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Contamination of hospital surfaces with respiratory pathogens in Bangladesh

  • Md. Zakiul Hassan ,

    Roles Conceptualization, Data curation, Formal analysis, Investigation, Methodology, Project administration, Supervision, Writing – original draft

    Affiliation icddr,b (formerly, International Centre for Diarrheal Disease Research, Bangladesh), Dhaka, Bangladesh

  • Katharine Sturm-Ramirez,

    Roles Conceptualization, Formal analysis, Methodology, Writing – review & editing

    Affiliation icddr,b (formerly, International Centre for Diarrheal Disease Research, Bangladesh), Dhaka, Bangladesh

  • Mohammad Ziaur Rahman,

    Roles Data curation, Formal analysis, Methodology, Writing – review & editing

    Affiliation icddr,b (formerly, International Centre for Diarrheal Disease Research, Bangladesh), Dhaka, Bangladesh

  • Kamal Hossain,

    Roles Formal analysis, Methodology, Validation, Writing – review & editing

    Affiliation icddr,b (formerly, International Centre for Diarrheal Disease Research, Bangladesh), Dhaka, Bangladesh

  • Mohammad Abdul Aleem,

    Roles Formal analysis, Methodology, Project administration, Writing – review & editing

    Affiliation School of Public Health and Community Medicine, University of New South Wales, Sydney, NSW, Australia

  • Mejbah Uddin Bhuiyan,

    Roles Methodology, Project administration, Supervision, Writing – review & editing

    Affiliation Division of Paediatrics, School of Medicine, The University of Western Australia, Perth, WA, Australia

  • Md. Muzahidul Islam,

    Roles Data curation, Formal analysis, Methodology, Writing – review & editing

    Affiliation icddr,b (formerly, International Centre for Diarrheal Disease Research, Bangladesh), Dhaka, Bangladesh

  • Mahmudur Rahman,

    Roles Data curation, Formal analysis, Methodology, Supervision, Writing – review & editing

    Affiliation Institute of Epidemiology, Disease Control and Research (IEDCR), Dhaka, Bangladesh

  • Emily S. Gurley

    Roles Conceptualization, Formal analysis, Funding acquisition, Methodology, Project administration, Supervision, Writing – review & editing

    Affiliation Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, United States of America

Contamination of hospital surfaces with respiratory pathogens in Bangladesh

  • Md. Zakiul Hassan, 
  • Katharine Sturm-Ramirez, 
  • Mohammad Ziaur Rahman, 
  • Kamal Hossain, 
  • Mohammad Abdul Aleem, 
  • Mejbah Uddin Bhuiyan, 
  • Md. Muzahidul Islam, 
  • Mahmudur Rahman, 
  • Emily S. Gurley


With limited infection control practices in overcrowded Bangladeshi hospitals, surfaces may play an important role in the transmission of respiratory pathogens in hospital wards and pose a serious risk of infection for patients, health care workers, caregivers and visitors. In this study, we aimed to identify if surfaces near hospitalized patients with respiratory infections were contaminated with respiratory pathogens and to identify which surfaces were most commonly contaminated. Between September-November 2013, we collected respiratory (nasopharyngeal and oropharyngeal) swabs from patients hospitalized with respiratory illness in adult medicine and paediatric medicine wards at two public tertiary care hospitals in Bangladesh. We collected surface swabs from up to five surfaces near each case-patient including: the wall, bed rail, bed sheet, clinical file, and multipurpose towel used for care giving purposes. We tested swabs using real-time multiplex PCR for 19 viral and 12 bacterial pathogens. Case-patients with at least one pathogen detected had corresponding surface swabs tested for those same pathogens. Of 104 patients tested, 79 had a laboratory-confirmed respiratory pathogen. Of the 287 swabs collected from surfaces near these patients, 133 (46%) had evidence of contamination with at least one pathogen. The most commonly contaminated surfaces were the bed sheet and the towel. Sixty-two percent of patients with a laboratory-confirmed respiratory pathgen (49/79) had detectable viral or bacterial nucleic acid on at least one surface. Klebsiella pneumoniae was the most frequently detected pathogen on both respiratory swabs (32%, 33/104) and on surfaces near patients positive for this organism (97%, 32/33). Surfaces near patients hospitalized with respiratory infections were frequently contaminated by pathogens, with Klebsiella pneumoniae being most common, highlighting the potential for transmission of respiratory pathogens via surfaces. Efforts to introduce routine cleaning in wards may be a feasible strategy to improve infection control, given that severe space constraints prohibit cohorting patients with respiratory illness.


