Next Article in Journal
Evaluation of Antioxidant, Antimicrobial and Tyrosinase Inhibitory Activities of Extracts from Tricholosporum goniospermum, an Edible Wild Mushroom
Next Article in Special Issue
Antibiogram, Prevalence of OXA Carbapenemase Encoding Genes, and RAPD-Genotyping of Multidrug-Resistant Acinetobacter baumannii Incriminated in Hidden Community-Acquired Infections
Previous Article in Journal
Content and Mechanism of Action of National Antimicrobial Stewardship Interventions on Management of Respiratory Tract Infections in Primary and Community Care
Previous Article in Special Issue
Impact of Colistin Dosing on the Incidence of Nephrotoxicity in a Tertiary Care Hospital in Saudi Arabia
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Clinical and Economic Burden of Carbapenem-Resistant Infection or Colonization Caused by Klebsiella pneumoniae, Pseudomonas aeruginosa, Acinetobacter baumannii: A Multicenter Study in China

1
Centre for Health Management and Policy Research, School of Public Health, Cheeloo College of Medicine, Shandong University, (NHC Key Lab of Health Economics and Policy Research, Shandong University), Jinan 250012, China
2
Center for Health Policy Studies, School of Public Health, Zhejiang University School of Medicine, Hangzhou 310058, China
3
Department of Global Public Health, Karolinska Institutet, 17177 Stockholm, Sweden
4
Center for Health Policy and Management Studies, School of Government, Nanjing University, Nanjing 210023, China
*
Author to whom correspondence should be addressed.
Antibiotics 2020, 9(8), 514; https://doi.org/10.3390/antibiotics9080514
Submission received: 14 July 2020 / Revised: 10 August 2020 / Accepted: 11 August 2020 / Published: 13 August 2020
(This article belongs to the Special Issue Antibiotics Use and Antimicrobial Resistance in Hospital)

Abstract

:
Background: Carbapenem resistant Klebsiella pneumoniae (CRKP), Pseudomonas aeruginosa (CRPA), and Acinetobacter baumannii (CRAB) pose significant threats to public health. However, the clinical and economic impacts of CRKP, CRPA, and CRAB remain largely uninvestigated in China. This study aimed to examine the clinical and economic burden of CRKP, CRPA, and CRAB compared with carbapenem susceptible cases in China. Method: We conducted a retrospective and multicenter study among inpatients hospitalized at four tertiary hospitals between 2013 and 2015 who had K. pneumoniae, P. aeruginosa, and A. baumannii positive clinical samples. Propensity score matching (PSM) was used to balance the impact of potential confounding variables, including age, sex, insurance, number of diagnosis, comorbidities (disease diagnosis, and Charlson comorbidity index), admission to intensive care unit, and surgeries. The main indicators included economic costs, length of stay (LOS), and mortality rate. Results: We included 12,022 inpatients infected or colonized with K. pneumoniae, P. aeruginosa, and A. baumannii between 2013 and 2015, including 831 with CRKP and 4328 with carbapenem susceptible K. pneumoniae (CSKP), 1244 with CRPA and 2674 with carbapenem susceptible P. aeruginosa (CSPA), 1665 with CRAB and 1280 with carbapenem susceptible A. baumannii (CSAB). After PSM, 822 pairs, 1155 pairs, and 682 pairs, respectively were generated. Compared with carbapenem-susceptible cases, those with CRKP, CRPA, and CRAB were associated with statistically significantly increased total hospital cost ($14,252, p < 0.0001; $4605, p < 0.0001; $7277, p < 0.0001) and excess LOS (13.2 days, p < 0.0001; 5.4 days, p = 0.0003; 15.8 days, p = 0.0004). In addition, there were statistically significantly differences in hospital mortality rate between CRKP and CSKP, and CRAB and CSAB group (2.94%, p = 0.024; 4.03%, p = 0.03); however, the difference between CRPA and CSPA group was marginal significant (2.03%, p = 0.052). Conclusion: It highlights the clinical and economic impact of CRKP, CRPA, and CRAB to justify more resources for implementing antibiotic stewardship practices to improve clinical outcomes and to reduce economic costs.

1. Introduction

Carbapenem resistance poses a significant threat to public health globally. It occurs mainly among gram-negative bacteria such as Klebsiella pneumoniae, Pseudomonas aeruginosa, and Acinetobacter baumannii, which are the most concerning bacteria with a propensity toward multi-drug resistance and cause the life-threatening healthcare associated infections amongst critically ill and immunocompromised individuals [1]. Carbapenem resistant K. pneumoniae (CRKP), P. aeruginosa (CRPA), and A. baumannii (CRAB) were recognized as critical-priority bacteria, by the World Health Organization (WHO), which was mainly based on the associated increasing clinical and economic burden, unavailability of effective therapy, and antibiotic resistant characteristics [2].
In the European countries, the population-weighted mean proportions of CRKP, CRPA, and CRAB were 7.5%, 17.2%, and 31.9% in 2018, respectively [3]. In China, there were marked increases in the proportion of CRKP from 3.0% in 2005 to 26.3% in 2018, and in the prevalence of CRAB from 39.0% in 2005 to 73.9% in 2018. The proportion of CRPA showed a downward trend during between 2005 and 2014, but deteriorated from 2015 and reached 30.7% in 2018 [4,5,6,7,8].
Recently published studies mainly focus on gram-positive bacteria [9], while only few studies estimated the burden of CRKP, CRPA, and CRAB in terms of mortality, length of stay (LOS), and cost [10,11,12,13,14]. It was reported that patients with CRKP, CRPA, and CRAB infections were associated with higher mortality, longer hospital stay, and higher hospital costs compared with carbapenem susceptible cases [9,15,16,17]. In addition, hospital costs incurred by colonized patients with CRKP were also high [18]. However, it was also found that there were no significant differences in hospital mortality between CRPA and carbapenem susceptible P. aeruginosa (CSPA) cases [10,15], in total hospital cost between CRAB and carbapenem susceptible A. baumannii (CSAB) cases [14].
In China, there were some studies exploring the mortality and LOS associated with CRKP [19,20,21,22,23], CRPA [24,25,26], or CRAB [27,28,29,30], and exploring the economic burden attributed by CRKP [19], CRPA [24], or CRAB [27,31]. Although hospitalized patients with carbapenem resistance appeared to have increased hospitality mortality, hospital stay, and hospital costs, no significant differences in hospital mortality and hospital stay between CRKP and carbapenem susceptible K. pneumoniae (CSKP) cases were showed as well [19,21]. In addition, majority of studies were conducted in a single hospital setting, and using univariate analyses regardless of confounding risk factors [32]. Therefore, there are limited published data and the clinical and economic impacts of CRKP, CRPA, and CRAB remain largely uninvestigated in China. In this study, we aimed to examine the clinical and economic burden of carbapenem resistance in K. pneumoniae, P. aeruginosa, and A. baumannii compared with carbapenem susceptible cases in China.

