Cryptorchidism in Sweden: A Nationwide Study of Prevalence, Operative Management, and Complications

To review the cumulative prevalence, operative management, and complications of treatment for cryptorchidism in Sweden. A nationwide observational study from longitudinal register data of all Swedish-born boys 0-18 years of age, diagnosed with cryptorchidism from 2001 to 2014. Primary outcomes were...

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Published inThe Journal of pediatrics Vol. 194; pp. 197 - 203.e6
Main Authors Bergbrant, Susanna, Omling, Erik, Björk, Jonas, Hagander, Lars
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.03.2018
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Summary:To review the cumulative prevalence, operative management, and complications of treatment for cryptorchidism in Sweden. A nationwide observational study from longitudinal register data of all Swedish-born boys 0-18 years of age, diagnosed with cryptorchidism from 2001 to 2014. Primary outcomes were occurrence and age at primary surgery. Secondary outcomes included type of procedure and surgical site infection. Of 20 375 boys diagnosed with cryptorchidism in 2001-2014, 12 766 were surgically treated. The cumulative childhood prevalence was 1.8% (95% CI, 1.5-2.0), with a higher prevalence in boys born prematurely, small for gestational age, or with low birth weight. The median age at treatment decreased from 6.2 years in 2001 to 3.4 years in 2014 (P < .001). Still, 94.1% (95% CI, 92.7-95.6) had surgery after the recommended 1 year of age in 2014. Variations in age at surgery between Swedish counties were great (range, 2.9-5.9 years of age). There were no deaths within 30 days after surgery and the frequency of surgical site infection was low (1.4%; 95% CI, 1.1-1.6). The cumulative childhood prevalence of cryptorchidism was high, and complications were rare. Few boys underwent surgery in a timely manner according to clinical guidelines, and standards of care varied considerably across the country. Further research and collective actions are needed to improve the detection and management of congenital cryptorchidism.
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ISSN:0022-3476
1097-6833
DOI:10.1016/j.jpeds.2017.09.062