The Effect of Combination Therapy on Mortality and Adverse Events in Patients with Staphylococcus aureus Bacteraemia: A Systematic Review and Meta-analysis of Randomized Controlled Trials

Abstract

Introduction

The findings of randomized controlled trials (RCTs), observational studies, and meta-analyses vary regarding the effectiveness and safety of combination therapy for patients with Staphylococcus aureus bacteraemia (SAB). We aimed to identify the effectiveness and safety of combination therapy in patients with SAB compared with those of monotherapy.

Methods

We performed a systematic review and meta-analysis to compare combination therapy versus monotherapy in patients with SAB. Two authors independently searched PubMed, Embase, and the Cochrane Library of clinical trials until 17 February 2021. Any RCT comparing mortality or adverse events (AEs) of combination therapy versus monotherapy for patients with SAB was eligible. Summary risk ratios (RRs) and 95% confidence intervals (CIs) were evaluated using a random-effects model. The primary outcome was all-cause mortality at any time point. This meta-analysis is registered with the PROSPERO database (CRD42020188176) and reported according to PRISMA guidelines.

Results

In total, 1906 articles were identified and screened, and 14 studies (2367 patients) were included in the meta-analysis. There was no significant difference in the risk of all-cause mortality between the two groups (RR = 1.00; 95% CI 0.83–1.20; P = 0.99; I² = 0%). Similar results were obtained by subgroup analysis of mortality recording time, endocarditis, pathogen resistance, article publication time, number of patients, and adjuvant antibiotics. Notably, combination treatment might significantly increase the risk of drug-related AEs (RR = 1.68; 95% CI 1.06–2.66; P = 0.03; I² = 67%) and nephrotoxicity (RR = 2.30; 95% CI 1.68–3.16; P < 0.00001; I² = 0%), although the occurrences of AEs leading to treatment discontinuation and serious AEs were not significantly different between the two groups.

Conclusions

The meta-analysis suggested that combination therapy could not reduce mortality but might increase the risk of drug-related AEs and nephrotoxicity and should be applied very cautiously. Future studies on combined drug therapy for SAB need careful and rigorous design for specific antibiotic combinations.

Supplementary Information

The online version contains supplementary material available at 10.1007/s40121-021-00539-y.

Key Summary Points

Fourteen eligible RCTs involving 2367 patients were included for the final analysis

Meta-analyses showed that there was no significant difference in the risk of all-cause mortality between combination therapy and monotherapy groups

Combination therapy may increase the risk of nephrotoxicity and drug-related AEs, which will limit its clinical application

Future studies on combined drug therapy for SAB need careful and rigorous design for specific antibiotic combinations

Introduction

Staphylococcus aureus is among the leading causes of infections in hospital- and community-acquired infection patients and is associated with significant morbidity. Enhanced infection control efforts have helped reduce the rate of S. aureus bacteraemia (SAB) over the past decade, but case fatality rates for SAB have improved only modestly in recent decades. During this time, the incidence of SAB in the general population has ranged from 20 to 25 episodes per 10⁵ patient-years, with mortality rates of approximately 20–30% [1–4].

Despite straightforward evidence-based combination interventions for SAB, doubts remain regarding the best antimicrobial therapy [5]. For decades, treatment has included anti-staphylococcal penicillins (ASPs) or first-generation cephalosporins (such as cefazolin) for methicillin-sensitive S. aureus bacteraemia (MSSAB) and vancomycin or daptomycin for methicillin-resistant S. aureus bacteraemia (MRSAB) [6, 7]. Due to the potential severity of SAB, there remains active interest in novel treatment strategies to improve clinical outcomes.

