ,non tender.
• Skin over abdomen-Normal.
• No dilated vein over abdomen.
• No organomegaly,no palpable mass.
• Anal opening patent.
• Bowel sounds-heard.2-3/min
CVS:
• S1 S2 heard.
• Systolic murmur best heard Lt lower sternal
border @ 4th ICS.
R/S:
• No retractions ,B/L air entry adequate.
• No crepitations.
CNS:
• AF-2*2 cm open at level
• Cry refelex and activity –Good.
• Moro reflex-Complete and symetrical
S/L/T/AGA/F WITH ACUTE INTESTINAL
OBSTRUCTION-SMALL INTESTINAL
?MALROTATION ?DUODENAL
ATRESIA/STENOSIS
WITHOUT PERFORATION OR PERITONITIS,
WITH CAHD –SMALL VSD ,LT TO RT
SHUNT,IN SINUS RHYTHM WITHOUT CCF.
PROVISONAL DIAGNOSIS:
Course in hospital and Investigations:
• Baby was kept NPO and ryle tube was inserted
• Baby was started on first line antibiotics.
• Surgical reference was taken and as per advice
2hrly RTA aspirate was done and barium meal
follow through was planned for next day.
CBC:
• Hb-13.6 gm/dl,TLC-1580/mm3,
PMN-53%,Platelet count-3.45 lakh/mm3
• Serum sodium-142.9mEq/L,Pottasium-3.8mEq/L
• CRP-20.6mg/L
• RFT-WNL.
• Chest X ray-R UL opacity.
• Echo-Small ASD with Small PDA,normal
biventricular function.
• In view of positive septic screen and upper lobe
opacity baby was changed to second line
antibiotics.
• Barium meal done on D2 of admission
showed no e/o malrotation or intestinal
obstruction.
• Baby had no further episodes of vomiting but
continued to have bilious RTA of 60 ml/24hr
on D2 of admission.
• Baby continued to pass 3-4 stools/day.
With these findings:Normal Barium meal and
positive septic screen.Diagnosis was revised
to:
TERM/AGA/LATE ONSET SEPSIS WITH
Rt UPPER LOBE CONSOLIDATION ?
Aspiration WITH SEPTIC PARALYTIC
ILEUS with ASD and Small PDA
• Baby was contiued on 2nd line antibiotics.
• At D6 of admission RTA aspirate was bilious
8ml/24 hrs and abdomen was soft and non
distended.
• Stomach wash was given and baby started on
small feeds 5ml through spoon along with cover
of motility agent domperidone.
• Baby had abdominal distension after 20ml feeds
,2 feeds were skipped and then again restarted.
• Feeds gradually increased and baby was directly
BF at D9 of admission.
• On D10 of admission baby had multiple
episodes of bilious vomiting.
• Baby was kept NPO and USG abdomen was
planned .
With report of USG repeat contrast meal
follow through was planned
.
TERM/AGA/SMALL INTESTINAL PARTIAL
OBSTRUCTION?STENOSIS-WEB WITH
ASPIRATION PNEUMONIA OF RT UL
WITH CAHD –ASD WITH SMALL PDA
WITHOUT CCF
• Baby was operated on D12 of admission.
• On table findings-proximal duodenal dilation
found.Dodenal web was found near DJ
junction.
• Procedure:Explorative laprotomy+web
excision+duodenoplasty
Post op course
• Baby had RTA about 30-40 ml/day which
gradually decreased on POD5.
• Baby was started on spoon feeds on POD6.
• Baby was discharged on 30/08/16 at POD 10 .
• Duration of hospital stay-22 days.
• Admission wt-2.7kg
• Discharg wt-2.63kg(@ D27 of life)
Follow up:
• Baby is admiited 3 days(28 DOL) back with c/o
of bilious vomiting.
• Admissiion weight-2.5kg
• Antenatal scan were reveiwed at this
admission.
“HINDSIGHT IS ALWAYS BETTER
THAN FORESIGHT”
“Before ,you are wise;after, you
are wise .In between you are
otherwise”-
Looking back was everything done
perfectly???
• Delivery at tertiary care center.
• Missed antenatal USG scan.
• First barium meal was reported as normal???
• Delayed diagnosis –prolonged stay.
Intestinal obstruction in newborn
• Congenital intestinal obstruction occurs
approximately 1 :2000 live births.
• Accounts upto 1/3 of admissions to neonatal
surgical units.
• Success or failure in terms of morbidity or
mortality depends not much on pinpointing the
exact location of lesion but on correctly
diagnosing obstruction as cause of clinical
symptoms and instituting prompt operative
intervention.
Causes of intestinal obstruction
Congenital Acquired Functional
Atresia NEC Hirschprung disease
Stenosis Intusucception Meconium plug
syndrome
Meconium ileus Peritoneal
adhesions
Ileus
Anorectal
malformations
Peritonitis
Enteric duplications
Volvulus
Peritoneal bands
Annular pancreas
Cyst and tumors
When to suspect Intestinal
obstruction????