Pathogens present in ill patients' respiratory secretions can contaminate nearby hospital surfaces, such as floors, walls, bedrails and mattresses, through coughing, sneezing and touching [14]. Respiratory viral and bacterial pathogens, including Staphylococcus aureus, Streptococcus pyogenes, influenza viruses, respiratory syncytial virus, adenovirus, rhinoviruses and novel coronavirus strains, can survive on hospital surfaces for days, weeks or even months. Furthermore, touching contaminated surfaces may lead to nosocomial transmission of pathogens between patients, family caregivers, visitors, and healthcare workers [1, 5, 6].

Patient care areas in Bangladeshi hospitals are open wards with multiple beds in a room and are frequently overcrowded with patients, family caregivers, and visitors [7, 8]. A previous study by Rimi et al. found a median of four people per 100 sq. feet of floor space in hospital wards in Bangladesh and observed a median of five uncovered coughs or sneezes per 100 sq feet per hour [7]. Due to shortage of health care workers, family caregivers (family members who provides 24 hour hands on care to sick patient, including bedside nursing and cleaning) are integral part of inpatient care in Bangladeshi public hospitals, contributing crowding of hospital wards [8, 9]. The World Bank estimated that in 2014 only $32 of public funds per capita were spent annually on health infrastructure in Bangladesh. Thus, resources for infection control are severely limited in Bangladeshi hospitals [7, 10], making it difficult to implement international infection control guidelines [11].

The lack of routine infection control practices, including no regular surface cleaning, may increase the transmission of respiratory pathogens via hospital surfaces [3, 5, 6, 8]. Family caregivers, visitors, and hospital staff may acquire respiratory infections either through direct contact with infected patients or via droplets, aerosols or contaminated surfaces. Contaminated hospital surfaces can pose a serious risk of infection for patients, health care workers, caregivers and visitors.

Within this context of scarce resources, describing the magnitude of surface contamination in Bangladeshi hospitals, particularly identifying priority areas for decontamination, could influence infection control policy and practice. Our objective was to assess the frequency with which patients hospitalized for respiratory illnesses in Bangladeshi public hospitals contaminate nearby surfaces, to identify commonly contaminated surfaces, and to determine which pathogens are detected most frequently.

Materials and methods

Case identification and sample collection

We conducted the study in two public tertiary care teaching hospitals in Rajshahi and Jessore, Bangladesh between September and November 2013. Rajshahi Medical College Hospital contains approximately 1,200 beds with eight adult medicine wards and four pediatric wards. Jessore Medical College Hospital is a 250-bed hospital with two adult medicine wards and one pediatric ward. Paediatric wards typically admit patients <14 years of age and older patients are admitted to adult medicine wards. The mean bed occupancy proportion in these hospital wards are consistently >100% with patients being treated on the floor and in hallways when beds unavailable [8, 12]. Study physicians in adult medicine and pediatric wards identified patients aged ≥5 years who met the severe acute respiratory illness (SARI) case definition of subjective or measured fever (≥38 C°) within the past seven days with cough or sore throat [13]. In pediatric wards, physicians identified children <5 years of age who met the severe pneumonia (SP) case definition: cough or difficulty breathing and at least one danger sign (i.e. chest indrawing, stridor while calm, history of convulsions, inability to drink, lethargy or unconsciousness and/or intractable vomiting) with onset of symptoms within the last seven days [13]. Since case-patients were identified immediately after admission, their illnesses were mostly community acquired.

