Standardized Treatment and Assessment Pathway Improves Mortality in Adults With Methicillin-resistant Staphylococcus aureus Bacteremia: STAPH Study

被引:7
作者
Alosaimy, Sara [1 ]
Lagnf, Abdalhamid M. [1 ]
Morrisette, Taylor [1 ]
Jorgensen, Sarah C. J. [1 ,9 ]
Trinh, Trang D. [1 ,10 ]
Zasowski, Evan J. [1 ,11 ]
Scipione, Marco R. [2 ]
Zhao, Jing J. [3 ]
Mynatt, Ryan [4 ,5 ]
Herbin, Shelbye [2 ]
Dhar, Sorabh [5 ,6 ]
Chopra, Teena [5 ,7 ]
Janisse, James [8 ]
Rebold, Nicholas [1 ]
Pogue, Jason M. [5 ,12 ]
Rybak, Michael J. [1 ,2 ,8 ]
机构
[1] Wayne State Univ, Eugene Applebaum Coll Pharm & Hlth Sci, Dept Pharm Practice, Antiinfect Res Lab, Detroit, MI 48201 USA
[2] Detroit Receiving Hosp & Univ Hlth Ctr, Detroit Med Ctr, Dept Pharm, Detroit, MI USA
[3] Harper Univ Hosp, Detroit, MI USA
[4] Univ Kentucky, Lexington, KY USA
[5] Wayne State Univ, Sch Med, Dept Med, Div Infect Dis, Detroit, MI 48201 USA
[6] John D Dingell Vet Adm Med Ctr, Div Infect Dis, Detroit, MI USA
[7] Detroit Med Ctr, Detroit, MI USA
[8] Wayne State Univ, Sch Med, Dept Family Med & Publ Hlth Sci, Detroit, MI 48201 USA
[9] Mt Sinai Hosp, Dept Pharm, Toronto, ON, Canada
[10] Univ Calif San Francisco, Sch Pharm, Dept Clin Pharm, San Francisco, CA USA
[11] Touro Univ Calif, Coll Pharm, Dept Clin Sci, Vallejo, CA USA
[12] Univ Michigan, Coll Pharm, Dept Clin Pharm, 428 Church St, Ann Arbor, MI 48109 USA
来源
OPEN FORUM INFECTIOUS DISEASES | 2021年 / 8卷 / 07期
关键词
beta-lactams; bloodstream infections; combination therapy; gram-positive infections; MRSA; PIPERACILLIN-TAZOBACTAM; LACTAM THERAPY; BETA-LACTAM; VANCOMYCIN; COMBINATION; DAPTOMYCIN; INFECTIONS; RISK;
D O I
10.1093/ofid/ofab261
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Methicillin-resistant Staphylococcus aureus (MRSA) bloodstream infection (BSI) management remains challenging for clinicians. Numerous in vitro studies report synergy when vancomycin (VAN) and daptomycin (DAP) are combined with beta-lactams (BLs), which has led to clinical implementation of these combinations. While shorter durations of bacteremia have often been reported, there has been no significant impact on mortality. Methods. The Detroit Medical Center (DMC) developed and implemented a clinical pathway algorithm for MRSA BSI treatment in 2016 that included the early use of BL combination therapy with standard of care (VAN or DAP) and a mandatory Infectious Diseases consultation. This was a retrospective, quasi-experimental study at the DMC between 2013 and 2020. Multivariable logistic regression was used to assess the independent association between pathway implementation and 30-day mortality while adjusting for confounding variables. Results. Overall, 813 adult patients treated for MRSA BSI were evaluated. Compared with prepathway (PRE) patients (n = 379), those treated postpathway (POST; n = 434) had a significant reduction in 30-day and 90-day mortality: 9.7% in POST vs 15.6% in PRE (P = .011) and 12.2% in POST vs 19.0% in PRE (P = .007), respectively. The incidence of acute kidney injury (AKI) was higher in the PRE compared with the POST group: 9.6% vs 7.2% (P = .282), respectively. After adjusting for confounding variables including Infectious Diseases consult, POST was independently associated with a reduction in 30-day mortality (adjusted odds ratio [aOR], 0.608; 95% CI, 0.375-0.986). Conclusions. Implementation of an MRSA BSI treatment pathway with early use of BL reduced mortality with no increased rate of AKI. Further prospective evaluation of this pathway approach is warranted.
