- •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
36 N. Samnakay and A. Barker
4.1 Epidemiology
Urinary tract infections (UTIs) are a common childhood condition. It is estimated that 2% of boys and 7% of girls will be diagnosed with a urinary UTI by age 6.1, 2
Under 1 year of age, boys are more likely to present with a UTI than girls; after this age, girls get UTIs more commonly than boys.1
4.2 Presentation
The very young infant and the preverbal child with a UTI usually present generally unwell with fever, vomiting and lethargy. Up to 13% of infants with fever of unknown origin will have a UTI, so one must always suspect UTI as a possible diagnosis in the unwell child.3
The older child may present with localized signs and symptoms more specific to a UTI, such as loin pain, suprapubic pain or dysuria.
4.3 Diagnosis and Workup
Apart from the general history of the presenting complaint, specific aspects of history in a child with a UTI are important:
•Antenatal history
In particular, any antenatal hydroureteronephrosis or bladder abnormalities at any stage of gestation. As these findings are usually filed in the mother’s obstetric notes, they may not be available without an effort to trace them.
Management will change if there is a known antenatally diagnosed urinary tract anomaly. On the other hand, we feel that a normal antenatal scan does not obviate the need for a renal tract ultrasound in a child with a UTI.
•History of previous UTIs
•History of predisposing conditions such as renal stones, congenital structural anomalies and spina bifida
Chapter 4. Urinary Tract Infection: Australasia |
37 |
•Urinary stream and voiding pattern – is there dysfunctional voiding?
•History of constipation
•Family history of urinary tract anomalies and vesicoureteric reflux (VUR)
Examination should also include looking for loin tenderness, a palpable bladder or kidneys and the appearance of the external genitalia. The back should be inspected for evidence of occult spinal dysraphism.
The diagnosis of UTI is made with a urine sample. The acutely unwell baby or infant with fever and poor feeding in Australia is often referred to the emergency department of a secondary or tertiary centre, where a full septic screen is performed.As much as possible,a urine sample should be obtained as a clean catch. A bag specimen has a high false positive rate due to contamination from the skin. A bag specimen is useful to exclude a UTI if the collected urine is culture negative; however, one should be suspicious of a UTI if bacteria, protein and white cells are present in the bag specimen and obtain a clean catch if possible. If a clean catch cannot be obtained, a suprapubic aspirate or catheter specimen should be obtained.
Urine should be sent off for urgent microscopy and culture in the unwell young infant; in the older child, it may be sent off for routine microscopy, culture and sensitivities. Bacteria seen on microscopy are 93% sensitive and 95% specific for a UTI. Positive nitrites on a dipstick are 99% specific in predicting a UTI, but if nitrites are negative, they are only 60% sensitive in ruling out a UTI.4
4.4 Management
Empirical treatment with antibiotics is usually commenced after specimen collection, and adjusted accordingly once results are through. The majority of UTIs (>80%) are due to Escherichia coli, with the remaining being due to
Proteus, Klebsiella, and Enterococcus. Pseudomonas and
Staphylococcus UTIs are uncommon and considered atypical.5
38 N. Samnakay and A. Barker
Generally children with temperatures over 38°C, loin pain and tenderness with positive urine cultures are considered to have an upper tract infection and are treated with intravenous antibiotics; older children with temperatures under 38°C, dysuria and frequency with positive urine cultures and no loin pain or tenderness, are considered to have cystitis and treated with oral antibiotics.
4.5 Investigations after First UTI in a Child
Studies suggest that 21–50% of children with a UTI will have an underlying abnormality.3 It is estimated that about 10% of children presenting with a UTI will have an abnormal ultrasound finding which may or may not affect management.6 This includes abnormalities such as pelviureteric junction obstruction, vesicoureteric junction obstruction and posterior urethral valves in boys. For this reason, we recommend that all children presenting with an initial UTI should have a renal tract ultrasound (USS). A renal tract USS after initial UTI should be performed even if there is a history of normal antenatal ultrasound scans.
Up to 30% of children presenting with a UTI will have underlying vesicoureteric reflux (VUR).6 90% of this VUR is lower grades, I to III. USS is not useful for assessing the presence or grade of VUR. A micturating cystourethrogram or MCU is the most useful test to assess for and grade VUR. An MCU is performed by catheterizing the bladder urethrally and filling it with contrast, followed by imaging during voiding. Sedation may be required in some cases.
VUR and UTIs are associated with renal damage, scarring and hypertension. It is estimated that 5% of children presenting with UTI will have associated renal scarring.7 Delay in the diagnosis and treatment of UTIs, and recurrent UTIs correlate more with renal scarring. However, it is now well known that renal scarring in children with VUR may be present even before a clinical UTI, suggesting pre-existing scarring or dysplasia of the kidney. This is especially
Chapter 4. Urinary Tract Infection: Australasia |
39 |
common in young male infants with VUR. On the other hand, children with VUR and UTIs may not acquire renal scarring, whilst some children with no proven VUR may acquire renal scarring after UTIs. With these variations, it is difficult to obtain data about the true risks of UTIs and the true role of associated VUR in the development of renal scarring.
The American Academy of Pediatrics recommends USS and MCU for all children presenting with their first UTI between ages of 2 months and 2 years.8 When significant VUR is found it is treated surgically with either endoscopic ureteric injection or open ureteric reimplantation.
The Royal College of Physicians in the UK in 1991 recommended screening children under 1 year of age with a renal USS, MCU as well as a Dimercaptosuccinic acid scan (DMSA) after a first UTI.9 The more recent UK NICE guidelines from 2007 have changed this traditional view. In essence, the guidelines recommend imaging after a first UTI in children should be more directed and selective, based on factors such as the age of the child, whether the UTI was typical or atypical and the response to treatment.10 One must remember that guidelines such as NICE are guides and are not meant to be prescriptive, so individual cases must be dealt with on their merits.
There are no set guidelines in Australia, and Australian practice in terms of imaging children after their first UTI varies from centre to centre and practitioner to practitioner.11
Our practice currently is to always obtain a renal USS after an initial UTI. An MCU should also be obtained in the following situations:
•Known anomaly on antenatal ultrasound scan – especially if dilated ureters are visible or a bladder or urethral abnormality is suspected
•Abnormality noted on the post-UTI renal ultrasound scan
•In any boy with any degree of bilateral hydronephrosis, or history of poor stream or voiding difficulties – to exclude the possibility of posterior urethral valves (Fig. 4.1)
40 N. Samnakay and A. Barker
•Strong family history of VUR and reflux nephropathy
•Recurrent UTIs
•Atypical UTI organism
•Severe UTI requiring IV antibiotics
•Geographical factors – Children in rural and remote areas of Australia who have to travel long distances to specialist health care, often need to be transferred to regional centers for their post-UTI investigations. In such children, it may be prudent to perform an MCU whilst they are at the regional centre even if they have a normal USS after a first UTI.
A DMSA scan is performed in children who have documented VUR on the MCU or the appearance of renal scarring suggested on ultrasound scan. The DMSA scan will give
FIGURE 4.1. MCU of 6 year old boy whose first UTI in infancy was treated but not followed up with imaging. It shows a severely dilated posterior urethra (PU), trabeculated bladder (B) and VUR on the left (V). The boy had posterior urethral valves.