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Cryptorchidism in Sweden: A Nationwide Study of Prevalence, Operative Management, and Complications
Susanna Bergbrant1, Erik Omling1, Jonas Björk2
1Lund University, Skåne University Hospital, World Health Organization Collaborating Center for Surgery and Public Health, Department of Clinical Sciences Lund, Pediatric Surgery, Lund, Sweden.
Insights
The cumulative prevalence of cryptorchidism (undescended testes) in Swedish children is 1.8%. Most boys with cryptorchidism had surgery after one year of age, and care standards varied regionally.
Area of Science:
- Pediatric Surgery
- Urology
- Public Health
Background:
- Cryptorchidism, the failure of one or both testes to descend into the scrotum, affects a significant number of male infants.
- Timely surgical intervention (orchiopexy) is crucial for optimal outcomes and fertility preservation.
Purpose of the Study:
- To determine the cumulative prevalence of cryptorchidism in Sweden.
- To analyze the operative management, including age at surgery and procedure type.
- To assess complications, such as surgical site infections, following treatment.
Main Methods:
- A nationwide observational study utilizing longitudinal register data.
- Inclusion of all Swedish-born boys aged 0-18 diagnosed with cryptorchidism between 2001 and 2014.
- Primary outcomes: occurrence and age at primary surgery; Secondary outcomes: procedure type and surgical site infection.
Main Results:
- The cumulative childhood prevalence of cryptorchidism was 1.8%, with higher rates in premature or low birth weight infants.
- Median age at surgery decreased but remained significantly delayed (3.4 years in 2014), with 94.1% operated after the recommended age of 1 year.
- Surgical site infection rate was low (1.4%), with no 30-day post-operative mortality.
Conclusions:
- Cryptorchidism prevalence is substantial, though surgical complications are infrequent.
- A significant proportion of boys undergo delayed surgery, indicating suboptimal adherence to clinical guidelines.
- Considerable regional variations in surgical timing highlight the need for improved, standardized care pathways for congenital cryptorchidism.
Objectives:
To review the cumulative prevalence, operative management, and complications of treatment for cryptorchidism in Sweden.
Study Design:
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.
Results:
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).
Conclusions:
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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