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页数:12
相关论文
共 38 条
[1]   Monotherapy with Vancomycin or Daptomycin versus Combination Therapy with β-Lactams in the Treatment of Methicillin-Resistant Staphylococcus Aureus Bloodstream Infections: A Retrospective Cohort Analysis [J].
Alosaimy, Sara ;
Sabagha, Noor L. ;
Lagnf, Abdalhamid M. ;
Zasowski, Evan J. ;
Morrisette, Taylor ;
Jorgensen, Sarah C. J. ;
Trinh, Trang D. ;
Mynatt, Ryan P. ;
Rybak, Michael J. .
INFECTIOUS DISEASES AND THERAPY, 2020, 9 (02) :325-339
[2]   Early Administration of Adjuvant -Lactam Therapy in Combination with Vancomycin among Patients with Methicillin-Resistant Staphylococcus aureus Bloodstream Infection: A Retrospective, Multicenter Analysis [J].
Casapao, Anthony M. ;
Jacobs, David M. ;
Bowers, Dana R. ;
Beyda, Nicholas D. ;
Dilworth, Thomas J. .
PHARMACOTHERAPY, 2017, 37 (11) :1347-1356
[3]  
Centers for Disease Control and Prevention, 2020, WEEKL COUNTS DEATHS
[4]   The Effect of Infectious Diseases Consultation on Mortality in Hospitalized Patients With Methicillin-Resistant Staphylococcus aureus, Candida, and Pseudomonas Bloodstream Infections [J].
Chesdachai, Supavit ;
Kline, Susan ;
Helmin, Derrek ;
Rajasingham, Radha .
OPEN FORUM INFECTIOUS DISEASES, 2020, 7 (01)
[5]   Daptomycin Improves Outcomes Regardless of Vancomycin MIC in a Propensity-Matched Analysis of Methicillin-Resistant Staphylococcus aureus Bloodstream Infections [J].
Claeys, Kimberly C. ;
Zasowski, Evan J. ;
Casapao, Anthony M. ;
Lagnf, Abdalhamid M. ;
Nagel, Jerod L. ;
Nguyen, Cynthia T. ;
Hallesy, Jessica A. ;
Compton, Mathew T. ;
Kaye, Keith S. ;
Levine, Donald P. ;
Davis, Susan L. ;
Rybak, Michael J. .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2016, 60 (10) :5841-5848
[6]   Combinations of vancomycin and β-lactams are synergistic against staphylococci with reduced susceptibilities to vancomycin [J].
Climo, MW ;
Patron, RL ;
Archer, GL .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1999, 43 (07) :1747-1753
[7]   Combination of Vancomycin and β-Lactam Therapy for Methicillin-Resistant Staphylococcus aureus Bacteremia: A Pilot Multicenter Randomized Controlled Trial [J].
Davis, Joshua S. ;
Sud, Archana ;
O'Sullivan, Matthew V. N. ;
Robinson, James O. ;
Ferguson, Patricia E. ;
Foo, Hong ;
van Hal, Sebastiaan J. ;
Ralph, Anna P. ;
Howden, Benjamin P. ;
Binks, Paula M. ;
Kirby, Adrienne ;
Tong, Steven Y. C. .
CLINICAL INFECTIOUS DISEASES, 2016, 62 (02) :173-180
[8]  
Detroit Medical Center, 2021, GUIDELINES TREATMENT
[9]   Vancomycin and Piperacillin-Tazobactam Against Methicillin-Resistant Staphylococcus aureus and Vancomycin-Intermediate Staphylococcus aureus in an In Vitro Pharmacokinetic/Pharmacodynamic Model [J].
Dilworth, Thomas J. ;
Leonard, Steve N. ;
Vilay, A. Mary ;
Mercier, Renee-Claude .
CLINICAL THERAPEUTICS, 2014, 36 (10) :1334-1344
[10]  
Finch NA, 2017, ANTIMICROB AGENTS CH, V61, DOI [10.1128/AAC.01293-17, 10.1128/aac.01293-17]