key: cord-0840818-09ijsdqb authors: Moosa, Shazia; Muhammad, Ammar Ali; Dogar, Sohail; Iftikhar, Sundus; Johnson, Walter; Latif, Asad; Samad, Lubna title: Implementation of an infant male circumcision programme, Pakistan date: 2021-04-01 journal: Bull World Health Organ DOI: 10.2471/blt.19.249656 sha: c8ff57b07b7d88368cc58451d68de9501d128a44 doc_id: 840818 cord_uid: 09ijsdqb OBJECTIVE: To retrospectively review outcomes of a health provider-led infant circumcision programme in Pakistan. METHODS: Based on World Health Organization guidelines, we trained surgical technicians and midwives to perform circumcisions using the Plastibell device at two Indus Health Network facilities. Programme tools include a training manual for health providers, information brochures for families, an enrolment form and standardized forms for documenting details of the procedure and outcomes. Infants aged 1–92 days were eligible for the study. Health workers contacted families on days 1 and 7 after the procedure to record any adverse events. We compared the characteristics of infants experiencing adverse events with infants facing no complications using multivariate logistic regression. FINDINGS: Between August 2016 and August 2018, 2822 circumcised male infants with mean age 22.8 days were eligible for the study. Of these, 2617 infants (92.7%) were followed up by telephone interviews of caretakers. Older infants were more likely to experience adverse events than infants circumcised between 1–30 days of age: 31–60 days: adjusted odds ratio, aOR: 2.03; 95% confidence interval, CI: 1.31–3.15; 61–92 days: aOR: 2.14; 95% CI: 1.13–4.05. Minor adverse events (100 infants; 3.8%) included failure of the bell to shed (90 infants) and minimal bleeding (10 infants). Major adverse events (eight infants; 0.3%) included bleeding that required intervention (four infants), infection (three infants) and skin tear (one infant). CONCLUSION: Standardized training protocols and close monitoring enabled nonphysician health providers to perform safe circumcisions on infants aged three months or younger. Male circumcision is one of the most common surgical procedures performed, with an estimated 38.7% of males circumcised worldwide. 1 Given an annual global birth rate of 70 million boys, 2 around 27 million male circumcisions are performed per year, of which half are religiously or culturally motivated. 3 In recent years, increasing evidence has linked male circumcision to lower rates of asymptomatic urinary tract infections, especially during infancy, 4, 5 and to a lower risk of sexually transmitted diseases, notably human immunodeficiency virus (HIV). 6 This evidence has led to global attention on the prophylactic role of circumcision, with scale-up strategies being advocated in many countries with a high prevalence of HIV and acquired immunodeficiency syndrome, 7 especially in sub-Saharan Africa. In Muslim-majority countries like Pakistan, male circumcision is considered an essential religious practice. 3 This obligation contributes to large surgical volumes, making it even more important that circumcisions should be performed safely with the lowest possible risk of adverse events. An estimated 3.2 million male infants are born in Pakistan every year, 8 almost all of whom undergo circumcision in their infancy or childhood. 3 The mean number of paediatric surgeons is 0.4 per million population in Pakistan 9 and the number of paediatric surgeons in the country is about 200. 10 Therefore, relying exclusively on specialists and general practitioners to meet the need for safe circumcisions is unfeasible. Currently, only 5-10% of boys are presented to qualified surgeons and physicians for circumcision. 11 The remainder of caretakers approach traditional circumcisers, barbers and untrained paramedical staff, 12, 13 who often use unsterilized instruments and unsafe techniques with no follow-up or recording of adverse events. 11 To promote safe circumcision, the World Health Organization (WHO) and the Johns Hopkins Program for International Education in Gynecology and Obstetrics developed a manual with technical guidance for structuring an infant circumcision programme. This manual recommends that infant male circumcision should be the primary task of nonphysician health-care workers. 14 This is an example of task-sharing, where health providers, defined as nonphysician health-care workers by WHO, are trained to perform high volume, technically less demanding tasks, under close supervision and monitoring with a referral system in place. 14, 15 Such task-sharing between surgeons or physicians and trained health providers is not yet well-established in Pakistan, despite insufficient health-care resources. The country therefore needs a public health strategy in which appropriate nonphysician health providers are trained to perform circumcisions safely, using correct techniques and modern infection control practices. 