Oral Antimicrobial Therapy: Efficacy and Safety for Methicillin-Resistant Staphylococcus aureus Infections and Its Impact on the Length of Hospital Stay
2
조회
0
다운로드
0
인용
0
참고문헌
키워드
초록
Background: Carefully switching from intravenous to oral antibiotic therapy has shown to reduce treatment costs and lengths ofhospital stay as well as increase safety and comfort in patients with infections. The aim of this study was to compare the clinicalefficacy and safety between the patients treated with glycopeptides (case group), and the patients given oral antibiotics, as theinitial or step-down therapy (control group), in the treatment of patients with methicillin-resistant Staphylococcus aureus (MRSA)infection. Materials and Methods: A multicenter observational study was retrospectively performed in 7 teaching hospitals in Korea fromJanuary to December 2012. The study included adult patients (≥ 18 years) with infection caused by MRSA isolates, susceptibleto clindamycin, erythromycin, and ciprofloxacin. The primary end point was treatment outcome, including all-cause mortalityand switching of antibiotics. Drug-related adverse events and the lengths of hospital stay were also compared between the twotreatment groups. Results: During the study period, 107 patients (43 cases and 64 controls) with MRSA infections were enrolled from the participatinghospitals. The most common sites of MRSA infection were skin and soft tissue (n = 28) and bone and joint (n = 26). Themedian Charlson comorbidity index (P = 0. 560), the frequency of severe sepsis (P = 0.682) or thrombocytopenia (P = 1.000),and median level of serum C-reactive protein (P = 0.157) at the onset of MRSA infections were not significantly different betweenthe case and control groups. The oral antibiotics most frequently prescribed in the case group, were fluoroquinolones(n = 29) and clindamycin (n = 8). The median duration of antibiotic treatment (P = 0.090) and the occurrence of drug-relatedadverse events (P = 0.460) did not reach statistically significant difference between the two groups, whereas the total length ofhospital stay after the onset of MRSA infection was significantly shorter in the case group than the control group [median (in-terquartile range), 23 days (8-41) vs. 32 days (15-54), P = 0.017]. In multivariate analyses, the type of antibiotic used was notan independent risk factor for treatment failure. The statistically significant factors associated with treatment failure includedunderlying hepatic diseases, prior receipt of antibiotics, and foreign body retention. Conclusions: This study indicates that oral antibiotic therapy with active agents against MRSA isolates can be considered as theinitial or step-down therapy for the treatment of MRSA infections and also reduce the length of hospital stay.
Abstract
Background: Carefully switching from intravenous to oral antibiotic therapy has shown to reduce treatment costs and lengths ofhospital stay as well as increase safety and comfort in patients with infections. The aim of this study was to compare the clinicalefficacy and safety between the patients treated with glycopeptides (case group), and the patients given oral antibiotics, as theinitial or step-down therapy (control group), in the treatment of patients with methicillin-resistant Staphylococcus aureus (MRSA)infection. Materials and Methods: A multicenter observational study was retrospectively performed in 7 teaching hospitals in Korea fromJanuary to December 2012. The study included adult patients (≥ 18 years) with infection caused by MRSA isolates, susceptibleto clindamycin, erythromycin, and ciprofloxacin. The primary end point was treatment outcome, including all-cause mortalityand switching of antibiotics. Drug-related adverse events and the lengths of hospital stay were also compared between the twotreatment groups. Results: During the study period, 107 patients (43 cases and 64 controls) with MRSA infections were enrolled from the participatinghospitals. The most common sites of MRSA infection were skin and soft tissue (n = 28) and bone and joint (n = 26). Themedian Charlson comorbidity index (P = 0. 560), the frequency of severe sepsis (P = 0.682) or thrombocytopenia (P = 1.000),and median level of serum C-reactive protein (P = 0.157) at the onset of MRSA infections were not significantly different betweenthe case and control groups. The oral antibiotics most frequently prescribed in the case group, were fluoroquinolones(n = 29) and clindamycin (n = 8). The median duration of antibiotic treatment (P = 0.090) and the occurrence of drug-relatedadverse events (P = 0.460) did not reach statistically significant difference between the two groups, whereas the total length ofhospital stay after the onset of MRSA infection was significantly shorter in the case group than the control group [median (in-terquartile range), 23 days (8-41) vs. 32 days (15-54), P = 0.017]. In multivariate analyses, the type of antibiotic used was notan independent risk factor for treatment failure. The statistically significant factors associated with treatment failure includedunderlying hepatic diseases, prior receipt of antibiotics, and foreign body retention. Conclusions: This study indicates that oral antibiotic therapy with active agents against MRSA isolates can be considered as theinitial or step-down therapy for the treatment of MRSA infections and also reduce the length of hospital stay.