2. Material and Methods

2.1. Study Site

This study was conducted in four tertiary hospitals in China. Hospital site 1 and site 2 are general provincial hospitals in Zhejiang province and Shandong province, respectively. Hospital site 3 and site 4 are general county hospital and combined traditional Chinese and Western medicine provincial hospital in Zhejiang province, respectively. Hospital site 1–4 are with 3200, 3500, 1727, 2100 of hospital beds, and with 170,000, 160,000, 80,000, 50,000 of inpatients per year, respectively.

2.2. Study Design and Patients

It was a retrospective and multicenter study. Patients were identified from the records of the clinical microbiology laboratory. 100% of inpatients in hospital site 2–4, and 60% of inpatients in hospital site 1 between 2013–2015 who had clinical samples positive for CRKP, CRPA, CRAB infection or colonization were included. The control group comprised of patients with CSKP, carbapenem susceptible P. aeruginosa (CSPA), and CSAB-positive clinical samples with the same percentages who were hospitalized during the same study period. Only 60% of inpatients were randomly selected from hospital site 1 due to the large inpatient population [31]. The interpretation of carbapenem susceptibility was based on the Clinical and Laboratory Standards Institute (CLSI) definitions and reported as resistant (R), susceptible (S), and intermediate (I). K. pneumoniae, P. aeruginosa, and A. baumannii isolates, were considered resistant to carbapenems if they were resistant or intermediate to any carbapenem (imipenem, meropenem, panipenem or ertapenem) [31], and the control group was defined as patients infected or colonized by K. pneumoniae, P. aeruginosa, and A. baumannii susceptible to all carbapenems. To avoid duplication, cases with the first episode detected in any clinical specimen (e.g., blood, stool, cervical, urethral sources) were included. If multiple samples were taken from a patient during the study period, only the first sample was included in this study.

2.3. Data Collection

Data were obtained from patients’ medical records. Patients’ characteristics included demographics (age, sex, and insurance), comorbidities (disease diagnosis, and Charlson comorbidity index (CCI), hospital events (admitting service, surgical services, and dates of hospital and intensive care unit (ICU) admission/discharge), and clinical outcomes (discharged alive or death during hospitalization). We also noted any related laboratory results when isolation of K. pneumoniae, P. aeruginosa, and A. baumannii was recorded in the inspection system, and recorded the antibiotic susceptibility test results obtained from the microbiology laboratory. In addition, economic costs associated with these patients were obtained from the financial system. The economic costs included total hospital cost, medication cost (antibiotic cost), diagnostic cost, treatment cost, material cost, and other costs, including out-of pocket payment and payment covered by health insurers. Values of the economic costs were converted from Chinese Yuan to United States dollars in 2015 [33,34].

2.4. Propensity Score Matching

To eliminate the impact of potential confounding variables, propensity score matching (PSM) with 1:1 nearest-neighbor matching using STATA was conducted. For logistic regression modeling with carbapenem resistant and carbapenem susceptible as dependent variables, independent variables included age, sex, insurance, number of diagnosis, CCI, admission to ICU, surgery, and comorbidities, but not clinical and economic outcomes (economic costs, LOS, and in-hospital mortality). The generated pairs, who were matched for all included variables, were subjected to further analyses of economic costs, LOS, and in-hospital mortality.

2.5. Indicators and Statistical Analyses

In this study, the main indicators included economic costs, LOS, and in-hospital mortality. We performed 1000 iterations of Monte Carlo simulations to calculate the 95% uncertainty interval for each indicator with normal distribution using SAS [35]. We compared the main indicators between CRKP and CSKP group, between CRPA and CSPA group, between CRAB and CSAB group using t test and χ2 test for quantitative and qualitative variables, respectively. All p-values were two-tailed, <0.05 were deemed statistically significant, and ≥0.05 and <0.10 were considered marginally significant.

2.6. Ethical Approval and Informed Consent

The study was approved by the institutional review board of Zhejiang University School of Public Health, who waived the need for informed consent. All inpatients data were anonymized prior to analysis.

3. Results

We included 12,022 inpatients infected or colonized with K. pneumoniae, P. aeruginosa, and A. baumannii between 2013 and 2015, including 5159 K. pneumoniae, 3918 P. aeruginosa, and 2945 A. baumannii. Of these, a total of 831 with CRKP and 4328 with CSKP, 1244 with CRPA and 2674 with CSPA, 1665 with CRAB and 1280 with CSAB were included. Significant differences were found in insurance, admission to ICU, surgery between CRKP and CSKP group, in age, sex, number of diagnosis, CCI, admission to ICU between CRPA and CSPA group, in age, sex, insurance, number of diagnosis, CCI, admission to ICU, surgery between CRAB and CSAB group. Some comorbidities between the three groups were significantly different as well. After PSM, there were no differences in patients’ characteristics between the three groups, and generated 822 pairs, 1155 pairs, and 682 pairs, respectively (Table 1, Table 2 and Table 3).
Inpatients with carbapenem resistance were significantly associated with higher economic costs than carbapenem susceptible cases. For patients with K. pneumoniae, the mean differences (95% UI) in total hospital cost, antibiotic cost, medication cost including antibiotics, diagnostic cost, treatment cost and material cost were $14,251 ($13,852–$14,653), $3296 ($3202–$3390), $9132 ($8910–$9354), $1517 ($1465–$1570), $2574 ($2462–$2686), and $899 ($826–$971), respectively (Table 4). For patients with P. aeruginosa, the mean differences (95% UI) in economic costs were $4,605 ($4249–$4960), $1078 ($1007–$1149), $3053 ($2867–$3238), $370 ($323–416), $1174 ($1043–$1305), and $76 ($19–$132), respectively (Table 5). For patients with A. baumannii, the mean differences (95% UI) in economic costs were $7277 ($6897–$7657), $1537 ($1468–$1605), $3902 ($3731–$4074), $628 ($585–$670), $2156 ($1967–$2344), $421 ($351–$491), respectively (Table 6).
Compared with inpatients with CSKP, CSPA, and CSAB, those with CRKP, CRPA, and CRAB were significantly associated with longer LOS, with mean differences (95% UI) of 13.2 days (12.7–13.7days), 5.4 days (4.4–6.5 days), and 15.8 days (13.9–17.7 days), respectively (Table 7).
There were statistical differences in in-hospital mortality rate between CRKP and CSKP group (9.59% (9.33–9.85%) vs. 6.65% (6.43–6.87%)), and CRAB and CSAB group (8.28% (8.04–8.53%) vs. 4.25% (4.07–4.43%)). The difference in in-hospital mortality rate between CRPA and CSPA group was marginal significant, with the difference rate of 2.03% (1.75–2.32%) (p = 0.052) (Table 8).