16 With these considerations in mind, the Safe Circumcision Programme was implemented at the Indus Hospital in Karachi to demonstrate a strategic approach for providing safe circumcisions to male infants in Pakistan. The programme provides training for surgical technicians and midwives to perform safe, 17 This study aims to evaluate outcomes during the first 26 months of programme delivery. After a 4-month preparation phase (February through June 2016), the programme started in July 2016 at the Indus Health Network's main campus, Indus Hospital, Karachi, Pakistan. In December 2017, the programme expanded to the network's semi-urban facility in Muzaffargarh in Punjab Province, Pakistan. All Indus Health Network's services, including circumcisions at the daily circumcision clinic, are provided free of charge. While the programme is ongoing, all procedures until 31 August 2018 were included in the present study. We obtained ethical approval for the study from Indus Hospital's Institutional Review Board. The programme has a coordinator responsible for the development of programme tools, training of health workers, data analysis and overall programme management. The training includes how to counsel caretakers, screen infants according to inclusion criteria and collect and enter data on paper forms and electronically using a computer software package. Paediatric surgeons train the health providers to perform circumcisions. Programme tools include a training manual for health providers, information brochures for families, an enrolment form and standardized forms for documenting details of the procedure and outcomes. We developed visual aids, including pictorial representations of the procedure with possible adverse events and an animated video encouraging families to opt for early circumcisions. The video was played in the waiting rooms in the hospital to inform caretakers. The training manual contains information about the programme's background, related anatomy and surgical technique. 11, 14, 15, [18] [19] [20] The Plastibell method of circumcision is used since it is simple, easily taught, recommended by WHO 14 and associated with few adverse events. 16, [21] [22] [23] [24] Practical training started with observing circumcisions, followed by performing the procedure under supervision. We required each trainee to perform a minimum of 20 procedures independently to the trainer's satisfaction. Upon completion of training, a paediatric surgeon assessed the trainee's knowledge and skills. If the skills were suboptimal, the trainee needed to perform additional procedures until they reached a satisfactory level for certification. Once certified, each health provider received a procedural fee of 200 Pakistani rupees (1.2 United States dollars, US$) per circumcision. For Karachi, we trained two surgical technicians, while for Muzaffargarh we initially trained three surgical technicians, who were later replaced by two trained midwives. Caretakers of male infants born at facilities where the programme is established were counselled about early circumcision using programme brochures, while parents of infants born elsewhere spontaneously approached the facility for circumcision. Only healthy infants weighing at least 2.5 kg were included in the programme. Since circumcisions done in younger infants are simpler to perform, heal better, have fewer adverse events and provide health benefits earlier than when done in older infants, 25, 26 we originally set the upper age limit at 60 days, following WHO's recommendations. 14 Later, we extended this limit to 3 months, in agreement with the recommendation of Pakistani surgeons that circumcision should be performed within the first few months of life in the absence of contraindications. 13 In underweight or unwell infants, we deferred circumcision until resolution of the underlying cause. We screened infants for genital anomalies, including hypospadias, epispadias, ambiguous genitalia, congenital buried penis, congenital chordee, micropenis or penoscrotal web, and asked questions for any signs or family history of bleeding disorders. We referred infants with an abnormality to a specialist. Preprocedure investigations, such as coagulation profile, are not routinely performed. 13 We did not consider physiological jaundice as a contraindication; however, we deferred circumcision in infants with visually assessed deep jaundice. 12, 27 We avoided circumcision in the first 24 h after birth to ensure that the infant was stable, had time to void and had started to feed, as well as to give time for any abnormalities to become apparent. 14 At the daily circumcision clinic, a health worker enrolled the infant, obtaining demographic information, medical history and informed consent from parents. 14, 17 The health worker recorded the infant's vital signs. If documentation was not present regarding vitamin K administration at birth, the infant received one dose 30 minutes before the procedure. 