Study physicians collected respiratory swabs (nasopharyngeal and oropharyngeal) from identified cases using the World Health Organization's laboratory safety manual protocol [14] and pooled them into a single cryovial containing viral transport media (VTM). Trained research assistants in each hospital collected one swab sample from five different surfaces near each enrolled case patient: the wall next to the patient’s bed, bed rail, bed sheet, clinical record files, and a multipurpose towel. The multipurpose towel is a cloth brought from home by family caregivers and used to clean patient respiratory secretions, wiping the patient’s face or head, and to dry caregivers’ hands and face [8]. We selected these surfaces because patients, caregivers, and healthcare workers (HCWs) frequently come into contact with them in the hospital wards [6, 7, 15]. The research assistants collected surface swabs between 12–72 hours after the case-patients’ admission to the hospital. This allowed for adequate time for hospital surfaces to be exposed to possible contamination by respiratory pathogens, while also making sure that surfaces were swabbed before the enrolled patients were discharged or died, as patient turnover in wards was high with a median hospital stay of three days [16]. The risk for infection from these potentially contaminated surfaces between patients within a room, between patients and healthcare workers, or between patients and family caregivers would vary based on the particular surface and how these different risk groups interacted with the surface. With one sterile rayon swab stick per surface, the research assistant swabbed the area of the wall in contact with the bed 45 cm high from the level of the bed sheet, all surfaces of the bed rail located in the area near the patients’ head, half of the bed sheet where the patient’s head was including underneath the patient, front and back cover of the patient file and both sides of the multi-purpose towel. Not all patients had a wall or bedrail nearby as some patients were cared for on the floor, due to overcrowding. Swab samples from each surface area were put into individual cryovials containing VTM and kept in a cool box for up to 30 minutes with a temperature between 2°-8°C. Both the respiratory swabs and surface swab samples were labelled, packaged, stored in a nitrogen dry shipper (-150°C) and sent to the icddr,b virology laboratory by batch twice a month.

Testing of respiratory and surface swabs

The swab samples were thawed and the cryovials containing the sample were vortexed. About 200 μL of the swab supernatant was used for nucleic acid extraction using InviMag® Pathogen Kit/KF 96 (STRATEC Molecular, Berlin, Germany) and the final eluted volume of nucleic acid solution was 200 μL, as per the manufacturer’s instruction [17]. The real-time multiplex PCR assay was performed as per the manufacturer’s instructions using an AgPath-ID  One-Step RT-PCR kit (Ambion) with the Fast Track Diagnostic (FTD) respiratory pathogens 33 kit (Fast Track Diagnostics, Luxembourg) for 19 different viruses and 12 bacterial pathogens [18]. Case-patients with at least one pathogen detected in their respiratory swab had corresponding surface swabs tested for those same pathogens. Detection of nucleic acid of at least one similar pathogen on respiratory swab and a nearby surface was defined as contamination of that surface. To investigate wider hospital contamination, we also tested the surface swabs collected near case-patients with no pathogens detected in their respiratory swabs for the most commonly detected pathogens identified on surfaces near patients with detected respiratory pathogens.

Statistical analysis

We summarized the data using descriptive statistics. We assessed the difference in proportion of pathogen detection in respiratory swabs and surface swabs between adult and paediatric ward patients using Chi-Square test considering Fisher exact test where appropriate. Any association with a p value <0.05 was considered statistically significant.

Ethical consideration

Study participants (aged ≥18 years) or their legal guardians (if aged <18 years) provided informed written consent. The institutional review board of icddr,b reviewed and approved the study protocol. The Institutional Review Board at the Centers for Disease Control and Prevention (Atlanta, GA, USA) deferred to icddr,b's approval.


