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100+ Free ABU Pediatric Urology Practice Questions

Pass your ABU Pediatric Urology Subspecialty Certification exam on the first try — instant access, no signup required.

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~85-90% first-time among pediatric urology fellowship graduates (ABU annual statistics) Pass Rate
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Using the Society for Fetal Urology (SFU) grading system for antenatal hydronephrosis, Grade 3 is defined by which finding?

A
B
C
D
to track
2026 Statistics

Key Facts: ABU Pediatric Urology Exam

~150-200

Total MCQ Items

ABU Pediatric Urology Subspecialty Examination

~4-6 hr

Total Exam Time

1-day computer-based test including breaks

~8%

VUR Weight

Largest single domain tied with oncology on 2026 ABU outline

~$1,800

2026 Subspecialty Exam Fee

ABU (verify current schedule)

1-2 yr

Fellowship Length

ACGME-accredited pediatric urology fellowship

~85-90%

First-Time Pass Rate

ABU annual subspecialty statistics (fellowship graduates)

The ABU Pediatric Urology Subspecialty Exam is a 1-day computer-based test from the American Board of Urology comprising ~150-200 single-best-answer MCQs over ~4-6 hours at Pearson VUE. Content spans VUR (~8%), pediatric GU oncology (~8%), neurogenic bladder (~7%), DSD (~7%), PUV (~6%), cryptorchidism (~6%), hypospadias (~6%), UTI (~5%), GU trauma (~5%), voiding dysfunction (~4%), exstrophy (~4%), duplication (~4%), hydronephrosis/UPJ (~3%), stones (~3%), acute scrotum (~3%), and circumcision (~3%). Subspecialty Examination fee is ~$1,800; requires ABU primary certification plus an ACGME-accredited pediatric urology fellowship.

Sample ABU Pediatric Urology Practice Questions

Try these sample questions to test your ABU Pediatric Urology exam readiness. Each question includes a detailed explanation. Start the interactive quiz above for the full 100+ question experience with AI tutoring.

