Z Geburtshilfe Neonatol 2014; 218(01): 18-26
DOI: 10.1055/s-0034-1367042
Übersicht
© Georg Thieme Verlag KG Stuttgart · New York

Lower Urinary Tract Obstruction (LUTO) – Krankheitsbild, pränatale Diagnostik und Therapiemöglichkeiten

Lower Urinary Tract Obstruction (LUTO) – Clinical Picture, Prenatal Diagnostics and Therapeutic Options
J. Bildau
1   Frauenklinik, Asklepios Klinik Lich, akademisches Lehrkrankenhaus der Justus-Liebig Universität Gießen
,
C. Enzensberger
2   Abteilung für Pränatalmedizin und gynäkologische Sonografie, Zentrum für Frauenheilkunde und Geburtshilfe, Justus-Liebig Universität Gießen und UKGM
,
J. Degenhardt
2   Abteilung für Pränatalmedizin und gynäkologische Sonografie, Zentrum für Frauenheilkunde und Geburtshilfe, Justus-Liebig Universität Gießen und UKGM
,
A. Kawecki
2   Abteilung für Pränatalmedizin und gynäkologische Sonografie, Zentrum für Frauenheilkunde und Geburtshilfe, Justus-Liebig Universität Gießen und UKGM
,
A. Tenzer
2   Abteilung für Pränatalmedizin und gynäkologische Sonografie, Zentrum für Frauenheilkunde und Geburtshilfe, Justus-Liebig Universität Gießen und UKGM
,
T. Kohl
3   Deutsches Zentrum für Fetalchirurgie & minimal-invasive Therapie (DZFT)
,
R. Stressig
4   Praxis für Praenatalmedizin und Genetik Köln/Düsseldorf, Praenatal.de
,
J. Ritgen
4   Praxis für Praenatalmedizin und Genetik Köln/Düsseldorf, Praenatal.de
,
B. Utsch
5   Zentrum für Kinderheilkunde und Jugendmedizin, Abteilung für Allgemeine Pädiatrie und Neonatologie, Jusustus-Liebig-Universität Gießen und UKGM
,
R. Axt-Fliedner
2   Abteilung für Pränatalmedizin und gynäkologische Sonografie, Zentrum für Frauenheilkunde und Geburtshilfe, Justus-Liebig Universität Gießen und UKGM
› Author Affiliations
Further Information

Publication History

eingereicht 13 September 2013

angenommen nach Überarbeitung16 January 2014

Publication Date:
04 March 2014 (online)

