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Towards understanding global patterns of antimicrobial use and resistance in neonatal sepsis: insights from the NeoAMR network
  1. Grace Li1,
  2. Julia Anna Bielicki1,2,
  3. A S M Nawshad Uddin Ahmed3,
  4. Mohammad Shahidul Islam3,
  5. Eitan Naaman Berezin4,
  6. Clery B Gallacci4,
  7. Ruth Guinsburg5,
  8. Carlos Eduardo da Silva Figueiredo6,
  9. Rosilene Santarone Vieira6,
  10. Andre Ricardo Silva7,
  11. Cristiane Teixeira8,
  12. Paul Turner9,
  13. Ladin Nhan10,
  14. Jaime Orrego11,
  15. Paola Marsela Pérez11,
  16. Lifeng Qi12,
  17. Vassiliki Papaevangelou13,
  18. Pinelope Triantafyllidou14,
  19. Elias Iosifidis15,
  20. Emmanuel Roilides15,
  21. Kosmas Sarafidis15,
  22. Dasaratha Ramaiah Jinka16,
  23. Raghuprakash Reddy Nayakanti16,
  24. Praveen Kumar17,
  25. Vikas Gautam17,
  26. Vinayagam Prakash18,
  27. Arasar Seeralar18,
  28. Srinivas Murki19,
  29. Hemasree Kandraju19,
  30. Sanjeev Singh20,
  31. Anil Kumar20,
  32. Leslie Lewis21,
  33. Jayashree Pukayastha21,
  34. Sushma Nangia22,
  35. Yogesha K N22,
  36. Suman Chaurasia23,
  37. Harish Chellani24,
  38. Stephen Obaro25,
  39. Angela Dramowski26,
  40. Adrie Bekker26,
  41. Andrew Whitelaw27,28,
  42. Reenu Thomas29,
  43. Sithembiso Christopher Velaphi29,
  44. Daynia Elizabeth Ballot29,
  45. Trusha Nana29,
  46. Gary Reubenson29,
  47. Joy Fredericks29,
  48. Suvaporn Anugulruengkitt30,
  49. Anongnart Sirisub30,
  50. Pimol Wong31,
  51. Sorasak Lochindarat32,
  52. Suppawat Boonkasidecha32,
  53. Kanchana Preedisripipat33,
  54. Tim R Cressey33,
  55. Pongsatorn Paopongsawan34,
  56. Pagakrong Lumbiganon34,
  57. Dounghatai Pongpanut35,
  58. Pra-ornsuda Sukrakanchana35,
  59. Philippa Musoke36,37,
  60. Linus Olson38,
  61. Mattias Larsson38,
  62. Paul T Heath1,
  63. Michael Sharland1
  1. 1 Paediatric Infectious Diseases Research Group, Institute of Infection and Immunity, St George's, University of London, London, UK
  2. 2 Paediatric Pharmacology and Pharmacometrics Research, University of Basel Children's Hospital, Basel, Switzerland
  3. 3 Child Health Research Foundation, Dhaka Shishu Hospital, Dhaka, Bangladesh
  4. 4 Santa Casa Medical School, São Paulo, Brazil
  5. 5 Escola Paulista de Medicina, Universidade Federal de São Paulo, São Paulo, Brazil
  6. 6 Instituto Fernandes Figueira, Rio de Janeiro, Brazil
  7. 7 Federal Fluminense University, Rio de Janeiro, Brazil
  8. 8 Prontobaby Children’s Hospital, Rio de Janeiro, Brazil
  9. 9 Cambodia Oxford Medical Research Unit, Siem Reap, Cambodia
  10. 10 Angkor Hospital for Children, Siem Reap, Cambodia
  11. 11 Fundación Valle del Lili, Santiago de Cali, Colombia
  12. 12 Shenzhen Children’s Hospital, Shenzhen, China
  13. 13 Third Department of Pediatrics, National and Kapodistrian University of Athens, Athens, Greece
  14. 14 Attikon University General Hospital, Athens, Greece
  15. 15 School of Health Sciences, Aristotle University, Thessaloniki, Greece
  16. 16 Department of Paediatrics, Rural Development Trust Hospital, Bathalapalli, India
  17. 17 Paediatrics, Post Graduate Institute of Medical Education and Research, Chandigarh, India
  18. 18 Institute of Obstetrics and Gynaecology and Government Hospital for Women and Children, Chennai, India
  19. 19 Department of Neonatology, Fernandez Hospital, Hyderabad, India
  20. 20 Amrita Institute of Medical Sciences, Kochi, India
  21. 21 Kasturba Medical College, Manipal, India
  22. 22 Lady Hardinge Medical College, New Delhi, India
  23. 23 All India Institute of Medical Sciences, New Delhi, India
  24. 24 Vardhman Mahavir Medical College and Safdarjung Hospital, New Delhi, India
  25. 25 International Foundation Against Infectious Disease in Nigeria, Omaha, Nebraska, USA
  26. 26 Department of Paediatrics and Child Health, Faculty of Medicine and Health Sciences, Stellenbosch University, Stellenbosch, South Africa
  27. 27 Division of Medical Microbiology, Faculty of Medicine and Health Sciences, Stellenbosch University, Stellenbosch, South Africa
  28. 28 National Health Laboratory Service, Tygerberg Hospital, Cape Town, South Africa
  29. 29 University of the Witwatersrand, Johannesburg, South Africa
  30. 30 Chulalongkorn University, Bangkok, Thailand
  31. 31 Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand
  32. 32 Queen Sirikit National Institute of Child Health, Bangkok, Thailand
  33. 33 Chiangrai Prachanukroh Hospital, Chiang Rai, Thailand
  34. 34 Department of Paediatrics, Khon Kaen University, Khon Kaen, Thailand
  35. 35 Phayao Hospital, Phayao, Thailand
  36. 36 Paediatrics and Child Health, Makerere University, Kampala, Kampala, Uganda
  37. 37 Mulago Hospital, Kampala, Uganda
  38. 38 Karolinska Institute in collaboration with Vietnam National Children's Hospital within Training and Research Academic Collaboration (TRAC) Sweden – Vietnam, Hanoi, Vietnam
  1. Correspondence to Professor Michael Sharland, Institute of Infection and Immunity, St George's, University of London, London SW17 0RE, UK; msharlan{at}


