Urethrocutaneous fistulas after voluntary medical male circumcision for HIV prevention-15 African Countries, 2015-2019.


Journal

BMC urology
ISSN: 1471-2490
Titre abrégé: BMC Urol
Pays: England
ID NLM: 100968571

Informations de publication

Date de publication:
12 Feb 2021
Historique:
received: 15 10 2020
accepted: 01 02 2021
entrez: 13 2 2021
pubmed: 14 2 2021
medline: 23 7 2021
Statut: epublish

Résumé

Voluntary medical male circumcision (VMMC) is an HIV prevention strategy recommended to partially protect men from heterosexually acquired HIV. From 2015 to 2019, the President's Emergency Plan for AIDS Relief (PEPFAR) has supported approximately 14.9 million VMMCs in 15 African countries. Urethrocutaneous fistulas, abnormal openings between the urethra and penile skin through which urine can escape, are rare, severe adverse events (AEs) that can occur with VMMC. This analysis describes fistula cases, identifies possible risks and mechanisms of injury, and offers mitigation actions. Demographic and clinical program data were reviewed from all reported fistula cases during 2015 to 2019, descriptive analyses were performed, and an odds ratio was calculated by patient age group. In total, 41 fistula cases were reported. Median patient age for fistula cases was 11 years and 40/41 (98%) occurred in patients aged < 15 years. Fistulas were more often reported among patients < 15 compared to ≥ 15 years old (0.61 vs. 0.01 fistulas per 100,000 VMMCs, odds ratio 50.9 (95% confidence interval [CI] = 8.6-2060.0)). Median time from VMMC surgery to appearance of fistula was 20 days (interquartile range (IQR) 14-27). Urethral fistulas were significantly more common in patients under age 15 years. Thinner tissue overlying the urethra in immature genitalia may predispose boys to injury. The delay between procedure and symptom onset of 2-3 weeks indicates partial thickness injury or suture violation of the urethral wall as more likely mechanisms of injury than intra-operative urethral transection. This analysis helped to inform PEPFAR's recent decision to change VMMC eligibility policy in 2020, raising the minimum age to 15 years.

Sections du résumé

BACKGROUND BACKGROUND
Voluntary medical male circumcision (VMMC) is an HIV prevention strategy recommended to partially protect men from heterosexually acquired HIV. From 2015 to 2019, the President's Emergency Plan for AIDS Relief (PEPFAR) has supported approximately 14.9 million VMMCs in 15 African countries. Urethrocutaneous fistulas, abnormal openings between the urethra and penile skin through which urine can escape, are rare, severe adverse events (AEs) that can occur with VMMC. This analysis describes fistula cases, identifies possible risks and mechanisms of injury, and offers mitigation actions.
METHODS METHODS
Demographic and clinical program data were reviewed from all reported fistula cases during 2015 to 2019, descriptive analyses were performed, and an odds ratio was calculated by patient age group.
RESULTS RESULTS
In total, 41 fistula cases were reported. Median patient age for fistula cases was 11 years and 40/41 (98%) occurred in patients aged < 15 years. Fistulas were more often reported among patients < 15 compared to ≥ 15 years old (0.61 vs. 0.01 fistulas per 100,000 VMMCs, odds ratio 50.9 (95% confidence interval [CI] = 8.6-2060.0)). Median time from VMMC surgery to appearance of fistula was 20 days (interquartile range (IQR) 14-27).
CONCLUSIONS CONCLUSIONS
Urethral fistulas were significantly more common in patients under age 15 years. Thinner tissue overlying the urethra in immature genitalia may predispose boys to injury. The delay between procedure and symptom onset of 2-3 weeks indicates partial thickness injury or suture violation of the urethral wall as more likely mechanisms of injury than intra-operative urethral transection. This analysis helped to inform PEPFAR's recent decision to change VMMC eligibility policy in 2020, raising the minimum age to 15 years.

Identifiants

pubmed: 33579261
doi: 10.1186/s12894-021-00790-y
pii: 10.1186/s12894-021-00790-y
pmc: PMC7881669
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

23

Subventions

Organisme : World Health Organization
ID : 001
Pays : International

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Auteurs

Todd Lucas (T)

Division of Global HIV and Tuberculosis, Centers for Disease Control and Prevention, Atlanta, GA, USA. tlucas@cdc.gov.