In vitro laboratory data, animal models, and observational studies have suggested that combination antimicrobial therapy may be beneficial for S. aureus [8–12]. Over the past several years, there has been an increase in the number of randomized controlled trials (RCTs) involving patients with SAB, including the use of adjunctive rifampicin, fosfomycin, or ceftaroline for SAB [13–16]; however, the evidence supporting combination therapy in SAB is unclear. Several efforts have been made through meta-analyses to investigate whether combination antibiotic therapy is associated with better clinical outcomes than monotherapy. However, these meta-analyses either included a small number of patients with S. aureus infections or most of the included studies were non-RCTs with large heterogeneity that affected the reliability of the results [17–19]. We aimed to systematically review and synthesize the published RCTs via meta-analysis methodology to examine whether combination antibiotic therapy was associated with more favourable clinical outcomes than monotherapy in patients with SAB.

Methods

Information Sources and Key Word Search

Using the PubMed, Embase, and Cochrane databases, searches for relevant articles were performed with the following items: ‘Staphylococcus aureus’ and ‘bacteraemia or septicaemia or bloodstream infection’ and ‘randomized controlled trial’. The search used a combination of subject words and free words. Searches were limited to articles published in English up to 17 February 2021. References from clinical trials were searched manually to identify potentially relevant studies. The review protocol is registered at the Prospero international prospective register of systematic reviews (registration no. CRD42020188176), and the article is reported according to PRISMA guidelines.

Inclusion and Exclusion Criteria

Only full-length published trials in adult patients with SAB were included in the analysis. Studies were included if they met the following criteria. (1) They compared the efficacy or safety of treatment between monotherapy and combination therapy in two groups of patients. Usually, monotherapy was defined as therapy with ASPs or first-generation cephalosporins for MSSAB. If the patients were allergic to the above agents, clindamycin, vancomycin, or daptomycin was used as alternative treatment; vancomycin or daptomycin was used for MRSAB. Any one of the above primary drugs plus another antibiotic was considered combination therapy. (2) The included studies were all RCTs. (3) At least one of the following outcomes was reported: mortality and adverse effects (AEs). Articles were excluded if outcomes were not reported, outcome data were not readily extractable for each treatment group, or the article was not available in English.

Data Extraction and Quality Assessment

Two researchers independently reviewed the included studies and extracted the relevant information from each study. Disagreement between the two reviewers was resolved by discussion until consensus was reached. We used a standard form to extract relevant data from the included articles, including author name, study period, type of pathogen, study country, publication year, patient population, characteristics of bacteraemia, data relevant to therapy (antimicrobials used), mortality and AE outcome, and numbers of different groups. Risk of bias and study quality were assessed using the Cochrane Risk of Bias 2 tool [20]. This was applied to each study independently by two reviewers, with disagreements resolved by involvement of a third reviewer [20].

Outcomes and Definitions

The primary outcome was all-cause mortality. If multiple time points were reported, mortality at the latest time point (i.e., reporting the highest number of deaths) was included in the main analysis. When mortality was provided for both the intention-to-treat (ITT) and the per-protocol populations, we used the ITT population. Only if ITT data were not available did we include per-protocol data in the meta-analysis. The safety outcomes included any adverse event (AEs), any serious adverse events (SAEs), drug-related AEs, and any AEs leading to treatment discontinuation and nephrotoxicity. These definitions were the same as the definitions described in each publication.

Statistical Methods

Data were analysed using Review Manager (RevMan 5.3; The Nordic Cochrane Centre, Cochrane Collaboration, 2008). We calculated pooled risk ratios (RRs) and 95% confidence intervals (CIs) using the Mantel-Haenszel random-effects model and considered a P value < 0.05 to be statistically significant [21, 22]. Statistical heterogeneity among studies was assessed by χ² test (P < 0.10 indicated significant heterogeneity) and I². RevMan or STATA software (version 15.1; Stata Corp., University City, TX, USA) was used to create a funnel chart to assess publication bias. Publication bias of the included studies was analysed using Egger’s test [23]. A P value ≤ 0.05 for any of those tests was indicative of the presence of bias. We performed subgroup analyses to assess the effect of mortality recording time, endocarditis, pathogen resistance, article publication time, number of patients, and adjuvant antibiotics on the primary outcome.