Objective To gain an understanding of the variation in available resources and clinical practices between neonatal units (NNUs) in the low-income and middle-income country (LMIC) setting to inform the design of an observational study on the burden of unit-level antimicrobial resistance (AMR).

Design A web-based survey using a REDCap database was circulated to NNUs participating in the Neonatal AMR research network. The survey included questions about NNU funding structure, size, admission rates, access to supportive therapies, empirical antimicrobial guidelines and period prevalence of neonatal blood culture isolates and their resistance patterns.

Setting 39 NNUs from 12 countries.

Patients Any neonate admitted to one of the participating NNUs.

Interventions This was an observational cohort study.

Results The number of live births per unit ranged from 513 to 27 700 over the 12-month study period, with the number of neonatal cots ranging from 12 to 110. The proportion of preterm admissions <32 weeks ranged from 0% to 19%, and the majority of units (26/39, 66%) use Essential Medicines List ‘Access’ antimicrobials as their first-line treatment in neonatal sepsis. Cephalosporin resistance rates in Gram-negative isolates ranged from 26% to 84%, and carbapenem resistance rates ranged from 0% to 81%. Glycopeptide resistance rates among Gram-positive isolates ranged from 0% to 45%.

Conclusion AMR is already a significant issue in NNUs worldwide. The apparent burden of AMR in a given NNU in the LMIC setting can be influenced by a range of factors which will vary substantially between NNUs. These variations must be considered when designing interventions to improve neonatal mortality globally.

  • antimicrobial resistance
  • neonatal sepsis

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What is already known on this topic?

  • The majority of neonatal pathogens in the UK setting are susceptible to antimicrobials used as empirical treatment for neonatal sepsis.