1Using the Society for Fetal Urology (SFU) grading system for antenatal hydronephrosis, Grade 3 is defined by which finding?
A.Mild dilation of the renal pelvis only with no calyceal involvement
B.Dilation of the renal pelvis plus all of the calyces with preserved renal parenchymal thickness
C.Dilation of the renal pelvis, all calyces, and associated parenchymal thinning
D.A normal renal pelvis of less than 4 mm
Explanation: SFU grading: Grade 0 (no dilation), Grade 1 (pelvis only), Grade 2 (pelvis + some calyces), Grade 3 (pelvis + all calyces with normal parenchyma), Grade 4 (pelvis + all calyces + parenchymal thinning). Grade 3-4 warrant additional imaging such as MAG3 diuretic renography.
2When should the first postnatal renal-bladder ultrasound be obtained in a neonate with antenatal hydronephrosis who has no high-risk features?
A.Within the first 24 hours of life
B.At 48 hours to 1 week, and repeated at 4-6 weeks
C.Only at 6 months of age
D.At 1 year of age
Explanation: The first 24-48 hours after birth is a period of relative oliguria and can falsely underestimate dilation. Consensus recommendations (SFU/AUA) obtain the first RBUS after 48 hours (often 3-7 days), then repeat at 4-6 weeks. Exceptions (obtain urgently) include bilateral severe hydronephrosis, solitary kidney, oligohydramnios, or suspected PUV.
3What is the most common cause of antenatal hydronephrosis?
A.Posterior urethral valves
B.Ureterocele
C.Transient/physiologic hydronephrosis
D.Multicystic dysplastic kidney
Explanation: Transient or physiologic hydronephrosis accounts for 50-70% of cases and typically resolves spontaneously. UPJ obstruction is the most common pathologic cause, followed by VUR, megaureter, multicystic dysplastic kidney, ureterocele/duplex, and posterior urethral valves.
4A 3-month-old has SFU grade 4 unilateral hydronephrosis with a MAG3 t1/2 of 45 minutes and a differential renal function of 38% on the affected side. What is the most appropriate management?
A.Immediate pyeloplasty
B.Observation with serial ultrasound and renal function studies
C.Percutaneous nephrostomy
D.Nephrectomy
Explanation: Indications for pyeloplasty in UPJ obstruction include differential function <40% with declining trend, decrease of >10% on serial scans, worsening hydronephrosis, symptomatic obstruction, or febrile UTIs. An initial DRF of 38% with only one study is not an absolute indication; observation with close follow-up is reasonable while monitoring for deterioration.
5Which surgical technique is considered the gold standard open repair for UPJ obstruction in children?
A.Anderson-Hynes dismembered pyeloplasty
B.Culp-DeWeerd spiral flap
C.Foley Y-V plasty
D.Endopyelotomy
Explanation: The Anderson-Hynes dismembered pyeloplasty (excision of the UPJ, spatulation, and dependent anastomosis) has >95% success and is considered the reference standard. It can be performed open, laparoscopically, or robotically. Endopyelotomy is less successful in children and reserved for select secondary cases.
6The RIVUR trial (2014, NEJM) demonstrated which outcome for children with vesicoureteral reflux randomized to trimethoprim-sulfamethoxazole prophylaxis?
A.A 90% reduction in renal scarring
B.No difference in recurrent UTI rates
C.Approximately a 50% reduction in recurrent UTIs but no significant reduction in new renal scarring
D.Increased rate of renal scarring
Explanation: The NIH-funded RIVUR trial enrolled 607 children with VUR (grades I-IV) after febrile/symptomatic UTI. Prophylaxis reduced recurrent UTI by ~50% (HR ~0.50) but did not significantly reduce new renal scarring. The trade-off is an increased prevalence of resistant organisms in breakthrough infections.
7According to the AUA VUR guideline, which grade of reflux is defined by dilation of the ureter, pelvis, and calyces with preservation of papillary impressions?
A.Grade I
B.Grade II
C.Grade III
D.Grade V
Explanation: International Reflux Study grading: Grade I (ureter only, no dilation), Grade II (ureter, pelvis, calyces, no dilation), Grade III (mild/moderate dilation, papillary impressions preserved), Grade IV (moderate dilation, blunted fornices, maintained papillary impressions in the majority), Grade V (gross dilation and tortuosity, papillary impressions lost).
8What is the approximate spontaneous resolution rate by age 5 for unilateral grade II vesicoureteral reflux in children?
A.10-15%
B.30-40%
C.60-80%
D.Virtually 0%
Explanation: Spontaneous resolution depends on grade, laterality, and age. Low grade unilateral VUR (grades I-II) resolves in roughly 70-80% of children by age 5. Grades III-IV resolve in ~30-50%, and grade V rarely resolves without intervention.
9Which surgical technique for ureteral reimplantation uses a transvesical, cross-trigonal submucosal tunnel?
A.Cohen cross-trigonal
B.Politano-Leadbetter
C.Lich-Gregoir
D.Glenn-Anderson
Explanation: Cohen cross-trigonal reimplantation creates a transverse submucosal tunnel across the trigone. Politano-Leadbetter uses a combined intra/extravesical approach with a new hiatus. Lich-Gregoir is a purely extravesical detrusorrhaphy. Glenn-Anderson uses a distal submucosal advancement.
10Endoscopic subureteric injection (e.g., Deflux — dextranomer/hyaluronic acid) has approximately what single-session success rate for grade III VUR?
A.~30%
B.~50-70%
C.~95%
D.Less than 10%
Explanation: Single-injection success varies by grade: ~80-90% for grade I-II, ~70% for grade III, ~60% for grade IV, and 30-50% for grade V. Open ureteral reimplantation success is ~98-99% across grades and remains the definitive option.

