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Unilateral renal agenesis: a systematic review on associated anomalies and renal injury.
Westland, Rik; Schreuder, Michiel F; Ket, Johannes C F; van Wijk, Joanna A E.
Afiliación
  • Westland R; Department of Pediatric Nephrology, VU University Medical Center, Amsterdam, The Netherlands. r.westland@vumc.nl
Nephrol Dial Transplant ; 28(7): 1844-55, 2013 Jul.
Article en En | MEDLINE | ID: mdl-23449343
ABSTRACT

BACKGROUND:

Unilateral renal agenesis (URA) is associated with other congenital anomalies of the kidney and urinary tract (CAKUT) and extra-renal anomalies. However, the reported prevalences of these anomalies are highly variable. We estimated the prevalence of associated CAKUT and extra-renal anomalies in patients with URA. Furthermore, we determined the prevalence of renal injury in URA patients.

METHODS:

We conducted a systematic review of English and non-English articles using PubMed and Embase.com. Included studies reported at least one of the following items incidence of URA, gender, side of URA, prenatal diagnosis, performance of micturating cystourethrogram, associated CAKUT, urinary tract infection or extra-renal anomalies. Studies that described a mean/median glomerular filtration rate (GFR) and proportions of patients with hypertension, micro-albuminuria or a decreased GFR were also included.

RESULTS:

Analyses were based on 43 included studies (total number of patients 2684, 63% male). The general incidence of URA was 1 in ∼2000. Associated CAKUT were identified in 32% of patients, of which vesicoureteral reflux was most frequently identified (24% of patients). Extra-renal anomalies were found in 31% of patients. Hypertension could be identified in 16% of patients, whereas 21% of patients had micro-albuminuria. Ten per cent of patients had a GFR<60 mL/min/1.73 m2;.

CONCLUSIONS:

These aggregate results provide insight in the prevalence of associated anomalies and renal injury in patients with URA. Our systematic review implicates that URA is not a harmless malformation by definition. Therefore, we emphasize the need for clinical follow-up in URA patients starting at birth.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Anomalías Congénitas / Sistema Urinario / Riñón / Enfermedades Renales Tipo de estudio: Prognostic_studies / Risk_factors_studies / Systematic_reviews Límite: Humans Idioma: En Revista: Nephrol Dial Transplant Asunto de la revista: NEFROLOGIA / TRANSPLANTE Año: 2013 Tipo del documento: Article País de afiliación: Países Bajos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Anomalías Congénitas / Sistema Urinario / Riñón / Enfermedades Renales Tipo de estudio: Prognostic_studies / Risk_factors_studies / Systematic_reviews Límite: Humans Idioma: En Revista: Nephrol Dial Transplant Asunto de la revista: NEFROLOGIA / TRANSPLANTE Año: 2013 Tipo del documento: Article País de afiliación: Países Bajos