SYSTEMATIC REVIEW article

Front. Glob. Women’s Health, 01 July 2025

Sec. Infectious Diseases in Women

Volume 6 - 2025 | https://doi.org/10.3389/fgwh.2025.1605049

Surgical site infections after caesarean section across sub-Sahara Africa: a scoping review of prevalence and associated factors

  • 1. Centre for International Health Protection, Robert Koch Institute, Berlin, Germany

  • 2. University Hospital Bouaké, Bouaké, Côte d'Ivoire

  • 3. Faranah Regional Hospital, Faranah, Guinea

  • 4. Methods Development, Research Infrastructure and Information Technology, Robert Koch Institute, Berlin, Germany

Abstract

Surgical site infections are among the most common healthcare associated infections worldwide and pose a significant risk in cesarean section procedures, which are the most frequently performed surgical operations globally. Our scoping review aimed to synthesize available literature from studies conducted in sub-Saharan Africa on the prevalence of post-caesarean surgical site infections, as well as on reported associated factors. In this scoping review we included studies retrieved in OVID from January 2014 to January 15, 2024 without restrictions on the language of publication or publication status focusing on studies from sub-Saharan African countries. The review was registered on the Open Science Framework platform. The reported rates of surgical site infection across the 73 included studies ranged from 2.0%–56.0%. A forest plot showed that the studies were highly heterogeneous, whereby only 11.0% showed a surgical site infection rate above 20.0%. Most surgical site infections surfaced within two-weeks after a caesarean section. The strongest and most frequently cited risk factors were: duration of labour ≥8 h, surgical duration, multiple vaginal examinations, stored water usage, and premature rupture of membrane. The following protective factors were also determined: Pfannenstiel/transversal incisions, caesarean section at term, having health insurance, normal body mass index, <1 h of surgical intervention, <24 h of premature rupture of membrane, low intraoperative blood loss and absorbable sutures. Staphylococcus aureus was the most commonly isolated pathogen among studies with bacteriological reporting. Our scoping review provides first guidance for regions with limited resources for surveillance, such as sub-Saharan Africa, by outlining most common associated factors and a minimum screening period of two weeks. While utilizing minimal resources effectively, this targeted surveillance could capture the majority of cases and thereby enhancing maternal patient safety.

Systematic Review Registration:

https://osf.io/qe7bf/

Introduction

Surgical site infections (SSIs) in general are a major cause for post-surgical mortality and morbidity (). With a global incidence between 3.0 and 15.0% (), SSIs are among the most common healthcare associated infections worldwide (). In low-resource settings, there are limited surveillance systems and hence scarce data on prevalence and associated factors of SSIs (), but existing evidence suggests highest prevalence rates up to 30.9% in the African region (). The most commonly performed operations around the world are caesarean sections (CSs) (). In the African region, up to 20.0% of CSs result in SSIs leading to increased maternal morbidity and mortality, longer hospital stays and higher treatment costs (). A recent systematic review and meta analysis on SSIs after CS reports global risk factors related to comorbidities. These reported risk factors were obesity, diabetes, hypertension, prolonged hospital stays, inappropriate timing of antibiotics, and environmental factors such as overcrowded living conditions and improper hygiene (). In the African region, there is currently no comprehensive review on SSIs and their risk factors following caesarean section. For the African region, up to now there is no review on SSIs and associated risk factors after CS.

Our scoping review aims to synthesize literature on prevalence of SSIs after CS across sub-Saharan Africa (SSA), while elucidating associated risk and protective factors. This summarization of available evidence and hence deeper understanding of associated factors can potentially guide SSA healthcare stakeholders such as hospitals and practitioners in risk assessment and mitigation for increased maternal patient safety.

Methods

We conducted a scoping review following the Preferred Reporting Items for Systematic Reviews and Meta-Analysis extension for Scoping Reviews (PRISMA-ScR) () and the Joanna Briggs Institute (JBI) methodology for scoping reviews (). We adapted our search strategy for the African continent from the strategy used by Barth and colleagues () in conjunction with the definition of SSA from the World Bank (). The protocol including the search strategy was published on Open Science Framework (OSF) (). At the time the protocol was uploaded, no similar reviews were registered in either OSF or PROSPERO. We searched the platform OVID for publications between January 2014 and January 15, 2024 without restrictions on the language of publication or publication status. We used Rayyan () for deduplication and EndNote X7 (Clarivate Analytics, PA, USA) for screening and study selection (conducted by AB, RW and SM). Screening of titles and abstracts for assessment as well as screening of full text against the inclusion criteria for the review was done in pairs by the research team (AB, RW, SM, SW). Any disagreement arising at each stage of the selection process was resolved through discussion with first and supervisory authors. Studies were considered eligible if they included women who received CSs in health settings in SSA. All types of studies, including clinical trials, cohort or case-control studies were included. In the case of intervention studies, reported sample size and prevalence for the baseline were used in order to show generalisable prevalence rates. Articles in English and French were included.

Data extraction was done in double and independently by the research team (AB, RW, SM, SW) into a structured form in Microsoft Excel. The extracted variables included: author, publication year, title, journal, publication status, study type, study period, City/Country, sample size, sampling strategy, response rate, inclusion criteria, exclusion criteria, age, SSI prevalence, clinical appearance, sample collection, testing strategy, testing rate, type of infection, type of test, test name, factors investigated, factors associated, level of analysis and additional data. A forest plot was used to display results descriptively and given the hetereogeneity of included studies, a meta analysis was not performed.

Results

Selection of studies

The search identified a total of 395 articles; following the removal of duplicates and critical assessment of title and abstracts, 117 potentially relevant articles were identified for full-text screening (Figure 1). Application of the pre-set eligibility criteria resulted in a final inclusion of 73 articles. All included studies were conducted between January 2009 and March 2023.

Figure 1

Study characteristics

The included studies contain SSI prevalence data on 51,695 women from 20 countries across SSA, with most studies from Ethiopia (17/73), Nigeria (12/73), Rwanda (11/73) and Tanzania (9/73) (Figure 2, Table 1). The most frequently analyzed health settings were university, teaching or tertiary hospitals 37.0% (27/73), followed by referral, district or regional hospitals 32.9% (24/73). No study included private hospitals. The majority of studies included women who underwent CS at the study site regardless of the indication, whereby 5.5% (4/73) focused on emergency and 2.7% (2/73) on elective CSs only (Table 1).