About the ABU Pediatric Urology Exam

The ABU Pediatric Urology Subspecialty Certification Examination validates advanced knowledge for independent pediatric urology practice. Content spans vesicoureteral reflux (AUA VUR Guideline, RIVUR trial, Deflux, ureteral reimplantation), posterior urethral valves (antenatal diagnosis, valve ablation, valve bladder syndrome), hypospadias (TIP/Snodgrass, MAGPI, two-stage Bracka), cryptorchidism (AUA guideline — orchiopexy 6-18 months, Fowler-Stephens), disorders of sex development (Chicago 2006 consensus, CAH, AIS, gonadal dysgenesis, Y-material gonadectomy), bladder exstrophy-epispadias complex (MSRE vs CPRE, pelvic osteotomy), pediatric GU oncology (Wilms/COG AREN, rhabdomyosarcoma, testicular tumors), neurogenic bladder (spina bifida, urodynamics, CIC, augmentation, Mitrofanoff), pediatric UTI (AAP 2011/2016 Guideline), GU trauma (AAST), antenatal hydronephrosis (SFU 0-4), UPJ obstruction, ureteral duplication (Weigert-Meyer), pediatric stones, acute scrotum and torsion, circumcision (AAP 2012), voiding dysfunction/enuresis, varicocele, pediatric renal transplantation, and female pediatric GU anomalies. Requires ABU primary certification plus an ACGME-accredited pediatric urology fellowship.

Questions

175 scored questions

Time Limit

1-day CBT (~4-6 hours including breaks)

Passing Score

Criterion-referenced scaled score set by ABU (modified Angoff standard)

Exam Fee

~$1,800 Pediatric Urology Subspecialty Examination fee (ABU 2026 — verify current schedule) (American Board of Urology (ABU) / Pearson VUE)

ABU Pediatric Urology Exam Content Outline

~8%

Vesicoureteral Reflux (VUR)

International Reflux Study Grade I-V, AUA VUR Guideline, RIVUR trial (NEJM 2014 — TMP-SMX or nitrofurantoin prophylaxis reduces recurrent febrile UTI ~50% in Grade I-IV VUR), endoscopic injection of dextranomer/hyaluronic acid (Deflux), ureteral reimplantation (Cohen cross-trigonal, Politano-Leadbetter, Lich-Gregoir extravesical), robotic-assisted reimplantation, top-down DMSA vs bottom-up VCUG, BBD (bladder-bowel dysfunction) treatment required before surgical correction.

~8%

Pediatric GU Oncology

Wilms tumor (COG AREN protocols — stage-based vincristine/dactinomycin ± doxorubicin ± radiation, WT1/WAGR 11p13/Denys-Drash/Beckwith-Wiedemann, favorable vs anaplastic histology, nephron-sparing for bilateral/syndromic), rhabdomyosarcoma GU (bladder/prostate/paratesticular, IRS Group I-IV, embryonal better than alveolar PAX3/7-FOXO1), neuroblastoma (MYCN amplification, INRG stage L1/L2/M/MS), testicular tumors (yolk sac — AFP elevated, teratoma, gonadoblastoma in DSD), Xp11 translocation RCC.

~7%

Neurogenic Bladder

Spina bifida/myelomeningocele, tethered cord, sacral agenesis, urodynamics (detrusor leak point pressure ≥40 cm H2O predicts upper-tract deterioration), CIC (clean intermittent catheterization) cornerstone, oxybutynin/anticholinergics, intradetrusor onabotulinumtoxinA, augmentation cystoplasty (ileal, sigmoid; complications — mucus, stones, perforation, electrolyte imbalance, long-term malignancy), Mitrofanoff appendicovesicostomy/Monti, MACE Malone antegrade continence enema, transitional urology.

~7%

Disorders of Sex Development (DSD)

Chicago 2006 consensus nomenclature, 46,XX DSD (CAH — 21-hydroxylase deficiency most common; salt-wasting with hyponatremia/hyperkalemia; elevated 17-OHP), 46,XY DSD (complete/partial androgen insensitivity — AR gene; 5-alpha-reductase deficiency — DHT deficiency; gonadal dysgenesis — Swyer SRY), sex chromosome DSD (mixed gonadal dysgenesis 45,X/46,XY; Klinefelter 47,XXY), ovotesticular DSD, Y-chromosome material and gonadoblastoma risk — prophylactic gonadectomy indicated, multidisciplinary team, genitoplasty timing controversy.