1.Antenatally diagnosed intestinal obstruction
a)Antenatal USG showing double bubble
appearance.
b)Dilated bowel loops >15mm in length and
7mm in diameter
c)Whirlpool appearance to bowel and mesentry
may indicate malrotation with volvulus.
d)Polyhydramnios
2)Family history of Hirschprung disease and jejunal
atresia.
3)Gastric aspirate >20 ml at birth.
4)Delayed passage of meconium in term or near
term baby-Hirschprung ,meconium
ileus,meconium plug syndrome,SLCS.
5)Vomiting-
• Neonates with bilious vomiting are supposed to
have intestinal obstruction unless proved
otherwise.
• Onset after birth is delayed the more distal
obstructuion is preceded by progressive
abdominal distension
6)Mass abdomen-Duplication cysts,pouch colon
Nature of vomiting and D/D s
Non bile stained with
abdominal distension
Pyloric atresia/stenosis,pre
duodenal variety of duodenal
atresia
Non bilious without abdominal
distension
GER,CDH,prematurity ,sepsis
Bilious vomiting-Surgical causes Malrotation,duodenal stenosis
or atresia,
Proximal jejunal atresia
Bilious vomiting-other causes Intestinal ileus due to
electrolyte imbalance or sepsis
Approach to intestinal obstruction
Radiological diagnosis
• Obtain AXR- AP and cross table lateral view.
• Erect abdominal view is done in case of non
sick babies.
• A prone cross table lateral view should be
done at >24 hrs after birth for suspected ARM
Normal progression of air in intestine:
Stomach First breath
Duodenum Second or third breath
Proximal small bowel 1 hour
Distal small bowel 3 hour
Caecum 6hour
Rectum 18-24 hour
Characteristic signs of AXR
Double Bubble appearance Duodenal atresia
Triple bubble appearance Proximal jejunal atresia
Uniformly dilated bowel loops
with multiple air fluid levels
Distal obstruction
Ground glass or soap bubble
appearnce.
NEC,meconium ileus
Speckled calcification Meconium ileus
Mild double bubble with distal
gas with 2nd part of duodenum
to left of spine
Malrotation
Contrast enema:if clinical scenario and
AXR suggest distal obstruction
Microcolon Meconium ileus and SLCS
Abnormal caecal position Malrotation
Right sided colonic
breaking
Volvulus
Abnormal rectosigmoid
index
Hirschprung disease
Upper GI series:
• Procedure of choice in diagnosing malrotation
1)Abnormally located D-J flexure-to the right of
spine.
2)Proximal jejunum located in right side of
abdomen.
3)Spiral corckscrew course of distal duodenum
and proximal jejunum.
Abdominal USG
• Reversal of relation of SMA and SMV in
malrotation.
• Can also diagnose intussusception and free
fluid in peritoneal cavity.
Pre operative management
• NPO and head end elevation.
• Insert OG tube and ensure continous
aspiration.
• If drainage is more than 10ml/kg per 12 hr
shift,replace the volume loss with equal
volume of NS.
Post operative management:
• IVF at maintenance level from 2nd POD along
with parenteral nutrition.
• Titrate fluids based on RFT ,weight and urine
specific gravity.
• Maintain Ng tube to contious suction and
measure output.Tube to be removed when
drainage is minimal and non bilious.
• After baby has pased stools start feeding with
small volumes and look abdominal distension .
References:
• Ashcrafts Pediatric Surgery, George W.
Holcomb, III, MD and Jerry D Murphy-5th
ed.p400-424.
• Avery’s Diseases of Newborn:Christine A
Gleason,Sherin Devaskar,9e.
• The PGI NICU,Handbook of Protocols,4e.
• Nelson Textbook of Pediatrics,20e.
THANK YOU

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Intestinal obstruction Neonates

  • 2. • B/O Shivamma • 6 days /Female • Holalkere,Chitradurga • Was referred to our hospital from Basaveshwara Medical college,Chitradurga with provisional diagnosis of Malnourishment with Intestinal obstruction.
  • 3. • Chief complaints:Vomiting from D5 of life • Baby had 8-10 episodes of vomiting which was not associated with feeding,non projectile,bilious in nature. • No h/o constipation,delayed passage of meconium or abdominal distension. • No h/o poor feeding ,lethargy,convulsion,hurried breathing,dcereased urine output.
  • 4. Birth history: • G2P2L1. • Married life-4 ½ years,NCM,Elder sibling 3 yr old male ,apparently healthy. • Concieved spontaneously.Had regular ANC in C’durga Govt hospital.Taken iron and folic acid suuplements.Immunised with 2 doses of TT. • Antenatal USG- was not reviewed at admission • No h/o maternal GDM,PE or Hypothyroidism.