4. Discussion

To the best of our knowledge, this is the first large and multicenter study quantifying the clinical and economic impact of CRKP, CRPA, and CRAB in mainland China using the PSM method. We found that after PSM, compared with carbapenem susceptible cases, those with CRKP, CRPA, and CRAB were associated with significantly increased economic costs, excess LOS, and attributable in-hospital mortality rate. A marginal difference in hospital mortality rate existed between CRPA and CSPA group.
It was clearly demonstrated that economic costs for infection or colonization caused by carbapenem resistance were higher than in case of carbapenem susceptible bacteria, suggesting that carbapenem resistance indeed incurs excessive economic costs on patients infected or colonized with K. pneumoniae, P. aeruginosa, and A. baumannii. It also shows that the impact of carbapenem resistance on economic costs might depend on the type of gram-negative bacteria, with resistance in K. pneumoniae having a larger impact, followed by A. baumannii and P. aeruginosa. This finding is consistent with several previous studies, in which carbapenem resistance was associated with higher economic costs for infection or colonization caused by gram-negative bacteria, including K. pneumonia [19], P. aeruginosa [10,12,24], and A. baumannii [11,13,27,31]. However, one study did not find a statistically significant association in total hospital cost among infants with ventilator associated pneumonia in the ICU between CRAB and CSAB group [14], which might be because that critical illness can attenuate the effect of carbapenem resistance [36]. Effective control of carbapenem resistance would result in cost savings and could be useful for assessing the cost-effectiveness of interventions to reduce the development and spread of carbapenem resistance in hospital settings [19].
We indeed found that carbapenem resistance was associated with longer LOS, which is similar with other investigations that patients with resistant bacteria requires increases in the number of hospitalization days [19,24,37]. Prolonged LOS associated with carbapenem resistance might be independent of the type of gram-negative bacteria, with resistance in A. baumannii having a larger influence, followed by K. pneumoniae, and P. aeruginosa. Hospital stay is the major contributor to the additional economic costs in carbapenem resistant infection or colonization, as patients with longer hospital stay were associated with more antibiotic therapy and more surgeries [19,24,37]; therefore, LOS was not included in PSM analyses [38].
The poorest clinical outcomes were observed for CRAB, followed by CRKP and CRPA. In-hospital mortality rate was significantly higher for patients with CRKP and CRAB than for carbapenem susceptible cases, which is similar with other studies [16,39,40]. A 2.03% increase in mortality rate for the CRPA patients is clinically meaningful, and the non-significant p-value (p = 0.052) is too low to confidently rule out an effect of CRPA on mortality rate, which is different with other findings [16,39,40], however, several studies reported non-significant association between mortality and CRPA as well [10,15]. Spending on medical services was associated with a reduction in the mortality rate, therefore, it is critical to consider the clinical and economic burden posed by CRKP, CRPA, and CRAB when shirting resource allocation [41].
The proportions of CRKP, CRPA, and CRAB in the four sampled hospitals were 10.29%, 31.75%, and 56.54%, respectively, which were approximate the national levels reported in China Antimicrobial Resistance Surveillance System (CARSS) (8.03%, 22.61%, and 58.05%) [42]. In addition, the mean total hospital cost, length of hospital stay, and hospital mortality were $3042 and $2470, 10.1 days and 9.4 days, 0.3% and 0.4% in Zhejiang and Shandong province in 2015, respectively, which were similar to the national levels ($2378, 9.6 days, and 0.4%). Therefore, we assumed that the antibiotic resistant level, and clinical and economic burden due to CRKP, CRPA, and CRAB from four sampled hospitals in China were approximate results representing the national level.
Our study has some limitations. First, due to the retrospective nature of our study, it is difficult to distinguish infection or colonization, which may underestimate the clinical and economic outcome of carbapenem resistant infection. However, colonization is an important reservoir for bacteria causing infection, therefore, it is important to identify the burden of patients with CRKP, CRPA and CRAB, either infected or colonized, in order to contain the spread of these bacteria. In this study, we explored the clinical and economic outcomes for CRKP, CRPA and CRAB isolation and not specifically infection. Studies on clinical infection or colonization separate should be considered in the future as well. Secondly, this is a retrospective study, inherently resulting in bias and confounding, thus, PSM was conducted to balance potential confounding factors in order to minimize the risk of bias. However, PSM is not without its own limitations, which ignore unmeasured confounders that could potentially impact outcomes. Moreover, although it is a multicenter study that was conducted in four tertiary hospitals, the antibiotic resistant levels and the main indicators approximate the national levels, it is necessary to expand this study to different types of hospitals in different areas in the future. Finally, as we had data between 2013 and 2015 only, Monte Carlo simulations with 1000 iterations were conducted and mean values during the study period were reported. Although study period did not influence the conclusions, future studies with update data are warranted.

5. Conclusions

This study underscores the substantial clinical and economic burden associated with CRKP, CRPA, and CRAB in hospitalized patients. The input of more resources to control carbapenem resistance in K. pneumoniae, P. aeruginosa, and A. baumannii can be justified both for improving clinical outcomes, and for reducing economic costs, thus maximized benefit with available resources. In addition, urgent need for implementing antibiotic stewardship practices across the continuum of hospital settings will hopefully help to curb the emergency and spread of carbapenem resistance and K. pneumoniae, P. aeruginosa, and A. baumannii.

Author Contributions

X.Z. participated in the conception and design of this study, data collection, data analysis, and interpretation of data, drafted and revised the manuscript. C.S.L. participated in the conception and design of the study and helped in the revising the manuscript. X.S. and S.G. performed the data analysis, and interpretation of data, drafted and revised the manuscript. H.D. participated in the conception, design of the study, data collection and interpretation of data, and drafted and revised the manuscript. All authors read and approved the final manuscript.