~6%

Posterior Urethral Valves (PUV)

Young Type I (>95%), antenatal findings (keyhole sign, bilateral hydroureteronephrosis, oligohydramnios/anhydramnios → Potter sequence with pulmonary hypoplasia), VCUG diagnostic gold standard postnatal, primary valve ablation (cold knife, Bugbee electrode), temporary vesicostomy or high diversion in small/sick neonates, valve bladder syndrome (noncompliant small-capacity, then myogenic failure with large-capacity hypocontractile bladder), POP-OFF mechanisms (VURD — unilateral reflux with dysplastic kidney), progression to CKD/ESRD, transplantation.

~6%

Cryptorchidism

AUA Cryptorchidism Guideline — orchiopexy by 6-18 months of age to optimize fertility and reduce malignancy risk; palpable (inguinal canal, superficial pouch) vs nonpalpable (laparoscopic exploration gold standard); Fowler-Stephens two-stage for high intra-abdominal testis; malignancy relative risk ~2-4x (seminoma most common; germ cell neoplasia in situ precursor); no preoperative imaging needed; retractile testis has normal exam cremasteric reflex; hCG and GnRH analogs rarely used.

~6%

Hypospadias

Classification — glanular, coronal, distal shaft (most common), midshaft, proximal/penoscrotal/perineal; chordee correction (degloving, dorsal plication, ventral grafting); TIP/Snodgrass tubularized incised plate (workhorse for distal); MAGPI meatal advancement; Mathieu flip-flap; onlay island flap; two-stage Bracka for severe proximal with severe chordee; staged buccal mucosa graft for redo; complications (urethrocutaneous fistula most common, meatal stenosis, urethral diverticulum, glans dehiscence, urethral stricture); optimal age 6-18 months.

~5%

Pediatric UTI

AAP 2011 UTI Guideline (reaffirmed 2016) — febrile UTI in age 2-24 months requires catheterized or suprapubic urine culture and renal-bladder ultrasound; VCUG reserved for recurrent febrile UTI or abnormal ultrasound; RIVUR trial supports prophylaxis in VUR I-IV; pathogens (E. coli >80%; Proteus in uncircumcised boys); circumcision reduces infant UTI risk ~10-fold; BBD evaluation and bowel regimen; DMSA for renal scarring assessment.

~5%

Genitourinary Trauma

AAST renal injury scale (Grade I-V); children more susceptible (less rib protection, proportionately larger kidneys, less perinephric fat, softer ribs); nonoperative management preferred for hemodynamically stable blunt injury even high-grade; contrast CT with 10-minute delayed phase to assess collecting system; pediatric pelvic fracture with posterior urethral injury (retrograde urethrogram, suprapubic cystostomy + delayed repair); straddle injury to anterior urethra; testicular rupture requires ultrasound then surgical exploration within 72 hours for salvage.

~4%

Voiding Dysfunction & Enuresis

ICCS terminology, primary monosymptomatic nocturnal enuresis (desmopressin short-term, enuresis alarm for durable response — first-line behavioral), dysfunctional voiding (staccato/interrupted flow, pelvic floor discoordination), Hinman syndrome (non-neurogenic neurogenic bladder), overactive bladder/urge incontinence (oxybutynin), underactive bladder, BBD (constipation management — PEG 3350 critical), biofeedback, pelvic floor physical therapy.

~4%

Bladder Exstrophy–Epispadias Complex

Spectrum from epispadias → classic bladder exstrophy → cloacal exstrophy (OEIS — omphalocele/exstrophy/imperforate anus/spinal); modern staged repair of exstrophy (MSRE — closure → epispadias repair → bladder neck reconstruction) vs complete primary repair of exstrophy (CPRE — Mitchell single-stage); pelvic osteotomy (anterior innominate or posterior iliac) for tension-free closure; Young-Dees-Leadbetter bladder neck for continence; augmentation if inadequate capacity; fertility and sexual function considerations; increased malignancy risk (adenocarcinoma).

