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Effect of 4 % chlorhexidine on cord colonization among hospital and community births in India: a randomized controlled study
© The Author(s). 2016
Received: 6 October 2015
Accepted: 6 July 2016
Published: 2 August 2016
Infections are the single most important cause of neonatal mortality in developing countries. Results from trials in Asia evaluating the effect of chlorhexidine on neonatal mortality have been encouraging but limited data are available on the impact of cord cleansing on bacterial colonization. Further, no data from facility deliveries and impact with time is available. This pilot study was aimed to evaluate the impact of 4 % commercially prepared chlorhexidine on cord colonization and density of colonization among newborns in India.
Three hundred twenty-six newborns (hospital-247; community-79) were enrolled within 24 h of birth and randomly assigned to one of three groups: chlorhexidine, placebo or dry cord care. Umbilical swabs were collected at baseline, 2- and 48- hours after intervention application.
At baseline, growth positivity (any bacterial growth) was 20 % (50 of 247 swabs) and 81 % (64 of 79 swabs) among hospital and community born neonates, respectively. In both settings, chlorhexidine compared to placebo and dry cord care, reduced colonization following 2- and 48-hour post application. Chlorhexidine significantly reduced 48-hour post application colony counts in comparison to placebo [Hospital: mean difference = −1.01; 95 % CI: −1.72, −0.30 Community: mean difference = −1.76; 95 % CI: −2.60, −0.93] and dry cord care [Hospital: mean difference = −1.16; 95 % CI: −1.93, −0.39 Community: mean difference = −2.23; 95 % CI: −3.18, −1.29]. Differences were similar for gram-positive and gram-negative bacteria.
Cord cleansing with 4 % chlorhexidine soon after birth reduced colonization as well as density of colonization significantly; however this pilot study does not address the impact of chlorhexidine on mortality. The control preparation neither increased or decreased colonization.
Clinical Trial Registration: clinicaltrials.gov: NCT01528852, Registered February 7, 2012.
Neonatal deaths account for 40 % of global under-five mortality [1–3] and are a major health concern in the developing countries, particularly in the south Asian and sub-Saharan countries [4, 5]. Each year serious infections account for nearly 13 % of the 3 million neonatal deaths, this proportion is closer to 50 % in settings with high mortality risk . Five countries namely India, Nigeria, Democratic Republic of the Congo, Pakistan and China alone account for half (2.440 million) of the global deaths from infections and 53.3 % (1.636 million) of neonatal deaths . Community based studies from developing world suggest that infections are responsible for 8 to 80 % of all neonatal deaths and as many as 42 % deaths in first week of life [5, 6].
In neonates, umbilicus acts as a bacterial reservoir and a potential entry point for the infection, especially in first few days of life, when umbilical vein is patent. This may lead to sepsis with or without omphalitis [7, 8]. The responsible organisms most likely originate in maternal genital tract and are acquired during labor and delivery . In low income countries, many neonatal infections are environmentally acquired because of higher number of home deliveries, unsafe traditional practices, untrained birth attendants and unclean living conditions, all of which pose an increased risk of umbilical cord infection . The local signs of umbilical cord infection include pus, redness, swelling, warmth, tenderness and foul odour  and seem to be associated with increased risk of mortality . Infectious organisms may get directly transmitted from patent umbilical cord to the blood stream without evident signs of local cord infection .
Recommendations for umbilical cord care, particularly in regard to prevention of umbilical cord infection, are controversial. In developing countries, World Health Organization (WHO) [10, 14] promotes dry cord care. These recommendations were based on lack of evidence for alternative approaches . Based on currently available evidence, the WHO recommends 7.1 % chlorhexidine digluconate solution or gel, (delivering 4 % chlorhexidine) among home deliveries in settings with neonatal mortality rate more than 30 . This interim recommendation awaits review of further data especially the results of two large trials in Africa.