We collected and tested respiratory swabs from 104 patients hospitalized with respiratory illness: 50 SARI cases from adult medicine wards and 54 severe pneumonia cases from paediatric medicine wards. The median age of patients in the adult wards was 32 years (IQR 25–48) and in paediatric wards three months (IQR 2–6). The male-to-female ratio was 2.6:1 (Table 1). Of the 104 patients, 79 (75%) had detectable viral and/or bacterial nucleic acid in their respiratory swabs. Paediatric patients more frequently had one or more detectable pathogen in their respiratory swabs than adult patients (91% versus 60%, p = 0.001). Bacterial pathogens were identified in 76% of adult respiratory swabs. Klebsiella pneumoniae, Streptococcus pneumoniae and Staphylococcus aureus were most commonly detected during the study period. In contrast, viral pathogens were commonly detected among paediatric patients, including human cytomegalovirus, respiratory syncytial viruses, and human rhinoviruses (Table 1). Clinical features, mean duration of symptom onset to sample collection (3.2 days Vs 3 days) did not vary between patients with a detectable viral and a detectable bacterial nucleic acid in respiratory swabs. Two patients, one with Klebsiella pneumoniae and one with Streptococcus pneumoniae detected in their respiratory swabs, had been hospitalized at other facilities within two weeks prior to admission to the study hospital, suggesting that these organisms could have been hospital-acquired. Both these patients had abnormal chest X-rays and were diagnosed with severe pneumonia in the study hospital.

Table 1. Demographic characteristics of study patients and proportion of patients with a detectable nucleic acid for a specific pathogen in respiratory swabs in two tertiary care hospitals in Bangladesh, September-November, 2013.

We tested the surrounding hospital surface swabs for each of the 79 patients with evidence of respiratory pathogens for the same viral/bacterial nucleic acid detected in their respiratory swabs. We collected and tested 287 surface swabs near the 79 patients as not all these patients had a wall or bedrail near them. Nearly half of the hospital surface swabs (46% [133/287]) had evidence of contamination by at least one pathogen included in the testing panel. The most commonly contaminated surfaces were the bed sheet, the multipurpose towel, and the bed rail. We infrequently detected bacterial or viral nucleic acid on wall surfaces or on patients’ clinical record files (Fig 1). Sixty-two percent of patients (49/79) had detectable viral and/or bacterial nucleic acid on at least one (range: 1–5) nearby surface, including 60% of adults (18/30) and 63% (31/49) of pediatric patients. The most common bacterial pathogen detected on surface swabs was Klebsiella pneumoniae and 97% (32/33) of patients positive for Klebsiella pneumoniae had at least one surface with detectable DNA. The most frequently detected viral pathogen on surfaces was human cytomegalovirus and 86% (18/21) of patients positive for human cytomegalovirus had detectable DNA on nearby surfaces (Table 2).

Fig 1. Percentage of different hospital surfaces* tested with detectable nucleic acid for common respiratory pathogens in two tertiary care hospitals in Bangladesh, September-November, 2013.

*Surfaces collected nearby patients with at least one detectable pathogen in respiratory swabs.

Table 2. Frequency of surface contamination with detectable nucleic acid for specific pathogen near patients with detectable nucleic acid in respiratory swab of the same pathogen, in two tertiary care hospitals in Bangladesh, September-November, 2013.

We tested nearby surfaces for 22 patients (18 patients from adult wards and 4 from pediatric wards) without detectable viral/bacterial nucleic acid in their respiratory swabs. We tested these surfaces for six frequently identified pathogens in respiratory swabs of case-patients: Klebsiella pneumoniae, Streptococcus pneumoniae, Staphylococcus aureus, human cytomegalovirus, respiratory syncytial viruses and human rhinoviruses. Klebsiella pneumoniae was detected on at least one nearby surface in 95% (21/22) of these patients, Staphylococcus aureus in 18% (4/22), and Streptococcus pneumoniae in 14% (3/22) patients. Viruses, including, human cytomegalovirus (4/22), respiratory syncytial viruses A and B (1/22) and human rhinoviruses (0/22), were rarely detected nearby these patients.