~4%

Ureteral Duplication & Ectopia

Weigert-Meyer rule — upper pole moiety inserts inferomedial/ectopic (often obstructed or drains ectopically), lower pole inserts superolateral (typically refluxing); ectopic ureter (female — insertion below sphincter → continuous incontinence; male — always above sphincter, may cause epididymitis/seminal vesicle cyst); ureterocele (intravesical simple vs ectopic/extravesical complex); duplex management (endoscopic ureterocele incision, upper-pole heminephrectomy, ipsilateral ureteroureterostomy, common-sheath reimplantation).

~3%

UPJ Obstruction & Hydronephrosis

Antenatal hydronephrosis (SFU grading 0-4; Urinary Tract Dilation UTD classification — A1/A2-3 postnatal), MAG3 diuretic renography (T1/2 >20 min obstructive, 10-20 equivocal, <10 nonobstructive), Anderson-Hynes dismembered pyeloplasty (open, laparoscopic, robotic-assisted — now standard in many centers), indications for intervention (symptomatic, split function <40%, progressive hydronephrosis, UTI, stones), crossing lower-pole vessel, horseshoe kidney association.

~3%

Pediatric Stone Disease

Metabolic evaluation critical (24-hour urine Ca/Ox/Cit/Cys/Na; plasma bicarbonate for distal RTA; cystinuria SLC3A1/SLC7A9; primary hyperoxaluria type I AGXT; hypocitraturia); imaging (ultrasound first-line for children; low-dose CT if needed; MRU research); SWL, ureteroscopy with miniaturized scopes (4.5-6 Fr semirigid, flexible), mini-PCNL/micro-PCNL, increasing incidence in adolescents, dietary therapy (fluid, normal calcium, low sodium).

~3%

Acute Scrotum

Testicular torsion (6-hour window for viability; bell-clapper deformity bilateral risk; emergent scrotal exploration with contralateral orchidopexy; manual detorsion outward/lateral — open book), torsion of appendix testis (blue dot sign, self-limited NSAIDs), epididymitis (uncommon prepubertal — always evaluate for structural anomaly like ectopic ureter), idiopathic scrotal edema, incarcerated hernia, HSP (Henoch-Schönlein purpura), post-pubertal epididymo-orchitis (sexually transmitted — N. gonorrhoeae, C. trachomatis).

~3%

Circumcision & Foreskin Disorders

AAP 2012 Circumcision Policy — benefits outweigh risks (UTI, HIV/STI, penile cancer reduction); not routine recommendation, family decision; phimosis (physiologic — resolves by age 5; pathologic BXO/lichen sclerosus requires circumcision); paraphimosis (urologic emergency — manual reduction, dorsal slit if needed); complications (bleeding most common, infection, meatal stenosis, glans/urethral injury, skin bridges, buried penis); techniques — Gomco clamp, Mogen clamp, Plastibell, sleeve resection.

~2%

Varicocele & Renal Transplant

Adolescent varicocele ~15%, predominantly left-sided (left gonadal vein drains into left renal vein at 90 degrees; right varicocele — evaluate for retroperitoneal pathology); indications for repair (testicular size discrepancy >20% or 2 mL, pain, bilateral, abnormal semen analysis in older adolescents); microsurgical subinguinal preferred (lowest recurrence/hydrocele). Pediatric transplant indications (CAKUT — PUV/reflux nephropathy/dysplasia; FSGS; Alport); preemptive transplant preferred; small-child intraperitoneal approach; bladder optimization pre-transplant (CIC, augmentation) in valve/neurogenic patients.

~2%

Renal Anomalies, Megaureter & Female Pediatric GU

Multicystic dysplastic kidney (nonfunctioning, typically involutes; contralateral anomaly ~30% — VUR, UPJ); bilateral renal agenesis (Potter sequence fatal); horseshoe kidney (isthmus at L3, increased UPJ/Wilms/stones); ARPKD (PKHD1) and ADPKD (PKD1/PKD2); primary obstructive megaureter (distal adynamic segment — observation first, many resolve; tapering/plication with reimplant if persistent); labial adhesions (topical estrogen); MRKH vaginal agenesis; cloacal malformation (PSARP, total urogenital mobilization); OHVIRA/Herlyn-Werner-Wunderlich.

