The impact of inpatient bloodstream infections caused by antibiotic-resistant bacteria in low- and middle-income countries: A systematic review and meta-analysis

被引:34
作者
Allel, Kasim [1 ,2 ,3 ,4 ]
Stone, Jennifer [5 ]
Undurraga, Eduardo A. [4 ,6 ,7 ,8 ]
Day, Lucy [1 ]
Moore, Catrin E. [9 ]
Lin, Leesa [10 ,11 ,12 ]
Furuya-Kanamori, Luis [13 ]
Yakob, Laith [1 ,2 ]
机构
[1] London Sch Hyg & Trop Med, Fac Infect & Trop Dis, Dept Dis Control, London, England
[2] London Sch Hyg & Trop Med, Antimicrobial Resistance Ctr, London, England
[3] UCL, Inst Global Hlth, London, England
[4] Multidisciplinary Initiat Collaborat Res Bacterial, Santiago, Chile
[5] Univ Adelaide, Fac Hlth & Med Sci, JBI, Adelaide, SA, Australia
[6] Pontificia Univ Catolica Chile, Escuela Gobierno, Santiago, Chile
[7] CIFAR, CIFAR Azrieli Global Scholars Program, Toronto, ON, Canada
[8] Res Ctr Integrated Disaster Risk Management CIGIDE, Santiago, Chile
[9] St Georges Univ London, Infect & Immun Inst, Ctr Neonatal & Paediat Infect, London, England
[10] London Sch Hyg & Trop Med, Fac Epidemiol & Populat Hlth, Dept Infect Dis Epidemiol, London, England
[11] Hong Kong Sci Pk, Lab Data Discovery Hlth D24H, Hong Kong, Peoples R China
[12] Univ Hong Kong, Hong Kong, Peoples R China
[13] Univ Queensland, Fac Med, UQ Ctr Clin Res, Herston, Australia
关键词
STAPHYLOCOCCUS-AUREUS BACTEREMIA; LENGTH-OF-STAY; SUSCEPTIBLE PSEUDOMONAS-AERUGINOSA; ENTEROCOCCUS-FAECALIS BACTEREMIA; HOSPITALIZED CANCER-PATIENTS; GRAM-NEGATIVE BACTEREMIA; RISK-FACTORS; CARBAPENEM-RESISTANT; INTENSIVE-CARE; ACINETOBACTER-BAUMANNII;
D O I
10.1371/journal.pmed.1004199
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BackgroundBloodstream infections (BSIs) produced by antibiotic-resistant bacteria (ARB) cause a substantial disease burden worldwide. However, most estimates come from high-income settings and thus are not globally representative. This study quantifies the excess mortality, length of hospital stay (LOS), intensive care unit (ICU) admission, and economic costs associated with ARB BSIs, compared to antibiotic-sensitive bacteria (ASB), among adult inpatients in low- and middle-income countries (LMICs). Methods and findingsWe conducted a systematic review by searching 4 medical databases (PubMed, SCIELO, Scopus, and WHO's Global Index Medicus; initial search n = 13,012 from their inception to August 1, 2022). We only included quantitative studies. Our final sample consisted of n = 109 articles, excluding studies from high-income countries, without our outcomes of interest, or without a clear source of bloodstream infection. Crude mortality, ICU admission, and LOS were meta-analysed using the inverse variance heterogeneity model for the general and subgroup analyses including bacterial Gram type, family, and resistance type. For economic costs, direct medical costs per bed-day were sourced from WHO-CHOICE. Mortality costs were estimated based on productivity loss from years of potential life lost due to premature mortality. All costs were in 2020 USD. We assessed studies' quality and risk of publication bias using the MASTER framework. Multivariable meta-regressions were employed for the mortality and ICU admission outcomes only. Most included studies showed a significant increase in crude mortality (odds ratio (OR) 1.58, 95% CI [1.35 to 1.80], p < 0.001), total LOS (standardised mean difference "SMD" 0.49, 95% CI [0.20 to 0.78], p < 0.001), and ICU admission (OR 1.96, 95% CI [1.56 to 2.47], p < 0.001) for ARB versus ASB BSIs. Studies analysing Enterobacteriaceae, Acinetobacter baumanii, and Staphylococcus aureus in upper-middle-income countries from the African and Western Pacific regions showed the highest excess mortality, LOS, and ICU admission for ARB versus ASB BSIs per patient. Multivariable meta-regressions indicated that patients with resistant Acinetobacter baumanii BSIs had higher mortality odds when comparing ARB versus ASB BSI patients (OR 1.67, 95% CI [1.18 to 2.36], p 0.004). Excess direct medical costs were estimated at $12,442 (95% CI [$6,693 to $18,191]) for ARB versus ASB BSI per patient, with an average cost of $41,103 (95% CI [$30,931 to $51,274]) due to premature mortality. Limitations included the poor quality of some of the reviewed studies regarding the high risk of selective sampling or failure to adequately account for relevant confounders. ConclusionsWe provide an overview of the impact ARB BSIs in limited resource settings derived from the existing literature. Drug resistance was associated with a substantial disease and economic burden in LMICs. Although, our results show wide heterogeneity between WHO regions, income groups, and pathogen-drug combinations. Overall, there is a paucity of BSI data from LMICs, which hinders implementation of country-specific policies and tracking of health progress. Author summary Why was this study done? Bloodstream infections (BSIs) caused by antibiotic-resistant bacteria (ARB) have multifaceted impacts, including higher admission to intensive care units (ICUs), prolonged hospitalisations, and high economic and societal costs worldwide.Despite the global burden, most evidence on the excess burden of ARB BSIs has been derived from high-income countries; comparatively, there are limited data from low- and middle-income countries (LMICs). What did the researchers do and find? We employed a systematic literature review and subsequent meta-analysis of 109 individual studies to quantify the impact of ARB BSIs in hospitalised patients from LMICs.Based mostly on crude data comparisons ignoring the possible influence of confounding factors, we found that ARB BSIs, compared to BSIs caused by antibiotic-sensitive bacteria (ASB), were associated with substantially longer stays in hospitals and ICUs, higher mortality, and increased direct medical and productivity costs. What do these findings mean? Our findings highlight the excess morbidity, mortality, and costs associated with ARB BSIs and the sparsity of data from LMICs.Targeted strategies to improve the prevention, detection, and treatment of resistant BSIs in LMICs are required to reduce the economic and disease burden.
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