Funding

This work was supported by “Pfizer Investment Co. Ltd. (Burden of multi-drug resistant infections in China and associated risk factors)”, “The Fundamental Research Funds of Shandong University”, and “The Joint Research Funds for Shandong University and Karolinska Institutet”.

Acknowledgments

We want to thank the Center for Health Policy Studies, School of Medicine, Zhejiang University for the assistance in primary data collection.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. World Health Organization. Guidelines for the Prevention and Control of Carbapenem-Resistant Enterobacteriaceae, Acinetobacter Baumannii and Pseudomonas Aeruginosa in Health Care Facilities. 2017. Available online: https://www.who.int/infection-prevention/publications/guidelines-cre/en/ (accessed on 20 May 2020).
  2. World Health Organization. Global Priority List of Antibiotic Resistant Bacteria to Guide Research, Discovery, and Development of New Antibiotics. 2017. Available online: https://www.who.int/medicines/publications/WHO-PPL-Short_Summary_25Feb-ET_NM_WHO.pdf (accessed on 6 February 2019).
  3. European Centre for Disease Prevention and Control. Surveillance Atlas of Infectious Diseases. 2019. Available online: http://atlas.ecdc.europa.eu/public/index.aspx (accessed on 20 May 2020).
  4. Hu, F.; Guo, Y.; Zhu, D.; Wang, F.; Jiang, X.; Xu, Y.; Zhang, X.; Zhang, Z.; Ji, P.; Xie, Y.; et al. Chinet surveillance of bacterial resistance in China: 2018 report. Chin. J. Infect. Chemother. 2020, 20, 1–10. [Google Scholar]
  5. Hu, F.; Guo, Y.; Zhu, D.; Wang, F.; Jiang, X.; Xu, Y.; Zhang, X.; Zhang, Z.; Ji, P.; Xie, Y.; et al. Antimicrobial resistance profile of clinical isolates in hospitals across China: Report from the CHINET surveillance program, 2017. Chin. J. Infect. Chemother. 2018, 18, 241–251. [Google Scholar]
  6. Hu, F.; Guo, Y.; Zhu, D.; Wang, F.; Jiang, X.; Xu, Y.; Zhang, X.; Zhang, Z.; Ji, P.; Xie, Y.; et al. CHINET surveillance of bacterial resistance across China: Report of the results in 2016. Chin. J. Infect. Chemother. 2017, 17, 481–491. [Google Scholar]
  7. Hu, F.; Zhu, D.; Wang, F.; Jiang, X.; Xu, Y.; Zhang, X.; Zhang, Z.; Ji, P.; Xie, Y.; Kang, M.; et al. Report of CHINET antimicrobial resistance surveillance program in 2015. Chin. J. Infect. Chemother. 2016, 685–694. [Google Scholar]
  8. Hu, F.; Guo, Y.; Zhu, D.; Wang, F.; Jiang, X.; Xu, Y.; Zhang, X.; Zhang, C.; Ji, P.; Xie, Y.; et al. Resistance trends among clinical isolates in China reported from CHINET surveillance of bacterial resistance, 2005–2014. Clin. Microbiol. Infec. 2016, 221, S9–S14. [Google Scholar] [CrossRef] [Green Version]
  9. Zhen, X.; Stålsby Lundborg, C.; Sun, X.; Hu, X.; Dong, H. Economic burden of antibiotic resistance in ESKAPE organisms: A systematic review. Antimicrob. Resist. Infect. Control 2019, 8, 137. [Google Scholar] [CrossRef] [Green Version]
  10. Eagye, K.J.; Kuti, J.L.; Nicolau, D.P. Risk factors and outcomes associated with isolation of meropenem high-level-resistant Pseudomonas aeruginosa. Infect. Cont. Hosp. Epidemiol. 2009, 30, 746–752. [Google Scholar] [CrossRef]
  11. Lautenbach, E.; Synnestvedt, M.; Weiner, M.G.; Bilker, W.B.; Vo, L.; Schein, J.; Kim, M. Epidemiology and impact of imipenem resistance in Acinetobacter baumannii. Infect. Cont. Hosp. Epidemiol. 2009, 30, 1186–1192. [Google Scholar] [CrossRef]
  12. Lautenbach, E.; Synnestvedt, M.; Weiner, M.G.; Bilker, W.B.; Vo, L.; Schein, J.; Kim, M. Imipenem resistance in Pseudomonas aeruginosa: Emergence, epidemiology, and impact on clinical and economic outcomes. Infect. Cont. Hosp. Epidemiol. 2010, 31, 47–53. [Google Scholar] [CrossRef]
  13. Lemos, E.V.; de la Hoz, F.P.; Alvis, N.; Einarson, T.R.; Quevedo, E.; Castaneda, C.; Leon, Y.; Amado, C.; Canon, O.; Kawai, K. Impact of carbapenem resistance on clinical and economic outcomes among patients with Acinetobacter baumannii infection in Colombia. Clin. Microbiol. Infec. 2014, 20, 174–180. [Google Scholar] [CrossRef] [Green Version]
  14. Thatrimontrichai, A.; Techato, C.; Dissaneevate, S.; Janjindamai, W.; Maneenil, G.; Kritsaneepaiboon, S.; Tanaanantarak, P. Risk factors and outcomes of carbapenem-resistant Acinetobacter baumannii ventilator-associated pneumonia in the neonate: A case-case-control study. J. Infect. Chemother. 2016, 22, 444–449. [Google Scholar] [CrossRef]
  15. Tabak, Y.P.; Sung, A.H.; Ye, G.; Vankeepuram, L.; Gupta, V.; McCann, E. Attributable clinical and economic burden of carbapenem-non-susceptible Gram-negative infections in patients hospitalized with complicated urinary tract infections. J. Hosp. Infect. 2019, 102, 37–44. [Google Scholar] [CrossRef] [Green Version]
  16. Rodriguez-Acevedo, A.J.; Lee, X.J.; Elliott, T.M.; Gordon, L.G. Hospitalization costs for patients colonized with carbapenemase-producing Enterobacterales during an Australian outbreak. J. Hosp. Infect. 2020, 105, 146–153. [Google Scholar] [CrossRef] [PubMed]
  17. The Brooklyn Antibiotic Resistance Task Force. The cost of antibiotic resistance: Effect of resistance among Staphylococcus aureus, Klebsiella pneumoniae, Acinetobacter baumannii, and Pseudmonas aeruginosa on length of hospital stay. Infect. Cont. Hosp. Epidemiol. 2002, 23, 106–108. [Google Scholar] [CrossRef] [PubMed]
  18. Huang, W.; Qiao, F.; Zhang, Y.; Huang, J.; Deng, Y.; Li, J.; Zong, Z. In-hospital medical costs of infections caused by carbapenem-resistant Klebsiella pneumoniae. Clin. Infect. Dis. 2018, 672, S225–S230. [Google Scholar] [CrossRef] [PubMed]
  19. Tian, L.; Tan, R.; Chen, Y.; Sun, J.; Liu, J.; Qu, H.; Wang, X. Epidemiology of Klebsiella pneumoniae bloodstream infections in a teaching hospital: Factors related to the carbapenem resistance and patient mortality. Antimicrob. Resist. Infect. Control 2016, 5, 1–12. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  20. Jiao, Y.; Qin, Y.; Liu, J.; Li, Q.; Dong, Y.; Shang, Y.; Huang, Y.; Liu, R. Risk factors for carbapenem-resistant Klebsiella pneumoniae infection/colonization and predictors of mortality: A retrospective study. Pathog. Glob. Health. 2015, 109, 68–74. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  21. Huang, J. Risk Factors and Clinical Outcomes of Carbapenem-Resistant Klebsiella Pneumoniae Infections of Critically Ill Patients; Zhejiang University: Zhejiang, China, 2015; p. 44. [Google Scholar]