How to Pass the ABU Pediatric Urology Exam

What You Need to Know

  • Passing score: Criterion-referenced scaled score set by ABU (modified Angoff standard)
  • Exam length: 175 questions
  • Time limit: 1-day CBT (~4-6 hours including breaks)
  • Exam fee: ~$1,800 Pediatric Urology Subspecialty Examination fee (ABU 2026 — verify current schedule)

Keys to Passing

  • Complete 500+ practice questions
  • Score 80%+ consistently before scheduling
  • Focus on highest-weighted sections
  • Use our AI tutor for tough concepts

ABU Pediatric Urology Study Tips from Top Performers

1VUR and the RIVUR trial: International Reflux Study Grade I (ureter only) → V (grossly dilated ureter with loss of renal parenchyma). RIVUR (NEJM 2014) — children with Grade I-IV VUR on continuous antimicrobial prophylaxis (TMP-SMX or nitrofurantoin) had ~50% reduction in recurrent febrile UTI, though no difference in renal scarring. AUA VUR Guideline supports prophylaxis in younger children and BBD treatment; surgical options include endoscopic Deflux (dextranomer/hyaluronic acid) and open reimplantation (Cohen cross-trigonal most common, Lich-Gregoir extravesical, Politano-Leadbetter).
2AUA Cryptorchidism Guideline — orchiopexy between 6 and 18 months of age for optimal fertility preservation and reduced malignancy risk. Palpable undescended testis → inguinal orchiopexy (dartos pouch). Nonpalpable → diagnostic laparoscopy (no preoperative imaging indicated). High intra-abdominal testis → Fowler-Stephens (stage 1 clip spermatic vessels, stage 2 at 6 months mobilize on deferential/cremasteric collaterals). Malignancy risk ~2-4x (seminoma most common; germ cell neoplasia in situ). Retractile testis (normal cremasteric reflex, reducible to scrotum) does NOT require surgery.
3Posterior urethral valves — Young Type I >95%. Antenatal: keyhole sign on ultrasound, bilateral hydroureteronephrosis, oligohydramnios → Potter (pulmonary hypoplasia, limb contractures). Postnatal: VCUG is diagnostic gold standard (dilated posterior urethra proximal to obstruction). Primary valve ablation (cold knife or Bugbee electrode) when urethral size permits; otherwise vesicostomy. Valve bladder syndrome: initial small-capacity noncompliant bladder → evolves to large-capacity hypocontractile myogenic failure requiring CIC ± augmentation. ~30% progress to CKD/ESRD.
4SFU hydronephrosis grading (0-4): 0 no dilation; 1 renal pelvis only; 2 pelvis + some calyces; 3 pelvis + all calyces with normal parenchyma; 4 pelvis + all calyces + parenchymal thinning. MAG3 diuretic renography: T1/2 >20 minutes obstructive, 10-20 equivocal, <10 nonobstructive. Anderson-Hynes dismembered pyeloplasty is the gold standard for symptomatic UPJ obstruction; robotic approach is now standard in many pediatric centers. Split function <40% or symptoms/stones/UTI are surgical indications.
5DSD high-yield (Chicago 2006 consensus): 46,XX DSD — CAH 21-hydroxylase deficiency most common (salt-wasting with hyponatremia/hyperkalemia, elevated 17-OHP, give hydrocortisone/fludrocortisone). 46,XY DSD — complete androgen insensitivity (AR mutation, female phenotype, intra-abdominal testes, no Müllerian structures), 5-alpha-reductase deficiency (ambiguous → virilizes at puberty, low DHT, high testosterone), Swyer syndrome (SRY mutation 46,XY pure gonadal dysgenesis). Sex chromosome DSD — mixed gonadal dysgenesis 45,X/46,XY. Any DSD with Y-chromosome material has gonadoblastoma risk → prophylactic gonadectomy indicated for streak/dysgenetic gonads.

