- Letter to the Editor
- Open Access
Effect of handrubbing using locally-manufactured alcohol-based handrubs in paediatric wards in Harare, Zimbabwe
Antimicrobial Resistance & Infection Control volume 6, Article number: 8 (2017)
We assessed bacterial contamination of hands of adults present in paediatric wards in two tertiary-care hospitals in Harare, Zimbabwe and the microbiologic efficacy of locally-manufactured alcohol-based hand rub (ABHR). During unannounced visits, samples were collected using hand-print and hand-rinse methods. Samples were collected from 152 individuals (16 nurses, 10 doctors, 28 students, 86 parents/guardians, 12 others). Contamination of hands with Gram-negative bacteria was found in 91% of adults tested with a mean of 14.6 CFU (hand-rinse method; IQR 3–65), representing a high risk for transmission of pathogens potentially leading to nosocomial infections. A single application of ABHR under controlled conditions achieved an average of 82% (or 0.72 log) reduction in detectable counts. Amongst 49 Enterobacteriaceae isolates from hands, 53% were resistant to gentamicin and 63% were resistant to cefpodoxime. Use of ABHR represents an attractive intervention for reducing nosocomial infections in this setting.
Health-care workers’ (HCWs) hands have frequently been found to be colonized with potential pathogens during routine patient care . These organisms survive if hand hygiene by HCWs is inadequate or omitted entirely. Infections are transmitted  when contaminated hands come in direct contact with another patient or an object used for patient care [3, 4].
Zimbabwe has been undergoing strenuous economic challenges for more than a decade. Amongst other difficulties, this has led to intermittent water supply in many hospitals. Alcohol-based hand-rub (ABHR) is recommended as an effective method of hand decontamination during routine patient care [5, 6] and is locally-produced in many hospitals in low-income countries .
This study was a cross-sectional evaluation ahead of a planned trial of an ABHR-based intervention. We focused on the detection of Gram-negative Enterobacteriaceae on the hands of adults to determine whether this potentially represented a major vector for transmission of antibiotic-resistant Enterobacteriaceae between paediatric patients in this setting.
Study participants were recruited from the paediatrics wards of two tertiary government-sector hospitals in Harare, Zimbabwe. These hospitals have established hospital infection programs, but no routine data on hand-hygiene performance was being collected at the time of the study.
After relevant ethics approvals, all adults present in wards on unannounced study dates were approached for participation. After informed consent was obtained, one hand (either left or right) was tested before and after ABHR use . Four fingers of the selected hand were lightly pressed to an agar plate to make a print (hand-print method). The same hand was then rinsed in a bag containing 200 ml of sterile water by inserting the entire hand, shaking vigorously and rubbing fingers and thumb together for 15 s (hand-rinse method). Plastic bags (Zipwave, Multix, Australia) were sterilized between uses by immersion in boiling water. From each hand-rinse sample, 100 ml of liquid was filtered using paper with 0.45 μm apertures (Millipore, UK). A 0.5 MacFarland suspension of ATCC 25923 E.coli and sterile water were used as controls.
Alcohol-based hand rub prepared at Parirenyatwa Hospital Pharmacy following the WHO guidelines  was used. For quality control in production, the percentage alcohol content was routinely tested using a hydrometer . Additionally, a sample of ABHR from the same production batch as used in this study was analysed by spectrography in University Hospital Geneva Pharmacy, Switzerland in June 2015. Approximately 5 ml of ABHR was dispensed onto both the hands of the participant and the investigator showed how to rub the hands together according to standard WHO method for hand-cleansing . After ABHR use, samples were immediately collected from the opposite hand using the same methods as described above.
Samples from both methods were cultured aerobically on MacConkey agar at 37 °C for 18–24 h. Plates were read and the Gram-negative colonies were counted manually. Fifty oxidase-negative isolates identified to the level of family/genus and species using API10S strips (Biomerieux, France). Enterobacteriaceae isolates were tested for resistance to six antibiotics according to the British Society of Antimicrobial Chemotherapy standard method . Analysis of data was performed using a Microsoft Excel spreadsheet and statistical tests were performed using STATA v14.1.
The study took place over a 2-week period in May 2015. Samples were collected from 152 individuals in the participating wards (16 nurses, 10 doctors, 86 parents/guardians, 28 students, 12 others). Before the use of ABHR, Gram-negative bacteria were detected on the hands of 91% (138/152) of adults tested by either the hand-print or hand-rinse method. The mean recovery rate for Gram-negative bacteria was high, with a geometric mean of 6.8 CFU (IQR 1–21) and 14.6 CFU (IQR 3–65) detected by the hand-print and hand-rinse method respectively. Immediately after ABHR use, the mean recovery rate for Gram-negative bacteria from the opposite hand was 1.2 CFU (IQR 0–2) and 2.4 CFU (IQR 0–5 CFU) by hand-print and hand-rinse methods (Table 1).
