Abstract
We conducted a prospective population-basedstudy in Kuwait to determine the prevalence andpattern of previously undiagnosed congenitalanomalies of urinary tract in patientsundergoing intravenous urography (IVU) and toexamine the demographic factors associated withthese anomalies. The study included 2398consecutive patients undergoing IVU, forvarious indications, in all the six publichospitals in Kuwait, during the period 1 June1999–30 September 2000. Patients were alsointerviewed to obtain selected demographicinformation. Multiple logistic regression wasused to identify factors associated with theanomalies. The average age (± SD) of thepatients (1623 males, 775 females) was 39.2± 15.1 years. A total of 335 anomalies(12.1% in males, 17.9% in females;p < 0.001) were detected in 300 (12.5%)patients (10.9% males, 15.9% females; p < 0.01). About half (47.2%) of the anomaliesinvolved the kidney, 28.4% renal pelvis,22.4% ureters, and 2.1% bladder. Multipleregression analysis showed that age < 20 years(odds ratio (OR) = 12.5; 95% confidenceinterval (95% CI): 7.0–22.3) female gender (OR= 1.5; 95% CI: 1.2–2.0) Kuwaiti nationality(OR = 1.7; 95% CI: 1.2–2.3) and family historyof congenital malformation (OR = 3.8; 95% CI:2.2–6.6) were independently associated with theanomalies of the urinary tract. Overall, 42%of the patients reported a consanguineousmarriage between their parents. The frequencyof anomalies was higher in individuals who hadconsanguineous parents (13.8 vs. 11.6%; OR =1.2) but this positive association did notreach statistical significance. Considering therelatively high prevalence of previouslyundiagnosed congenital anomalies of the urinarytract, it is important to establish clinicalguidelines for early detection and managementof these conditions to decrease the associatedmorbidity and mortality.
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References
Annual Statistical Abstract. Kuwait: Ministry of Planning, Statistics and Information Sector, 2000.
Al-Awadi SA, Moussa MA, Naguib KK et al. Consanguinity among the Kuwaiti population. Clin Genet 1985; 27: 483–486.
Al-Gazali LI, Dawodu AH, Sabarinathan K, Varghese M. The profile of major congenital abnormalities in the United Arab Emirates population. J Med Genet 1995; 32: 7–13.
Barakat AJ, Drougas JG. Occurrence of congenital abnormalities of kidney and urinary tract in 13,775 autopsies. Urology 1991; 38: 347–350.
Berry CA, Channtler C. Urogenital malformations and disease. Br Med Bull 1986; 42: 181–186.
Bittar Z. Major congenital malformations presenting in the first 24 hours of life in 3865 consecutive births south of Beirut. Incidence and pattern. Lebanese Med. J 1998; 46: 256–260.
Bois E, Feingold J, Benmaiz H, Briard ML. Congenital urinary tract malformations: Epidemiologic and genetic aspects. Clin Genet 1975; 8: 37–47.
Calzolari E, Cavazutti GB, Cocci G et al. Congenital malformations in 100,000 consecutive births in Emilia Romagna region of northern Italy: Comparison with the Eurocat data. Eur J Epidemiol 1987; 3: 423–430.
Hashmi MA. Frequency of consanguinity and its effect on congenital malformation - A hospital based study. J Pak Med Assoc 1997; 47: 75–78.
Helin I, Winberg J. Chronic renal failure in Swedish children. Acta Paediat Scand 1980; 69: 607–611.
Jain VK, Nalini P, Chandra R, Srinivasan S. Congenital malformations, reproductive wastage and consanguineous mating. Aust N Z J Obstet Gynaecol 1993; 33: 33–36.
Mihara M, Ito Y, Fukushima K et al. Ultrasonographic screening for renal abnormalities in three-year-old children. Acta Paediatr 1992; 81: 326–328.
Radovanovic Z, Shah N, Behbehani J. Prevalence and social correlates of consanguinity in Kuwait. Annals of Saudi Med 1999; 19: 206–210.
Rubentein M, Meyer R, Bernstein J. Congenital abnormalities of the urinary system. I. A postmortem survey of devel-opmental anomalies and acquired congenital lesions in a children's hospital. J Pediatr 1961; 58: 356–366.
Sheih CP, Liu MS, Hung CS et al. Renal abnormalities in schoolchildren. Pediatrics 1989; 84: 1086–1090.
Simpson JL, German J. Familial urinary tract anomalies. JAMA 1970; 212: 2264–2268.
Stoll C, Alembik Y, Roth MP et al. Risk factors in internal urinary system malformations. Pediat. Nephrol 1990; 4: 319–323.
Stoll C, Alembik Y, Dott B, Feingold J. Parental consanguinity as a cause of increased incidence of birth defects in a study of 131,760 consecutive births. Am J Med Genet 1994; 49: 114–117.
Wals de P, Dolk E, Gillerot Y. Base-line prevalence of congenital anomalies in 17 EUROCAT Registers, 1980-1983. In: De Wals P, Lechat MF, eds. Surveillance of Congenital Anoma-lies, 1980-1983. Bruxelles: Department of Epidemiology, University of Louvain, 1986: 8–101.
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Gupta, R., Memon, A., Al-Khawari, H. et al. The prevalence and pattern of congenital anomalies of the urinary tract detected by intravenous urography in Kuwait. Int Urol Nephrol 34, 477–483 (2002). https://doi.org/10.1023/A:1025600219402
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DOI: https://doi.org/10.1023/A:1025600219402