Of topical antiseptics (eg, ethanol, silver sulfadiazine, triple dye, gentian violet, chlorhexidine, povidine iodine), chlorhexidine with strong residual activity has shown potential as an effective cord care agent during the neonatal period against both gram-positive and gram-negative organisms [16–18]. It has an excellent safety profile, is rarely associated with bacterial resistance, is easy to administer and costs few cents per application [9, 19, 20]. Available high-quality evidence from the recently conducted Cochrane review indicates that cord cleansing with 4 % chlorhexidine reduces the risk of neonatal mortality by 12 % and sepsis (omphalitis)/infections by 50 % in low-resource community settings including Nepal, Bangladesh, and Pakistan . However, in hospital settings, chlorhexidine cord cleansing reduces the risk of omphalitis/infections by 52 % and may lead to no difference in neonatal mortality as compared to dry cord care. Despite all these data, limited evidence is available on the mechanism of this protective effect [22–24] and only one study  published recently suggested an impact on bacterial colonization of the cord and provided information on early neonatal colonization dynamics in community setting. There are no data available evaluating impact of chlorhexidine on colonization among facility births, and spectrum of chlorhexidine overtime. In all the earlier chlorhexidine trials evaluating impact on mortality and/or cord infections, 4.0 % free chlorhexidine were prepared by diluting 20 % chlorhexidine digluconate to the appropriate concentration with purified water at the study sites. As there was no data available from Africa, two large trials in Africa (Pemba, Tanzania and Zambia) were funded by Bill and Melinda gates Foundation to evaluate the mortality impact of the intervention. In the present pilot study, we tested the antimicrobial activity of the commercially prepared 4 % chlorhexidine solution as a cord-cleansing agent, and evaluated its impact on bacterial colonization and colony counts after 2- and 48-hour post-application in hospital- and community born neonates in comparison to placebo (same solution without active ingredients) and dry cord care. The aim of this pilot study was to ensure and document the efficacy of preparation before evaluating mortality and sepsis impact in large trials (more than 60,000 newborns in African setting). In addition, the pilot study provided data on potential cord colonizing pathogens that could be responsible for sepsis, apart from regular skin flora.
This pilot study was a prospective, randomized, controlled trial conducted in New Delhi, India. There could be significant differences in environmental cleanliness and bacteriologic profile in the community and hospital settings; study subjects from both the settings were included in order to have a representative sample.
The hospital component of the pilot study was conducted at Kalawati Saran Children’s Hospital, New Delhi while the community component was undertaken at Sangam Vihar, New Delhi.
Kalawati Saran Children’s Hospital is a government hospital catering to patients from the lower socio-economic strata. Approximately 40–60 deliveries take place daily in this hospital.
Sangam Vihar is a resettlement colony mainly comprising of migrants from rural areas of the country. Its population is predominantly from the low socio-economic strata of the society. Almost 60 % of the births in Sangam Vihar take place at home (20–25 deliveries daily).
Training and reliability
Training sessions were organized for the field workers, supervisors and hospital staff who were apprised of the study protocol and the various forms that need to be filled at different time points. Swab sample collection from the umbilical cord as well as cleaning of cord using the assigned intervention method was demonstrated using a dummy doll. This was followed by practice and return demonstration by trainees on the dummy. Subsequently, dry run sessions were undertaken by the staff to ensure reliability and effective implementation of study protocol.
Recruitment and enrollment
Enrollment in hospital
Study team was stationed outside the maternity ward from 8.00 am to 5.30 pm. After birth, the study team comprising of hospital staff and study supervisor visited the mother baby duo and screened the newborn for eligibility to participate in the study. If the newborn was found eligible (normal delivery, full term healthy newborns of both sexes with birth weight >2500 g, first contact ≤48 h), the study purpose and procedure were explained to the mother once she was stable or else to the nearest kin and the consent for their newborn’s participation in the study was sought. The newborn was enrolled in the study after the consent was obtained from the parents. Neonates requiring resuscitation and admission to NICU and also those with major congenital malformation were excluded.