Nearly two-thirds of the patients hospitalized with laboratory-confirmed acute respiratory infection had at least one nearby contaminated surface. Klebsiella pneumoniae was the most commonly detected pathogen in patients' respiratory swabs, and was detected in nearly every environmental swab testing, suggesting widespread hospital contamination from current and previously hospitalized patients. With the ability to spread rapidly in the hospital environment, Klebsiella pneumoniae has been linked to several nosocomial outbreaks [19, 20]. The most frequently contaminated surfaces were the bed sheet, towel, and bed rail, further highlighting the perils of no routine surface cleaning practices in these hospitals. Studies in tertiary care hospitals of Bangladesh have shown that one in 20 patients with a hospital stay greater than three days developed a hospital-acquired respiratory infection, and that only 21% of those infections had a viral aetiology, suggesting a large proportion of these infections might be bacterial [21, 22]. Since, future work should further investigate the role of Klebsiella pneumoniae may be an important nosocomial pathogen in these hospitals.

Several other studies have identified multidrug resistant Klebsiella pneumoniae in hospital environments and its association with severe infections, prolonged hospital stays and increased mortality rates, particularly in debilitated and immunocompromised patients [23, 24]. A 2004 study in an urban tertiary care hospital in Dhaka, Bangladesh, reported that 40% of the clinical specimens (sputum, pus, urine, throat, and vaginal swabs) collected from hospitalized patients were drug resistant [25]. Moreover, our study findings were consistent between the two hospitals despite being located in different geographical areas and may suggest surface contamination with Klebsiella pneumoniae as a wider public health problem. The predominant bacterial pathogens we identified, Klebsiella pneumoniae, Streptococcus pneumoniae, and Staphylococcus aureus, can survive on surfaces from a few days to a few months [5, 26, 27]. Bacteria, in the presence of low humidity, forms biofilms protecting microorganisms from harsh environmental influences and are difficult to eradicate [28, 29]. In Bangladesh, hospital surfaces are not adequately cleaned and hospitals report insufficient supplies of cleaning agents [7, 8, 30]. To remove and prevent biofilm formation, hospital decontamination protocols should include strategies such as daily cleaning of surfaces with disinfectant (e.g. 0.3% sodium hypochlorite or 2% chlorhexidine solutions).

Among the most commonly detected viral pathogens, RSV was prevalent in respiratory swab of paediatric patients and nearby surfaces. RSV has been a major nosocomial hazard on pediatric wards and has been linked with hospital outbreaks [31, 32]. With reported higher case fatality among patient with nosocomial RSV infections (OR 4.46, 95% CI 1.1–18), widespread surface contamination with RSV is concerning for low income hospitals (34, 35).

We identified, that towel, was frequently contaminated with respiratory secretions. [8]. Islam et al. reported that family caregivers frequently used a multipurpose towel for patient secretions and for their own use, without cleaning it in between these uses [8].This suggests that the towel may act as a potential vehicle for transmission of respiratory viral and bacterial pathogens from patient to caregiver [33]. Infection control could target care giving practices associated with the use of the towel and should test feasible low-cost interventions such as the supply of low cost disinfectant by hospitals that encourage caregivers to clean the towels more frequently and to improve hand washing practices, including the use of hand sanitizer.

An important limitation of our study is that we only identified the presence of viral or bacterial nucleic acid on different hospital surfaces, and cannot be sure that the pathogens we detected were viable. A second limitation is that we conducted the study in only two public hospitals, so the findings may not be representative of all public hospitals. However, our findings were consistent between the two typical tertiary care hospitals we studied, located in completely different parts of the country. A third limitation is that we only sampled surfaces once, which limits our ability to comment on duration of contamination, and did not have the ability to observe contamination from seasonal infections. Influenza, for example, has a known seasonal pattern in Bangladesh, circulating usually between May and September, potentially explaining the low detection rate in our study [34, 35]. Lastly, we did not investigate drug resistance patterns of the bacteria we detected due to resource constraints. Based on evidence from other studies, however, it is likely that many of the pathogens we detected on surfaces were drug resistant and future studies should consider including investigations about drug resistance [25].