  • 5. • Baby born via naturalis at 6:15 am on 03/08/16 in C’durga govt hospital. • B. wt-2.85kg. • Cried immediately after birth,was breast fed within one hour of birth. • Baby passed meconium and urine within 24 hours . • Baby has passed stool around 2-3 times/day. • No episode of vomiting noted upto D5 of life.
  • 6. On Examination: • PR-148/min Good volume and regular, RR-52/min , CRT<3 sec .Temp- 99 F. • Icterus upto Zone 3. • No pallor, cyanosis or edema. • Cry reflex and activity-Good. • Anthropometry:Wt-2.7kg, Length-49cm,OFC- 34cm. • Head to toe examination-No dysphormic features.
  • 7. Systemic examination: Per Abdomen Examination: • RTA-3ml of bilious aspirate. • Soft ,mildly distended ,non tender. • Skin over abdomen-Normal. • No dilated vein over abdomen. • No organomegaly,no palpable mass. • Anal opening patent. • Bowel sounds-heard.2-3/min
  • 8. CVS: • S1 S2 heard. • Systolic murmur best heard Lt lower sternal border @ 4th ICS. R/S: • No retractions ,B/L air entry adequate. • No crepitations. CNS: • AF-2*2 cm open at level • Cry refelex and activity –Good. • Moro reflex-Complete and symetrical
  • 9. S/L/T/AGA/F WITH ACUTE INTESTINAL OBSTRUCTION-SMALL INTESTINAL ?MALROTATION ?DUODENAL ATRESIA/STENOSIS WITHOUT PERFORATION OR PERITONITIS, WITH CAHD –SMALL VSD ,LT TO RT SHUNT,IN SINUS RHYTHM WITHOUT CCF. PROVISONAL DIAGNOSIS:
  • 10. Course in hospital and Investigations: • Baby was kept NPO and ryle tube was inserted • Baby was started on first line antibiotics. • Surgical reference was taken and as per advice 2hrly RTA aspirate was done and barium meal follow through was planned for next day.
  • 11. CBC: • Hb-13.6 gm/dl,TLC-1580/mm3, PMN-53%,Platelet count-3.45 lakh/mm3 • Serum sodium-142.9mEq/L,Pottasium-3.8mEq/L • CRP-20.6mg/L • RFT-WNL. • Chest X ray-R UL opacity. • Echo-Small ASD with Small PDA,normal biventricular function. • In view of positive septic screen and upper lobe opacity baby was changed to second line antibiotics.
  • 12.
  • 13. • Barium meal done on D2 of admission showed no e/o malrotation or intestinal obstruction. • Baby had no further episodes of vomiting but continued to have bilious RTA of 60 ml/24hr on D2 of admission. • Baby continued to pass 3-4 stools/day.
  • 14. With these findings:Normal Barium meal and positive septic screen.Diagnosis was revised to: TERM/AGA/LATE ONSET SEPSIS WITH Rt UPPER LOBE CONSOLIDATION ? Aspiration WITH SEPTIC PARALYTIC ILEUS with ASD and Small PDA
  • 15. • Baby was contiued on 2nd line antibiotics. • At D6 of admission RTA aspirate was bilious 8ml/24 hrs and abdomen was soft and non distended. • Stomach wash was given and baby started on small feeds 5ml through spoon along with cover of motility agent domperidone. • Baby had abdominal distension after 20ml feeds ,2 feeds were skipped and then again restarted. • Feeds gradually increased and baby was directly BF at D9 of admission.
  • 16. • On D10 of admission baby had multiple episodes of bilious vomiting. • Baby was kept NPO and USG abdomen was planned .
  • 17.
  • 18. With report of USG repeat contrast meal follow through was planned .
  • 19. TERM/AGA/SMALL INTESTINAL PARTIAL OBSTRUCTION?STENOSIS-WEB WITH ASPIRATION PNEUMONIA OF RT UL WITH CAHD –ASD WITH SMALL PDA WITHOUT CCF
  • 20. • Baby was operated on D12 of admission. • On table findings-proximal duodenal dilation found.Dodenal web was found near DJ junction. • Procedure:Explorative laprotomy+web excision+duodenoplasty
  • 21. Post op course • Baby had RTA about 30-40 ml/day which gradually decreased on POD5. • Baby was started on spoon feeds on POD6. • Baby was discharged on 30/08/16 at POD 10 . • Duration of hospital stay-22 days. • Admission wt-2.7kg • Discharg wt-2.63kg(@ D27 of life)
  • 22. Follow up: • Baby is admiited 3 days(28 DOL) back with c/o of bilious vomiting. • Admissiion weight-2.5kg • Antenatal scan were reveiwed at this admission.
  • 23.
