- •Guide to Pediatric Urology and Surgery in Clinical Practice
- •Preface
- •Contributors
- •Key Points
- •1.1 Introduction
- •1.2 Risk Factors
- •1.3 Presentation
- •1.4 Diagnosis
- •1.5 Common Pathogens
- •1.6 Treatment
- •1.7 Imaging
- •1.8 Indications for Referral
- •Suggested Reading
- •Key Points
- •2.1 Introduction
- •2.2 Pathogenesis
- •2.3 Establishing the Diagnosis
- •2.4 Acute Management
- •2.5 Once the Diagnosis Is Established
- •2.6 Long Term Management
- •References
- •Key Points
- •3.1 Introduction
- •3.2 Aetiology
- •3.3 Pathogenesis and Risk Factors
- •3.4 Classification
- •3.5 Signs and Symptoms
- •3.6 Diagnosis
- •3.7 Imaging Studies
- •3.8 Ultrasound Scan (USG)
- •3.9 Voiding Cystourethrography (VCUG)
- •3.10 Dimercapto-Succinic Acid Scan (DMSA)
- •3.11 Treatment
- •3.12 Prophylaxis and Prevention
- •References
- •Key Points
- •4.1 Epidemiology
- •4.2 Presentation
- •4.3 Diagnosis and Workup
- •4.4 Management
- •4.5 Investigations after First UTI in a Child
- •4.6 Prevention of UTIs
- •4.7 Managing VUR and UTIs
- •References
- •Key Points
- •5.1 Introduction
- •5.2 Common Abnormalities of the Scrotum
- •5.4 Indications for Referral
- •Suggested Readings
- •Key Points
- •6.1 Introduction
- •6.2 Common Foreskin Conditions
- •6.3 Treatment of Conditions of the Foreskin
- •6.4 Indications for Referral
- •References
- •Key Points
- •7.1 Hypospadias
- •7.1.1 Introduction
- •7.1.2 Management Issues
- •7.1.3 Indications and Timing of Referral
- •7.1.4 Complications of Surgery
- •7.2 Epispadias
- •Key Points
- •7.2.1 Introduction
- •7.2.2 Management Issues
- •7.2.3 Surgery, Common complications, and Postoperative Issues
- •7.3 Concealed Penis
- •7.3.1 Introduction
- •7.3.2 Referral and Treatment
- •7.3.3 Complications
- •7.3.4 Benign Urethral Lesions in Boys
- •7.3.5 Treatment
- •7.3.6 Follow-Up After Treatment
- •Key Points
- •References
- •Key Points
- •8.1 Introduction
- •8.2 Common Conditions
- •8.3 Treatment of Undescended Testis
- •8.4 Indications for Referral
- •References
- •Key Points
- •9.1 Natural History of the Prepuce
- •9.2 Benefits of Circumcision
- •9.3 Absolute Indications for Circumcision
- •9.4 Relative Indications for Circumcision
- •9.5 Surgical Options
- •9.6 Contraindications to Circumcision
- •9.7 Complications of Circumcision
- •9.8 Conclusion
- •References
- •Key Points
- •10.1 Introduction
- •10.2 Labial Adhesions
- •10.3 Interlabial Masses
- •10.4 Paraurethral (Skene’s Duct) Cyst
- •10.5 Imperforate Hymen with Hydrocolpos
- •10.6 Prolapsed Ectopic Ureterocele
- •10.7 Urethral Prolapse
- •10.8 Urethral Polyp
- •10.10 Vaginal Discharge and Vaginal Bleeding
- •References
- •Key Points
- •11.1 Introduction
- •11.2 Functional LUTS
- •11.2.1 Overactive Bladder
- •11.2.2 Dysfunctional Voiding
- •11.2.3 Underactive Bladder
- •11.2.4 Uroflowmetry
- •11.2.5 Treatment
- •11.2.5.1 Standard Outpatient Urotherapy
- •11.2.5.2 The Failed Training
- •11.2.6 Giggle Incontinence, Incontinentia Risoria
- •References
- •Key Points
- •12.1 Introduction
- •12.1.1 Definition
- •12.1.2 Prevalence
- •12.1.3 Causes
- •12.1.4 Monosymptomatic Enuresis
- •12.1.4.1 Genetics
- •12.1.4.2 Sleep
- •12.1.4.3 Sleep-Disordered Breathing
- •12.1.4.4 Small Functional Bladder Capacity
- •12.1.4.5 Psychological/Behavioral
- •12.1.5 Nonmonosymptomatic (Organic) Enuresis
- •12.1.5.2 Polyuria
- •12.1.5.3 ADH Secretion
- •12.1.5.4 Food Sensitivity
- •12.2 Investigations
- •12.2.1 History
- •12.2.2 Physical Examination
- •12.2.3 Laboratory Tests
- •12.2.4 Imaging Studies
- •12.2.5 Evaluation of Functional Capacity
- •12.3 Conventional Treatment
- •12.3.1 Behavioral Therapy
- •12.3.2 Alarm Therapy
- •12.3.3 Pharmacologic Therapy
- •12.4 Alternative Treatment
- •12.5 Conclusion
- •12.5.1 Areas of Uncertainty
- •12.5.2 Guidelines
- •References
- •Key Points
- •13.1 Introduction
- •13.2 Definition of Constipation
- •13.3 Evaluation
- •13.4 Treatment of Constipation
- •13.5 Indications for Referral
- •Suggested Readings
- •Key Points
- •14.1 Hematuria
- •14.1.1 Important Points in the History
- •14.1.2 Causes of Hematuria
- •14.1.3 Investigations
- •14.1.4 Management
- •14.2 Proteinuria
- •14.2.1 Quantification of Proteinuria
- •14.2.2 Causes of Proteinuria
- •14.2.2.1 Non-Pathological Proteinuria
- •14.2.2.2 Orthostatic Proteinuria (Postural Proteinuria)
- •14.2.2.3 Pathological Proteinuria
- •14.2.3 Investigations
- •References
- •Key Points
- •15.1 Introduction
- •15.2 Indications for Referral
- •References
- •Key Points
- •16.1 Introduction
- •16.2 Treatment of Angular Dermoid
- •16.3 Indications for Referral
- •16.4.1 Introduction
- •Suggested Reading
- •Key Points
- •17.1 Introduction
- •17.2.1 Thryoglossal Duct Cyst
- •17.2.2 Midline Dermoid Cyst
- •17.2.3 Lymph Nodes
- •17.2.4 Thyroid Nodule
- •17.2.5 “Plunging” Ranula
- •17.2.6 Investigations
- •17.3 Treatment
- •17.3.1 Thryoglossal Duct Cyst
- •17.3.2 Midline Dermoid Cyst
- •17.3.3 Lymph Nodes
- •17.3.4 Plunging Ranula
- •Key Points
- •18.1 Introduction
- •18.2.1 Lymph Nodes
- •18.2.1.1 Infective
- •18.2.1.2 Inflammatory
- •18.2.1.3 Neoplastic
- •18.2.2.1 Investigations
- •Key Points
- •19.1 Introduction
- •19.2 Etiology and Types of Torticollis
- •19.3 Treatment of Torticollis
- •19.4 Indications for Referral
- •Suggested Readings
- •Key Points
- •20.1 Introduction
- •20.2 Common Umbilical Conditions
- •20.4 Indications for Referral
- •20.5 Epigastric Hernia
- •20.5.1 Introduction
- •References
- •Key Points
- •21.1 Introduction
- •21.2 Common Sources of Abdominal Pain
- •21.2.1 Children
- •21.2.2 Infants
- •21.3 Treatment of Conditions
- •21.4 Indications for Surgical Referral in Children with Abdominal Pain
- •References
- •Key Points
- •22.1 Introduction
- •22.2 History
- •22.3 Physical Examination
- •22.4 Laboratory Tests
- •22.5 Diagnostic Imaging
- •Suggested Readings
- •Key Points
- •23.1 Introduction
- •23.2 Investigations
- •23.3 Treatment
- •References
- •Key Points
- •24.1 General Principles
- •24.2 Neonates and Newborn
- •24.3 Infants and Young Toddlers
- •24.4 Older Children
- •24.5 Conclusion
- •References
- •Key Points
- •25.1 Introduction
- •25.3 Neonatal Intestinal Obstruction (Distal)
- •25.4 Childhood Intestinal Obstruction
- •References
- •26.1 Introduction
- •26.3 Initial Management
- •26.4 Causes of Neonatal Bilious Vomiting
- •Key Points
- •26.6 Necrotizing Enterocolitis
- •26.7 Duodenal Atresia
- •26.8 Small Bowel Atresia
- •26.9 Meconium Ileus
- •26.10 Hirschsprung’s Disease
- •26.11 Anorectal Malformations
- •26.12 Conclusion
- •References
- •Key Points
- •27.1 Introduction
- •27.2 Presentation
- •27.3 Investigations
- •27.4 Management
- •References
- •Key Points
- •28.1 Introduction
- •28.2 Presentation
- •28.3 Investigations
- •28.4 Management
- •28.5 Surgical Management
- •References
- •Key Points
- •29.1 Introduction
- •29.2 Types of Vascular Anomalies
- •29.3 Investigation of Vascular Anomalies
- •29.4 Treatment of Vascular Anomalies
- •29.5 Indications for Referral
- •Suggested Readings
- •Index
Chapter 26. Unique Considerations in the Neonate and Infant |
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Ninety-five percent of term neonates pass meconium within the first 24 h and almost all by 48 h. Premature babies may have delayed passage of meconium. A neonate born in meconium-stained liquor has passed meconium but beware of green stained liquor. This may represent fetal vomiting of green bile into the amniotic fluid and therefore obstruction.