Zusammenfassung

Die Ätiologie der Obstruktion des Blasenhalses (LUTO) ist heterogen. Die häufigsten Entitäten sind isolierte posteriore Urethralklappen oder eine Urethralatresie beim männlichen Feten. LUTO bei weiblichen Feten ist häufig Teil eines komplexeren Fehlbildungsgeschehens. Der natürliche Verlauf bei LUTO ist charakterisiert durch eine hohe Mortalität und Morbidität aufgrund sich entwickelnden Lungenhypoplasie, die im Zusammenhang mit einer ausgeprägten Oligo- oder Anhydramnie zum Zeitpunkt der kannaliculären Phase der Lungenentwicklung (16.-24. SSW) steht. Die begleitende Nierenschädigung ist variabel und reicht von geringen Einschränkungen der Nierenfunktion im Kleinkindalter bis hin zur Dialysepflichtigkeit und Notwendigkeit der Nierentransplantation. Die Möglichkeit der pränatalen Intervention zur Umgehung der Obstruktion ist biologisch plausibel und technisch erfolgreich durchführbar. Vesiko-amniales Shunting und, zur Zeit noch seltener, die fetoskopische Zystoskopie mit Laserablation der posterioren Urethralklappen sind mögliche minimal-invasive Therapieverfahren. Die bisherigen Ergebnisse zeigen, daß die perinatale Sterblichkeit durch die pränatale Therapie (vesiko-amniales Shunting oder fetoskopische Zystoskopie mit Laserablation der posterioren Urethralklappen) verringert werden kann, jedoch derzeit keine Verbesserung der Anzahl der Kinder mit postnatal normaler Nierenfunktion zu erreichen ist. Die Auswahl der betroffenen Ungeborenen mit LUTO die von einer fetalen Therapie profitieren können, wird derzeit dadurch beeinträchtigt, dass durch die Sonografie und die serielle fetale Urinanalytik keine definitiv verlässlichen Prognosekriterien für die postpartale Nierenfunktion abgeleitet werden können. Eine Schwäche der derzeit vorliegenden Untersuchungen ist die fehlende Randomisierung. Aufgrund einer relevanten Komplikationsrate der intrauterinen Eingriffe bei nicht klar belegter Effektivität sollten derartige Eingriffe nur in hochspezialisierten Zentren erfolgen. Weitere Studien zur verbesserten Auswahl betroffener Feten und zur früheren Therapie in der Schwangerschaft sind erforderlich. Die Daten der prospektiv randomisierten multizentrischen PLUTO Studie der Universität Birmingham, England (percutaneous shunting in lower urinary tract obstruction) könnten zu diesen Fragen Aufschluss geben. Bis dahin sollte die Indikation zur intrauterinen Harnableitung mit größter Sorgfalt und nach interdisziplinärer Beratung gemeinsam mit den Neonatologen, den Kindernephrologen und den werdenden Eltern gestellt werden. Eine allgemeingültige Handlungsanweisung zur fetalen Therapie bei LUTO kann auf dem Boden der derzeitigen Daten nicht gegeben werden.

Abstract

The aetiology of urinary tract obstructions (LUTO) is heterogeneous. The most common entities are isolated posterior urethral valves or urethral atresia in male foetuses. In female foetuses LUTO is frequently a part of complex malformations. The natural history of LUTO is characterised by high morbidity and mortality due to the development of severe pulmonary hypoplasia caused by oligo- or anhydramnios affecting the cannalicular phase (16–24 weeks of gestation) of pulmonary development. The degree of renal damage is variable and ranges from mild renal impairment in infancy to end-stage renal insufficiency, necessitating dialysis and transplantation. Foetal interventions in order to bypass the obstruction are biologically plausible and technically feasible. Vesico-amniotic shunting as well as (currently less frequent) foetoscopic cystoscopy and laser ablation of posterior urethral valves are minimally invasive treatment options. Previous reports indicate that prenatal therapy is suitable to reduce perinatal mortality but does not improve postnatal renal function. Selection of foetuses who may profit from prenatal intervention is aggravated by the lack of reliable prognostic criteria for the prediction of postnatal renal function in both ultrasound and foetal urine analysis. Furthermore, there is no randomised trial available at the time of writing. Because of a relevant complication rate and still no clear evidence for foetal benefit, interventions should be performed in specialised centres. Further studies are necessary to improve case selection of affected foetuses and to evaluate the impact of interventions in earlier gestational weeks. The data from the PLUTO trial (percutaneous shunting in lower urinary tract obstruction) conducted by the University of Birmingham may help to answer these questions. In the meantime selection of foetuses for prenatal intervention puts high requirements on interdisciplinary counselling in every case. A general treatment algorithm for foetal therapy is not available at the moment.