This study identified that hospital surfaces in these Bangladeshi hospitals, were frequently contaminated with respiratory pathogens and pose a potential threat for fomite-borne transmission of respiratory infections to patients, healthcare workers and family caregivers. To prevent the spread of Klebsiella and other infections between patients, healthcare personnel must follow specific infection control precautions including strict adherence to hand hygiene and the use of gloves. In addition, our data clearly indicate that efforts to regularly disinfect environmental surfaces and ensure clean towels for patient caregiving could reduce risk of exposure to patients, healthcare staff and visitors. The government of Bangladesh has taken a number of initiatives to improve infection control in hospitals [36]. Despite this, a 2013 nationally representative survey of healthcare facilities showed that healthcare workers performed recommended hand hygiene in only 9% of 919 opportunities, suggesting low adherence to international standards [30]. Barriers include awareness, training, accountability and appropriate infrastructure (among 875 health facilities, 10% handwashing locations had no water, 20% had no soap and 50–80% had no alcohol based sanitizer) to support these behaviours [30, 37, 38] This study highlighted the gaps in practice, as well as the substantial barriers to improvement that will require widespread investments to address. In 2018, the Directorate of Hospital Infection Control, Directorate General of Health Services (DGHS) at the Ministry of Health and Family Welfare in Bangladesh has communicated the intention to form infection control committees in each district and tertiary care hospital across the country to improve the safe care [39]. Further investigation to identify the true contribution of fomites in the transmission of respiratory pathogens within hospital settings could be useful to help these committees prioritize efforts to improve hand and surface cleaning.


We would like to thank authorities of participating hospitals, all the study participants, the study physicians, field staff and laboratory staff for their contribution. We acknowledge Gladys Leterme for reviewing and editing this manuscript.

icddr,b acknowledges with gratitude the commitment of CDC to its research effort. icddr,b is also grateful to the Governments of Bangladesh, Canada, Sweden and the UK for providing core/unrestricted support.


