Treatment for chronic methicillin-sensitive Staphylococcus aureus pulmonary infection in people with cystic fibrosis

被引:2
|
作者
Ahmed, Molla I. [1 ]
Mukherjee, Saptarshi [2 ]
机构
[1] Univ Hosp Leicester, Leicester Royal Infirm, Dept Pediat, Infirm Sq, Leicester LE1 5WW, Leics, England
[2] Cardiff Univ, Sch Med, Wales Heart Res Inst, Cardiff CF10 3AX, S Glam, Wales
关键词
LEVOFLOXACIN INHALATION SOLUTION; 2 DOSAGE REGIMENS; MAINTENANCE-TREATMENT; CONTROLLED TRIAL; YOUNG-CHILDREN; UNITED-STATES; PHARMACOKINETICS; CIPROFLOXACIN; PSEUDOMONAS; ADULTS;
D O I
10.1002/14651858.CD011581.pub2
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Cystic fibrosis is an inherited life-threatening multisystem disorder with lung disease characterized by abnormally thick airway secretions and persistent bacterial infection. Chronic, progressive lung disease is the most important cause of morbidity and mortality in the condition and is therefore the main focus of clinical care and research. Staphylococcus aureus is a major cause of chest infection in people with cystic fibrosis. Early onset, as well as chronic, lung infection with this organism in young children and adults results in worsening lung function, poorer nutrition and increases the airway inflammatory response, thus leading to a poor overall clinical outcome. There are currently no evidence-based guidelines for chronic suppressive therapy for Staphylococcus aureus infection in cystic fibrosis such as those used for Pseudomonas aeruginosa infection. Objectives To assess the evidence regarding the effectiveness of long-term antibiotic treatment regimens for chronic infection with methicillin-sensitive Staphylococcus aureus (MSSA) infection in people with cystic fibrosis and to determine whether this leads to improved clinical and microbiological outcomes. Search methods Trials were identified by searching the Cochrane Cystic Fibrosis and Genetic Disorders Group's Cystic Fibrosis Trials Register, MEDLINE, Embase, handsearching article reference lists and through contact with local and international experts in the field. We also searched ongoing trials databases. Date of the last search of the Group's Cystic Fibrosis Trials Register: 03 March 2016. Selection criteria Randomised or quasi-randomised controlled trials comparing any combinations of topical, inhaled, oral or intravenous antimicrobials used as suppressive therapy for chronic infection withmethicillin-sensitive Staphylococcus aureus compared with placebo or no treatment. Data collection and analysis The authors independently assessed all search results for eligibility. No eligible trials were identified. Main results The searches identified 55 trials, but none were eligible for inclusion in the current version of this review. Authors' conclusions No randomised controlled trials were identified which met the inclusion criteria for this review. Although methicillin-sensitive Staphylococcus aureus is an important and common cause of lung infection in people with cystic fibrosis, there is no agreement on how best to treat long-term infection. The review highlights the need to organise well-designed trials that can provide evidence to support the best management strategy for chronic methicillin-sensitive Staphylococcus aureus infection in people with cystic fibrosis.
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页数:23
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