 
  • Literatur

  • 1 Vanderheyden T, Kumar S, Fisk NM. Fetal renal impairment. Semin Neonatol 2003; 8: 279-289
  • 2 Lissauer D, Morris RK, Kilby MD. Fetal lower urinary tract obstruction. Semin Fetal Neonatal Med 2007; 12: 464-470
  • 3 Kerecuk L, Schreuder MF, Woolf AS. Renal tract malformations: perspectives for nephrologists. Nat Clin Pract Nephrol 2008; 4: 312-325
  • 4 Robyr R, Benachi A, Daikha-Dahmane F et al. Correlation between ultrasound and anatomical findings in fetuses with lower urinary tract obstruction in the first half of pregnancy. Ultrasound Obstet Gynecol 2005; 25: 478-482
  • 5 Freedman AL, Johnson MP, Gonzalez R. Fetal therapy for obstructive uropathy: past, present, future?. Pediatr Nephrol 2000; 14: 167-176
  • 6 Freedman AL, Johnson MP, Smith CA et al. Longterm outcome in children after antenatal intervention for obstructive uropathies. Lancet 1999; 354: 374-377
  • 7 Parkhouse HF, Barratt TM. Investigation of the dilated urinary tract. Pediatr Nephrol 1988; 2: 43-47
  • 8 Harrison MR, Golbus MS, Filly RA et al. Fetal surgery for congenital hydronephrosis. N Engl J Med 1982; 306: 591-593
  • 9 Harrison MR, Golbus MS, Filly RA et al. Management of the fetus with congenital hydronephrosis. J Pediatr Surg 1982; 17: 728-742
  • 10 Harrison MR, Golbus MS, Filly RA et al. Fetal surgical treatment. Pediatr Ann 1982; 11 (896/899) 901-903
  • 11 Golbus MS, Harrison MR, Filly RA et al. In utero treatment of urinary tract obstruction. Am J Obstet Gynecol 1982; 142: 383-388
  • 12 Harrison MR, Ross N, Noall R et al. Correction of congenital hydronephrosis and pulmonary hypoplasia in fetal lambs. J Pediatr Surg 1983; 18: 247-256
  • 13 Agarwal SK, Fisk NM. In utero therapy for lower urinary tract obstruction. Prenat Diagn 2001; 21: 970-976
  • 14 Clark TJ, Martin WL, Divakaran TG et al. Prenatal bladder drainage in the management of fetal lower urinary tract obstruction: a systematic review and meta-analysis. Obstet Gynecol 2003; 102: 367-382
  • 15 McLorie G, Farhat W, Khoury A et al. Outcome analysis of vesicomaniotic shunting in a comprehensive population. J Urol 2001; 166: 1036-1040
  • 16 Hutton KA, Thomas DF, Davies BW. Prenatally detected posterior urethral valves: qualitative assessment of second trimester scans and prediction of outcome. J Urol 1997; 158: 1022-1025
  • 17 Anumba DO, Scott JE, Plant ND et al. Diagnosis and outcome of fetal lower urinary tract obstruction in the northern region of England. Prenat Diagn 2005; 25: 7-13
  • 18 Malin G, Tonks AM, Morris RK et al. Congenital lower urinary tract obstruction: a population-based epidemiological study. BJOG 2012; 119: 1455-1464
  • 19 Morris RK, Kilby MD. Long-term renal and neurodevelopmental outcome in infants with LUTO, with and without fetal intervention. Early Hum Development 2011; 87: 607-610
  • 20 Ruano R. Fetal surgery for severe lower urinary tract obstruction. Prenat Diagn 2011; 31: 667-674
  • 21 Parkhouse HF, Barratt TM. Investigation of the dilated urinary tract. Pediatr Nephrol 1988; 2: 43-47
  • 22 Merill DC, Weiner CP. Urinary tract obstruction. In: Fisk NM, Moise Jr KJ. eds. Fetal Therapy: Invasive and Transplacental. Cambridge, UK: Cambridge University Press; 1997: 273-276
  • 23 Mahoney BS, Callen PW, Filly RA. Fetal urethral obstruction: US evaluation. Radiology. 1985. 157. 221-224
