Correlation of anorectal malformation complexity and associated urologic abnormalities

被引:23
作者
Fuchs, Molly E. [1 ]
Halleran, Devin R. [1 ]
Bourgeois, Tran [1 ]
Sebastiao, Yuri [1 ]
Weaver, Laura [1 ]
Farrell, Nolan [1 ]
Vilanova-Sanchez, Alejandra [1 ]
Gasior, Alessandra [1 ]
Halaweish, Ihab [1 ]
Jayanthi, Venkata R. [1 ]
Wood, Richard J. [1 ]
Dajusta, Daniel G. [1 ]
机构
[1] Nationwide Childrens Hosp, Ctr Colorectal & Pelv Reconstruct, 700 Childrens Dr, Columbus, OH 43205 USA
关键词
Anorectal malformation; Cloaca; Urologic; ANOMALIES; EMBRYOLOGY;
D O I
10.1016/j.jpedsurg.2021.02.051
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Background: Patients with anorectal malformations (ARM) commonly have associated urologic anomalies. Few large studies exist to accurately characterize the incidence or associations between severity of malformation and urologic diagnosis. The purpose of our study was to determine the incidence of urologic diagnoses in a large cohort of children with ARM and evaluate for any correlation between severity of ARM and the incidence and number of associated urologic diagnoses. Methods: A retrospective review was performed of patients with ARM treated at our pediatric colorectal center. All patients underwent protocolized urologic screening . ARM subtypes were ordered with increasing severity as follows in males: perineal, bulbar, prostatic and bladder neck fistulae. Females were similarly categorized as perineal, vestibular and vaginal fistulae followed by cloaca with < 3 cm common channel and cloaca with > 3 cm common channel. The following urologic diagnoses were assessed to determine whether a correlation existed with the severity of the ARM subtype: hydronephrosis, vesicoureteral reflux (VUR), solitary kidney, renal ascent anomalies (ectopic or pelvic), renal fusion anomalies (horseshoe or cross fused kidney), duplex kidney, hypospadias and undescended testicle. ARM subtypes were defined by distal rectal anatomy. Results: A total of 712 patients were included in our study with a mean age of 4 years and of whom 45% were male. The overall rate of urologic anomalies was greater in males than females (65% vs 56% p < 0.026). In both sexes, the rate of urologic anomalies increased with increasing severity of ARM subtype ( p < 0.0 0 010) finding that males with bladder neck fistula and females with cloacal malformations, particularly with long common channels, being the highest incidence. In males and females, the rate of hydronephrosis increased as the complexity of ARM increased and this correlated significantly ( p < 0.0 0 01 vs p < 0.0 0 03 respectively). Similarly, the incidence of VUR also increased as complexity of ARM increased in both males and females ( p = 0.01 and p < 0.0 0 01 respectively). The remaining urologic diagnoses were not significantly correlated with severity of ARM. Conclusions: Urologic anomalies occur at a high rate in children with ARM and appear to increase in frequency with increasing complexity of ARM subtype. These findings stress the importance of proper ARM screening and proactive collaboration with a clinician with expertise in pediatric urology early in the management of such children to improve early recognition of urologic diagnoses. Level of evidence: Level III. (c) 2021 Elsevier Inc. All rights reserved.
引用
收藏
页码:1988 / 1992
页数:5
相关论文
共 16 条
[1]   Urologic problems in anorectal malformations .2. Functional urologic sequelae [J].
Boemers, TML ;
deJong, TPVM ;
vanGool, JD ;
Bax, KMA .
JOURNAL OF PEDIATRIC SURGERY, 1996, 31 (05) :634-637
[2]   Urological anomalies in anorectal malformations in The Netherlands: effects of screening all patients on long-term outcome [J].
Goossens, W. J. H. ;
de Blaauw, I. ;
Wijnen, M. H. ;
de Gier, R. P. E. ;
Kortmann, B. ;
Feitz, W. F. J. .
PEDIATRIC SURGERY INTERNATIONAL, 2011, 27 (10) :1091-1097
[3]   Research electronic data capture (REDCap)-A metadata-driven methodology and workflow process for providing translational research informatics support [J].
Harris, Paul A. ;
Taylor, Robert ;
Thielke, Robert ;
Payne, Jonathon ;
Gonzalez, Nathaniel ;
Conde, Jose G. .
JOURNAL OF BIOMEDICAL INFORMATICS, 2009, 42 (02) :377-381
[4]   Preliminary report on the international conference for the development of standards for the treatment of anorectal malformations [J].
Holschneider, A ;
Hutson, J ;
Peña, A ;
Bekhit, E ;
Chatterjee, S ;
Coran, A ;
Davies, M ;
Georgeson, K ;
Grosfeld, J ;
Gupta, D ;
Iwai, N ;
Kluth, D ;
Martucciello, G ;
Moore, S ;
Rintala, R ;
Smith, ED ;
Sripathi, DV ;
Stephens, D ;
Sen, S ;
Ure, B ;
Grasshoff, S ;
Boemers, T ;
Murphy, F ;
Söylet, Y ;
Dübbers, M ;
Kunst, M .
JOURNAL OF PEDIATRIC SURGERY, 2005, 40 (10) :1521-1526
[5]   Embryology of the hindgut [J].
Kluth, Dietrich ;
Fiegel, Henning C. ;
Metzger, Roman .
SEMINARS IN PEDIATRIC SURGERY, 2011, 20 (03) :152-160
[6]   Embryology of anorectal malformations [J].
Kluth, Dietrich .
SEMINARS IN PEDIATRIC SURGERY, 2010, 19 (03) :201-208
[7]   Anorectal malformations [J].
Levitt, Marc A. ;
Pena, Alberto .
ORPHANET JOURNAL OF RARE DISEASES, 2007, 2
[8]   THE GENITOURINARY SYSTEM IN PATIENTS WITH IMPERFORATE ANUS [J].
MCLORIE, GA ;
SHELDON, CA ;
FLEISHER, M ;
CHURCHILL, BM .
JOURNAL OF PEDIATRIC SURGERY, 1987, 22 (12) :1100-1104
[9]   Genital malformations and coexistent urinary tract or spinal anomalies in patients with imperforate anus [J].
Metts, JC ;
Kotkin, L ;
Kasper, S ;
Shyr, Y ;
Adams, MC ;
Brock, JW .
JOURNAL OF UROLOGY, 1997, 158 (03) :1298-1300
[10]   Screening practices and associated anomalies in infants with anorectal malformations: Results from the Midwest Pediatric Surgery Consortium [J].
Minneci, Peter C. ;
Kabre, Rashmi S. ;
Mak, Grace Z. ;
Halleran, Devin R. ;
Cooper, Jennifer N. ;
Afrazi, Amin ;
Calkins, Casey M. ;
Downard, Cynthia D. ;
Ehrlich, Peter ;
Fraser, Jason ;
Gadepalli, Samir K. ;
Helmrath, Michael A. ;
Kohler, Jonathan E. ;
Landisch, Rachel ;
Landman, Matthew P. ;
Lee, Constance ;
Leys, Charles M. ;
Lodwick, Daniel L. ;
Mon, Rodrigo ;
McClure, Beth ;
Rymeski, Beth ;
Saito, Jacqueline M. ;
Sato, Thomas T. ;
Peter, Shawn D. St. ;
Wood, Richard ;
Levitt, Marc A. ;
Deans, Katherine J. .
JOURNAL OF PEDIATRIC SURGERY, 2018, 53 (06) :1163-1167