Compliance with Ethics Guidelines

This article is based on previously conducted studies and does not contain any new studies with human participants or animals performed by any of the authors.

Results

Study Selection and Characteristics

As shown in Fig. 1, the literature search strategy initially identified 1906 articles (390 from PubMed, 917 from EMBASE, 596 from The Cochrane Library, and 3 from other sources). Five hundred ninety-seven studies were excluded because they were duplicated studies. A total of 1261 articles were removed after initial screening of titles and abstracts. Of the remaining 48 studies, we excluded 34 studies from the full-text evaluation for five main reasons. In total, after the full-text screening, we included 14 RCTs [13–16, 24–33] in the qualitative synthesis. Of these 14 studies, 9 were multicentre studies [13–16, 24–27, 30] and 5 were single-centre studies [28, 29, 31–33]. Only one of the nine multicentre studies was transnationally conducted in Australia, Singapore, Israel, and New Zealand [14]. Of the 13 non-transnational studies, five were from the USA, six were from Europe (two from Spain, two from Belgium, one from England and one from Finland), one was from Canada, and one was from Australia. Five of the 14 studies evaluated only MRSAB [14–16, 25, 29] and MSSAB [24, 27, 28, 32, 33], while the other 4 studies included both MRSAB and MSSAB [13, 26, 30, 31]. Standard therapy varied; ASPs were usually the most commonly used agent for MSSAB, whereas others included cefazolin and clindamycin, and vancomycin or daptomycin was the main agent for MRSAB. The adjuvant agents in the combined treatment group also varied, with gentamicin as an additive in four studies [26, 28, 32, 33], rifampicin as an additive in four studies [13, 29–31], and daptomycin [24], levofloxacin [27], fosfomycin [15], or ceftaroline [16] as an additive in one study. In the other two studies, ASPs or cefazolin was used as additives [14, 25]. Other characteristics included in the study, such as the age of the patients, the definition of outcome indicators, and the number of patients in the two groups, are shown in Table 1. The source of infection sites of the two groups, Charlson comfort index, and Sequential Organ Failure Assessment (SOFA) score are shown in Table S1.

Fig. 1.

Flow diagram of the selection of studies for inclusion in the meta-analysis

Table 1.