  22. Xiao, T.; Yu, W.; Niu, T.; Huang, C.; Xiao, Y. A retrospective, comparative analysis of risk factors and outcomes in carbapenem-susceptible and carbapenem-nonsusceptible Klebsiella pneumoniae bloodstream infections: Tigecycline significantly increases the mortality. Infect. Drug Resist. 2018, 11, 595–606. [Google Scholar] [CrossRef] [Green Version]
  23. Chen, Z.; Xu, Z.; Wu, H.; Chen, L.; Gao, S.; Chen, Y. The impact of carbapenem-resistant Pseudomonas aeruginosa on clinical and economic outcomes in a Chinese tertiary care hospital: A propensity score-matched analysis. Am. J. Infect. Control. 2018, 47, 677–682. [Google Scholar] [CrossRef]
  24. Lv, Q.; Ruan, Z.; Wang, J.; Ma, Q.; Dai, Y. Clinical characteristics and prognosis of patients with carbapenem resistant Pseudomonas aeruginosa infection. Chin. J. Nosocomiol. 2015, 25, 5570–5571. [Google Scholar]
  25. Yuan, L.; Ding, B.; Shen, Z.; Wu, H.; Xu, X.; Li, G. Clinical investigation of infections caused by carbapenem-resistant Pseudomonas aeruginosa in huashan hospital. Chin. J. Infect. Chemother. 2017, 17, 121–126. [Google Scholar]
  26. Cui, N.; Cao, B.; Liu, Y.; Liang, L.; Gu, L.; Song, S. The impact of imipenem-resistant Acinetobacter baumannii infection on clinical outcomes and medical care costs. Chin. J. Infect. Dis. 2012, 30, 209–214. [Google Scholar]
  27. Wang, Y.; Fu, R.; Zheng, Y.; Wan, Y.; Zhou, L. Risk factors and mortality of patients with nosocomial carbapenem-resistant Acinetobacter baumannii pneumonia. J. Clin. Pulm. Med. 2016, 21, 784–788. [Google Scholar]
  28. Zheng, Y.; Wan, Y.; Zhou, L.; Ye, M.; Liu, S.; Xu, C.; He, Y.; Chen, J. Risk factors and mortality of patients with nosocomial carbapenem-resistant Acinetobacter baumannii pneumonia. Am. J. Infect. Control. 2013, 41, E59–E63. [Google Scholar] [CrossRef]
  29. Yang, S.; Sun, J.; Wu, X.; Zhang, L. Determinants of mortality in patients with nosocomial Acinetobacter baumannii bacteremia in southwest China: A five-year case-control study. Can. J. Infect. Dis. Med. 2018, 1–9. [Google Scholar] [CrossRef] [Green Version]
  30. Zhen, X.; Chen, Y.; Hu, X.; Dong, P.; Gu, S.; Sheng, Y.Y.; Dong, H. The difference in medical costs between carbapenem-resistant Acinetobacter baumannii and non-resistant groups: A case study from a hospital in Zhejiang province, China. Eur. J. Clin. Microbiol. 2017, 36, 1989–1994. [Google Scholar] [CrossRef]
  31. Zhen, X.; Stålsby Lundborg, C.; Sun, X.; Hu, X.; Dong, H. The clinical and economic impact of antibiotic resistance in China: A systematic review and meta-analysis. Antibiotics 2019, 8, 115. [Google Scholar] [CrossRef] [Green Version]
  32. Organization for Economic Cooperation and Development. Purchasing Power Parities for GDP. 2019. Available online: https://stats.oecd.org/index.aspx?queryid=221# (accessed on 15 February 2019).
  33. Organization for Economic Cooperation and Development. Consumer Price Indices. 2019. Available online: https://stats.oecd.org/index.aspx?queryid=221# (accessed on 15 February 2019).
  34. Cassini, A.; Hogberg, L.D.; Plachouras, D.; Quattrocchi, A.; Hoxha, A.; Simonsen, G.S.; Colomb-Cotinat, M.; Kretzschmar, M.E.; Devleesschauwer, B.; Cecchini, M.; et al. Attributable deaths and disability-adjusted life-years caused by infections with antibiotic-resistant bacteria in the EU and the European Economic Area in 2015: A population-level modelling analysis. Lancet Infect. Dis. 2019, 19, 56–66. [Google Scholar] [CrossRef] [Green Version]
  35. Zhen, X.; Stålsby Lundborg, C.; Zhang, M.; Sun, X.; Li, Y.; Hu, X.; Gu, S.; Gu, Y.; Wei, J.; Dong, H. Clinical and economic impact of methicillin-resistant Staphylococcus aureus: A multicentre study in China. Sci. Rep. UK 2020, 10, 3900. [Google Scholar] [CrossRef] [Green Version]
  36. Vargas-Alzate, C.A.; Higuita-Gutierrez, L.F.; Lopez-Lopez, L.; Cienfuegos-Gallet, A.V.; Jimenez, Q.J. High excess costs of infections caused by carbapenem-resistant Gram-negative bacilli in an endemic region. Int. J. Antimicrob. Agents 2018, 51, 601–607. [Google Scholar] [CrossRef]
  37. Hemmige, V.; David, M.Z. Effects of including variables such as length of stay in a propensity score analysis with costs as outcome. Clin. Infect. Dis. 2019, 69, 2039–2040. [Google Scholar] [CrossRef] [PubMed]
  38. Balkhair, A.; Al-Muharrmi, Z.; Al’Adawi, B.; Al, B.I.; Taher, H.B.; Al-Siyabi, T.; Al, A.M.; Hassan, K.S. Prevalence and 30-day all-cause mortality of carbapenem-and colistin-resistant bacteraemia caused by Acinetobacter baumannii, Pseudomonas aeruginosa, and Klebsiella pneumoniae: Description of a decade-long trend. Int. J. Infect. Dis. 2019, 85, 10–15. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  39. Andria, N.; Henig, O.; Kotler, O.; Domchenko, A.; Oren, I.; Zuckerman, T.; Ofran, Y.; Fraser, D.; Paul, M. Mortality burden related to infection with carbapenem-resistant Gram-negative bacteria among haematological cancer patients: A retrospective cohort study. J. Antimicrob. Chemother. 2015, 70, 3146–3153. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  40. Persoon, M.C.; Voor, I.H.A.; Wielders, C.; Gommers, D.; Vos, M.C.; Severin, J.A. Mortality associated with carbapenem-susceptible and Verona Integron-encoded Metallo-beta-lactamase-positive Pseudomonas aeruginosa bacteremia. Antimicrob. Resist. Infect. Control 2020, 9, 25. [Google Scholar] [CrossRef] [PubMed]
  41. Golinelli, D.; Toscano, F.; Bucci, A.; Lenzi, J.; Fantini, M.P.; Nante, N.; Messina, G. Health expenditure and all-cause mortality in the ‘Galaxy’ of Italian regional healthcare systems: A 15-year panel data analysis. Appl. Health Econ. Health Policy 2017, 15, 773–783. [Google Scholar] [CrossRef]