Figure 2

Table 1

Reference and Publication yearSSI DefinitionCity, countryStudy TypeSample size (N)SSI prevalence % (n/N)Follow-up (d)Reported AppearanceFactors associated as reported (aOR, 95% CI, p-value)Highest level of analysisBacteriological Reporting Yes/No
Adane, A. et al. ()CDCHarar, Dire Dawa, Oromia, Somali, EthiopiaCohort336Overall: 7.7% (26/336)308/26 before dischargeRupture of the membrane before CS (aOR 3.75, 95% CI: 1.85–16.6)MultivariateYes
Emergency: 14.9% (17/114)18/26 through follow-up and readmission
Elective: 4.1% (9/222)
Alemye, T. et al. ()CDCHarar, EthiopiaCross-sectional1,069Overall: 12.3% (131/1,069)30NRGeneral anesthesia (aOR 2.02, 95% CI: 1.34–3.02), rupture of membrane before CS (aOR 1.91, 95% CI: 1.18–3.09), post-operative hospital stay > 7d (aOR 2.24, 95% CI: 1.61–3.64), blood transfusion (aOR 4.10, 95% CI: 2.61–6.44)MultivariateNo
Emergency: 12.9% (105/811)
Elective: 10.1% (26/258)
Ali, O. et al. ()Clinical DiagnosisGondar, EthiopiaCross-sectional818Overall: 12.2% (100/818)NR60/100 (60.0%) after dischargeChorioamnionitis (aOR 6.46, 95% CI: 1.82–22.71, p = 0.01), Diabetes Mellitus (aOR 6.02, 95% CI: 1.69–21.36, p = 0.005, rupture of membrane ≥ 12 h before CS (aOR 2.94, 95% CI: 1.52–5.67, p = 0.001), MSAF (aOR 2.43, 95% CI: 1.23–4.81, p = 0.011), anemia (aOR 3.44, 95% CI: 1.56–7.56, p = 0.002)MultivariateNo
Emergency: 14.0% (96/688)
100/100 (100.0%) within 14 days
Elective: 3.1% (4/130)
Alidina, S. et al. ()NRLake Zone, TanzaniaCase-controlPre-intervention: 1,120 (intervention) 1,113 (control)Pre-intervention: intervention: 6.5% (73/1,120)30NRNRNRNo
Control: 8.1% (90/1,113)
Overall Pre-intervention:(163/2,233)
Overall pre-intervention: 2,233
No follow-up after discharge
Post-intervention: intervention: 2.3% (23/980)
Post-intervention: 980 (intervention)
Control: 2.6% (11/427)
427 (control)
Aulakh, A. et al. ()CDCGambiaCase-control682Overall: 13.2% (90/682)3051/90 (58.0%) after dischargeDecision-to-incision time (p = 0.01), fetal status (p = 0.001), postoperative stay (p = 0.001), antibiotic regimen (p = 0.03)BivariateNo
Emergency: 12.3% (70/571)
Elective 9.1% (3/33)
Ayala, D. et al. ()CDCNekemte, EthiopiaCross-sectional382Overall: 8.9% (34/382)30NRAge > 35 years (aOR 5.03, 95% CI: 1.69–14.95, p = 0.004), pregnancy-induced hypertension (aOR 5.63, 95% CI: 1.88–16.79, p = 0.002), prolonged Labor (>24 h) (aOR 4.12, 95% CI: 1.01–32.19, p = 0.048), general anesthesia (aOR 3.96, 95% CI: 1.02–15.29, p = 0.040), post-operative hemoglobin <11 g/dl (aOR 4.51, 95% CI: 1.84–11.07, p = 0.001)MultivariateNo
Emergency: 8.5% (28/328)
Elective: 11.1% (6/54)
Azeze, G. ()NRDahir Dar, EthiopiaCross-sectional3837.8% (30/383)3022/30 (73.3%) after dischargeRupture of membrane before CS (aOR 13.9, 95% CI: 2.99–64.8, p = 0.002), vertical skin incision (longitudinal abdominal incision) (aOR 4.77, 95% CI: 1.74–13.06, p = 0.001), duration of surgery >30 m (aOR 4.9, 95% CI: 1.8–13.1, p = 0.001), Interrupted skin closure technique (aOR 6.29, 95% CI: 2.07–19.11, p = 0.002)MultivariateNo
Bizuayew, H. et al. ()CDCGojjam zone, Northwest EthiopiaCross-sectional62212.4% (77/622)30NRResidence (rural) (aOR 2.30, 95% CI: 1.29–4.09, p = 0.005), rupture of membrane >12 h (aOR 4.61, 95% CI: 2.34–9.09, p = 0.001), duration of labor >24 h (aOR 3.48, 95% CI: 1.50–8.09, p = 0.004), hypertension (aOR 3.14, 95% CI: 1.29–7.59, p = 0.011), preoperative hematocrit <30% (aOR 3.22, 95% CI: 1.25–8.31, p = 0.016)MultivariateNo
Brisibe, S. et al. ()NRPort Harcourt, South NigeriaCross-sectionalSite 1Site 1 baseline: 13.17% (54/410), follow up: 10.34% (43/416); Site 2 13.95% (42/301)NoneNRNoneBivariateNo
Baseline: 410, Follow up: 416 Site 2: 301
Buambo, J. et al. ()NRBrazzaville, CongoCross-sectional1,06338.4% (408/1,063)30NRAge <25 years (aOR 2.0, 95% CI: 1.01–4.1, p = 0.04), primary education (aOR 4.1, 95% CI: 1.4–11.8, p = 0.09), BMI > 30 kg/m2 (aOR 5.9, 95% CI: 1.2–27.1, p = 0.02), PROM >6 h (aOR 2.2, 95% CI: 1.1–4.1, p = 0.02), tinted amniotic fluid (aOR 3.6, 95% CI: 1.6–7.6, p = 0.001), duration of surgery >45 min (aOR 21.1, 95% CI: 11.3–39.4, p = 0.001), no dressing (aOR 2.5, 95% CI: 1.3–4.5, p = 0.004), antibiotics (aOR 3.9, 95% CI: 2.2–6.8, p = 0.001)MultivariateNo
Carshon-Marsh, R. et al. ()NRBo, Sierra LeoneCohort599Overall: 7.5% (45/599)30 (after discharge, telephone calls)NRNANANo
Mergency:7.4% (40/541)
Elective: 8.6% (5/58)
Cherian, T. et al. ()CDCKirehe, RwandaCross-sectional5259.9% (52/525)10 ± 3, call 30NRNAMultivariateNo
Chu, K. et al. ()CDCBurundi, DRC, Sierra LeoneCohort1,2767.3% (93/1,276)Until dischargeMedian: 6 days (range 2–17)Age <30 years (aOR 2.1, 95% CI: 1.2–3.6, p = 0.013), program site (Lubutu) (aOR 0.3, 95% CI: 0.1–0.9, p = 0.038), PROM (aOR 2.1, 95% CI: 1.3–3.4, p = 0.002), neonatal death (aOR 2.7, 95% CI: 1.5–5.0, p = 0.001), antenatal hemorrhage (aOR 0.2, 95% CI: 0.05–1.0, p = 0.050)MultivariateNo
Dayo-Dada, T. et al. ()NREkiti State, NigeriaCohort1,224Overall: 16.0% (196/1,224)NRNRAge (X²: 97.714, p < 0.000), Occupation (X²: 80.321, p < 0.000), Gravidity (X²: 175.768, p < 0.000), Parity (X²: 571.065, p < 0.000), Type of Cesarean Section (Emergency vs. Elective) (X²: 0.008, p < 0.000), Indication for CS (X²: 246.844, p < 0.000), Previous Scar (X²: 199.09, p < 0.000) Occupation (X²: 80.321, p < 0.000)BivariateNo
Emergency: 16.0% (146/915)
Elective: 16.2% (50/309)