  • 24 Parkhouse HF, Woodhouse CR. Long-term status of patients with posterior urethral valves. Urol Clin North Am 1990; 17: 373-378
  • 25 Parkhouse HF, Barrat TM, Dillon MJ et al. Long term outcome of boys with posterior urethral valves. Br J Urol 1988; 62: 59-62
  • 26 Favre R, Kohler M, Gasser B et al. Early fetal megacystis between 11 and 15 weeks of gestation. Ultrasound Obstet Gynecol 1999; 14: 402-406
  • 27 Young ID, Mckeever PA, Brown LA et al. Prenatal diagnosis of the megacystis-microcolon-intestinal hypoperistalsis syndrome. J Med Genet 1989; 26: 403-406
  • 28 Sepulveda W. Megacystis in the first trimester. Prenat Diagn 2004; 24: 144-149
  • 29 Jouannic JM, Hyett JA, Pandya PP et al. Perinatal outcome in fetuses with megacystis in the first half of pregnancy. Prenat Diagn 2003; 23: 340-344
  • 30 Liao AW, Sebire NJ, Geerts L et al. Megacystis at 10–14 weeks of gestation: chromosomal defects and outcome according to bladder length. Ultrasound Obstet Gynecol 2003; 21: 338-341
  • 31 Freedman AL, Qureshi F, Shapiro E et al. Smooth muscle development in the obstructed fetal bladder. Urology 1997; 49: 104-107
  • 32 Gloor JM, Ogburn PLJR, Breckle RJ et al. Urinary tract anomalies detected by prenatal ultrasound examination at Mayo Clinic Rochester. Mayo Clin Proc 1995; 70: 526-531
  • 33 Bunduki V, Saldanha LB, Sadek L et al. Fetal renal biopsies in obstructive uropathy: feasibility and clinical correlations—preliminary results. Prenat Diagn 1998; 18: 101-109
  • 34 Shimada K, Matsumoto F, Tohda A et al. Histological study of fetal kidney with urethral obstruction and vesicoureteral reflux: a consideration on the etiology of congenital reflux nephropathy. Int J Urol 2003; 10: 518-524
  • 35 Bernardes LS, Aksnes G, Saada J et al. Keyhole sign: how specific is it for the diagnosis of posterior urethral valves?. Ultrasound Obstet Gynecol 2009; 34: 419-423
  • 36 Ruano R, Duarte S, Bunduki V et al. Fetal cystoscopy for severe lower urinary tract obstruction – initial experience of a single center. Prenat Diagn 2010; 30: 30-39
  • 37 Hutton KA, Thomas DF, Arthur RJ et al. Prenatally detected posterior urethral valves: is gestational age at detection a predictor of outcome?. J Urol 1994; 152: 698-701
  • 38 Dinneen MD, Dhillon HK, Ward HC et al. Antenatal diagnosis of posterior urethral valves. Br J Urol 1993; 72: 364-369
  • 39 Peters CA. Lower urinary tract obstruction: clinical and experimental aspects. Br J Urol 1998; 81: 22-32
  • 40 Wu S, Johnson MP. Fetal lower urinary tract obstruction. Clin Perinatol 2009; 36: 377-390
  • 41 Miller OF, Lashley DB, Mcaleer IM et al. Diagnosis of urethral obstruction with prenatal magnetic resonance imaging. J Urol 2002; 168: 1158-1159
  • 42 Quintero RA, Hume R, Smith C et al. Percutaneous fetal cystoscopy and endoscopic fulguration of posterior urethral valves. Am J Obstet Gynecol 1995; 172: 206-209
  • 43 Quintero RA, Johnson MP, Romero R et al. In-utero percutaneous cystoscopy in the management of fetal lower obstructive uropathy. Lancet 1995; 346: 537-540
  • 44 Welsh A, Agarwal S, Kumar S et al. Fetal cystoscopy in the management of fetal obstructive uropathy: experience in a single European centre. Prenat Diagn 2003; 23: 1033-1041
  • 45 Oliveira EA, Diniz JS, Cabral AC et al. Predicitve factors of uretra obstruction: a multivariate analysis. Fetal Diagn Ther 2000; 15: 180-186