  42. China Antimicrobial Resistance Surveillance System. Annual Report of the China Antimicrobial Resistance Surveillance, 2014–2017. 2018. Available online: http://www.carss.cn/Report/Details?aId=552 (accessed on 14 February 2019).
Table 1. Characteristics of the patients with CRKP and CSKP before and after PSM.
Table 1. Characteristics of the patients with CRKP and CSKP before and after PSM.
Baseline CharacteristicsBefore PSMAfter PSM
CSKPCRKPp-ValueCSKPCRKPp-Value
Number of inpatient, n4328831 822822
Age in years, median (range)72 (0–100)73 (0–98)0.32370 (0–100)73 (0–98)0.602
Sex male, n (%)2963 (68.46)554 (66.67)0.309554 (67.40)547 (66.55)0.714
Insurance, n (%)3568 (82.44)658 (79.18)0.025644 (78.35)650 (79.08)0.718
Number of diagnosis, median (range)6 (1–30)7 (1–23)0.1296 (1–30)6.5 (1–23)0.481
Charlson comorbidity index, median (range)5 (1–34)5 (1–18)0.0745 (1–24)5 (1–18)0.710
Admission to ICU, n (%)503 (11.62)321 (38.63)<0.0001310 (37.71)312 (37.96)0.919
Surgery, n (%)1106 (25.55)277 (33.33)<0.0001300 (36.50)276 (33.58)0.215
Myocardial infarction, n (%)124 (2.87)19 (2.29)0.35222 (2.68)19 (2.31)0.635
Congestive heart failure, n (%)764 (17.65)121 (14.56)0.03125 (15.21)119 (14.48)0.677
Peripheral vascular disease, n (%)54 (1.25)11 (1.32)0.85712 (1.46)11 (1.34)0.834
Cerebrovascular diseases, n (%)2178 (50.32)484 (58.24)<0.0001462 (56.20)476 (57.91)0.485
Dementia, n (%)130 (3.00)24 (2.89)0.85823 (2.80)24 (2.92)0.882
Chronic pulmonary disease, n (%)1084 (25.05)154 (18.53)<0.0001139 (16.91)154 (18.73)0.334
Connective tissue disease, n (%)83 (1.92)9 (1.08)0.09611 (1.34)9 (1.09)0.653
Mild liver disease, n (%)163 (3.77)24 (2.89)0.21525 (3.04)24 (2.92)0.885
Peptic ulcer disease, n (%)29 (2.98)31 (3.73)0.25340 (4.87)31 (3.77)0.275
Diabetes mellitus, n (%)1206 (27.87)194 (23.35)0.007175 (21.29)193 (23.48)0.287
Diabetes mellitus with chronic complications, n (%)163 (3.77)15 (1.81)0.00513 (1.58)15 (1.82)0.703
Moderate to severe chronic kidney disease, n (%)322 (7.44)102 (12.27)<0.0001116 (14.11)97 (11.80)0.163
Hemiplegia, n (%)38 (0.88)8 (0.96)0.8126 (0.73)8 (0.97)0.591
Solid tumor without metastases, n (%)298 (6.89)52 (6.26)0.5159 (7.18)50 (6.08)0.372
Leukemia, n (%)67 (1.55)24 (2.89)0.00727 (3.28)24 (2.92)0.670
Malignant lymphoma, n (%)46 (1.06)15 (1.81)0.0719 (2.31)15 (1.82)0.488
Severe liver disease, n (%)57 (1.32)13 (1.56)0.57211 (1.34)13 (1.58)0.681
Metastatic tumor, n (%)249 (5.75)16 (1.93)<0.000115 (1.82)16 (1.95)0.856
CRKP: carbapenem resistant Klebsiella pneumoniae, CSKP: carbapenem susceptible K. pneumoniae, PSM: propensity score matching, ICU: intensive care unit.
Table 2. Characteristics of the patients with CRPA and CSPA before and after PSM.
Table 2. Characteristics of the patients with CRPA and CSPA before and after PSM.
Baseline CharacteristicsBefore PSMAfter PSM
CSPACRPAp-ValueCSPACRPAp-Value
Number of inpatient, n26741244 11551155
Age in years, median (range)73 (0–100)79 (0–98)<0.000177 (0–100)79 (0–98)0.994
Sex male, n (%)1775 (66.38)877 (70.50)0.01803 (69.52)812 (70.30)0.683
Insurance, n (%)2322 (86.84)1084 (87.14)0.7941007 (87.19)1007 (87.19)1.000
Number of diagnosis, median (range)6 (1–36)7 (1–21)0.0027 (1–36)7 (1–21)0.444
Charlson comorbidity index, median (range)5 (1–34)5 (1–22)0.0075 (1–34)5 (1–22)0.468
Admission to ICU, n (%)282 (10.55)283 (22.75)<0.0001252 (21.82)221 (19.13)0.110
Surgery, n (%)554 (20.72)275 (22.11)0.322272 (23.55)245 (21.21)0.178
Myocardial infarction, n (%)65 (2.43)46 (3.70)0.02640 (3.46)40 (3.46)1.000
Congestive heart failure, n (%)504 (18.85)196 (15.76)0.019192 (16.62)178 (15.41)0.427
Peripheral vascular disease, n (%)24 (0.90)20 (1.61)0.0519 (1.65)17 (1.47)0.737
Cerebrovascular diseases, n (%)1360 (50.86)813 (65.35)<0.0001732 (63.38)735 (63.64)0.897
Dementia, n (%)169 (6.32)86 (6.91)0.48482 (7.10)85 (7.36)0.810
Chronic pulmonary disease, n (%)1113 (41.62)292 (23.47)<0.0001268 (23.20)289 (25.02)0.307
Connective tissue disease, n (%)55 (2.06)16 (1.29)0.09217 (1.47)16 (1.39)0.861
Mild liver disease, n (%)40 (1.50)23 (1.85)0.41421 (1.82)22 (1.90)0.878
Peptic ulcer disease, n (%)57 (2.13)37 (2.97)0.10937 (3.20)33 (2.86)0.627
Diabetes mellitus, n (%)614 (22.96)310 (24.92)0.179309 (26.75)291 (25.19)0.393
Diabetes mellitus with chronic complications, n (%)52 (1.94)23 (1.85)0.83921 (1.82)22 (1.90)0.878
Moderate to severe chronic kidney disease, n (%)191 (7.14)105 (8.44)0.15393 (8.05)94 (8.14)0.939
Hemiplegia, n (%)37 (1.38)21 (1.69)0.46320 (1.73)20 (1.73)1.000
Solid tumor without metastases, n (%)117 (4.38)59 (4.74)0.60556 (4.85)50 (4.33)0.551
Leukemia, n (%)21 (0.79)15 (1.21)0.19913 (1.13)11 (0.95)0.682
Malignant lymphoma, n (%)17 (0.64)8 (0.64)0.97910 (0.87)8 (0.69)0.636
Severe liver disease, n (%)23 (0.86)9 (0.72)0.65811 (0.95)8 (0.69)0.490
Metastatic tumor, n (%)70 (2.62)24 (1.93)0.1924 (2.08)23 (1.99)0.883
CRKP: carbapenem resistant Pseudomonas aeruginosa, CSKP: carbapenem susceptible P. aeruginosa, PSM: propensity score matching, ICU: intensive care unit.
Table 3. Characteristics of the patients with CRAB and CSAB before and after PSM.
Table 3. Characteristics of the patients with CRAB and CSAB before and after PSM.
Baseline CharacteristicsBefore PSMAfter PSM
CSABCRABp-ValueCSABCRABp-Value
Number of inpatient, n12801665 682682
Age in years, median (range)73 (0–100)68 (0–102)<0.000170.5 (0–100)71 (0–102)0.845
Sex male, n (%)917 (71.64)1127 (67.69)0.021480 (70.38)480 (70.38)1.000
Insurance, n (%)1030 (80.47)1167 (70.09)<0.0001500 (73.31)510 (74.78)0.537
Number of diagnosis, median (range)6 (1–23)6 (1–24)0.026 (1–23)6 (1–24)0.243
Charlson comorbidity index, median (range)5 (1–28)4 (1–18)<0.00015 (1–16)5 (1–17)0.352
Admission to ICU, n (%)160 (12.50)825 (49.55)<0.0001160 (23.46)170 (24.93)0.527
Surgery, n (%)380 (29.69)753 (45.23)<0.0001250 (36.66)246 (36.07)0.822
Myocardial infarction, n (%)34 (2.66)47 (2.82)0.78424 (3.52)22 (3.23)0.764