  • The Delhi Neonatal Infection Study demonstrated high levels of resistance of neonatal pathogens to antimicrobials used as empirical treatment for neonatal sepsis in Delhi.

  • The prevalence of extended-spectrum beta-lactamase (ESBL) Gram-negative infections in neonates is increasing worldwide.

What this study adds?

  • For the first time, this study describes multinational, multicentre variation in empirical antimicrobial choice for neonatal sepsis, with a focus on low-income and middle-income settings.

  • This study is the first to describe multinational, multicentre rates of antimicrobial resistance in both Gram-negative and Gram-positive isolates from neonatal units.

  • This study is the first to show high rates of cephalosporin and carbapenem resistance in isolates, particularly those from Bangladesh and South Africa.


Between 2000 and 2015 there was a significant decline in global neonatal mortality, from 36 to 19 per 1000 live births (5.1–2.7 million cases annually).1 This was less pronounced than the reduction seen in childhood (<5 years) mortality, highlighting room for improvement. Antimicrobial resistance (AMR) threatens progress towards this goal.

Laxminarayan et al 2 previously estimated the global AMR population-attributable fraction for neonatal mortality. It was assumed that low-income and middle-income countries (LMICs) consistently use a combination of a narrow-spectrum penicillin (benzylpenicillin/ampicillin) and aminoglycoside (gentamicin/amikacin) as empirical therapy for neonatal sepsis (in line with the WHO guidelines), and local resistance rates to either antimicrobial drug could be used as a proxy for risk of mortality attributable to AMR. Mortality rates for AMR neonatal infections were taken from the published literature. Their analysis suggested that 214 000 of 690 000 annual neonatal deaths (31%) associated with sepsis are potentially attributable to AMR. Morbidity and mortality due to AMR have since been added to the Global Burden of Disease Study.3

These estimates are likely to represent an overestimate of mortality attributable to AMR, as blood cultures are usually taken in an inpatient setting where infants are more unwell; it is difficult to accurately estimate mortality from AMR sepsis in the community setting. The limited availability of global microbiological data means that national estimates of resistance may be extrapolated from one or two studies only. Resistance patterns are also known to vary widely between units within cities, particularly when prescribing practices differ substantially.4 These factors illustrate the need for detailed multicountry, patient-level data to better characterise the relationship between AMR and mortality.

A number of factors may affect the burden of resistant infections in the neonatal setting (figure 1). They can be divided into three broad categories: resource availability, clinical presentation and clinical decision-making.

Figure 1

Factors affecting the apparent burden of antimicrobial resistance (AMR) in the neonatal setting.

The Neonatal AMR research network (NeoAMR) project was established in September 2017. It aims to ‘develop new, globally applicable, empiric antibiotic regimens and strategies for the treatment of neonatal sepsis in settings with varying prevalence of multidrug-resistant pathogens .5 These include establishing a global network of neonatal units (NNUs) to design and conduct studies on the optimal use of off-patent antibiotics and other clinical interventions to reduce AMR infection. NNUs should be a mix of neonatal intensive care and special care beds, depending on local demand and resource availability. To facilitate this, a web-based survey was designed to gain an understanding of how the above three factors varied between different settings.


The NeoAMR web-based survey collected data from 39 NNUs across 12 countries in four continents, with contact made through existing networks. Participating centres were provided with either a PDF (portable document format) copy of the survey or an online link to the REDCap6 database, with questions focused on issues concerning unit capacity, staffing ratios, availability of services, use of antimicrobial guidelines, choice of empirical antimicrobial regimens, local laboratory facilities and antimicrobial susceptibility rates. NNUs also provided information about the total number of positive blood cultures, species isolated and antimicrobial sensitivity testing performed over 12 months. We did not collect data on the rate of culture collection.

The WHO Essential Medicines List (EML) 2017 was revised to include three new categories for antimicrobials—‘Access’, ‘Watch’ and ‘Reserve’, to denote the order (first-line, second-line or last resort) in which antimicrobials should be used to ensure that the appropriate antibiotics are prescribed for a given infection.7 We analysed our results according to these categories.

