Children's Surgery in Sub-Saharan Africa
PaedSurgAfrica
Paediatric Surgery Across Sub-Saharan Africa: A Multi-Centre Prospective Cohort Study
1 other identifier
observational
1,407
1 country
1
Brief Summary
Background: Five billion people worldwide do not have access to safe, affordable surgical care. A significant proportion live in sub-Saharan Africa (SSA), where up to 50% of the population are children. There is limited literature on neonatal and paediatric surgery in SSA and children's surgery does not appear on any of the National Health Strategic Plans for the 47 independent countries across SSA. Objectives: To form a collaboration of surgeons and allied health professionals involved in children's surgery across SSA and collectively undertake the largest prospective cohort study of paediatric surgery in this region. Materials and Methods: Data will be collected via REDCap website on all patients with gastroschisis, anorectal malformation, appendicitis, inguinal hernia and intussusception, during a 1-month period of collaborators choice between October 2016 to April 2017, with a 30-day follow up until the end of May 2017. Estimated study population: 1450 patients from 50 institutions. Full ethical approval has been granted by the host centre; local ethical approval will be required at collaborating centres for participation. All collaborators will be co-authors. Primary outcome will be in-hospital all-cause mortality. Secondary outcomes will include post-intervention complications. Data will be collected on institutional facilities, patient demographics, duration from condition onset to presentation, peri-operative resuscitation, intervention and outcome. Differences in outcomes between SSA and benchmark data from high-income countries will be calculated using chi-squared analysis. Multi-level multivariate logistic regression analysis will be used to identify interventions and peri-operative factors associated with improved outcomes; p\<0.05 will be deemed significant. Outcome: Results will be used to advocate for enhanced children's surgical services in SSA. We shall identify context-appropriate interventions associated with improved outcome. The collaboration will help to enhance research capacity in the region.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Oct 2016
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
October 1, 2016
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 31, 2017
CompletedFirst Submitted
Initial submission to the registry
June 12, 2017
CompletedFirst Posted
Study publicly available on registry
June 14, 2017
CompletedStudy Completion
Last participant's last visit for all outcomes
June 30, 2017
CompletedAugust 21, 2017
June 1, 2017
8 months
June 12, 2017
August 16, 2017
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
All-cause in-hospital mortality
In-hospital (if in the patient is still in hospital at 30-days post-intervention, a 30-day mortality will be utilised)
Secondary Outcomes (5)
30-day mortality
30-days
Duration of hospital stay
Patients are followed up for a maximum of 30-days post-intervention
Surgical site infection
Within 30-days post-intervention
Full thickness wound dehiscence
Within 30-days post-intervention
Need for re-intervention
Within 30-days of the primary intervention
Study Arms (5)
Gastroschisis
All patients presenting primarily to the institution with gastroschisis during the data collection period will be included in the study.
Anorectal malformation
All patients presenting primarily to the institution with anorectal malformation during the data collection period will be included in the study.
Appendicitis
All patients under 16-years of age presenting primarily to the institution with appendicitis during the data collection period will be included in the study.
Intussusception
All patients under 16-years of age presenting primarily to the institution with intussusception during the data collection period will be included in the study.
Inguinal hernia
All patients under 16-years of age undergoing surgery for an inguinal hernia at the institution during the data collection period will be included in the study.
Interventions
This is an observational study. Patients were not allocated to different interventions. Common interventions for each of the conditions, which will be compared during analysis include the following: Gastroschisis - primary operative closure, surgical silo, preformed silo. Anorectal malformation - various types of stoma, anoplasty, PSARP, other. Appendicitis - antibiotics, open appendicectomy, laparoscopic appendicectomy. Intussusception - air enema reduction, hydro-enema reduction, laparotomy. Inguinal hernia - open repair, laparoscopic repair.
Eligibility Criteria
Collaborating centres were recruited using convenience sampling with snowballing. Centres include both tertiary paediatric surgery centres and district hospitals.