  1. 1. Boone SA, Gerba CP. Significance of fomites in the spread of respiratory and enteric viral disease. Applied and environmental microbiology. 2007;73(6):1687–96. pmid:17220247
  2. 2. Boyce JM. Environmental contamination makes an important contribution to hospital infection. Journal of Hospital infection. 2007;65(2):50–4.
  3. 3. Weinstein RA, Hota B. Contamination, disinfection, and cross-colonization: are hospital surfaces reservoirs for nosocomial infection? Clinical infectious diseases. 2004;39(8):1182–9. pmid:15486843
  4. 4. Hassan MZ, Sazzad HM, Luby SP, Sturm-Ramirez K, Bhuiyan MU, Rahman MZ, et al. Nipah Virus Contamination of Hospital Surfaces during Outbreaks, Bangladesh, 2013–2014. Emerging infectious diseases. 2018;24(1):15. pmid:29260663
  5. 5. Kramer A, Schwebke I, Kampf G. How long do nosocomial pathogens persist on inanimate surfaces? A systematic review. BMC Infectious Diseases. 2006;6(1):130.
  6. 6. Cheng V, Chau P, Lee W, Ho S, Lee D, So S, et al. Hand-touch contact assessment of high-touch and mutual-touch surfaces among healthcare workers, patients, and visitors. Journal of Hospital Infection. 2015;90(3):220–5. pmid:25929790
  7. 7. Rimi NA, Sultana R, Luby SP, Islam MS, Uddin M, Hossain MJ, et al. Infrastructure and contamination of the physical environment in three Bangladeshi hospitals: putting infection control into context. PloS one. 2014;9(2):e89085. pmid:24586516
  8. 8. Islam MS, Luby SP, Sultana R, Rimi NA, Zaman RU, Uddin M, et al. Family caregivers in public tertiary care hospitals in Bangladesh: risks and opportunities for infection control. American journal of infection control. 2014;42(3):305–10. pmid:24406254
  9. 9. Ahmed SM, Hossain MA, RajaChowdhury AM, Bhuiya AU. The health workforce crisis in Bangladesh: shortage, inappropriate skill-mix and inequitable distribution. Human resources for health. 2011;9(1):3.
  10. 10. Mustafa A, Begum T. Universal Health Coverage Assessment People’s Republic of Bangladesh. 2014.
  11. 11. Rosenthal VD, Al-Abdely HM, El-Kholy AA, AlKhawaja SAA, Leblebicioglu H, Mehta Y, et al. International Nosocomial Infection Control Consortium report, data summary of 50 countries for 2010–2015: Device-associated module. American journal of infection control. 2016;44(12):1495–504. pmid:27742143
  12. 12. Bhuiyan MU, Luby SP, Zaman RU, Rahman MW, Sharker MY, Hossain MJ, et al. Incidence of and risk factors for hospital-acquired diarrhea in three tertiary care public hospitals in Bangladesh. The American journal of tropical medicine and hygiene. 2014;91(1):165–72. pmid:24778198
  13. 13. Organization WH. WHO interim global epidemiological surveillance standards for influenza. 2012. 2013.
  14. 14. Organization WH. Manual for the laboratory diagnosis and virological surveillance of influenza. 2011.
  15. 15. Huslage K, Rutala WA, Sickbert-Bennett E, Weber DJ. A quantitative approach to defining “high-touch” surfaces in hospitals. Infection Control & Hospital Epidemiology. 2010;31(8):850–3.
  16. 16. Bhuiyan MU, Luby SP, Alamgir NI, Homaira N, Mamun AA, Khan JA, et al. Economic burden of influenza‐associated hospitalizations and outpatient visits in Bangladesh during 2010. Influenza and other respiratory viruses. 2014;8(4):406–13. pmid:24750586
  17. 17. Morris SK, Pell LG, Rahman MZ, Dimitris MC, Mahmud A, Islam MM, et al. Maternal vitamin D supplementation during pregnancy and lactation to prevent acute respiratory infections in infancy in Dhaka, Bangladesh (MDARI trial): protocol for a prospective cohort study nested within a randomized controlled trial. BMC pregnancy and childbirth. 2016;16(1):309. pmid:27737646
  18. 18. FTD Respiratory pathogens 33 Luxemburg: Fast track diagnostics. Available from:
  19. 19. Pena C, Pujol M, Ardanuy C, Ricart A, Pallares R, Linares J, et al. An outbreak of hospital-acquired Klebsiella pneumoniae bacteraemia, including strains producing extended-spectrum β-lactamase. Journal of Hospital Infection. 2001;47(1):53–9. pmid:11161899
  20. 20. Woodford N, Tierno PM, Young K, Tysall L, Palepou M-FI, Ward E, et al. Outbreak of Klebsiella pneumoniae producing a new carbapenem-hydrolyzing class A β-lactamase, KPC-3, in a New York medical center. Antimicrobial agents and chemotherapy. 2004;48(12):4793–9. pmid:15561858