The survey covered a timeframe of 12 months, where relevant, and data were collected between June and September 2017. All data were anonymised and hosted on a server at St George’s, University of London. All participating sites agreed to the remote hosting of clinical data.


Resource availability

Of the 39 units, 38 were university or teaching hospitals. Twenty-five were publicly funded, or free at the point of access, eight were funded by a mixture of public/private incomes, and six were private, that is, a fee for service was payable by the patient. The 39 units serve a total of 228 580 live births per year, of whom 84 140 babies were admitted (both inborn and outborn) and 37 500 (45%) were born preterm (<37 weeks). Summary statistics for the 39 centres are shown in table 1.

Table 1

Summary statistics for NeoAMR centres (per year)

Of the 39 units, 35 provided intubation and ventilation routinely (1 provided intubation and ventilation on a non-routine basis, 3 could provide non-invasive ventilation, of which 1 provided non-invasive ventilation on a non-routine basis). Thirty-six centres were capable of providing inotropic support, and 34 had the facilities to provide total parenteral nutrition. Thirty-three centres had routine support from a paediatric surgical team, three centres had non-routine support from a surgical team, and three centres had no access to a paediatric surgical team. Seven units were not associated with a maternity unit on site; the average percentage of preterm admissions <37 weeks was 26%. On this basis, the majority of units would be categorised as level 3 units, as defined by the American Academy of Pediatrics or the British Association of Perinatal Medicine (BAPM).8 On average, each unit had 38 admissions per cot per annum (IQR 22–50); however, the unit in Uganda was an outlier with 119 admissions per cot.

Access to laboratory facilities was good across the network, with blood culturing taking place at all sites apart from Uganda. Antimicrobial susceptibility testing was taking place at 31 of 39 sites.

Clinical presentation

The ratio of nurses to cots, as well as the proportion of preterm admissions, determines the workload and influences the ability of medical staff to recognise unwell infants. Table 1 demonstrates that there does not appear to be an association between units with higher nurse to cot ratios and those with higher proportions of preterm admissions. Although we do not have data on the intensity of bed usage (ie, whether they are used in a high-dependency or special care capacity), our data suggest that on average there is approximately one whole-time equivalent nurse employed per cot for the participating units. On average, participating units had on average 0.78 (IQR 0.52–1.25) full-time nurses per cot, and as our data included both intensive care and low dependency beds this would suggest that the 1:1 ratio for intensive care beds recommended by the BAPM8 is being met.

Clinical decision-making

Local or national guidelines for empirical antibiotic use in early-onset sepsis (EOS) or late-onset sepsis (LOS) were available in the majority of centres (29 of 38). Fewer guidelines were available for neonatal meningitis (22 of 38). Of 38 centres, 24 used the WHO-recommended combination of a broad-spectrum penicillin with aminoglycoside (benzylpenicillin/ampicillin with gentamicin/amikacin) as first-line therapy in EOS. Table 2 shows the empirical antibiotic regimens grouped according to the three EML categories. Choice of antimicrobials tended to cluster by geographical region; there was less compliance with WHO guidance overall in Bangladesh, China and India. There was no clear association between the level of preterm admissions and choice of antimicrobial regimen. Seventeen NeoAMR centres listed WHO ‘Reserve’ antibiotics as a choice on their empirical antimicrobial guidelines (for either EOS, LOS or meningitis). This suggests that use of ‘Reserve’ antibiotics is already established in NNUs as empirical therapy. A full list of empirical antibiotic regimens for NeoAMR centres can be found in online supplementary appendix 1.

Table 2

Empirical antimicrobial regimens, categorised by EML-C group

The majority of centres reserved the use of broader spectrum antibiotics for LOS and meningitis. However, there was significant variation in the use of ‘Watch’ antibiotics in particular. Overall, 43% of empirical antimicrobial regimens consist of ‘Access’ antibiotics, 37% of ‘Watch’ antibiotics and 20% consist of ‘Reserve’ antibiotics. Of intended ‘Reserve’ antibiotic usage, 4% was in EOS, 48% in LOS and 48% in meningitis. The use of Reserve antibiotics in the management of neonatal meningitis was particularly notable in India.

Although we do not have information about the blood culturing rate (ie, we do not know the positivity rate or the yield of pathogens), the ratio of positive blood cultures to admissions ranged from 0.2% (Bangladesh) to 40% (South Africa).

Of the 39 centres, 31 provided results of antimicrobial sensitivity testing for their positive blood cultures. Cephalosporin resistance is found in the majority of Gram-negative isolates, with Bangladeshi and South African centres having the highest rates of carbapenem resistance (table 3). Glycopeptide resistance among Gram-positive isolates is a particular problem in Brazilian and Nigerian centres. Choice of ‘Reserve’ antibiotics for a local empirical antimicrobial guideline was associated with a higher total number of positive blood cultures per admission, suggesting that use of Reserve antibiotics may be guided by local microbiology results rather than as broad-spectrum empirical therapy.

Table 3

Antimicrobial resistance patterns in the NeoAMR network


To our knowledge, this is the first study to quantify differences in NNU resource allocation and choice of empirical antimicrobial therapy primarily in LMICs on a global scale, accompanied by AMR patterns of local isolates. There is significant variation in factors affecting neonatal care which will impact on the design of future neonatal sepsis trials, including the ratio of live births to the number of cots available locally, the level of staffing on site, the proportion of preterm admissions, access to a choice of empirical antimicrobial therapies, local blood culture rates and availability of antimicrobial susceptibility testing.

We divided these factors into three categories (figure 1). In the first category, accurate estimation of the admission rate relative to the local birth rate is needed to estimate the incidence of AMR sepsis and ease of access to intensive care support. Choice of empirical antimicrobial regimen may be a reflection of wider access to medicines at a country level. Gestational age is recognised as a particularly significant variable as preterm infants are more vulnerable to infection than term infants.9 Additionally, the unique pharmacokinetic profile of antimicrobials in this population10 may increase the risk of treatment failure. Colonisation by resistant bacteria and previous use of antibiotics are two factors which are used in clinical prediction scores, for example, for vancomycin-resistant enterococcus infection in an adult intensive care unit setting.11

Our data demonstrate the challenges faced when attempting global multicentre neonatal sepsis studies in settings with varied resource availability. Our study did not collect data on the acuity of bed usage, which is a key factor in the relationship between NNU staffing and mortality. There is currently no international standard for neonatal nursing training, although the Council of International Neonatal Nurses is increasingly playing a role in this area. There are also no published international data comparing neonatal nursing staffing ratios in different LMIC settings. The BAPM8 recommends staffing ratios of 1:1 for intensive care beds, 1:2 for high dependency beds and 1:4 for special care baby unit admissions. While a recent systematic review12 found that three of four studies reported correlation between lower neonatal staffing to patient ratios and higher mortality, and a reduction in staffing ratios for intensive care beds has been shown to correlate with increased mortality in a UK setting,13 differences in the definition of staffing and a lack of evidence from an LMIC setting prevent the design of an optimal staffing approach.

When combined with results taken from the Global Antimicrobial Resistance, Prescribing, and Efficacy Among Neonates and Children (GARPEC) database,14 our data confirm that variation in choice of empirical antimicrobial regimens exists, despite the existence of global guidelines. One study of paediatric Gram-negative blood stream infection (BSI) in the Pacific region found that for 309 episodes of BSI, 95 different empirical regimens were prescribed (European Congress of Clinical Microbiology and Infectious Diseases 2018, abstract O0055). Future guidance emerging from a neonatal sepsis study to reduce global mortality from AMR-related sepsis is likely to be regional.

Our data show a worryingly high level of AMR, particularly in Gram-negative species. The findings suggest that particularly in Bangladesh and South Africa, choice of second-line antimicrobial therapy is increasingly limited. The WHO Access, Watch and Reserve (AWaRe) classification system of antimicrobials may be a useful guide to monitor usage of broad-spectrum antimicrobials; however, it is beyond the scope of our study to determine whether use of empirical antimicrobial regimens in particular categories is correlated with local AMR rates.

The total number of blood cultures taken at each site was not known, but the total number of positive cultures was assumed to be a proxy of blood culturing rates. Due to anonymisation of clinical data, we could not differentiate between positive cultures from the same patient or the same clinical episode. The relationship between blood culturing rates, contamination rate and BSI is unclear.15 Use of blood culture positivity with a resistant pathogen as a metric of exposure to AMR presents challenges, as blood culture positivity in neonates is low, even when a serious bacterial infection may be present.16 Underdetection of serious bacterial infection will result in novel interventions to reduce mortality being perceived as less effective in reducing neonatal mortality from AMR sepsis.

Neonatal colonisation status is affected by several factors, including maternal colonisation profile and immune function,17 and is associated with invasive infection by colonising species.18 Colonisation status may change during an inpatient stay on an NNU,19 and the precise relationship between colonisation and serious bacterial infection is not clearly understood, particularly in LMIC settings. The use of mortality as the endpoint in future trials of neonatal sepsis poses diagnostic challenges, as multiple pathologies are common in neonates and the differentiation of deaths with sepsis as opposed to attributable to sepsis will need to be considered. An emphasis on clinical presentations or physiological observations which have a high positive predictive value for blood culture-positive sepsis4 is needed, as well as ensuring that the most common causes of death in the NNU population (eg, respiratory failure, intraventricular haemorrhage, massive pulmonary haemorrhage) are captured in future studies.20 Mortality is also not the only outcome which should be considered. Neurodisability is a potentially preventable consequence of severe sepsis but much more difficult to assess because of the difficulties associated with long-term follow-up.21


Our data provide an important snapshot of how differences in NNU organisation and empirical antibiotic regimens may contribute to different clinical outcomes from AMR sepsis in different country settings. Further work is now required to understand how these differences can be captured in a future observational study designed to clarify how AMR influences neonatal mortality and, ultimately, how its impact can be reduced or prevented.


We would like to acknowledge the following contributors: Professor Bhadresh Vyas (Hospital MP Shah Government Medical College and GG Hospital, Jamnagar, Gujarat), Eyinade Olateju (University of Abuja Teaching Hospital, Gwagwalada), Jolly Nankunda (Mulago Hospital, Kampala), Siriporn Rachakhom (Siriraj Hospital, Thailand), Professor Suely Dornellas do Nascimento (Universidade Federal de São Paulo), Professor Yonghong Yang, Dr Shufeng Tian and Dr Ruizhen Zhao (Shenzhen Children’s Hospital, Shenzhen), Dr Dan Wang and Dr Ying Zhang (Tianjin Children’s Hospital, Tianjin), Dr Ping Wang and Dr Jing Liu (Beijing Obstetrics and Gynecology Hospital, Beijing), Dr Ping Zhou and Dr Lijuan Wu (Bao'an Maternal and Child Health Hospital, Jinan University, Shenzhen), Dr Changan Zhao and Dr Xiaoping Mu (Guangdong Women and Children’s Hospital, Guangdong), and Dr Yajuan Wang and Dr Fang Dong (Beijing Children’s Hospital, Beijing).



  • Contributors MS and PTH conceived this work. JB designed the survey. JB and GL analysed and interpreted the data. GL wrote a first draft. All other authors contributed equally to collection of data. All authors contributed to critical review of drafts and approved the final manuscript.

  • Funding This work was supported by the Global Antibiotic Research and Development Partnership, Geneva.

  • Competing interests None declared.

  • Patient consent for publication Not required.

  • Ethics approval This was an observational study. No unique patient identifiers were collected, no patient samples were collected and no interventions were performed.

  • Provenance and peer review Not commissioned; externally peer reviewed.

  • Data availability statement Data are available upon reasonable request.

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