You may qualify if:
- All patients under 16-years of age presenting primarily with one of the five study conditions during the data collection period. This includes those managed conservatively without surgery or intervention and those offered palliative care, except patients with an inguinal hernia who must receive surgery to be included.
You may not qualify if:
- Patients re-presenting with one of the five study conditions with a complication from a previous intervention or requiring further surgical intervention.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- King's College Londonlead
- Sylvanus Olympio University Teaching Hospital, Lome, Togo.collaborator
- National Hospital of Niameycollaborator
- Centre Hospitalier Universitaire de la Mère et de l Enfant, Cotonou, Benin.collaborator
- HEAL Africa Hospital, Goma, Democratic Republic of the Congo.collaborator
- Centre Hospitalier Universitaire Pédiatrique Charles de Gaullecollaborator
- University Hospital De Bouaké, Ivory Coast.collaborator
- Teaching Hospital Treichville, Abidjan, Ivory Coast.collaborator
- Harare Central Hospital, Zimbabwe.collaborator
- University Teaching Hospital, Lusaka, Zambiacollaborator
- Mulago Hospital, Ugandacollaborator
- Tikur Anbessa Specialized Hospital, Addis Ababa, Ethiopia.collaborator
- Mbingo Baptist Hospital, Cameroon.collaborator
- Ministry of Health, Ghanacollaborator
- Korle-Bu Teaching Hospital, Accra, Ghanacollaborator
- Edna Adan Maternity Hospital, Hargeisa, Somaliland.collaborator
- Embu Level 5 Hospital, Kenya.collaborator
- Tenwek Hospitalcollaborator
- Soba University Hospitalcollaborator
- Kamuzu Central Hospitalcollaborator
- Queen Elizabeth Central Hospital, Blantyre, Malawicollaborator
- Muhimbili National Hospital, Dar es Salaam, Tanzania.collaborator
- Grey's Hospitalcollaborator
- Stranger Hospital, Kwazulu-Natal, South Africa.collaborator
- Tygerberg Hospital, South Africa.collaborator
- Clinton Hospital, Johannesburgcollaborator
- Charlotte Maxeke Johannesburg Academic Hospitalcollaborator
- Chris Hani Baragwanath Academic Hospitalcollaborator
- East London Hospital Complex, South Africa.collaborator
- Red Cross War Memorial Childrens Hospitalcollaborator
- Delta State University Teaching Hospital Ogharracollaborator
- Bowen University Teaching Hospital, Ogbomosocollaborator
- Ondo State Trauma and Surgical Centrecollaborator
- Mnamdi Azikiwe University Teaching Hospitalcollaborator
- University Of Nigeria Teaching Hospitalcollaborator
- University of Port Harcourt Teaching Hospitalcollaborator
- University College Hospital, Ibadancollaborator
- Ahmadu Bello University Teaching Hospitalcollaborator
- University of Abuja Teaching Hospitalcollaborator
- National Hospital, Abujacollaborator
- University of Calabar Teaching Hospitalcollaborator
- Federal Medical Centre, Abeokutacollaborator
- Federal Medical Centre, Owocollaborator
- Benue State University Teaching Hospitalcollaborator
- Olabisi Onabanjo University Teaching Hospitalcollaborator
- University of Ilorin Teaching Hospitalcollaborator
- Federal Medical Centre Lokojacollaborator
- Lagos State Universitycollaborator
- Obafemi Awolowo University Teaching Hospitalcollaborator
- Aminu Kano Teaching Hospitalcollaborator
Study Sites (1)
King's Centre for Global Health and Health Partnerships
Denmark Hill, London, SE5 9RJ, United Kingdom
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PMID: 18929686BACKGROUND
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Target Duration
- 30 Days
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
June 12, 2017
First Posted
June 14, 2017
Study Start
October 1, 2016
Primary Completion
May 31, 2017
Study Completion
June 30, 2017
Last Updated
August 21, 2017
Record last verified: 2017-06
Data Sharing
- IPD Sharing
- Will share
Following publication, the full anonymous data set will be made publicly available.