28, 29 The health provider checked the equipment, verified the infant's identity and performed a genital examination. A health worker either hand-restrained the infant or strapped him onto a circumcision board. The health provider administered a weight-adjusted dose of lidocaine for a dorsal penile nerve block before circumcision. Half an hour after the procedure, the health provider assessed the infant for excessive pain, swelling or bleeding. Parents received verbal information and a brochure, which included a helpline number, on postoperative care, possible causes for concern and the process for seeking urgent care. As part of the programme, a health worker called the caretaker on day 1 and day 7 after the procedure to enquire about the general well-being of the infant, ring shedding and parental satisfaction. If the ring had not shed by day 7, the health worker called on day 10 to instruct the caretaker to bring the infant to the hospital for ring removal. At least three calls and one text message, preferably to two different contact numbers, were sent before the infant was designated as lost to follow-up. Each health provider received feedback regarding recorded adverse events arising from their work. We classified adverse events as minor (easily handled by health providers); major (requiring specialist intervention); or serious (with life-threatening or long-term sequelae). To minimize bias, the health workers who collected outcome information differed from the health providers who performed the procedure. For monitoring and evaluation, the coordinator Research Safe circumcision programme, Pakistan Shazia Moosa et al. conducted periodic verification on randomly selected patients, by calling a few families every month to ask if they had received the follow-up calls and what their experience had been with the service being offered. Participants were de-identified by assigning programme identifiers, with personal data accessible to the programme team only. We entered all enrolment data in SPSS version 21.0 (IBM Corp., Armonk, New York, United States of America, USA). We expressed categorical variables as proportions, while quantitative variables were described by median and interquartile range, or mean and standard deviation (SD). To compare quantitative variables, we calculated Pearson's correlation coefficients and for categorical variables we used χ 2 tests. The primary outcome variable was adverse events, scored as a binary response variable with yes = 1 and no = 0. We performed univariate and multivariate analyses, using logistic regression. All variables with P < 0.25 in univariate analyses were included in the final multivariable model. All analyses were performed with Stata version 14 (StataCorp LP, College Station, USA). A two-tailed P < 0.05 was considered significant. A total of 4270 boys were born at the two facilities during the study period and the caretakers of 80.3% (3427) of these were counselled about circumcision. During the screening process, 700 infants were excluded, of which 84 caretakers refused circumcision ( Fig. 1 ). Reasons for refusal or deferral at the time of counselling included religious preference (i.e. non-Muslim parents), preference for local circumcisers, unwell mothers, mothers unable to decide independently or parents perceiving their infant too young for circumcision. Fifteen infants with genital abnormalities were referred to specialists. Fourteen infants with undescended testes, minimal chordee, minimal penile torsion, inguinal hernia or unilateral hydrocele were referred to a paediatric surgeon following circumcision. Of the 2822 infants circumcised, 2108 (74.7%) were born in a facility, whereas 714 were outpatients whose caretakers sought to circumcise their baby through the programme. Table 1 shows demographic data of the 2822 enrolled infants. The age of circumcised infants ranged from 1 to 92 days (mean: 22.8; SD: 20.3) and their weight ranged from 2.5-6.7 kg (mean: 3.5; SD: 0.7). Most (2082 infants; 73.8%) were circumcised during the first month of life. Mean age at circumcision depended on the place of delivery and was 17.9 days (SD: 17.1) for inpatients, 36.9 days (SD: 22.1) for infants born at other health facilities, and 39.2 days (SD: 23.0) for infants delivered at home. Mild jaundice was noted in 320 infants (11.3%) at the time of procedure. Infants of Muslim caretakers comprised 96.1% (2712) of our study population, reflecting national statistics. 8 Religious obligation was cited as a reason for undergoing circumcision by 96.2% (2716) of parents. The most common Plastibell size used had a diameter of 1.2 cm (1076 infants; 38.1%), followed by 1.1 cm (750 infants; 26.6%) and 1.3 cm (587 infants; 20.8%). Telephone follow-up was possible for 2617 infants (92.7%). The ring shed spontaneously in 2520 infants (96.3%), with mean shedding day of 6.4 days (SD: 1.7). In 26 infants (1.0%) the ring hung by a small skin tag which shed spontaneously after day 10. Following the procedure, 151 infants (5.4%) presented, spontaneously or after we telephoned the parents, to either the clinic or the emergency department. Of these, 43 caretakers required reassurance, mainly for concerns about ring impaction, bleeding, infection, swelling or unsatisfactory cosmesis. We documented adverse events in 108 (4.1%) infants of contactable caretakers, of which eight (0.3%) infants experienced major adverse events ( Table 2 ). The most frequent adverse event was failure of the bell to shed (90 infants; 83.3%). Table 3 shows the comparison of different characteristics between infants experiencing an adverse event compared with infants who did not. After adjustment for other variables and compared with infants circumcised between 1-30 days after birth, infants circumcised when older were more likely to experience adverse events (31-60 days adjusted odds ratio, aOR: 2.03; 95% confidence interval, CI: 1.31-3.15; 61-92 days; aOR: 2.14; 95% CI: 1.13-4.05). Infants circumcised at the Muzaffargarh facility were more likely to experience adverse events than infants circumcised at the Karachi facility (aOR: 1.67, 95% CI: 1.09-2.54; Table 4 ). The rate of parental satisfaction with the programme was 99.8% (2611/2617). While some believe that the Plastibell circumcision method is only safe when performed by experienced surgeons, 30 task-sharing is needed to provide safe circumcision for infants in countries with large volumes due to high birth rate and increased demands mainly due to religious considerations. To meet the demand in Pakistan, we used the WHO task-sharing recommendations for infant male circumcision services 14 to train nonphysician health providers to circumcise boys aged 3 months or younger. Such task-sharing has also been successfully implemented in African countries where nurses and trained paramedical staff routinely perform adult male circumcisions [31] [32] [33] and in Bradford, the United Kingdom of Great Britain and Northern Ireland, to cater to the Muslim population. 19, 34 Our study shows an overall proportion of adverse events of 4.1%, of which only 0.3% required specialist intervention and none were life-threatening. This proportion is lower than reported proportions for similar studies in other settings. In two studies based in the United Kingdom, infants aged 6 to 14 weeks underwent Plastibell circumcisions by trained nurses and the reported proportions of adverse events were 8.2% (93/1129) and 18.5% (31/168). 19, 34 In a large-scale study in Nigeria, where trained doctors employed the Plastibell method of circumcision in neonates and infants, the proportion was 1.1% (25/2276). 22 In contrast, a single-surgeon series of 381 infants undergoing Plastibell circumcisions in the Islamic Republic of Iran showed a proportion of adverse events of 7.1% (27/381), 35 whereas 386 infants circumcised by the same method by a paediatrician in the United Republic of Tanzania showed only minor adverse events in 2.8% (11/386) of infants. 24 Postoperative adverse events seem to be independent of technique, whether procedures are performed in high-or low-income settings, or if done by a surgeon, paediatrician, nurse or health worker. 17 Thorough training of the health provider, meticulous technique when performing the circumcision and close monitoring of outcomes to ensure consistent quality of care appear to be key for preventing adverse events. 11, [18] [19] [20] The risk of adverse events using the Plastibell method increases with age of the infant, 21,36 which can be attributed to increasing thickness and vascularity of preputial skin and difficulty in restraining larger infants. 24 Our results indicate that infants circumcised within their first month of life experienced the least number of adverse events. Although higher, the proportion of adverse events remained constant in infants after the neonatal period till 3 months of age. By extending the age limit to 3 months in our programme, we were able to perform safe circumcisions for infants who had surpassed the 60 days age limit set by WHO. 14 The mean age at circumcision was lower for inpatient infants, indicating that partnering circumcision clinics with maternity services or vaccination centres facilitates counselling and earlier referral. Adverse events arising after Plastibell circumcision range from trivial to consequential. 20 The most common adverse event in our study was failure of the ring to shed or ring impaction, similar to other studies (3.6%; 41/1129 and 6.1%; 75/1223 respectively). 19 [38] [39] [40] [41] Post-procedure bleeding was reported in 1.1% (30/2625) of children in a large retrospective review; 42 our study showed an incidence of 0.5% which also included minor bleeds that were controlled by application of direct pressure with gauze or gauze sprayed with adrenaline. While oral antibiotics are prescribed routinely in some centres, 22 the nominal infection rate observed in our programme justifies our practice of avoiding the prophylactic use of postoperative oral antibiotics. The significant difference observed in proportions of adverse events between the Karachi and Muzaffargarh sites may be attributed to the fact that the programme team remotely monitored this site, while the Karachi site received close support, as the programme team was based in Karachi. Additionally, unlike the Muzaffargarh site, on-campus paediatric surgeons were available in Karachi to intervene early in complicated cases. In our opinion, factors critical to the programme's success are thorough training of health providers, close monitoring of outcomes and a reliable referral system. Additionally, strict adherence to programme protocols, which was ensured by monitoring, and provision of clear follow-up instructions to families provided a safety net for patient care. Key challenges during implementation were to maintain an uninterrupted supply of Plastibells, continuous availability of sterilized instruments and to obtain permission from provincial governments