De Nardo, P. et al. ()CDCDodoma, TanzaniaCohort467Overall: 48.2% (225/467)30Median: 8 daysSenior doctor (OR 0.64, 95% CI: 0.43–0.97, p < 0.04), Pfannenstiel (incision) (OR 0.30, 95% CI: 0.18–0.5, p < 0.001), continuous intradermic (OR 0.26, 95% CI: 0.15–0.45, p < 0.001)Bivariate, none significant in multivariateYes
Emergency: 48.7% (207/425)
Elective: 43% (18/42)
Delamou, A. et al. ()CDCMultiple districts, GuineaCohort7,394Overall: 7.7% (570/7,394)NRNRYear of surgery:2,014 (aOR 0.70, 95% CI: 0.57–0.84, p = 0.001) 2,015 (aOR 0.43, 95% CI: 0.34–0.55, p < 0.001) comorbidities (aOR 1.54, 95% CI: 1.25–1.90, p < 0.001)MultivariateNo
2013: 10.0% (331/3,331)
2014: 7.0% (138/1,971)
2015: 5.0% (101/2,020)
Dessu, S. et al. ()CDCDire Dawa, EthiopiaCases: 119 Controls: 357476NAHospital dischargeNRAge 20–34 years (aOR 5.4, 95% CI: 2.35–12.7), age >35 years (aOR: 8.9, 95% CI: 1.8–43.9), <4 vaginal examinations (aOR 4.2, 95% CI: 2.16–8.22), history of chorioamnionitis (aOR 5, 95% CI: 1.05–23.9), previous CS (aOR 6.2, 95% CI: 2.72–14.36), antibiotic prophylaxis (aOR 3.2, 95% CI: 1.81–5.62), perioperative haematocrit level <30% (aOR 6.9, 95% CI: 3.45–14.1), rupture of membrane >12 h (aOR 5.4, 95% CI: 1.84–15.87)MultivariateNo
Cases: 119
Controls: 357
Di Genarro, F. et al. ()CDCFreetown, Sierra LeoneCase-control2,32310.9% (254/2,323)NRMean 4.4 ± 1.8 daysBeing single (aOR 1.48, 95% CI: 1.36–1.66), abnormal BMI, low BMI (aOR 1.42, 95% CI: 1.18–1.72), high BMI (aOR 1.85, 95% CI: 1.02–2.68), admitted from home (aOR 2.35, 95% CI: 2.18–2.59), unemployed (aOR 1.74, 95% CI: 1.24–2.21), low education level (aOR 1.68, 95% CI: 1.55–1.84), presenting with PROM (aOR 1.49, 95% CI: 1.18–1.88), long decision–incision time (aOR 2.08, 95% CI: 1.74–2.24), frequent missing post CS antibiotic doses (aOR 2.52, 95% CI: 2.10–2.85), previous CS (aOR 1.27, 95% CI: 1.10–1.52)MultivariateNo
Dlamini, L. et al.* ()CDCKampala, UgandaRandomized Clinical Trial432Overall: 56.5% (244/432)10NRNRBivariateNo
Elbur, A. et al. ()CDCKhartoum, SudanCross-sectional5788.3% (48/578)30NRNRMultivariateNo
Eleje, G. et al. ()NRItuku Ozalla/Enugu, NigeriaCross-sectionalOverall: 607Overall: 6.1% (37/607)NRNRNoneBivariateNo
During COVID-19: 228During COVID-19: 6.6% (15/228)
Pre-COVID-19: 379Pre-COVID-19: 8% (22/379)
Ernest, E. et al. ()CDCKagera/Mara regions, TanzaniaCross-sectional279Baseline 13.9% (19/136)Until dischargeNRImplementation of the safe surgery interventions in both health care center (p = 0.006) and hospitals (p < 0.001)BivariateNo
Follow-up 0.7% (1/143)
Fletcher, R. et al. ()Clinical DiagnosisKirehe, RwandaCohort5305.7% (30/530)±3 (with Thermal Camera)NRNRNRNo
Fletcher, R. et al. ()NRKirehe, RwandaCohort57210.8% (62/572)10 ± 3NRNRNRNo
Gajewski, J. et al. ()NRZambiaRandomized Control Trial1,3141.6% (21/1,314)NRNRNoneBivariateNo
Gashaw, A. et al.# ()CDCHawassa, EthiopiaCohort431All Emergency: 11.8% (51/431)NR<7 daysMultiple vaginal examinations >5 (aOR 6.10, 95% CI: 2.15–17.35, p = 0.001), estimated blood loss >500 ml (aOR 3.16, 95% CI: 1.19–8.38, p = 0.021) duration of labor ≥12 h (aOR 4.05, 95% CI: 1.12–13.7, p = 0.001), rupture of membrane ≥12 h (aOR 4.12, 95% CI: 1.50–11.27, p = 0.006)MultivariateNo
22/51 (43,1%)
7–14 days
28/51 (54,9%)
>14 days
1/51 (2.0%)
Gelaw, K. et al. ()Clinical DiagnosisMaichew, EthiopiaCross-sectional3846.8% (26/384)3020/26 (76.9%) before dischargeLabor >24 h (aOR 3.48, 95% CI: 1.25–9.68), rupture of membrane before CS (aOR 3.68, 95% CI: 1.13–11.96) midline incision compared to Pfannestiel (aOR = 5.73, 95% CI: 2.05–16.00)MultivariateNo
6/26 (23.0%) after discharge
Gentilotti, E. et al. ()CDCDodoma, TanzaniaCohortTotal: 1,040Overall: 30.8% (320/1,040)30NROverall/pre-intervention: Pfannenstiel incision (OR 0.29, 95% CI: 0.20–0.42, p < 0.001), continuous intradermic/semi-subcutaneous suture (OR 0.32, 95% CI: 0.23–0.46, p < 0.001); Pre-intervention: higher experience of the surgeon (OR 0.64, 95% CI: 0.43–0.97, p = 0.038)MultivariateYes
Emergency: 31% (299/964)
Pre: 467Elective: 27.6% (21/76)
Pre-Intervention: 48.2% (225/467)
Post: 573
Post-Intervention: 16.6% (95/573)
Post-intervention: younger age (OR 2.38, 95% CI: 1.38–4.09, p = 0.001), absorbable stiches (OR 0.47, 95% CI: 0.27–0.81, p = 0.006)
multivariate: lack of pre-incision antibiotic prophylaxis (OR 3.59, 95% CI: 1.92–6.70, p < 0.001), skin disinfection with Dettol/Ethanol (OR 2.40, 95% CI: 1.00–5.74, p = 0.050), absorbable suture (OR 0.52, 95% CI: 0.28–0.97, p = 0.040), normal BMI (18,5–24,9) (OR 0.63, 95% CI: 0.40–0.99, p = 0.045)
Gidiri, M./Ziruma, A. ()NRPartirenyatwa/Harare, ZimbabweRandomized Control Trial2324.7% (11/232)42NRNoneBivariateNo
Hedt-Gauthier, B. et al. ()Clinical DiagnosisKirehe District, RwandaCohort56910.7% (61/569)10NRNRNRNo
Igwemadu, G. et al. ()NRKeffi, NigeriaRandomized Control Trial1627.0% (11/162)14 after dischargeNRNoneBivariateNo
Kabore, B. et al. ()NRFada N'Gourma/Diapage, Burkina FasoCase-control198: cases: 99, controls: 99NRNRNRHyperthermia upon admittance (aOR 2.37, 95% CI: 1.9–5.3, p = 0.035), caput succedaneum (aOR 7.0, 95% CI: 2.5–16.7, p = 0.001) difficult extraction of the fetus (aOR 3.69, 95% CI: 1.26–6.3, p = 0.02)MultivariateNo