Congestive heart failure, n (%)250 (19.53)247 (14.83)0.001115 (16.86)123 (18.04)0.568
Peripheral vascular disease, n (%)21 (1.64)36 (2.16)0.30920 (2.93)18 (2.64)0.742
Cerebrovascular diseases, n (%)676 (52.81)1002 (60.18)<0.0001389 (57.04)380 (55.72)0.623
Dementia, n (%)42 (3.28)41 (2.46)0.18333 (4.84)21 (3.08)0.096
Chronic pulmonary disease, n (%)342 (26.72)306 (18.38)<0.0001138 (20.23)163 (23.90)0.103
Connective tissue disease, n (%)21 (1.64)22 (1.32)0.47410 (1.47)6 (0.88)0.314
Mild liver disease, n (%)42 (3.28)56 (3.36)0.90226 (3.81)22 (3.23)0.557
Peptic ulcer disease, n (%)34 (2.66)51 (3.06)0.51321 (3.08)20 (2.93)0.874
Diabetes mellitus, n (%)295 (23.05)354 (21.26)0.247160 (23.46)152 (22.29)0.606
Diabetes mellitus with chronic complications, n (%)39 (3.05)19 (1.14)<0.000110 (1.47)14 (2.05)0.410
Moderate to severe chronic kidney disease, n (%)100 (7.81)160 (9.61)0.08861 (8.94)54 (7.92)0.495
Hemiplegia, n (%)15 (1.17)31 (1.86)0.13412 (1.76)11 (1.61)0.833
Solid tumor without metastases, n (%)121 (9.45)72 (4.32)<0.000132 (4.69)45 (6.60)0.127
Leukemia, n (%)18 (1.41)4 (0.24)<0.00012 (0.29)3 (0.44)1.000
Malignant lymphoma, n (%)13 (1.02)7 (0.42)0.0511 (0.15)3 (0.44)0.624
Severe liver disease, n (%)15 (1.17)25 (1.50)0.44411 (1.61)6 (0.88)0.222
Metastatic tumor, n (%)94 (7.34)26 (1.56)<0.000112 (1.76)21 (3.08)0.113
CRKP: carbapenem resistant Acinetobacter baumannii, CSKP: carbapenem susceptible A. baumannii, PSM: propensity score matching, ICU: intensive care unit.
Table 4. Economic costs of patients with CRKP and CSKP after PSM for potential confounding variables.
Table 4. Economic costs of patients with CRKP and CSKP after PSM for potential confounding variables.
Hospital Cost ($)CSKPCRKPDifferencep-Value
Mean95% UIMean95% UIMean95% UI
Total hospital cost21,22921,00521,45335,48035,14935,81114,25213,85214,653<0.0001
Antibiotic cost287828242932617560976252329632023390<0.0001
Medication cost10,081996010,20219,21319,02719,399913289109354<0.0001
Diagnostic cost286828362900438543434426151714651570<0.0001
Treatment cost511250475176768675957776257424622686<0.0001
Material cost309630513140399339374050899826971<0.0001
Other cost706873626264−8−11−50.0028
CRKP: carbapenem resistant Klebsiella pneumoniae, CSKP: carbapenem susceptible K. pneumoniae, PSM: propensity score matching, UI: uncertainty interval.
Table 5. Economic costs of patients with CRPA and CSPA after PSM for potential confounding variables.
Table 5. Economic costs of patients with CRPA and CSPA after PSM for potential confounding variables.
Hospital Cost ($)CSPACRPADifferencep-Value
Mean95% UIMean95% UIMean95% UI
Total hospital cost20,90820,67021,14625,50825,24425,771460542494960<0.0001
Antibiotic cost242623802472350434503558107810071149<0.0001
Medication cost10,082995910,20313,13512,99613,273305328673238<0.0001
Diagnostic cost2759272827903129309431633703234160.0001
Treatment cost551254345591668365786789117410431305<0.0001
Material cost2397235424402472243525087619132<0.0001
Other cost6260638481872319260.3252
CRKP: carbapenem resistant Pseudomonas aeruginosa, CSKP: carbapenem susceptible P. aeruginosa, PSM: propensity score matching, UI: uncertainty interval.
Table 6. Economic costs of patients with CRAB and CSAB after PSM for potential confounding variables.
Table 6. Economic costs of patients with CRAB and CSAB after PSM for potential confounding variables.
Hospital Cost ($)CSABCRABDifferencep-Value
Mean95% UIMean95% UIMean95% UI
Total hospital cost20,34920,10320,59527,63027,34227,919727768977657<0.0001
Antibiotic cost238023312428391738683965153714681605<0.0001
Medication cost91609036928313,06512,94813,183390237314074<0.0001
Diagnostic cost284028092870346834393497628585670<0.0001
Treatment cost515550735237731371437482215619672344<0.0001
Material cost310230503153352134733569421351491<0.0001
Other cost9189939390962−260.0001
CRAB: carbapenem resistant Acinetobacter baumannii, CSAB: carbapenem susceptible A. baumannii, PSM: propensity score matching, UI: uncertainty interval.
Table 7. Length of stay among patients with CRKP and CSKP, among patients with CRPA and CSPA, and among patients with CRAB and CSAB after PSM for potential confounding variables.
Table 7. Length of stay among patients with CRKP and CSKP, among patients with CRPA and CSPA, and among patients with CRAB and CSAB after PSM for potential confounding variables.
Length of Stay (Days)Carbapenem Susceptible-Carbapenem Resistant-Differencep-Value
Mean95% UIMean95% UIMean95% UI
CRKP vs. CSKP32.932.633.246.145.746.513.212.713.7<0.0001
CRPA vs. CSPA41.140.641.646.545.647.45.44.46.50.0003
CRAB vs. CSAB33.733.434.149.647.751.415.813.917.70.0004
CRKP: carbapenem resistant Klebsiella pneumoniae, CSKP: carbapenem susceptible K. pneumoniae, CRKP: carbapenem resistant Pseudomonas aeruginosa, CSKP: carbapenem susceptible P. aeruginosa, CRAB: carbapenem resistant Acinetobacter baumannii, CSAB: carbapenem susceptible A. baumannii, PSM: propensity score matching, UI: uncertainty interval.
Table 8. In hospital mortality among patients with CRKP and CSKP, among patients with CRPA and CSPA, and among patients with CRAB and CSAB after PSM for potential confounding variables.
Table 8. In hospital mortality among patients with CRKP and CSKP, among patients with CRPA and CSPA, and among patients with CRAB and CSAB after PSM for potential confounding variables.
In Hospital Mortality Rate (%)Carbapenem Susceptible-Carbapenem Resistant-Differencep-Value
Rate95% UIRate95% UIRate95% UI
CRKP vs. CSKP6.656.436.879.599.339.852.942.63.280.024
CRPA vs. CSPA4.734.544.916.776.556.992.031.752.320.052
CRAB vs. CSAB4.254.074.438.288.048.534.033.734.330.003
CRKP: carbapenem resistant Klebsiella pneumoniae, CSKP: carbapenem susceptible K. pneumoniae, CRKP: carbapenem resistant Pseudomonas aeruginosa, CSKP: carbapenem susceptible P. aeruginosa, CRAB: carbapenem resistant Acinetobacter baumannii, CSAB: carbapenem susceptible A. baumannii, PSM: propensity score matching, UI: uncertainty interval.