Enrollment in community
A survey was carried out by trained birth attendants (TBAs) to identify the pregnant women in the six blocks of Sangam Vihar. A record of all identified pregnancies with their tentative due delivery dates was prepared. The family members and TBAs were instructed to contact the study supervisor at the time of delivery or immediately thereafter. The study supervisor and fieldworker along with the TBA visited the newborn within 48 h of delivery. They screened the newborn for eligibility (vaginally delivered, term healthy newborns, first contact ≤48 h) and if found eligible, the study purpose and procedure were explained to the mother and the consent for their newborn’s participation in the study was sought.
Sample size estimations
Based on Nepal hospital data (Hodgins et al ) the sample size was estimated to be 80 in each intervention group for the hospital setting, with an alpha of 0.05 and power of 80 %, to detect a reduction in bacterial colonization from 29 to 11 % in the chlorhexidine group. Based on Bangladesh study (Mullany et al, personal communication), the sample size was estimated to be 44 in each intervention group in the community setting, with an alpha of 0.05 and power of 80 %, to detect a reduction in bacterial colonization from 93 to 69 % in the chlorhexidine group.
Masking and randomization
All enrolled neonates were randomly allocated to 1 of the 3 intervention groups: (a) 4 % chlorhexidine or (b) placebo (mild soap water) or (c) dry cord care group. Both the chlorhexidine and the placebo groups were blinded and the preparations were identical in packaging, appearance, colour, consistency and odour. It was not possible to blind the allocation to the dry cord care group. Each intervention group was identified by a letter code. The manager in the manufacturing unit decided the codes to be used for the solutions and kept the information secret till the data analysis was complete. Thus, neither the mothers of the neonates nor the hospital/field staff knew which intervention was being used. Two separate randomization lists were prepared; one for the hospital and other for the community births. For the hospital, a randomization list containing running serial number and randomly allocated code (A through I) was generated. These letter codes were used to identify three intervention groups. In order to ensure equalization of groups, six letter codes for the solution (3 codes for chlorhexidine and 3 for placebo groups) and three letter codes for the dry cord care were used. In-house computer software generated a random sequence of group codes with permuted block length of 18. Neonates were allocated to one of the groups in the order in which they got enrolled. For the community births, similar randomization procedure was used.
Composition of chlorhexidine and chlorhexidine placebo
Chlorhexidine 4 % solution (% v/v)
Placebo solution (% v/v)
Chlorhexidine gluconate 20 % w/v solution BP
Polyoxyl 40 hydrogenated castor oil NF (RH 40)
Purified water BP
Q.S to 100.00
Q.S to 100.00
Isopropyl alcohol BP
Mild soap [Sodium lauryl sulphatea (STEROCARE SLS (L))]
Silicon antifoaming agenta
Baseline (0 h) swab collection
For hospital births, soon after delivery, hospital supervisor checked the hospital records to record birth related information. Before beginning the procedures, the resident doctor washed his/her hands and donned sterile gloves. The resident doctor on duty collected the swab using HIMEDIA HiCultureTM transport swabs with amies medium with charcoal (Cat no: MS 651) from the tip, stump and base of the umbilicus and peri-umbilical region (2.5 cm radius around umbilicus) and the hospital supervisor immediately put the bar-coded sticker on the swab tube and pasted the corresponding duplicate sticker on the form. The date and time of the collection of each swab was recorded on a form. Within 4 h of collection, the swabs were transferred to the laboratory for culture analysis. Field/study worker used the same procedure to collect swabs among the community births.
Application of intervention (immediately following the collection of swab)
After the collection of swab for culture analysis, hospital staff/fieldworker applied the assigned intervention immediately. She/he opened the designated intervention pack and applied the intervention to cleanse the tip, stump and base of the umbilicus and peri-umbilical region. The intervention was applied twice: first after the collection of baseline swab and second 24 h after first application. In dry cord group, no intervention was applied and the standard WHO guidelines for cord care were followed .
Swab collection after 2-hours and 48-hours of application of intervention
In both settings, 2-hours and 48-hours post application, the study staff collected the umbilical swab, following the same procedure used for pre-application swab collection. In case of dry cord, the sample collection and timing was matched i.e. it was taken 2- and 48- h after the first sample.
The culture analysis for umbilical cord swabs was performed at Dr Dang’s Medical Diagnostic Center, Hauz Khas, New Delhi, India. Umbilical swabs collected using HiCultureTM Transport Swabs (Cat No. MS651) were transported to laboratory for aerobic culture. All samples (i.e. 10 μL of the neat specimen) were inoculated in 3 media plates i.e. McConkey Agar, Blood Agar and Chocolate Agar. The plates were incubated as per recommended time and temperature and were checked for absence or presence of bacterial isolates. Smear was prepared for identifying gram-negative and gram-positive bacteria. Based on the morphology and colour of the stain taken by the bacteria, they were classified into gram-positive or gram-negative organisms. Samples were further tested for species identification using standard manual methods and Vitek 2 compact system from BioMerieux France. For colony counts, the samples were put in 1 ml of normal saline for 3 log dilution and sub-cultured using standard subculture technique . Presence of bacterial growth, identification to gram-positive/-negative bacterial organisms and semi-quantitative colony count was estimated for all samples. Laboratory staff members were blinded to the formulation used; the swabs and the accompanying forms were labeled with bar-coded stickers. In addition, various quality control measures were followed using standard American Type Culture Collection strains during each step and inter/intra observer reliability tests in microscopy.
We used Visual Basic 6.0/ASP.net and Oracle 8i to manage the data, with stringent range, consistency, and logical checks. To ensure data quality and accuracy, real time data entry was done using netbook. Data were analyzed separately for the hospital and community births using Statistical Package of Social Sciences (SPSS Inc., Chicago, Illinois, USA, SPSS, Version 19.0 for Windows) and Stata (Stata Corp., College Station, Texas, USA, Intercooled Stata 12.0 Version), P ≤ 0.05 was considered statistically significant for all analyses. Descriptive statistics (frequencies, percentages, means and standard deviation) were calculated. We examined the characteristics of newborns and mothers across the allocated groups on a range of variables to determine the degree of balance achieved by the randomization. We analyzed colonization positivity data by intervention groups and follow-up time. Among those that were positive, we further estimated distribution of colony counts by intervention groups and follow-up time. A paired analysis comparing the baseline positivity/colony count of the child with his 2- and 48-hours post intervention positivity/counts was performed to study any group differences as well as changes over follow-up time within group. The chi square, t- test and OR with 95 % CI were used to estimate statistics and significance.
The primary outcome was culture positivity at 2-hours and 48-hours post application and the secondary outcome was bacterial colony count from umbilical and peri-umbilical region to estimate the concentration of viable bacteria. The reduction in bacterial colonization was assessed as proportion of neonates with positive culture (from umbilical and peri-umbilical area) 2-hours and 48-hours after application of 4 % chlorhexidine solution as compared to dry cord care and control groups. The reduction in density of bacterial colonization (limited to samples with growth) after 2-hours and 48-hours of application of 4 % chlorhexidine solution as compared to dry cord care and control groups was assessed in terms of mean reduction in bacterial colony counts. The risk of colonization stratified by gram-positive and gram-negative organisms was estimated by intervention groups.
Baseline characteristics and risk factors for infectiona
(n = 86)
(n = 86)
(n = 75)
Age of mother (years, mean ± SD)
23.87 ± 2.54
23.77 ± 2.86
25.12 ± 3.24
Birth weight (grams, mean ± SD)
2728.3 ± 479.5
2684.3 ± 453.6
2794.8 ± 437.6
No. of pelvic examinations (mean ± SD)
2.37 ± 1.25
2.07 ± 1.00
2.00 ± 0.97
Problems during delivery
Maternal risk factors for infection
LPVb > 24 h
Fever in mother
Time since birth (hrs:min, mean ± SD)
4:39 ± 2.31
4:35 ± 2:49
4:12 ± 2:37
(n = 36)
(n = 24)
(n = 19)
Age of mother (years, mean ± SD)
24.42 ± 3.95
24.62 ± 4.13
25.79 ± 3.91
Did the person clean hands before conducting delivery
New razor blade for cutting the cord
Baby given bath immediately after delivery
Of the 79 neonates enrolled in the community; 36 were assigned to chlorhexidine, 24 to placebo and 19 to dry cord care groups. At baseline, no significant differences were seen in a variety of variables measured, such as age of the mother, cord cutting methods, hand cleaning before conducting delivery and babies receiving bath immediately after delivery. The proportion of males was lower in chlorhexidine group (Table 2).
Bacterial colonization and density of colonization among positive cultures
Bacterial colonization (proportion with positive culture) and colony counts by intervention group and time of swab collection
2-hour post intervention
48-hour post intervention
Chlorhexidine (n-86, 86, 63)
Placebo (n-86, 86, 64)
Dry Cord (n-75, 75, 58)
Colony counts (Limited to samples with growth)c,d
3.67 ± 1.15
3.01 ± 0.88
3.96 ± 1.69
3.71 ± 0.75
3.77 ± 1.06
4.97 ± 0.97
Dry Cord (n-14, 24, 53)
3.88 ± 0.91
3.96 ± 1.69
5.12 ± 1.07
Chlorhexidine (n-36, 36, 36)
Placebo (n-24, 24, 24)
Dry Cord (n-19, 19, 19)
Colony Counts (Limited to samples with growth)c,d
Chlorhexidine (n-30, 16, 14)
5.28 ± 1.00
3.85 ± 1.15
3.32 ± 1.36
Placebo (n-20, 15, 16)
5.25 ± 1.10
5.35 ± 0.77
5.08 ± 0.80
Dry Cord (n-14, 14, 16)
5.85 ± 1.31
5.76 ± 1.24
5.55 ± 0.93
Comparison between chlorhexidine vs. placebo/dry cord care for the bacterial colonization and colony counts
Chlorhexidine vs. placebo
Chlorhexidine vs. dry cord
Odds ratio (95 % CI)
Odds ratio (95 % CI)
Paired comparison for bacterial colonization between-
Baseline and 2-hour post intervention
Baseline and 48-hour post intervention
Difference in mean of colony counts (95 % CI) at 48 h
−1.01 ( −1.72– −0.30)
−1.16 ( −1.93– −0.39)
Paired comparison for bacterial colonization between-
Baseline and 2-hour post intervention
Baseline and 48-hour post intervention
Difference in mean of colony counts (95 % CI) at 48 h
−1.76 ( −2.60– −0.93)
−2.23 ( −3.18– −1.29)
Among community births, baseline positivity was 81 % (64 of 79 swabs) (Table 3). Chlorhexidine showed a non-significant reduction of 53 % (OR = 0.47; p = 0.17) and a significant reduction of 86 % (OR = 0.14; p = 0.02) in change in bacterial colonization from baseline to 2 h sample as compared to placebo and dry cord care groups, respectively (Table 4). There was also a significant 83 % reduction in change in bacterial colonization from baseline to 48-hour post application in chlorhexidine group compared to placebo; 90 % compared to dry cord care. Change in mean colony counts from baseline to 48-hour post intervention among growth positives in chlorhexidine group were significantly reduced in comparison to placebo [difference in mean = −1.76; p < 0.001] and dry cord care [difference in mean = −2.23; p < 0.001].