Summary of the studies included in the qualitative synthesis

Author, year	Country	Type of pathogen	Study period	No. of centres	Ages (years)	Total included	STAN group	COMBO group	Mortality definition	Safety endpoint
Cheng (2021) [24]	Canada	MSSA	11/2016–06/2019	2	Median, STAN: 65 COMBO: 68	104	51 CFZ or CLOa	53 STAN + DAPb	③⑥	(2)(3)(5)
Pujol (2021) [15]	Spain	MRSA	11/2013–12/2017	18	Median, STAN: 72 COMBO: 74	155	81 DAPc	74 STAN + FOSd	①⑦	(1)
Tong (2020) [14]	Australia, Singapore, Israel, New Zealand	MRSA	08/2015–07/2018	27	Median, STAN: 63 COMBO: 65	352	178 VAN/DAPe	174 STAN + FLU or CLO or CFZf	②④⑥	(2)(3)(4)(5)
Geriak (2019) [16]	America	MRSA	01/2016–10/2017	3	Mean, STAN: 62 COMBO: 62	40	23 VAN/DAPg	17 DAP + CPTh	①②③④⑤⑥⑧	(5)
Thwaites (2018) [13]	England	MSSA or MRSA	11/2012–10/2016	29	Median, STAN: 66 COMBO: 64	758	388 FLU/VAN or TEC/othersi	370 STAN + RIFj	②③④⑤⑥	(2)(3)(4)(5)
Davis (2016) [25]	Australia	MRSA	01/2010–05/2014	7	Mean, STAN: 65 COMBO: 64	60	29 VANk	31 STAN + FLUl	③⑥⑧	Unable to extract
Fowler (2006) [26]	America	MSSA or MRSA	08/2002–02/2005	44	Median, STAN: 55.0 COMBO: 50.5	235	120 DAPm	115 VAN/ASPs + GENn	⑦	(2)(3)(4)(5)
Ruotsalainen (2006) [27]	Finland	MSSA	01/2000–08/2002	13	Mean, STAN: 58 COMBO: 58	381	190 ASPs/CXM/CLI/VAN/otherso	191 STAN + LEVp	①②③④⑤⑥	NR
Ribera (1996) [28]	Spain	MSSA	03/1988–02/1993	1	Mean, STAN: 26.5 COMBO: 27.1	90	45 CLO 2 g q 4 h	45 STAN + GENq	⑧	(5)
Levine (1991) [29]	America	MRSA	24 months	1	Median, STAN: 31 COMBO: 31	42	22 VAN 1 g q 12 h for 28 days	20 STAN + Rif 600 mg po. Qd for 28 days	⑧	NR
Vander Auwera (1985) [30]	Belgium	MSSA or MRSA	Unknown	3	Mean, STAN: 59.3 COMBO: 54.9	29	16 OXA or VAN + placebor	13 STAN + RIFs	⑧	NR
Vander Auwera (1983) [31]	Belgium	MSSA or MRSA	02/1980–07/1981	1	Mean, STAN: 58 COMBO: 48	19	9 OXA or VANt	10 STAN + RIFu	⑧	NR
Korzeniowski (1982) [32]	America	MSSA	Unknown	1	Unknown	78	35 NAFv	43 NAF + GENw	⑧	(5)
Abrams (1979) [33]	America	MSSA	08/1976–12/1977	1	Median, STAN: 27.5 COMBO: 27.5	24	12 OXA/PEN/CEPx	12 STAN + GENy	⑧	NR

ASPs anti-staphylococcal penicillins, CFZ cefazolin, CLO cloxacillin, CXM cefuroxime, CLI clindamycin, CPT ceftaroline, CEP cephalothin, COMBO combination treatment, DAP daptomycin, DIC dicloxacillin, FOS fosfomycin, FLU flucloxacillin, GEN gentamicin, LEV levofloxacin, MSSA methicillin-sensitive S. aureus, MRSA methicillin-resistant S. aureus, NAF nafcillin, NR not reported, OXA oxacillin, PEN penicillin G, RIF rifampin, STAN standard treatment, TEC teicoplanin, VAN vancomycin

^aReceived CFZ (68.6%), CLO (31.4%)

^bReceived CFZ (77.4%), CLO (22.6%), DAP (6 mg/kg/day) for a total of 5 days

^cReceived DAP 10 mg/kg/day

^dReceived DAP (10 mg/kg/day) + FOS 2 g q 6 h intravenously, antibiotic dosage was adjusted according to creatinine clearance

^eReceived VAN (100%), received DAP (3%)

^fReceived VAN (98%), received DAP (4%); FLU, 2 g q 6 h in Australia and New Zealand; CLO, 2 g q 6 h in Singapore and Israel for the first 7 calendar days following randomization

^gReceived VAN (21) or DAP (2, 6 to 8 mg/kg/day adjusted for renal function)

^h6–8 mg/kg/day DAP plus CPT 600 mg q 8 h (adjusted per renal function)

ⁱPrimary active antibiotic treatment (FLU was given to 82% of participants and VAN or TEC to 50% at some point in the primary treatment course)

^jRIF 600 mg or 900 mg for 14 days

^kReceived VAN with adjustment to maintain mean trough levels of 15 mg/l

^lVAN plus intravenous FLU 2 g q 4 h for the first 7 days after randomization

^mReceived DAP 6 mg/kg/day

ⁿVAN 1 g q 12 h or ASPs (NAF, OXA, FLU 2 g every 4 h). GEN (1 mg/kg q 8 h) was administered to the COMBO group (93.0%) and to the STAN group (0.8%) for a median of 4 days