Kasanga, M. et al. ()NRLusaka, ZambiaCross-sectional8386.0% (50/838)NRNRSecondary education (OR 0.38, 95% CI: 0.15–0.95, p < 0.038), emergency CS (OR 6.25, 95% CI: 2.83–13.80, p < 0.001), oral antibiotics post CS (OR 0.22, 95% CI: 0.05–0.96, p < 0.045), performing facility (OR 0.06, 95% CI: 0.02–0.17, p < 0.001), 8–15d IV antibiotic treatment (OR 18.04, 95% CI: 6.61–49.28, p < 0.001),BivariateNo
Kateera, F. et al. (45)NRKirehe, RwandaRandomized Control Trial87110.9% (95/871)30NRNoneBivariateNo
Ketema, D. et al. (46)CDCAmhara, EthiopiaCohort520Overall: 25.4% (132/520)30Median: 8 daysNot able to read and write (AHR 1.30, 95% CI: 1.19–2.11), no antenatal care (AHR 2.16, 95% CI: 1.05–4.53), previous CS (AHR 1.21, 95% CI: 1.11–2.31), HIV positive (AHR 1.39, 95% CI: 1.21–2.57), emergency procedure (AHR 1.13, 95% CI: 1.11–2.43), vertical skin incision (AHR 2.60, 95% CI: 1.05–6.44), rupture of membrane (AHR 1.50, 95% CI: 1.31–1.64), multiple vaginal examination (AHR 1.88, 95% CI: 1.71–3.20)MultivariateNo
Emergency: 26.3% (111/422)
Elective: 21.4% (21/98)
(IQR 5–13)
Kpagoi, S. et al. (47)WHO protocol for surgical site infectionBo, Sierra LeoneCross-sectional5962.5% (15/596)30NRNRNRNo
Lijaemiro, H. et al. (48)CDCAddis Ababa, EthiopiaCohort16615.1% (25/166)301–10 days (9.4%)One-year increment in age (aOR 1.50, 95% CI: 1.17–1.93, p < 0.001), gestational age (aOR 0.02, 95% CI: 0.00–0.29, p < 0.004), one-minute increment of duration of surgery (aOR 1.12, 95% CI: 1.03–1.20, p < 0.009), ≥5 vaginal examinations (aOR 13.08, 95% CI: 1.02–168.00, p < 0.048), CS at term (aOR 0.02, 95% CI: 0.00–0.29)MultivariateNo
11–17 days (15.6%)
25–30 days (1.4%)
Lukabwe, H. et al.* (49)NRMbarara, UgandaRandomized Control Trial9630.2% (29/96)30NRPre-operative baths with Chloroxylenol (adjusted RR 0.1, 95% CI: 0.03–0.33, p < 0.001)MultivariateNo
Mezemir, R. et al. (50)CDCAddis Abeba, EthiopiaCohort74111.6% (86/741)30Mean: 9 days2–3 antenatal care visits (aOR 3.11, 95% CI: 1.69–5.75), delayed antenatal booking (aOR 6.99, 95% CI: 2.09–23.32), PROM (aOR: 2.10, 95% CI: 1.0–4.24), multiple vaginal examinations (aOR 4.21, 95% CI: 1.35–6.92), public hospitals (aOR 11.1, 95% CI: 1.48–45.14), hospital stay <7 days (aOR 0.37, 95% CI: 0.15–0.91), transversal incisions (aOR 0.38, 95% CI: 0.15–0.91)MultivariateYes
(Range 8–10)
Mivumbi, V. et al. (51)NRKigali, RwandaRandomized Control Trial1323.8% (5/132)14All within 14 days (14 days was the study follow-up time)NRNRYes
Miyoshi, Y. et al. (52)*NRZimba, ZambiaCohort2662.3% (6/266)NRNRNoneBivariateNo
Mohammed, S. et al. (53)CDCKano, NigeriaRandomized Control Trial154Overall: 8.4% (13/154)30Mean: 7.9 ± 3.8 daysNoneBivariateNo
Emergency: 17.0% (8/47)
Elective: 4.7% (5/107)NR
Molla, M. et al. # (54)CDCDebretabor, EthiopiaCross-sectional3348.1% 27/334)30Before discharge: 3/27 (11.1%)Pregnancy induced hypertension (aOR 4.75, 95% CI: 1.62–13.92), chorioamnionitis (aOR 4.37, 95% CI: 1.53–12.50), midline skin incision (aOR 5.19, 95% CI: 1.87–14.37), post-operative hemoglobin l < 11 g/dc (aOR 5.28, 95% CI: 1.97–14.18)MultivariateNo
Post Discharge: 24/27 (88.9%)
Mothiba, M. et al. † (55)CDCPretoria, South AfricaRandomized Control Trial2070 (0/207)30NRNoneBivariateNo
Mpogoro, F. et al. # (56)CDCMwanza, TanzaniaCohort34510.9% (34/312)30Median: 7 daysHypertensive disorder (HR 2.9, 95% CI: 1.4–6.4, p < 0.006); contaminated wound (HR 2.5, 95% CI: 1.2–5.1, p < 0.016), multiple vaginal examinations (HR 2.6, 95% CI: 1.3–5.3, p < 0.008), operation done by intern doctor (HR 4.2,95% CI: 1.8–9.5, p < 0.001), severe anemia (HR 3.8, 95% CI: 1.2–12.4, p < 0.028), duration of procedure >1 h (HR 2.3, 95% CI: 1.1–4.8, p < 0.030)MultivariateYes
(IQR: 6–9)
Mukantwari, J. et al. (57)CDCKirehe, RwandaCohort67110.7% (72/671)3011 days: 33/671 (4.9%)Having health insurance (aOR 0.06, 95% CI: 0.01–0.58, p < 0.013), higher economic status (aOR 2.88, 95% CI: 1.39–5.97, p < 0.004)MultivariateNo
30 days: 39/671 (5.8%)
Ketemaw, N./ Dereje Zeleke, B. (58)CDCKaffa Zone, EthiopiaCohort36810.3% (38/368)NRNRNoneBivariateNo
Ngonzi, J. et al. (59)NRMbarara, UgandaCohort678Pre-intervention: 14.5% (29/200)Only pre-discharge follow-upNRNRBivariateNo
During intervention: 7.4% (17/230)
Post-intervention: 10.5% (26/248)
Ngowa, J. et al. (60)NRYaoundé, CamerounCohort4601.7% (8/460)30NRNRBivariateNo
Nguhuni, B. et al. (61)CDCDodoma, TanzaniaCohort37412.0% (45/374)30Median: 8 daysNoneNRNo
(IQR: 7–11)
Njoku, C. et al. (62)CDCCalabar, NigeriaCohort600Overall: 8.5% (51/600)30NREmergency CS (aOR 4.71, 95% CI: 3.19–5.35, p < 0.001), indication for CS (aOR 1.35, 95% CI: 1.00–1.65, p < 0.002), duration of membrane rupture (aOR 0.52, 95% CI: 0.32–0.95, p < 0.002), duration of labor (aOR 0.47, 95% CI: 0.20–0.79, p < 0.001), intra-operative blood loss >1 L (aOR 1.22, 95% CI: 1.17–2.90, p < 0.048), duration of surgery <1 h (aOR 0.03, 95% CI: 0.01–0.07, p < 0.028), post-operative packed cell volume <30% (aOR 2.60, 95% CI: 1.46–4.12, p < 0.002)MultivariateYes
Emergency: 11.0% (45/410)
Elective: 3.2% (6/190)
Nkurunziza, T. et al. (63)NICEKirehe, RwandaCohort55010.9% (60/550)10 ± 3All within 10 days (10 days was the study follow-up time)Transport cost >1.1 EUR (aOR 2.42, 95% CI: 1.31–4.49, p < 0.005), housewife (aOR 2.93, 95% CI: 1.08–7.97, p < 0.035), Skin preparation with one antiseptic (aOR 4.42, 95% CI: 1.05–18.57, p < 0.043)MultivariateNo
Nkurunziza, T. et al. (64)CDCKirehe, RwandaCohort787POD 10 ± 3: 4.2% (30/715)Home visit with telemedicine: 10 ± 3All within 10 days (10 days was the study follow-up time)NRNRNo
POD 11 ± 3: 5.4% (38/707)
Hospital visit: 11 ± 3,
Odada, D. et al. (65)NHSNNairobi, KenyaCase-controlTotal: 1,262Overall: 2.1% (27/1,262)30Out of the 27 SSI (4 dropped due to missing information)NoneBivariateYes
Out of 69 study participants: Emergency: 35.3% (12/34)
(69 study participants)14 days: 13/23 (56.0%)
Elective: 31.4% (11/35)
15–30 days: 10/23 (43.5%)
Ogah, C. et al. (66)*NRAbakaliki, NigeriaRandomized Control trial302 (152 control, 150 intervention)Overall: 7.3% (22/302)30Mean: 4.1 daysNoneBivariateYes
Intervention: wound infection: 5.3% (8/150)
Control: wound infection: 9.2% (14/152)
Onuzo, C. et al. (67)CDCAccra, GhanaCohort474Overall: 12.9% (61/474)30Before discharge from hospital: 13/61 (21.3%)Being single (aOR 4.81, 95% CI: 1.21–19.17, p < 0.03), alcohol consumption >3l/week (aOR 5.97, 95% CI: 1.32–26.98, p < 0.02), duration of labor ≥ 8 h (aOR 75.67, 95% CI: 6.61–866.24, p < 0.01), emergency CS (aOR 4.66, 95% CI: 1.22–17.75, p < 0.02), stored water used for pre-operative scrub rather than running water (aOR 18.60, 95% CI: 3.55–97.56, p < 0.01), vertical midline skin incision (aOR 12.55, 95% CI: 2.14—73.63, p < 0.05)MultivariateYes
Emergency: 16.5% (51/309)
Detected in post-discharge follow-up: 48/61 (78.8%)
Elective: 6.1% (10/165)
Median: 7 days
Onyegbule, O. et al. (68)NRNnewi, NigeriaCross-sectional120Overall: 12.5% (15/120)Follow-up and diagnosis done at day 4, additional follow-up not NRFollow-up and diagnosis done at day 4, additional follow-up not NRFor emergency CS: rupture of membrane <24 h (aOR 0.11, 95% CI: 0.03–0.47, p < 0.003), duration of labor <12 h (aOR 0.07, 95% CI: 0.01–0.32, p < 0.001), Pfannenstiel incision (aOR 0.21, 95% CI: 0.05–0.91, p < 0.038)MultivariateNo
Emergency: 20.0% (12/60)
Elective: 5.0% (3/60)
Oyeyem, N. et al. † (69)NRLagos, NigeriaRandomized Control Trial19021.6% (41/190)14 days and 6 weeksNRNoneBivariateNo
Peter, E./Ali Seif, S. (70)NRDodoma, TanzaniaCross-sectional18320.8% (38/183)14NRPoor wound care (aOR 5.95, 95% CI:1.76–20.17, p < 0.004), earth/sand houses (aOR 4.32, 95% CI: 1.11–16.83, p < 0.03)MultivariateYes
Rabiu, K. et al. (71)NRLagos, NigeriaCohort906Overall: 19.4% (176/906)Until DischargeNRPreoperative anemia (aOR 1.88, 95% CI: 1.03–3.41, p < 0.040, diabetes mellitus (aOR 7.94, 95% CI: 1.60–39.27, p < 0.011), HIV infection (aOR 6.34, 95% CI: 1.74–23.06, p < 0.005), prolonged operation time (aOR 2.30, 95% CI: 1.19–4.42, p < 0.013), excessive blood loss at surgery (aOR 5.05, 95% CI: 2.18–11.66, p < 0.000), chorioamnionitis (aOR 9.00, 95% CI: 1.37–59.32, p < 0.022)MultivariateNo
Emergency: 24.1% (143/594)
Elective: 10.6% (33/312)
Robb, K. et al. (72)screening protocolKirehe, RwandaCross-sectional1739.8% (17/173)30NRLack of water (OR 2.6, p < 0.027)BivariateNo
Sawadogo, Y. et al. (73)*Clinical DiagnosisOuagadougou, Burkina FasoCross-sectional1,9983.5% (70/1,998)NRMean: 6,7 ± 2.3 daysNoneNAYes
Scherbaum, M. et al. (74)RKI/CDCLambaréné, GabonCohort806.3% (5/80)Until dischargeAll detected before dischargeNRNRNo
Sway, A. et al. (75)CDCKiambu, KenyaCohort6006.7% (40/600)30NRAdministration of pre-operative antibiotic prophylaxis (OR 0.41, 95% CI: 0.20–0.82, p < 0.01)BivariateNo
Ugadu, I. et al. (76)CDCAbakaliki, NigeriaRandomized Control Trial2394.6% (11/239)14NRPreoperative cleansing on maternal infectious morbidity (RR 0.13, 95% CI: 0.05–0.36, p < 0.000)BivariateNo
Velin, L. et al. (77)CDCKirehe, RwandaCohort7955.7% (45/795)11 ± 3Range: 8—14 daysNRNRYes
Waalewijn, B. et al. (78)NRSierra LeoneCohort1,1743.7% (36/984)NRNRNRBivariateNo
Wae, M. et al. (79)NRArba Minch, EthiopiaCohort41612.0% (50/416)NRNRNRNRNo
Wendmagegn, T. et al. (80)CDCMekelle, EthiopiaCohort206Overall: 11.7% (24/206)NRNRPROM (aOR 8.82, 95% CI: 21.71–35.82, p < 0.002), prolonged labor (aOR 16.17, 95% CI: 2.85–91.82), p < 0.006), rural setting (aOR 5.67, 95% CI: 1.57–20.48), HIV positive (aOR 6.98, 95% CI: 1.38–35.27, p < 0.019), chorioamnionitis (aOR 16.17, 95% CI: 2.85–91.82, p < 0.002), blood loss <1000 ml (aOR 0.01 95% CI: 0.02–0.57, p < 0.01)MultivariateNo
Emergency: 12.4% (24/193)
Elective: 0.0% (0/13)
Westen, E. et al. (81)NRLindi/ Masasi, TanzaniaRandomized Control Trial1818.3% (15/181)30NRNRNRNo
Wodajo, S. et al. (82)CDCHawassa Town, EthiopiaCross-sectional59211.0% (65/592)NRBefore discharge: 64/65 (98.4%)Prolonged labor >24 h (aOR 6.78, 95% CI: 2.54–18.00), PROM < 12 h (aOR 5.83, 95% CI: 2.14–15.89), 1–4 digital vaginal examinations (aOR 2.91, 95% CI: 1.21–6.99), 5 digital examinations (aOR 8.59, 95% CI: 1.74–42.23), duration of surgery >1 h (aOR 12.32, 95% CI: 5.46–27.77), wound contamination class III (aOR 9.61, 95% CI: 1.84–50.06), conducted by junior professionals (GP) (aOR 7.06, 95% CI: 1.62–30.70) MSc students (aOR 8.31, 95% CI:1.79–28.52), postoperative hemoglobin <11 mg/dl (aOR 2.62, 95% CI: 1.21–5.69)MultivariateNo
Woodd, S. et al. (83)CDCDar es Salaam, TanzaniaCohort1468.2% (12/146)7telephone interviewNRNRMultivariateNo
Zubairu, U. et al. (84)CDCZaria, NigeriaRandomized Control Trial17011.2% (19/170)14Mean: 10.2 ± 3.6 daysLevel of education (tertiary) (aOR 0.24, 95% CI: 0.08–0.75, p < 0.014), parity <4 (aOR 0.23, 95% CI: 0.08–0.67, p < 0.007), no endometritis (aOR 0.10, 95% CI: 0.03–0.29, p < 0.000), no febrile morbidity (aOR 0.12, 95% CI: 0.02–0.72, p < 0.020)MultivariateNo
Emergency: 13.9% (14/101)
Elective: 7.2% (5/69)