Share and Cite

MDPI and ACS Style

Zhen, X.; Stålsby Lundborg, C.; Sun, X.; Gu, S.; Dong, H. Clinical and Economic Burden of Carbapenem-Resistant Infection or Colonization Caused by Klebsiella pneumoniae, Pseudomonas aeruginosa, Acinetobacter baumannii: A Multicenter Study in China. Antibiotics 2020, 9, 514. https://doi.org/10.3390/antibiotics9080514

AMA Style

Zhen X, Stålsby Lundborg C, Sun X, Gu S, Dong H. Clinical and Economic Burden of Carbapenem-Resistant Infection or Colonization Caused by Klebsiella pneumoniae, Pseudomonas aeruginosa, Acinetobacter baumannii: A Multicenter Study in China. Antibiotics. 2020; 9(8):514. https://doi.org/10.3390/antibiotics9080514

Chicago/Turabian Style

Zhen, Xuemei, Cecilia Stålsby Lundborg, Xueshan Sun, Shuyan Gu, and Hengjin Dong. 2020. "Clinical and Economic Burden of Carbapenem-Resistant Infection or Colonization Caused by Klebsiella pneumoniae, Pseudomonas aeruginosa, Acinetobacter baumannii: A Multicenter Study in China" Antibiotics 9, no. 8: 514. https://doi.org/10.3390/antibiotics9080514

APA Style

Zhen, X., Stålsby Lundborg, C., Sun, X., Gu, S., & Dong, H. (2020). Clinical and Economic Burden of Carbapenem-Resistant Infection or Colonization Caused by Klebsiella pneumoniae, Pseudomonas aeruginosa, Acinetobacter baumannii: A Multicenter Study in China. Antibiotics, 9(8), 514. https://doi.org/10.3390/antibiotics9080514

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop