Table 1.
Important outcomes | Clinical or microbiological cure, length of hospital stay, mortality, adverse effects | ||||||||
Number of studies (participants) | Outcome | Comparison | Type of evidence | Quality | Consistency | Directness | Effect size | GRADE | Comment |
What are the effects of treatment for MRSA infections at any body site? | |||||||||
5 (73) [15] | Mortality | Linezolid v vancomycin in bacteraemia | 4 | –3 | 0 | 0 | 0 | Very low | Quality points deducted for sparse data, methodological weaknesses (no blinding), and subgroup analysis |
7 (900) [13] [14] | Clinical or microbiological cure | Linezolid v vancomycin in infection at any body site | 4 | –2 | 0 | –2 | 0 | Very low | Quality points deducted for incomplete reporting and methodological weaknesses (no blinding). Directness points deducted for population issues (inclusion of people with non-MRSA infections in some studies), unclear/subjective outcome (clinical cure), and inclusion of co-intervention in one study (aztreonam) |
more than 1 RCT (>62 people) [13] [14] | Clinical or microbiological cure | Linezolid v vancomycin in nosocomial pneumonia | 4 | –3 | 0 | –2 | 0 | Very low | Quality points deducted for incomplete reporting, methodological weaknesses (no blinding), and subgroup analysis. Directness points deducted for population issues (inclusion of people with non-MRSA infections in some studies), unclear/subjective outcome (clinical cure), and inclusion of co-intervention in one study (aztreonam) |
more than 1 RCT (>80 people) [13] [14] | Clinical or microbiological cure | Linezolid v vancomycin in skin and soft-tissue infections | 4 | –3 | 0 | –2 | 0 | Very low | Quality points deducted for incomplete reporting, methodological weaknesses (no blinding) and subgroup analysis. Directness points deducted for population issues (inclusion of people with non-MRSA infections in some studies), unclear/subjective outcome (clinical cure), and inclusion of co-intervention in one study (aztreonam) |
12 (223) [15] [16] | Clinical or microbiological cure | Linezolid v vancomycin in bacteraemia | 4 | –2 | 0 | –2 | 0 | Very low | Quality points deducted for incomplete reporting and methodological weaknesses (no blinding). Directness points deducted for population issues (inclusion of people with non-MRSA infections in some studies, inclusion of children in some studies), and unclear/subjective outcome (clinical cure) |
1 (182)[17] | Clinical or microbiological cure | Linezolid v teicoplanin | 4 | –2 | 0 | –2 | 0 | Very low | Quality points deducted for sparse data and inclusion of people without MRSA. Directness points deducted for low follow-up and use of unclear/subjective outcome (clinical cure) |
1 (182)[17] | Mortality | Linezolid v teicoplanin | 4 | –2 | 0 | –1 | 0 | Very low | Quality points deducted for sparse data and inclusion of people without MRSA. Directness point deducted for highly selected population (on intensive care) |
1 (51)[25] | Clinical or microbiological cure | Quinupristin–dalfopristin v vancomycin | 4 | –2 | 0 | –1 | 0 | Very low | Quality points deducted for sparse data and subgroup analysis. Directness point deducted for use of unclear/subjective outcome (clinical cure) |
1 (298)[25] | Mortality | Quinupristin–dalfopristin v vancomycin | 4 | –1 | 0 | –1 | 0 | Low | Quality point deducted for inclusion of people without MRSA. Directness point deducted for lack of subgroup analysis in people with MRSA only, hence, limited generalisability to this population group |
1 (47)[26] | Clinical or microbiological cure | Trimethoprim–sulfamethoxazole (co-trimoxazole) v vancomycin | 4 | –2 | 0 | –2 | 0 | Very low | Quality points deducted for sparse data and subgroup analysis. Directness points deducted for highly selected population (injecting drug users) and for use of unclear/subjective outcome (clinical cure) |
1 (157) [24] | Clinical or microbiological cure | Tigecycline v vancomycin | 4 | –2 | 0 | 0 | 0 | Low | Quality points deducted for sparse data and no statistical assessment |
Type of evidence: 4 = RCT; Consistency: similarity of results across studies; Directness: generalisability of population or outcomes; Effect size: based on relative risk or odds ratio.