There was some indication that on the hand tested before the use of ABHR, the recovery rate for Gram-negative bacteria was higher on the non-dominant hand (mean for hand-rinse method = 33.4 CFU; n = 14) than on the dominant hand (mean = 13.7 CFU; n = 116) but the difference was not statistically significant (Wilcoxon rank sum test; p = 0.21).
Amongst sub-groups of people, the recovery of Gram-negative bacteria before use of ABHR was lowest amongst doctors (mean for hand-rinse method = 4.8 CFU; n = 10) and highest amongst parents/guardians (mean = 18.5 CFU; n = 86), although this difference did not reach statistical significance (Wilcoxon rank sum test; p = 0.15).
The reductions in Gram-negative bacteria counts with use of ABHR were 82% (or 0.75 log) according to the hand-print method and 84% (or 0.78 log) according to the hand-rinse method. Spectrographic analysis of ABHR used showed the correct alcohol concentration (83%; acceptable range 75-85%), but hydrogen peroxide was not detected (expected concentration 0.125%).
Amongst Gram-negative oxidase-negative bacterial isolates recovered from participants hands in this study, identification using API10S indicated that 49/50 were Enterobacteriaceae, with the most likely genus being Klebsiella (n = 21), Citrobacter (n = 15), Pantoea (n = 8), Escherichia (n = 4) and Yersinia (n = 1). Susceptibility testing indicated that antibiotic resistance was widespread in these isolates, including resistance to gentamicin (26/49; 53%) and cefpodoxime (34/49; 63%) (Table 2).
In paediatrics wards in government hospitals in Harare, we found that contamination of the hands of HCWs and parents with Gram-negative bacteria was extremely common (91% with detectable bacteria) and with a high burden of organisms, representing a high risk for transmission of pathogens which might cause infection. Interestingly, bacterial loads were found to be lowest amongst doctors and highest amongst the parents/guardians of paediatric patients and on non-dominant hands, though these were based on small numbers. We did not investigate whether specific ward-based tasks increased levels of contamination. Community-based work with mothers in Tanzania found that various activities including cleaning children’s faeces increased faecal indicator bacteria levels on hands . The organisms we isolated were frequently resistant to antibiotics routinely used for treatment, representing a direct risk to patients . The frequent resistance to cefpodoxime, an agent used to screen for the presence of Extended-Spectrum β-lactamases, and gentamicin suggests that transmission of this form of resistance might be occurring via the hands of adults in these wards . A single application of locally-manufactured ABHR achieved substantial but not complete reduction in detectable Gram-negative bacteria counts. Ideally, we should have tested equal numbers of dominant and non-dominant hands prior to ABHR use—this may have led to underestimation of the efficacy of ABHR. We cannot say with certainty whether the reductions in Gram-negative bacteria on hands demonstrated in this study would reflect on clinical outcomes in routine practice.
Repeated use of ABHR could be used as a strategy to prevent cross-infection between patients via the hands of staff and visitors in this setting . System changes to enable this practice must be addressed in Zimbabwean hospitals where ABHR use has not yet become a standard of care. In addition to making ABHR more widely available, there is an important need to instruct parents and HCWs in hospitals in Zimbabwe on the essential role of hand hygiene in care of hospitalized children.
Alcohol-based hand rub
World Health Organisation
Pittet D. Hand hygiene: improved standards and practice for hospital care’. Curr Opin Infect Dis. 2003;16(2003 SRC - GoogleScholar):327–35.
Chun JY, Seo HK, Kim MK, Shin MJ, Kim SY, Kim M, et al. Impact of a hand hygiene campaign in a tertiary hospital in South Korea on the rate of hospital-onset methicillin-resistant Staphylococcus aureus bacteremia and economic evaluation of the campaign. Am J Infect Control. 2016;44(12):1486–91.
Pessoa-Silva CL, Dharan S, Hugonnet S, Touveneau S, Posfay-Barbe K, Pfister R, et al. Dynamics of bacterial hand contamination during routine neonatal care. Infect Control Hosp Epidemiol. 2004;25(3):192–7.
Sax H, Allegranzi B, Uckay I, Larson E, Boyce J, Pittet D. ‘My five moments for hand hygiene’: a user-centred design approach to understand, train, monitor and report hand hygiene. J Hosp Infect. 2007;67(1):9–21. Epub 2007/08/28. Eng.