Results of included studies.

CDC, center for disease control and prevention; CI, confidence interval; AHR, adjusted hazard ratio; aOR, adjusted odds ratio; BMI, body mass index; CD, caesarean delivery; CS, c-section; GP, general practitioner; HIV, human immunodeficiency virus; HR, hazard ratio; Md, median; IQR, interquartile range; MSAF, meconium-stained amniotic fluid; MSc, master of science; NA, not applicable; NHSN, national healthcare safety work; NICE, national institute for health and care excellence; NR, not reported; PCV, pac,ed cell volume; POD, post-operative day; PROM, premature rupture of membrane; RKI, Robert-Koch-Institute; RR, relative risk; SD, standard deviation; SSI, surgical site infection; WHO, world health organization.

*

This study only included emergency C-sections.

#

Studies that had both elective/emergency C-sections included, whereby SSIs only appeared in those who had an emergency C-section.

†

Studies which only had elective C-sections included.

In terms of study type, 43.8% (32/73) of included studies were cohort, 28.8% (21/73) cross-sectional studies and 19.2% (14/73) randomized control studies and 8.2% (6/73) case control (Table 1).

Regarding the applied SSI definition, the majority of studies (54.5%, 40/74) reported to have used the Center for Disease Control guidelines (85), but only a slim majority of 52.5% (21/40) of these also conducted patient follow-up for the full recommended 30-day period. In total, a 37.0% (27/73) minority of studies reported full tracking of patients up to 30 days regardless of the definition applied (Table 1).

SSI rate and appearance time

Reported SSI rates among studies ranged from 2.0% ()–56.0% () (Figure 3). The forest plot showed that the studies were highly heterogeneous (I2 = 100.0%, p < 0.001), and only 11.0% (8/73) of studies showed an SSI rate above 20.0% (Table 1). Regarding the indication for CSs, SSI rates for emergency CS ranged between 7.4% () and 48.7% (), whereby SSI after elective CS from 3.1% ()–43.0% ().

Figure 3

Superficial SSIs had rates as high as 100.0% and were described in 32.3% (24/73) of studies followed by 24.7% (18/73) of studies reporting deep SSIs with highest rate of 32%, and 16.4% (12/73) detailing organ SSIs with rates up to 30.9% (Table 2).