참고문헌 (29)
- Kim ES, "A survey of community-associated methicillin-resistant Staphylococcus aureus in Korea", JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 60, pp.1108~1114 (2007), OXFORD UNIV PRESS
- Park SH, "Emergence of Community-Associated Methicillin-Resistant Staphylococcus aureus Strains as a Cause of Healthcare-Associated Bloodstream Infections in Korea", INFECTION CONTROL AND HOSPITAL EPIDEMIOLOGY, 30, pp.146~155 (2009), University of Chicago Press
- Charlebois ED, "Origins of community strains of methicillin-resistant Staphylococcus aureus", Clin Infect Dis, 39, pp.47~54 (2004)
- Almer LS, "Antimicrobial susceptibility and molecular characterization of community-acquired methicillin-resistant Staphylococcus aureus", Diagn Microbiol Infect Dis, 43, pp.225~232 (2002)
- Khawcharoenporn T, "Oral antibiotic treatment for methicillin-resistant Staphylococcus aureus skin and soft tissue infections: review of the literature", Hawaii Med J, 65, pp.290~293 (2006)
- Enoch DA, "Oral antimicrobial options for the treatment of skin and soft-tissue infections caused by methicillin-resistant Staphylococcus aureus (MRSA) in the UK", Int J Antimicrob Agents, 33, pp.497~502 (2009)
- Barnes EV 2nd, "Outcomes of community-acquired, methicillin-resistant Staphylococcus aureus, soft tissue infections treated with antibiotics other than vancomycin", Mil Med, 171, pp.504~507 (2006)
- Mathews CJ, "Bacterial septic arthritis in adults", Lancet, 375, pp.846~855 (2010)
- Lew DP, "Osteomyelitis", Lancet, 364, pp.369~379 (2004)
- Sabol KE, "Community-associated methicillin-resistant Staphylococcus aureus: new bug, old drugs", Ann Pharmacother, 40, pp.1125~1133 (2006)
- Zimmerli W, "Prosthetic-joint infections", N Engl J Med, 351, pp.1645~1654 (2004)
- Dryden M, "Antibiotic stewardship and early discharge from hospital: impact of a structured approach to antimicrobial management", J Antimicrob Chemother, 67, pp.2289~2296 (2012)
- Nathwani D, "Pan-European early switch", early discharge opportunities exist for hospitalised patients with methicillin-resistant Staphylococcus aureus complicated skin and soft-tissue infections, 2014, ~
- Daver NG, "Oral step-down therapy is comparable to intravenous therapy for Staphylococcus aureus osteomyelitis", J Infect, 54, pp.539~544 (2007)
- Itani KM, "Clinical efficacy of oral linezolid compared with intravenous vancomycin for the treatment of methicillin-resistant Staphylococcus aureus-complicated skin and soft tissue infections: a retrospective, propensity scorematched, case-control analysis", Clin Ther, 34, pp.1667~1673 (2012)
- O’Brien FG, "Diversity among community isolates of methicillin-resistant Staphylococcus aureus in Australia", J Clin Microbiol, 42, pp.3185~3190 (2004)
- David MZ, "What is community-associated methicillin-resistant Staphylococcus aureus?", J Infect Dis, 197, pp.1235~1243 (2008)
- Garner JS, "CDC definitions for nosocomial infections, 1988", Am J Infect Control, 16, pp.128~140 (1988)
- Charlson M, "Validation of a combined comorbidity index", J Clin Epidemiol, 47, pp.1245~1251 (1994)
- Longo DL, "Harrison’s principles of internal medicine, 18th ed" (2012), McGraw-Hill
- Moran GJ, "Methicillin-resistant S. aureus infections among patients in the emergency department", N Engl J Med, 355, pp.666~674 (2006)
- Francis JS, "Severe community-onset pneumonia in healthy adults caused by methicillin-resistant Staphylococcus aureus carrying the Panton-Valentine leukocidin genes", Clin Infect Dis, 40, pp.100~107 (2005)
- 고재훈, "First Imported Case of Skin Infection Caused by PVL-positive ST30 Community-Associated Methicillin-Resistant Staphylococcus aureus Clone in a Returning Korean Traveler from the Philippines", Journal of Korean Medical Science, 28(7), pp.1100~1102 (2013), 대한의학회
- Joo EJ, "Community-associated Panton-Valentine leukocidin-negative methicillin-resistant Staphylococcus aureus clone (ST72-MRSA-IV)causing healthcare-associated pneumonia and surgical site infection in Korea", J Hosp Infect, 81, pp.149~155 (2012)
- Kaka AS, "Bactericidal activity of orally available agents against methicillin-resistant Staphylococcus aureus", J Antimicrob Chemother, 58, pp.680~683 (2006)
- Markowitz N, "Trimethoprim-sulfamethoxazole compared with vancomycin for the treatment of Staphylococcus aureus infection", Ann Intern Med, 117, pp.390~398 (1992)
- Chen LF, "Community-acquired methicillin-resistant Staphylococcus aureus skin and soft tissue infections: management and prevention", Curr Infect Dis Rep, 13, pp.442~450 (2011)
- DeLeo FR, "Community-associated methicillin-resistant Staphylococcus aureus", Lancet, 375, pp.1557~1568 (2010)
- Kim BN, "Oral antibiotic treatment of staphylococcal bone and joint infections in adults", J Antimicrob Chemother, 69, pp.309~322 (2014)