Boyce JM, Pittet D. Guideline for Hand Hygiene in Health-Care Settings: recommendations of the Healthcare Infection Control Practices Advisory Committee and the HICPAC/SHEA/APIC/IDSA Hand Hygiene Task Force. Infect Control Hosp Epidemiol. 2002;23(12 Suppl):S3–40. Epub 2003/01/08. Eng.
Allegranzi B, Gayet-Ageron A, Damani N, Bengaly L, McLaws ML, Moro ML, et al. Global implementation of WHO’s multimodal strategy for improvement of hand hygiene: a quasi-experimental study. Lancet Infect Dis. 2013;13(10):843–51.
Chen JK, Wu KS, Lee SS, Lin HS, Tsai HC, Li CH, et al. Impact of implementation of the World Health Organization multimodal hand hygiene improvement strategy in a teaching hospital in Taiwan. Am J Infect Control. 2016;44(2):222–7.
WHO. Guide to Local Production: Who-Recommended Handrub Formulations. 2010. p. 1–9. SRC - GoogleScholar.
WHO. Hand Hygiene Why,How,and When Brochure. 2009. p. 1–7. SRC - GoogleScholar.
BSAC. BSAC methods for antimicrobial susceptibility testing. 2015.http://www.bsac.org.uk/wp-content/uploads/2012/02/BSAC-Susceptibility-testing-version-14.pdf.
Pickering AJ, Julian TR, Mamuya S, Boehm AB, Davis J. Bacterial hand contamination among Tanzanian mothers varies temporally and following household activities. Trop Med Int Health. 2011;16(2):233–9. Epub 2010/11/26. Eng.
de Kraker MEA, Wolkewitz M, Davey PG, Koller W, Berger J, Nagler J, et al. Burden of antimicrobial resistance in European hospitals: excess mortality and length of hospital stay associated with bloodstream infections due to Escherichia coli resistant to third-generation cephalosporins. J Antimicrob Chemother. 2011;66(2):398–407.
Magwenzi MT, Gudza-Mugabe M, Mujuru HA, Bwakura-Dangarembizi M, Robertson V, Aiken AM. Carriage of antibiotic-resistant Enterobacteriaceae in hospitalised children in tertiary hospitals in Harare, Zimbabwe. Antibiotic Resistance Infection Control. 2017;in press as of November 2016.
We acknowledge with thanks to all the participating healthcare personnel, parents/care givers for their participation in this study. We thank Memory Mucheka from Harare Central Hospital, and the laboratory staff in the Department of Medical Microbiology, University of Zimbabwe for assistance with sample collection and processing. We also thank Simbiso Midzi of Parirenyatwa Hospital Pharmacy for preparation of ABHR and Pascal Bonnabry for performance of ABHR quality testing in HUG, Switzerland.
This work was funded by an Academy of Medical Sciences Starter Grant for Clinical Lecturers (AA, grant reference AMS-SGCL11-AikenA). This work formed part of a pilot study ahead of a cluster-randomised trial of a hand-hygiene intervention in hospitals in sub-Saharan Africa.
Availability of data and materials
Data from this pilot study will be made available through the London School of Hygiene and Tropical Medicine Data Compass data repository.
Conceived and designed the experiments: MGM, MM, HAM, MBD, VR, AA. Performed the experiments: MGM, MM. Analysed the data: MGM AA. Contributed reagents/materials/analysis tools: VR, AA. Wrote the manuscript: MGM AA. All authors read and approved the manuscript.
The authors declare that they have no competing interests.
Consent for publication
Not applicable—the manuscript does not include details, images, or videos relating to individual participants but rather presents analysis of aggregated data on the study population.
Ethics approval and consent to participate
The study was reviewed and approved by the Harare Central Hospital Ethics Committee (ref HCHEC 031214/80), Joint Parirenyatwa Hospital and University of Zimbabwe College of Health Sciences Research Ethics Committee (ref 13/15), the Medical Research Council of Zimbabwe (ref MRCZ/A/1939) and the London School of Hygiene and Tropical Medicine (ref 8839). Health care workers, Parents or guardians gave written informed consent to participate in the study.
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Gudza-Mugabe, M., Magwenzi, M.T., Mujuru, H.A. et al. Effect of handrubbing using locally-manufactured alcohol-based handrubs in paediatric wards in Harare, Zimbabwe. Antimicrob Resist Infect Control 6, 8 (2017) doi:10.1186/s13756-016-0166-8
- Hand hygiene
- Gram negative bacteria
- Nosocomial infection
- Alcohol-based hand rub