to allow nonphysicians to perform the procedure. These challenges were addressed by advance planning, volume projections, close coordination with the supply chain and the Central Sterile Supply Department. Furthermore, to convince the government and regulatory bodies to allow task-sharing, we provided them with evidence-based results, including programme data. Notably, this programme could have potential cost savings for the health system and families. Cost of circumcision done by paediatric surgeons at local private hospitals ranges from 3600 to 9000 Pakistani rupees (US$ 22.4-55.9) per procedure, whereas public sector hospitals provide the same service free of cost, albeit with long waiting lists and overburdened teams. In comparison, one procedure in our programme costs 1550 Pakistani rupees (US$ 9.6), which includes the procedural fee plus cost of supplies, consumables and indirect cost. If scaled up to national level, our approach can ensure safe circumcisions at lower costs to both the health system and families. Between March and June 2020, health-care resources at the network's facilities were redirected to treat patients with coronavirus disease 2019 and all elective surgeries were suspended. This suspension created significant surgical backlog including circumcisions. When routine surgeries gradually resumed, the paediatric surgery team had to prioritize essential surgeries over circumcisions of infants who had surpassed the age limit of inclusion in our programme during the pause in routine services. We overcame this challenge by increasing the age limit to 6 months and included this cohort of infants in the Safe Circumcision Programme, while supported by the paediatric surgery team in case of any adverse event. This experience provides an excellent example of how task-sharing can fill a gap in the delivery of a key service at a time of critical need. This study had some limitations. We derived the data from a service delivery programme, which adopted a single method of circumcision most suited for our population. Outcome data are missing for 7% (205) of infants because their parents could not be contacted after the procedure. Adverse events may have been overreported in our study, since we counted all instances of bleeding, including minimal ooze, unlike previous studies. Since shedding of the ring was the end-point for follow-up, long-term sequelae are not reported here. We have shown that infant circumcisions are safely performed within 3 months of birth by trained health providers. In high-volume settings with in-sufficient numbers of surgeons, trained surgical technicians and midwives are a reliable resource for performing circumcisions if standardized training protocols and close monitoring systems are in place. ■ Вывод Стандартизованные протоколы обучения и тщательный мониторинг позволили провайдерам медико-санитарных услуг, которые не являются врачами, выполнять безопасное обрезание крайней плоти у младенцев в возрасте трех месяцев и младше. Objetivo Revisar retrospectivamente los resultados de un programa de circuncisión infantil temprana dirigido por proveedores sanitarios en Pakistán. Métodos Según las directrices de la OMS, hemos formado a técnicos quirúrgicos y matronas para que realizaran circuncisiones con el dispositivo Plastibell en dos centros de la Red de Salud Indus. Las herramientas del programa incluyen un manual de formación para los proveedores sanitarios, folletos informativos para las familias, un formulario de inscripción y formularios estandarizados para documentar los detalles del procedimiento y los resultados. Los lactantes de 1 a 92 días de edad eran elegibles para el estudio. Los trabajadores sanitarios se pusieron en contacto con las familias los días 1 y 7 después del procedimiento para registrar cualquier acontecimiento adverso. Se compararon las características de los lactantes que experimentaron acontecimientos adversos con las de los lactantes que no sufrieron complicaciones mediante una regresión logística multivariante. Resultados Entre agosto de 2016 y agosto de 2018, 2.822 bebés circuncidados con una media de edad de 22,8 días cumplieron los requisitos para participar en el estudio. De ellos, 2617 lactantes (92,7%) fueron objeto de seguimiento mediante entrevistas telefónicas por parte de los cuidadores. Los lactantes de más edad tuvieron más probabilidades de sufrir acontecimientos adversos que los circuncidados entre 1 y 30 días: 31-60 días: odds ratio ajustada, ORA: 2,03; intervalo de confianza del 95%, IC: 1,31-3,15; 61-92 días: ORA: 2,14; IC del 95%: 1,13-4,05. Los acontecimientos adversos menores (100 lactantes; 3,8%) incluyeron fallos en la separación del glande (90 lactantes) y hemorragias limitadas (10 lactantes). Los acontecimientos adversos importantes (ocho lactantes; 0,3%) incluyeron hemorragias que requirieron intervención (cuatro lactantes), infección (tres lactantes) y desgarro de la piel (un lactante). Conclusión Los protocolos de formación estandarizados y la estrecha vigilancia han permitido a los profesionales sanitarios distintos de los médicos realizar con seguridad circuncisiones en bebés de hasta los tres meses de edad. 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