Frequently Asked Questions

What is the ABU Pediatric Urology Subspecialty Examination?

The ABU Pediatric Urology Subspecialty Certification Examination is administered by the American Board of Urology for urologists seeking subspecialty certification in pediatric urology after fellowship. It validates advanced knowledge across vesicoureteral reflux, posterior urethral valves, hypospadias, cryptorchidism, disorders of sex development, bladder exstrophy-epispadias, pediatric GU oncology (Wilms, rhabdomyosarcoma), neurogenic bladder, pediatric UTI, GU trauma, UPJ obstruction, stones, acute scrotum, circumcision, and transitional urology.

Who is eligible to take the ABU Pediatric Urology Subspecialty Exam?

Candidates must hold current ABU primary certification in Urology in good standing and have completed an ACGME-accredited Pediatric Urology fellowship (1-2 years). A valid unrestricted medical license is required, and the fellowship program director must attest to satisfactory performance and ethics. Applications are submitted through the ABU on a schedule published annually.

What is the format of the ABU Pediatric Urology Subspecialty Exam?

The ABU Pediatric Urology Subspecialty Exam is a 1-day computer-based examination administered at Pearson VUE test centers, comprising approximately 150-200 single-best-answer multiple-choice questions over roughly 4-6 hours including breaks. Items frequently include VCUG, MAG3/DMSA renography, ultrasound, and intraoperative images. The exam is blueprinted to the ABU Pediatric Urology content outline.

How much does the 2026 ABU Pediatric Urology Subspecialty Exam cost?

The 2026 ABU Pediatric Urology Subspecialty Examination fee is approximately $1,800 — always verify the current schedule on the ABU website. Cancellation and refund policies follow the ABU schedule with decreasing refunds as the exam date approaches. Retakes require re-registration and full fee payment within the allowed qualification window following fellowship completion.

When is the 2026 exam administered?

The ABU Pediatric Urology Subspecialty Examination is typically offered once annually. Applications generally open earlier in the year with a submission deadline several months before the test. Candidates schedule specific appointments with Pearson VUE after application approval. Exact 2026 dates should be confirmed on the ABU subspecialty certification page.

How is the exam scored?

ABU uses criterion-referenced scaled scoring with a passing standard set by subject-matter experts using the modified Angoff method. A candidate's pass/fail result depends on performance relative to the fixed cut-score, not on other candidates. Score reports include domain-level feedback. Passing grants subspecialty certification in pediatric urology, maintained through the ABU Continuous Certification (CC) program.

What are the highest-yield topics?

Highest-yield topics include AUA VUR Guideline and the RIVUR trial findings, SFU hydronephrosis grading and MAG3 renogram interpretation, AAP 2011 UTI Guideline (urine collection, imaging algorithm), AUA Cryptorchidism Guideline (orchiopexy by 6-18 months; Fowler-Stephens), hypospadias techniques (TIP/Snodgrass, MAGPI, two-stage Bracka), posterior urethral valves and valve bladder syndrome, DSD (Chicago 2006 consensus, CAH, AIS, Y-material gonadectomy), bladder exstrophy repair (MSRE vs CPRE), Wilms tumor (COG AREN) and pediatric rhabdomyosarcoma, neurogenic bladder urodynamics (DLPP ≥40), and Weigert-Meyer rule for duplex systems.

How should I study for this exam?

Use a structured 12-18 month plan during and after pediatric urology fellowship. Map to the ABU Pediatric Urology content outline: begin with GU embryology and imaging (SFU, MAG3, VCUG), then VUR/UTI/PUV, neurogenic bladder and bladder augmentation, genital reconstruction (hypospadias, cryptorchidism, circumcision), DSD and exstrophy-epispadias, pediatric GU oncology, trauma and stones, and transitional urology. Core resources: Campbell-Walsh-Wein Pediatric Urology, Pediatric Urology by Gearhart/Rink/Mouriquand, AUA Guidelines (VUR, Cryptorchidism), AAP UTI Guideline, Chicago 2006 DSD consensus. Complete 2-3 full-length timed mock exams.