  21. 21. Bhuiyan MU. Incidence and viral aetiology of hospital-acquired respiratory infections at three tertiary care hospitals in Bangladesh, 2008–2011. Health and Science Bulletin. 2014;12(3):1–8.
  22. 22. Gurley ES, Zaman RU, Sultana R, Bell M, Fry AM, Srinivasan A, et al. Rates of hospital-acquired respiratory illness in Bangladeshi tertiary care hospitals: results from a low-cost pilot surveillance strategy. Clinical infectious diseases. 2010;50(8):1084–90. pmid:20210642
  23. 23. Hirsch EB, Tam VH. Detection and treatment options for Klebsiella pneumoniae carbapenemases (KPCs): an emerging cause of multidrug-resistant infection. Journal of Antimicrobial Chemotherapy. 2010;65(6):1119–25. pmid:20378670
  24. 24. Freeman JT, Nimmo J, Gregory E, Tiong A, De Almeida M, McAuliffe GN, et al. Predictors of hospital surface contamination with Extended-spectrum β-lactamase-producing Escherichia coli and Klebsiella pneumoniae: patient and organism factors. Antimicrobial resistance and infection control. 2014;3(1):5. pmid:24491119
  25. 25. Rahman MM, Haq JA, Hossain MA, Sultana R, Islam F, Islam AS. Prevalence of extended-spectrum β-lactamase-producing Escherichia coli and Klebsiella pneumoniae in an urban hospital in Dhaka, Bangladesh. International journal of antimicrobial agents. 2004;24(5):508–10. pmid:15519486
  26. 26. Neely AN, Maley MP. Survival of enterococci and staphylococci on hospital fabrics and plastic. Journal of clinical microbiology. 2000;38(2):724–6. pmid:10655374
  27. 27. Weemering ML. Survival of enterococci and staphylococci on hospital fabrics and plastic. Aorn Journal. 2001;73(2):515–.
  28. 28. Fux C, Costerton J, Stewart P, Stoodley P. Survival strategies of infectious biofilms. Trends in microbiology. 2005;13(1):34–40. pmid:15639630
  29. 29. Silva RC, Carver RA, Ojano‐Dirain CP, Antonelli PJ. Efficacy of disinfecting solutions in removing biofilms from polyvinyl chloride tracheostomy tubes. The Laryngoscope. 2013;123(1):259–63. pmid:22887035
  30. 30. Horng L, Unicomb L, Alam M-U, Halder A, Shoab A, Ghosh P, et al. Healthcare worker and family caregiver hand hygiene in Bangladeshi healthcare facilities: results from the Bangladesh National Hygiene Baseline Survey. Journal of Hospital Infection. 2016;94(3):286–94. pmid:27665311
  31. 31. French CE, McKenzie BC, Coope C, Rajanaidu S, Paranthaman K, Pebody R, et al. Risk of nosocomial respiratory syncytial virus infection and effectiveness of control measures to prevent transmission events: a systematic review. Influenza and other respiratory viruses. 2016;10(4):268–90. pmid:26901358
  32. 32. Nabeya D, Kinjo T, Parrott GL, Uehara A, Motooka D, Nakamura S, et al. The clinical and phylogenetic investigation for a nosocomial outbreak of respiratory syncytial virus infection in an adult hemato‐oncology unit. Journal of medical virology. 2017;89(8):1364–72. pmid:28240370
  33. 33. Hassan MZ SH, Luby SP, Sturm-Ramirez K, Bhuiyan MU, Rahman MZ, et al. Nipah virus contamination of hospital surfaces during outbreaks, Bangladesh, 2013–2014. Emerg Infect Dis. 24(1).
  34. 34. Zaman RU, Alamgir A, Rahman M, Azziz-Baumgartner E, Gurley ES, Sharker MAY, et al. Influenza in outpatient ILI case-patients in national hospital-based surveillance, Bangladesh, 2007–2008. PloS one. 2009;4(12):e8452. pmid:20041114
  35. 35. Ahmed M, Aleem MA, Roguski K, Abedin J, Islam A, Alam KF, et al. Estimates of seasonal influenza‐associated mortality in Bangladesh, 2010‐2012. Influenza and other respiratory viruses. 2017.
  36. 36. Services DGoH. Manual for implmentation of 5S in Hospital Setting. In: welfare MoHF, editor. Bangladesh: DGHS, Ministry of Health & Family welfare; 2015.
  37. 37. Gurley ES, Islam MS, Nahar N, Sultana R, Hossain MJ, Homaira N, et al. Behaviour change intervention to reduce caregivers’ exposure to patients’ oral and nasal secretions in Bangladesh. International Journal of Infection Control. 2013;9(2).
  38. 38. Horng L, Unicomb L, Alam M-U, Halder A, Ghosh P, Luby S, editors. Health Worker and Family Caregiver Hand Hygiene in Bangladesh Healthcare Facilities: Results From a Nationally Representative Survey. Open Forum Infectious Diseases; 2015: Oxford University Press.
  39. 39. (QIS) QiS. National Patient Safety Strategic Plan in Bangladesh. In: Welfare MoHF, editor. Bangladesh: Health Economics Unit, Health Sevices Division; 2018.