Specific organisms identified in the hospital and community setting
Among swabs with positive culture, the presence of specific organisms was assessed. In the hospital setting, Acinetobacter spp., Citrobacter diversus, Citrobacter spp., Coagulase-negative Staphylococcus, Escherichia coli, Klebsiella spp., Pseudomonas aeruginosa, Pseudomonas spp., Staphylococcus aureus, Staphylococcus spp. and Viridans streptococci were the most common organisms, constituting both gram-positive and gram-negative strains, identified on the umbilical stump, base and the peri-umbilical region. However, in the community, Acinetobacter iwoffii., Acinetobacter junii, Acinetobacter baumanii, Acinetobacter haemolyticus, Acinetobacter spp., Acinetobacter ursingii, Aeromonas hydrophilia, Aeromonas spp., Cedecea davisae, Citrobacter diversus, Citrobacter spp., Coagulase Negative Staphylococcus, Escherichia Coli, Enterobacter cloacae, Klebsiella pneumoniae, Klebsiella spp., Pseudomonas aeruginosa, Staphylococcus aureus, Staphylococcus lentus, and Staphylococcus sciuri were the most common pathogens identified on the umbilical cord.
When colonization positivity data was analyzed by gram-positive/gram-negative strains, intervention groups and follow-up time, the reductions with chlorhexidine persisted. In hospital born neonates, the overall reduction in colonization for gram-positive as well as gram-negative organisms remained significant for the chlorhexidine group compared to placebo or dry cord care groups for 2-hours and 48-hours post application samples. For the community births, there was a significant reduction in the chlorhexidine group compared to placebo and dry cord for gram-positive bacteria. For the gram-negative bacteria, although there was a trend of reduction, the differences were significant only at 48-hour post application (Additional file 1).
Chlorhexidine application over umbilical cord has been shown to reduce the risk of omphalitis and neonatal mortality in community settings in recent trials done in Nepal, Pakistan and Bangladesh [21, 28]. In this double blind randomized controlled trial with facility and community data, we evaluated the impact of 4 % chlorhexidine cord cleansing compared to placebo or dry cord care on cord colonization. Cord cleansing with 4 % chlorhexidine showed significant reduction in colonization and density of pathogens in both facility and community setting. As compared to dry cord care, the impact of 4 % chlorhexidine was greater in the first 48 h after birth suggesting that chlorhexidine may be a possible intervention for reducing omphalitis and sepsis arising from transmission of bacterial infections via the umbilical remnant. These findings are in line with observations reported in a study conducted in Bangladesh [29, 30].
The potential mechanisms for the chlorhexidine action in reducing the colonization rates could possibly be the result of the increased binding efficiency of the detergent form to the umbilical tissues, resulting in prolonged residual effect . This bactericidal effect of chlorhexidine could be attributed to its chemical structure, which is a positively charged hydrophobic and lipophilic molecule that interacts with phospholipids and lipopolysaccharides on the cell membrane of bacteria and enters the cell either through active or passive transport mechanism . Interaction of the positive charge of the molecule with the negatively charged phosphate groups on microbial cell wall [32, 33] alters the cells’ osmotic equilibrium, increasing the permeability of the cell wall thus allowing the chlorhexidine molecule to penetrate into the bacteria . Damage to this delicate membrane is followed by leakage of intracellular constituents, particularly phosphate entities such as adenosine triphosphate and nucleic acids. As a consequence, the cytoplasm becomes congealed, with resultant reduction in leakage; thus, there is a biphasic effect on membrane permeability. These early changes are beneficial during the critical first few hours and days of life when most neonatal deaths occur in resource-poor settings . Our data also suggests that mild soap and water solution (placebo) was not very effective in reducing bacterial colonization in comparison to dry cord care. This placebo solution only reduced the pathogens in immediate 2-hours post application swabs in the community setting and did not produce extended effect for 48 h. This could be a mere chance finding or cord cleansing process itself mechanically removed the organisms from the umbilical and peri-umbilical region, subsequently decreasing the bacterial load. This indicates that for residual and cumulative effects, antibacterial agents such as chlorhexidine are substantially more effective than non-antiseptic agents .
Bacteriologic colonization rates, profile, and dynamics in a community setting might differ substantially from that in the hospital setting . In the present study, the observed colonization positivity rate was higher in the community-setting (81 %) than in the hospital (20 %) which could be due to unhygienic environment, unclean delivery practices at homes and immediate post-delivery traditional practices. Further, as compared to other studies, the overall pre-application bacterial growth was low in the hospital setting which could be due to differences in neonate handling and infection prevention practices [26, 35, 36]. In the present study, the reported impact of 4 % chlorhexidine on the reduction of bacterial colonization was consistently high in both settings.