  • 46 Mandelbrot L, Dumez Y, Muller F et al. Prenatal prediction of renal function in fetal obstructive uropathies. J Perinat Med 1991; 19: 283-287
  • 47 Reinberg Y, De Castano I, Gonzalez R. Prognosis for patients with prenatally diagnosed posterior urethral valves. J Urol 1992; 148: 125-126
  • 48 Morris RK, Malin GL, Khan KS et al. Antenatal ultrasound to predict postnatal renal function in congenital lower urinary tract obstruction: systematic review of test accuracy. BJOG 2009; 116: 1290-1299
  • 49 Nicolini U, Spelzini F. Invasive assessment of fetal renal abnormalities: urinalysis, fetal blood sampling and biopsy. Prenat Diagn 2001; 21: 964-969
  • 50 Qureshi F, Jacques SM, Seifman B et al. In utero fetal urine analysis and renal histology correlate with the outcome in fetal obstructive uropathies. Fetal Diagn Ther 1996; 11: 306-312
  • 51 Burghard R, Pallacks R, Gjordani N et al. Microproteins in amniotic fluids as an index of changes in fetal renal function during development. Pediatr Nephrol 1987; 1: 574-580
  • 52 Bokenkamp A, Dieterich C, Dressler F et al. Fetal serum concentrations of cystatin C and beta2-microglobulin as predictors of postnatal kidney function. Am J Obstet Gynecol 2001; 185: 468-475
  • 53 Nolte S, Mueller B, Pringsheim W. Serum alpha-1-microglobulin and beta-2-microglobulin for the estimation of fetal glomerular renal function. Pediatr Nephrol 1991; 5: 573-577
  • 54 Mussap M, Fanos V, Pizzini C et al. Predicitve value of amniotic fluid costati C levels for the early identification of fetuses with obstructive uropathies. BJOG 2002; 109: 778-783
  • 55 Burghard R, Gjordani N, Leititis J et al. Protein analysis in amniotic fluid and fetal urine for the assessment of fetal renal function and dysfunction. Fetal Therapy 1987; 2: 188-196
  • 56 Burghard R, Leititis JU, Etzold S et al. Proteins in amniotic fluid as an index of kidney function and dysfunction in the fetus. Contributions to Nephrology 1988; 68: 250-258
  • 57 Crombleholme TM, Harrison MR, Golbus MS et al. Fetal intervention in obstructive uropathy: prognostic indicators and efficacy of intervention. Am J Obstet Gynecol 1990; 162: 1239-1244
  • 58 Glick PL, Harrison MR, Golbus MS et al. Management of the fetus with congenital hydronephrosis II: prognostic criteria and selection for treatment. J Pediatr Surg 1985; 20: 376-387
  • 59 Morris RK, Quinlan-Jones E, Kilby MD et al. Systematic review of accuracy of fetal urine analysis to predict poor postnatal renal function in cases of congenital urinary tract obstruction. Prenat Diagn 2007; 27: 900-911
  • 60 Eugene M, Muller F, Dommergues M et al. Evaluation of postnatal renal function in fetuses with bilateral obstructive uropathies by proton nuclear magnetic resonance spectroscopy. Am J Obstet Gynecol 1994; 170: 595-602
  • 61 Nicolini U, Tannirandorn Y, Vaughan J et al. Further predictors of renal dysplasia in fetal obstructive uropathy: bladder pressure and biochemistry of ‘fresh’ urine. Prenat Diagn 1991; 11: 159-166
  • 62 Kitagawa H, Pringle KC, Koike J et al. Early bladder wall changes after creation of obstructive uropathy in the fetal lamb. Pediatr Surg Int 2006; 22: 875-879
  • 63 Nagae H, Kitagawa H, Pringle KC et al. Pressure-limited vesicoamniotic shunt tube for fetal obstructive uropathy. J Pediatr Surg 2006; 41: 2086-2089
  • 64 Evans MI, Sacks AJ, Johnson MP et al. Sequential invasive assessment of fetal renal function and the intrauterine treatment of fetal obstructive uropathies. Obstet Gynecol 1991; 77: 545-550