  • 24. “HINDSIGHT IS ALWAYS BETTER THAN FORESIGHT” “Before ,you are wise;after, you are wise .In between you are otherwise”-
  • 25. Looking back was everything done perfectly??? • Delivery at tertiary care center. • Missed antenatal USG scan. • First barium meal was reported as normal??? • Delayed diagnosis –prolonged stay.
  • 26. Intestinal obstruction in newborn • Congenital intestinal obstruction occurs approximately 1 :2000 live births. • Accounts upto 1/3 of admissions to neonatal surgical units. • Success or failure in terms of morbidity or mortality depends not much on pinpointing the exact location of lesion but on correctly diagnosing obstruction as cause of clinical symptoms and instituting prompt operative intervention.
  • 27. Causes of intestinal obstruction Congenital Acquired Functional Atresia NEC Hirschprung disease Stenosis Intusucception Meconium plug syndrome Meconium ileus Peritoneal adhesions Ileus Anorectal malformations Peritonitis Enteric duplications Volvulus Peritoneal bands Annular pancreas Cyst and tumors
  • 28. When to suspect Intestinal obstruction???? 1.Antenatally diagnosed intestinal obstruction a)Antenatal USG showing double bubble appearance. b)Dilated bowel loops >15mm in length and 7mm in diameter c)Whirlpool appearance to bowel and mesentry may indicate malrotation with volvulus. d)Polyhydramnios
  • 29. 2)Family history of Hirschprung disease and jejunal atresia. 3)Gastric aspirate >20 ml at birth. 4)Delayed passage of meconium in term or near term baby-Hirschprung ,meconium ileus,meconium plug syndrome,SLCS. 5)Vomiting- • Neonates with bilious vomiting are supposed to have intestinal obstruction unless proved otherwise. • Onset after birth is delayed the more distal obstructuion is preceded by progressive abdominal distension 6)Mass abdomen-Duplication cysts,pouch colon
  • 30. Nature of vomiting and D/D s Non bile stained with abdominal distension Pyloric atresia/stenosis,pre duodenal variety of duodenal atresia Non bilious without abdominal distension GER,CDH,prematurity ,sepsis Bilious vomiting-Surgical causes Malrotation,duodenal stenosis or atresia, Proximal jejunal atresia Bilious vomiting-other causes Intestinal ileus due to electrolyte imbalance or sepsis
  • 31. Approach to intestinal obstruction
  • 32. Radiological diagnosis • Obtain AXR- AP and cross table lateral view. • Erect abdominal view is done in case of non sick babies. • A prone cross table lateral view should be done at >24 hrs after birth for suspected ARM
  • 33. Normal progression of air in intestine: Stomach First breath Duodenum Second or third breath Proximal small bowel 1 hour Distal small bowel 3 hour Caecum 6hour Rectum 18-24 hour
  • 34. Characteristic signs of AXR Double Bubble appearance Duodenal atresia Triple bubble appearance Proximal jejunal atresia Uniformly dilated bowel loops with multiple air fluid levels Distal obstruction Ground glass or soap bubble appearnce. NEC,meconium ileus Speckled calcification Meconium ileus Mild double bubble with distal gas with 2nd part of duodenum to left of spine Malrotation
  • 35.
  • 36.
  • 37.
  • 38.
  • 39. Contrast enema:if clinical scenario and AXR suggest distal obstruction Microcolon Meconium ileus and SLCS Abnormal caecal position Malrotation Right sided colonic breaking Volvulus Abnormal rectosigmoid index Hirschprung disease
  • 40.
  • 41.
  • 42. Upper GI series: • Procedure of choice in diagnosing malrotation 1)Abnormally located D-J flexure-to the right of spine. 2)Proximal jejunum located in right side of abdomen. 3)Spiral corckscrew course of distal duodenum and proximal jejunum.
  • 43.
  • 44. Abdominal USG • Reversal of relation of SMA and SMV in malrotation. • Can also diagnose intussusception and free fluid in peritoneal cavity.
  • 45. Pre operative management • NPO and head end elevation. • Insert OG tube and ensure continous aspiration. • If drainage is more than 10ml/kg per 12 hr shift,replace the volume loss with equal volume of NS.
  • 46. Post operative management: • IVF at maintenance level from 2nd POD along with parenteral nutrition. • Titrate fluids based on RFT ,weight and urine specific gravity. • Maintain Ng tube to contious suction and measure output.Tube to be removed when drainage is minimal and non bilious. • After baby has pased stools start feeding with small volumes and look abdominal distension .
  • 47. References: • Ashcrafts Pediatric Surgery, George W. Holcomb, III, MD and Jerry D Murphy-5th ed.p400-424. • Avery’s Diseases of Newborn:Christine A Gleason,Sherin Devaskar,9e. • The PGI NICU,Handbook of Protocols,4e. • Nelson Textbook of Pediatrics,20e.