Jonas Z Hines (JZ)

Division of Global HIV and Tuberculosis, Centers for Disease Control and Prevention, Atlanta, GA, USA.

Julia Samuelson (J)

Global HIV, Hepatitis, and STIs Programmes, World Health Organization, Geneva, Switzerland.

Timothy Hargreave (T)

Department of Surgery, Edinburgh University, Scotland, UK.

Stephanie M Davis (SM)

Division of Global HIV and Tuberculosis, Centers for Disease Control and Prevention, Atlanta, GA, USA.

Ian Fellows (I)

Fellows Statistics, Contractor, Centers for Disease Control and Prevention, San Diego, CA, USA.

Amber Prainito (A)

U.S. Office of the Global HIV/AIDS Coordinator, Washington, DC, USA.

D Heather Watts (DH)

U.S. Office of the Global HIV/AIDS Coordinator, Washington, DC, USA.

Valerian Kiggundu (V)

Office of HIV/AIDS, U.S. Agency for International Development, Washington, DC, USA.

Anne G Thomas (AG)

Department of Defense, Defense Health Agency, San Diego, CA, USA.

Onkemetse Conrad Ntsuape (OC)

Ministry of Health and Wellness, Gaborone, Botswana.

Kunle Dare (K)

Division of Global HIV and Tuberculosis, Centers for Disease Control and Prevention, Gaborone, Botswana.

Elijah Odoyo-June (E)

Division of Global HIV and Tuberculosis, Centers for Disease Control and Prevention, Nairobi, Kenya.

Leonard Soo (L)

U.S. Agency for International Development, Nairobi, Kenya.

Likabelo Toti-Mokoteli (L)

Ministry of Health, Maseru, Lesotho.

Robert Manda (R)

U.S. Agency for International Development, Maseru, Lesotho.

Martin Kapito (M)

Ministry of Health, Lilongwe, Malawi.

Wezi Msungama (W)

Division of Global HIV and Tuberculosis, Centers for Disease Control and Prevention, Lilongwe, Malawi.

James Odek (J)

U.S. Agency for International Development, Lilongwe, Malawi.

Jotamo Come (J)

Ministry of Health, Maputo, Mozambique.

Marcos Canda (M)

Division of Global HIV and Tuberculosis, Centers for Disease Control and Prevention, Maputo, Mozambique.

Nuno Gaspar (N)

U.S. Agency for International Development, Maputo, Mozambique.

Aupokolo Mekondjo (A)

Ministry of Health and Social Services, Windhoek, Namibia.

Brigitte Zemburuka (B)

Division of Global HIV and Tuberculosis, Centers for Disease Control and Prevention, Windhoek, Namibia.

Collen Bonnecwe (C)

National Department of Health, Pretoria, South Africa.

Peter Vranken (P)

Division of Global HIV and Tuberculosis, Centers for Disease Control and Prevention, Pretoria, South Africa.

Susan Mmbando (S)

Ministry of Health, Dar es Salaam, Tanzania.

Daimon Simbeye (D)

Division of Global HIV and Tuberculosis, Centers for Disease Control and Prevention, Dar es Salaam, Tanzania.

Fredrick Rwegerera (F)

U.S. Agency for International Development, Dar es Salaam, Tanzania.

Nafuna Wamai (N)

Division of Global HIV and Tuberculosis, Centers for Disease Control and Prevention, Kampala, Uganda.

Shelia Kyobutungi (S)

U.S. Agency for International Development, Kampala, Uganda.

James Exnobert Zulu (JE)

Ministry of Health, Lusaka, Zambia.

Omega Chituwo (O)

Division of Global HIV and Tuberculosis, Centers for Disease Control and Prevention, Lusaka, Zambia.

Sinokuthemba Xaba (S)

Ministry of Health and Child Care, Harare, Zimbabwe.

John Mandisarisa (J)

Division of Global HIV and Tuberculosis, Centers for Disease Control and Prevention, Harare, Zimbabwe.

Carlos Toledo (C)

Division of Global HIV and Tuberculosis, Centers for Disease Control and Prevention, Atlanta, GA, USA.

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