Table 2

PublicationSSI Classification (superficial/cutaneous/incisional, deep, and organ, other)
Adane, A. et al. ()Superficial: 19/26 (73.1%)
Deep: 3/26 (11.5%)
Organ: 4/26 (15.38%)
Ali. O. et al. ()Superficial: 88/100 (88.0%)
Deep: 12/100 (12.0%)
Organ: NA
Aulukah, A. et al. ()Superficial: 88/89 (98.9%)
Deep: NA
Organ: 1/89 (1.1%)
Azeze, G./Bizuneh, A. ()Superficial: 23 (76.7%)
Deep: 7 (23.3%)
Organ: NA
Brisibe, S. F. A. et al. ()Site 1
Superficial: 16/54 (29.6%)
Deep: 25/54 (46.3%)
Organ: 13/54 (24.1%)
Site 2
Superficial: 10/42 (23.8%)
Deep: 19/42 (45.2%)
Organ: 13/42 (31.0%)
Buambo, J. R. G. et al. ()Superficial: 90/408 (22.0%)
Other: Endometritis 163/408 (40.0%)
Pelviperitonitis: 65/408 (16.0%)
Chu, K. et al. ()Superficial: 85/93 (91.4%)
Deep: 7/93 (7.5%)
Unknown: 1/93 (1.1%)
De Nardo,P. et al. ()Superficial: 138/225 (61.4%)
Deep: 69/225 (30.6%)
Organ/spaces: 5/225 (2.3%)
Unknown: 13/225 (5.7%)
Delamou, A. et al. ()Cutaneous:
2013: 88.0%
2014: 93.0%
2015: 89.0%
Di Genarro, F. et al. ()Superficial: 90/254 (35.4%)
Deep: 98/254 (38.6%)
Organ/Space: 66/254 (26.0%)
Gashaw A, et al. ()Superficial: 33/51 (64.7%)
Deep: 15/51 (29.4%)
Organ/space: 3/51 (5.9%)
Gentilotti, E. et al. ()Pre:
Superficial: 138/225 (61.3%)
Deep/involving organ and/or space: 74/225 (32.9%)
Post:
Superficial: 80/95 (84.2%)
Deep/involving organ and/or spaces: 11/95 (11.6%)
Overall:
Superficial: 218/320 (68.1%)
Deep/Organ: 85/320 (26.6%)
Lijaemiro et al. (48)Superficial: 17/25 (68.0%)
Deep: 8/25 (32.0%)
Mezemir, R. et al. (50)Superficial: 81/86 (94.1%)
Molla, M. et al. (54)Superficial incisional: 7/27 (27.1%)
Mpogoro, F. et al. (56)Superficial: 21/34 (61.8%)
Organ space: 8/34 (23.5%)
Deep: 5/34 (14.7%)
Nguhuni, B. et al. (61)Superficial: 42/45 (93.3%)
Deep: 2/45 (4.4%)
Oragn/space: 1/45 (2.2%)
Nkurunziza, T. et al. (63)Superficial: 45/60 (75.0%)
Odada, D. et al. (65)Superficial: 18/23 (78.3%)
Deep: 5/23 (21.7%)
Onuzo, C. et al. (67)Superficial: 41/61 (67,2%)
Deep incisional: 18/61 (29.5%)
Organ space: 2/61 (3.3%)
Rabiu, K. A.et al. (71)Superficial: 139/176 (79.0%)
Deep: 37/176 (21.0%)
Sway, A. et al. (75)Thika:
Superficial: 11/12 (91.7)
Organ/space: 1/12 (8.3)
Kiambu:
Superficial: 18/28 (64.3%)
Deep: 7/28 (25.0%)
Organ/Space: 3/28 (10.7%)
Unknown: 1/28 (3.6%)
Velin, L. et al. (77)Superficial: 40/45 (88.9%)
Deep: 5/45 (11.1%)
Wodajo, S. et al. (82)Superficial: 46/65 (70.8%)
Deep: 17/65 (26.1%)
Organ: 2/65 (2.3%)

SSI classification in included studies.

Appearance time of an SSI was reported by 42.5% (31/73) of included studies. A majority 61.3% (19/31) of those studies stated that most SSIs appear during the first two weeks after CS. Additionally, some studies reported SSI appearance time terms of pre/post-discharge (8/31) out of which a 75% majority (6/8) of SSIs appeared during post-discharge (Table 1).

Associated factors

Associated factors in the development of SSIs were reported in 38.0% (28/73) of the studies (Table 1). Duration of labour ≥8 h presented as the strongest risk factor (aOR 75.6) (67) and was mentioned in 9.6% (7/73) of the included studies (Table 1). Extended surgical duration, mentioned six times as a risk factor, also presented a substantial risk (aOR 21.1) () (Table 1).

A high number (greater than five) of vaginal examinations was mentioned multiple times with a risk of up to 13.1 (48), as well as stored water with aOR of 18.6 (48).

Additionally, chorioamnionitis (aOR 16.2) (80), an infection of the amniotic fluid, also significantly elevated the risk of post-caesarean SSI and was mentioned in five of the included studies (Table 1).

Premature rupture of membrane (PROM), was observed in 14 of the included studies (Table 1), making it the most frequent risk factor with reported aOR of up to 13.9 (). Anaemia (also reported as low-haemoglobin/haematocrit/packed cell volume) throughout the surgical intervention was mentioned nine times (Table 1) with the highest aOR of 6.9 (). Vertical/midline skin incisions (aOR 12.6) (67) were also notably high-risk factors compared to Pfannenstiel/transversal incisions which were reported as protective factors (aOR 0.21) (68).

The analysis of protective factors for post-CS outcomes identified several key factors, whereby CS at term (aOR 0.02) (48) presented the strongest protective effect against SSIs.

Having health insurance (aOR 0.06) (57) as well as tertiary level of education (aOR 0.24) (84), demonstrated as protective factors. Within the same study, all other associated factors were found to be protective including parity <4 (aOR 0.23) (84). Women with a normal body mass index (18.5–24.9) showed a protective aOR of 0.63 ().

As opposed to the demonstrated risk factors of prolonged duration of labour, extended surgery duration and PROM, a <12 h duration of labour (aOR 0.07) (68), less than a 1 h surgical intervention (aOR 0.03) (62) and <24 h of membrane rupture (aOR 0.52) (62) were reported as protective factors.

Other surgical factors such as intraoperative blood loss of <1,000 ml (aOR 0.10) (80) and absorbable sutures (aOR 0.52) () were strong protective factors. Lastly, hospital stays of less than seven days had a protective aOR of 0.37 (50).

Bacteriological profiles

Only a minority of studies (17.8%; 13/73) reported bacteriological test results (Table 1). Staphylococcus aureus (S. aureus) was isolated in all thirteen of the studies with detection rates of up to 52.6% (70), and three of these studies also reported Methicillin-resistant S. aureus (MRSA) (, , 67) which in turn was detected in rates of up to 79.0% (, ). One study measuring a 79.0% MRSA rate was able to reduce to a rate of only 21.0% following interventive measures ().

Gram-negative bacteria were also prominent, particularly Escherichia coli which was identified in nine of the studies, and Klebsiella pneumoniae which was mentioned in seven studies, with two other studies also reporting Klebsiella species. Gram-negative bacteria was also reported as being resistant to ampicillin (100.0%), amoxicillin/clavulanate (93.0%), and trimethoprim/sulfamethoxazole (78.5%) (56) and susceptible or resistant to ceftriaxone (92.1%) and cefepime (84.6%) (77).

Discussion

This scoping review has a wide geographical representation with included data from 20 SSA countries, whereby most studies came from Ethiopia and Nigeria, possibly reflecting these countries as research epicenters in the region.

Our scoping review found a varying rate of SSIs. However, a large majority reported rates equal or below 20%, reflecting the WHO reporting for the African region ().

CS are the most commonly performed major operation globally (), thus surveillance of SSI after CS can be a good starting point for SSI surveillance (). However, full patient follow-up to day 30 was only conducted in a small minority of studies, demonstrating a possible discordance between international guidelines and their feasibility in resource-limited settings. Given that the majority of SSI were diagnosed within the first two weeks after CS, this time frame could potentially be taken into consideration in the pending update to the WHO SSI surveillance protocol for resource-limited settings (). Additionally, eight studies examined SSI occurrences in relation to discharge timing, with six reporting that SSIs primarily emerged post-discharge. This highlights the need to follow-up discharged patients, especially within the first two weeks after CS.