Neonates who may pass meconium but who may still have bowel obstruction include:
1.Babies with Hirchsprung’s may pass meconium, especially after rectal examination
2.Some sticky meconium pellets may be passed in meconium ileus
3.Onset of symptoms in malrotation with volvulus may be delayed for some time after birth3
4.A missed anorectal malformation with a fistula
26.3 Initial Management
At this stage the diagnosis may or may not be known but there are certain management steps that are common to all neonates with bilious vomiting:
Initial management
Pass a nasogastric tube |
Commence iv fluids |
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• |
8 or 10 Fr in a term baby |
Commence iv antibiotics |
• |
Aspirate and leave on free |
• as per local guidance |
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drainage |
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(Septic screen ± lumbar puncture)
26.4 Causes of Neonatal Bilious Vomiting
The following is a (non-exhaustive) list of causes of bilious vomiting in the neonate. If a malrotation with volvulus is missed then the consequences, i.e., dead midgut, are disastrous and it is for this reason that any child with bilious vomiting should be referred urgently to a pediatric surgeon.
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R.T. Peters and S.S. Marven |
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Causes |
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Medical |
High obstruction |
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• |
Necrotizing enterocolitis |
• |
Malrotation ± volvulus |
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• |
Sepsis |
• |
Duodenal atresia/stenosis |
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– |
Urinary tract infection |
• |
Proximal jejunal atresia |
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– |
Meningitis |
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– |
Group B streptococcus |
Low obstruction |
• |
Raised intracranial pressure |
• |
Hirschsprung’s disease |
• |
Hypothyroidism |
• |
Ileal/colonic atresia |
• |
Prematurity |
• |
Anorectal malformation |
• |
Idiopathic bilious vomiting |
• |
Meconium ileus |
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• |
Meconium plug |
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syndrome |
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• |
Small left colon |
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syndrome |
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• |
Hernia |
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26.5 Malrotation With/Without
Midgut Volvulus
Malrotation is failure of the gut to complete anti-clockwise rotation resulting in the entire small bowel lying attached by a narrow stalk rather than a broad based mesentery to the posterior abdominal wall. It is therefore prone to twist around on this stalk which compromises the blood supply (superior mesenteric vessels) of most of the small bowel - a midgut volvulus. Up to 80% of cases of malrotation present in the first month of life and most of these in the first week.4 Therefore a previously apparently normal neonate (or child of any age) can present with a midgut volvulus. This is one of the reasons for urgency of referral
Chapter 26. Unique Considerations in the Neonate and Infant |
245 |
in bilious vomiting. If a midgut volvulus is missed then the entire midgut can become unviable. At best this leads to short gut and lifelong parenteral nutrition, at worst, death. Plain abdominal x-ray may show dilated stomach and proximal duodenum but may also be entirely normal in malrotation. The diagnostic modality of choice is an upper GI contrast study. This demonstrates the duodenal-jejunal flexure lying to the right of the spine and inferior to the duodenal bulb. Treatment involves urgent laparotomy with resection of any dead gut and Ladd’s procedure (Figs. 26.2 and 26.3).
FIGURE 26.2. Upper gastrointestinal contrast study demonstrating malrotation. The duodenal-jejunal flexure lies to the right of the spine.
246 R.T. Peters and S.S. Marven
FIGURE 26.3. Dead gut found at operation for malrotation with midgut volvulus.
26.6 Necrotizing Enterocolitis
This is almost exclusively a disease of preterm infants (although it can occur at term) and is therefore uncommon outside of the neonatal unit. Necrotizing enterocolitis (NEC) consists of bowel wall inflammation and ulceration which may proceed to perforation. Neonates present generally unwell with apneas and bradycardias, green vomiting and temperature instability. The abdomen may be distended and shiny or erythematous and there may be rectal bleeding. Abdominal radiograph features include distended bowel loops, intramural gas (pneumatosis intestinalis), portal vein gas and pneumoperitoneum. Management is mostly undertaken by the neonatology team and consists of stopping enteral feeds, a nasogastric tube on free drainage and antibiotics. Complicated NEC may require surgical intervention including perforation and stricture formation. Mortality for NEC with perforation remains between 30% and 50%.5