This study also describes the specific pathogens colonizing the umbilical cord. Trends in colonization positivity data were assessed by intervention groups, follow-up time and gram stain status of organisms and it was observed that chlorhexidine showed high bactericidal activity. The evidence presented here for the immediate and extended effect of 4 % chlorhexidine on large and sustained reductions in colonization by gram-negative and gram-positive organisms due to early application with chlorhexidine complements the Cochrane conclusion  that colonization is substantially lower among infants receiving topical antiseptics compared with those with no specific treatment (OR = 0.28; 95 % CI: 0.22–0.36).
There were few limitations to our study. The sample size limited our ability to definitively determine whether any of the study outcomes could be influenced by one intervention or the other. But the encouraging findings in our study were that most of the results were statistically significant. Our results provide evidence that the application of 4 % chlorhexidine solution on the umbilical cord provides protection to the baby from bacterial colonization and growth. The findings of our pilot study are important but need to be confirmed in a large community based trial with adequate statistical power as reduction in colonization and colony count in small number of subjects does not have adequate power to evaluate the impact on mortality or sepsis but does provide data on possible mechanisms.
The study cannot address an impact that these changes can have on the microbiome and its implications. From a comparison study in Pemba and Zambia (personal communication and in submission) it is clear that reduction in omphalitis may not essentially result in reduction in sepsis and mortality.
Our study has shown that cord cleaning with the first time commercially produced 4 % chlorhexidine soon after birth can significantly reduce colonization as well as density of colonization among newborns. The study also demonstrated no impact of the control preparation compared to dry cord care on colonization (increase or decrease). The study showed impact of chlorhexidine on colonization in both hospital and community settings, but does not speak to relationship between this reduction and occurrence of sepsis or mortality. The findings of our pilot study are important but need to be tested in large community based trials to establish linkage between reduction in bacterial colonization and sepsis and or mortality. If the link between reduced colonization and reduction in neonatal mortality is established in larger trials in Africa, this intervention could have impact on neonatal mortality in developing country settings where there is limited availability of resources, stringent customs and poor environmental hygiene.
CI, confidence interval; GN, gram-negative; GP, gram-positive; OR, odds ratio; TBA, trained birth attendant
We are thankful to parents of enrolled children for their time and efforts to participate in the study. Further we acknowledge the efforts of the study team, physicians and staff at Kalawati Saran Children’s hospital, New Delhi, India for providing the necessary support to carry out the study. We duly acknowledge the contribution of Galentic Pharma (India) Pvt. Ltd, Mumbai, India for providing the chlorhexidine.
This study was supported by a grant from the Bill & Melinda Gates Foundation. The funder however did not have any role in study design, data collection, data analysis and interpretation, decision to publish or preparation of the manuscript.
Availability of data and materials
Data will not be put in the public domain for another year as we are still working on another manuscript from this data set and will wait for that manuscript to be published before putting the data in the public domain.
SN conceptualized and designed the study, critically reviewed and revised the manuscript. PD coordinated and supervised data collection, involved in data analysis, interpreted the results and drafted the initial manuscript. UD and AD designed the data collection instruments, carried out the initial analysis, reviewed and revised the manuscript. VPM and REB were involved in the conceptualization of the research, development of study protocol, and preparation of manuscript. SS conceptualized and designed the study, provided oversight for implementation, directed the analysis, critically reviewed and revised the manuscript. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
Consent for publication
Ethics approval and consent to participate
Ethical approval was obtained from the Annamalai University, Tamil Nadu, India and from the Lady Hardinge Medical College & Kalawati Saran Children’s Hospital, New Delhi, India. Verbal informed consent was obtained in local language from the parents of the newborns prior to the enrolment in the study.
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