Given the limited-resource setting in SSA, the introduction of surveillance systems could start by targeted SSI screening of patients with the risk factors identified as most frequent such as PROM, prolonged labor, duration of surgery, anemia and multiple vaginal examinations. In addition to this targeted surveillance, we would recommend considering measures to mitigate certain risk factors, such as, treating anemia, applying hygiene measures during vaginal examinations and ensuring the provision of clean water. Additionally, certain surgical techniques such as Pfannenstiel (horizontal/transversal) incisions and absorbable sutures should be prioritized given their potential to minimize foreign body reaction (86) and decrease the likelihood of SSIs. SSIs can lead to increased hospital stays, costs, morbidities and mortalities, making their prevention and prompt management a priority (87). Incorporating these protective factors into clinical practice can potentially enhance patient recovery and reduce complication rates and hospitalisation duration. Such incorporation should be done in accordance with the WHO global guidelines for SSI prevention which also specify known protective measures (88).

Our scoping review found a considerable lack in the provision of data on bacteriological profiles. This weakness is in line with recent literature, showing that only 1.0% of laboratories in SSA are formally assigned to deliver bacterial testing (). However, our synthesized data highlights Staphylococcus aureus as the most frequently reported pathogen causing SSI aligning with data from a recent meta-analysis (). This is an area of concern considering corresponding reported rates of Methicillin-resistant S. aureus. Prevalence of Gram-negative Klebsiella pneumonia and Escherichia coli also emphasizes the burden of enterobacteria in SSI.

Current literature promotes antibiotic stewardship measures such as selecting the proper antibiotic for prophylaxis in accordance with current resistance data, but acknowledges that stewardship recommendations can be difficult to implement in settings like SSA that have limited antibiotic resources and resistance data (89). These findings, therefore, highlight the urgent need for enhanced bacteriological surveillance and antimicrobial resistance monitoring to inform effective SSI management strategies in the SSA region.

Limitations

This scoping review has several limitations. Despite our inclusive approach and the inclusion of all studies conducted in SSA, only 20 out of 48 of SSA countries were represented with highest representation of Ethiopia and Nigeria. We did not limit our search to English articles, nevertheless, we were only able to retrieve two French publications. As such, we reran the OVID search using French terms, but still did not retrieve additional French articles. Our search strategy only included studies published from 2014 onwards, potentially excluding older but relevant data. Due to the lack of available data in included studies, as well as missing correlation between symptom data and SSI, and vague distinction between wound infection symptoms and other issues such as endometritis, we dropped the analysis of SSI symptom data. Lastly, no private hospitals were included in the selected studies, therefore our findings may not be applicable in those settings.

Conclusion

Findings from this study can aid those who wish to follow the WHO recommendations in using post-caesarean section SSIs as a practical entry point for healthcare associated infection surveillance. However, low reporting on aspects such as full 30-day follow-up and bacteriological testing from included studies suggests difficulty in implementation of some surveillance measures. As most reported SSIs surfaced within the first two-weeks, this time frame can be taken into consideration as a first step in surveillance implementation. Regions such as SSA that have limited-resources for surveillance and treatment can also consider targeted SSI screening of patients with frequent risk factors, and promotion of reported protective measures. Furthermore, bacteriological diagnostic capacity building is greatly needed in the region in order to improve data gaps and antibiotic treatment recommendations. Utilization of these recommendations can ideally contribute towards improved safety for women undergoing CS in SSA.

Statements

Data availability statement

The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author.

Author contributions

RW: Conceptualization, Data curation, Formal analysis, Funding acquisition, Investigation, Methodology, Project administration, Resources, Software, Supervision, Validation, Visualization, Writing – original draft, Writing – review & editing. AB: Conceptualization, Data curation, Formal analysis, Funding acquisition, Investigation, Methodology, Project administration, Resources, Software, Supervision, Validation, Visualization, Writing – original draft, Writing – review & editing. SW: Data curation, Formal analysis, Software, Writing – original draft. MN: Funding acquisition, Writing – review & editing. AD: Funding acquisition, Writing – review & editing. MD: Writing – review & editing. KH: Conceptualization, Investigation, Methodology, Software, Writing – original draft. CR: Conceptualization, Formal analysis, Methodology, Visualization, Writing – original draft, Writing – review & editing. IN: Conceptualization, Funding acquisition, Project administration, Writing – review & editing. BD: Conceptualization, Funding acquisition, Supervision, Writing – review & editing. MC: Funding acquisition, Writing – review & editing. SM: Conceptualization, Data curation, Formal analysis, Funding acquisition, Investigation, Methodology, Project administration, Resources, Software, Supervision, Validation, Visualization, Writing – original draft, Writing – review & editing.

Funding

The author(s) declare that financial support was received for the research and/or publication of this article. This study was funded by the Global Health Protection Program (# ZMI5-2523GHP029) under project PAcCI (Public Health Actions Ivory Coast) and (# ZMI5-2523GHP024) under project PASQUALE (Partnership to Improve Patient Safety and Quality of Care).

Acknowledgments

We would like to thank Dr. Francisco Pozo Martin for his experienced insight and guidance in the drafting of this review. Additionally, we thank all the past participants of the many studies included in this scoping review.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Generative AI statement

The author(s) declare that no Generative AI was used in the creation of this manuscript.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Abbreviations

aOR, adjusted odds ratio; BMI, body mass index; CDC, center for disease control and prevention; CI, confidence interval; CS, caesarean section; HIV, human immunodeficiency virus; JBI, Joanna Briggs institute; MRSA, methicillin-resistant staphylococcus aureus; OR, pdds ratio; OSF, open science framework; PRISMA-ScR, preferred reporting items for systematic reviews and meta-analysis extension for scoping reviews; SDGs, sustainable development Goals; SSA, sub-saharan Africa; SSI, surgical site infection; WBG, world bank group; WHO, world health organization.

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Summary

Keywords

surgical site infection, wound infection, caesarean, sub-Saharan Africa, scoping review

Citation

Wood R, Borodova A, Wolter S, N’Guessan M, Diallo AA, Diallo MK, Heldt K, Rocha C, Nabé I, Diané B, Cherif MS and Müller SA (2025) Surgical site infections after caesarean section across sub-Sahara Africa: a scoping review of prevalence and associated factors. Front. Glob. Women’s Health 6:1605049. doi: 10.3389/fgwh.2025.1605049

Received

15 April 2025

Accepted

12 June 2025

Published

01 July 2025

Volume

6 - 2025

Edited by

Bandit Chumworathayi, Khon Kaen University, Thailand

Reviewed by

Andrew Mgaya, Muhimbili National Hospital, Tanzania

Akmal El-Mazny, Cairo University, Egypt

Updates

Copyright

*Correspondence: Rebekah Wood

† These authors have contributed equally to this work and share first authorship

Disclaimer

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.

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