  • 65 Carroll SG, Soothill PW, Tizard J et al. Vesicocentesis at 10–14 weeks of gestation for treatment of fetal megacystis. Ultrasound Obstet Gynecol 2001; 18: 366-370
  • 66 Coplen DE. Prenatal intervention for hydronephrosis. J Urol 1997; 157: 2270-2277
  • 67 Holmes N, Harrison MR, Baskin LS. Fetal surgery for posterior urethral valves: long-term postnatal outcomes. Pediatrics 2001; 108: E7
  • 68 Lewis KM, Pinckert TL, Cain MP et al. Complications of intrauterine placement of a vesicoamniotic shunt. Obstet Gynecol 1998; 91: 825-827
  • 69 Springer A, Fartacek R, Reck CA et al. Major complication after intrauterine vesico-amniotic shunting. Afr J Paediatr Surg 2010; 7: 200-202
  • 70 Sato Y, Kitagawa H, Pringle KC et al. Effects of early vesicostomy in obstructive uropathy on bladder development. J Pediatr Surg 2004; 39: 1849-1852
  • 71 Quintero RA, Gomez Castro LA, Bermudez C et al. In utero management of fetal lower urinary tract obstruction with a novel shunt: a landmark development in fetal therapy. J Matern Fetal Neonatal Med 2010; 23: 806-812
  • 72 Quintero RA, Homsy Y, Bornick PW et al. 2001; In-utero treatment of fetal bladder-outlet obstruction by a ureterocele. Lancet 2001; 357 1947-1948
  • 73 Quintero RA, Morales WJ, Allen MH et al. Fetal hydrolaparoscopy and endoscopic cystotomy in complicated cases of lower urinary tract obstruction. Am J Obstet Gynecol 2000; 183: 324-330
  • 74 Quintero RA, Shukla AR, Homsy YL et al. Successful in utero endoscopic ablation of posterior urethral valves: a new dimension in fetal urology. Urology 2000; 55: 774
  • 75 Schmidt S, Hofmann R, Tekesin I et al. Operative fetoscopical management of intrauterine obstructive uropathia by urethral stent. J Perinat Med 2003; 31: 313-316
  • 76 Morris RK, Ruano R, Kilby MD. Effectiveness of fetal cystoscopy as a diagnostic and therapeutic intervention for lower urinary tract obstruction: a systematic review. Ultrasound Obstet Gynecol 2011; 37: 629-637
  • 77 Morris RK, Malin GL, Khan KS et al. Systematic review of the effectiveness of antenatal intervention for the treatment of congenital lower urinary tract obstruction. BJOG 2010; 117: 382-390
  • 78 Kilby M, Khan K, Morris K et al. PLUTO trial protocol: percutaneous shunting for lower urinary tract obstruction randomised controlled trial. BJOG 2007; 114: 904-905
  • 79 Davies JA.. Mesenchyme to epithelium transition during development of the mammalian kidney tubule. Acta Anat. 1996 156. 87-201
  • 80 Piscione TD, Rosenblum NG. The molecular control of renal branching morphogenesis: current knowledge and emerging insights. Differentiation 2002; 70: 227-246
  • 81 Shi Y, Pedersen M, Li C et al. early release of neonatal ureteral obstruction preserves renal function. Am J Physiol Renal Physiol 2004; 286: 1087-1099
  • 82 Biard J-M, Johnson MP, Carr MC et al. Long-term outcomes in children treated by prental vesicoamniotic shunting for lower urinary tract obstruction. Obstet Gynecol 2005; 106: 503-508
  • 83 Reinberg Y, De CI, Gonzalez R. Prognosis for patients with prenatally diagnosed posterior urethral valves. So J Urol 1992; 148: 125-126
  • 84 El-Ghoneimi A, Desgrippes A, Luton D et al. Outcome of posterior uretra valves: to what extent it is improved by prenatal diagnosis?. J Urol 1999; 162: 849-853