^oReceived ASPs, CLO, or DIC (2 g q 4 h) intravenously. Alternatively, CXM (1.5 g q 6 h), CLI (600 mg q 6–8 h), or VAN (1 g bid) was allowed if a contraindication against the use of penicillins was noted

^pLEV was administered at 500 mg once daily for patients < 60 kg and 500 mg bid for those > 60 kg in weight

^qReceived STAN + GEN (1 mg/kg q 8 h for the first 7 days)

^rReceived OXA (or VAN) plus placebo (150 mg of pyridium bid, orally)

^sReceived OXA 3 g qid or VAN 1 g bid plus RIF 600 mg bid orally

^tReceived OXA 3 g qid or VAN 1 g bid

^uSTAN + RIF 300 mg q 12 h

^vReceived NAF 9–112 g/day (q 4 h) for 6 weeks

^wSTAN + GEN (3 mg/kg/day, q 8 h for the initial 2 weeks)

^xReceived OXA 12 g/day or a cephalosporin (if a history of penicillin allergy existed) for 4 weeks, with PEN substituted if the organism proved sensitive

^ySTAN + GEN (80 mg every 8 h) for the first 2 weeks

Mortality ① all-cause mortality day 7; ② all-cause mortality day 14; ③ all-cause mortality day 28/30; ④ all-cause mortality day 42; ⑤ all-cause mortality day 60; ⑥ all-cause mortality day 90; ⑦ any-cause mortality at TOC (test of cure, visits 6 weeks after the end of therapy); ⑧ in-hospital mortality or death

Safety endpoints (1) any adverse event; (2) serious adverse event; (3) any adverse events leading to treatment discontinuation; (4) any drug-related adverse event; (5) nephrotoxicity

Quality Assessment

Two independent review authors independently assessed the risk of bias for each of the included studies and reached agreement. Figures 2 and 3 also provide a summary of the risk of bias in all included studies. Eleven trials described an adequate random sequence generation process with low risks for selection bias. Nine trials described the methods used for allocation concealment with low risks for selection bias. Three trials were designed in a double-blind model with low risks for performance bias. Four trials were designed with blinding of outcome assessment with low risks for detection bias. We determined that incomplete outcome data (attrition bias) introduced a low risk of bias in eight studies. We determined that seven of the included studies had a low risk of reporting bias, as the study protocols were available, and all outcomes of interest had been reported in the prespecified way.

Fig. 2.

Risk of bias graph: review authors' judgement about each risk of bias item presented as percentages across all included studies

Fig. 3.

Risk of bias summary: review authors' judgement about each risk of bias item for each included study

Primary Outcome

A meta-analysis of the 14 studies including 2360 patients suggested that there was no significant difference in the rate of all-cause mortality between the two groups (RR = 1.00; 95% CI 0.83–1.20; P = 0.99; I² = 0%) (Fig. 4). Subgroup analysis also suggested that there was no significant difference in all-cause mortality between the two groups at 7, 14, 30, 42, 60, and 90 days (Figure S1). Subgroup analysis of pathogen resistance suggested that there was no significant difference in mortality between the two groups, whether the infecting pathogen was MSSA (RR = 0.99; 95% CI 0.79–1.24; P = 0.93; I² = 0%) or MRSA (RR = 0.88; 95% CI 0.53–1.47; P = 0.62; I² = 27%) (Fig. 5). Finally, no statistically significant difference was found in all-cause mortality between the compared treatment arms when the five studies that examined patients with S. aureus endocarditis were analysed (RR = 1.11; 95% CI 0.62–1.99; P = 0.72; I² = 0%) (Fig. 6).

Fig. 4.

Forest plot of the risk ratio (RR) for all-cause mortality in patients with Staphylococcus aureus bacteraemia (SAB)

Fig. 5.

Forest plot of the risk ratio (RR) for all-cause mortality in patients with methicillin-sensitive S. aureus bacteraemia (MSSAB) or methicillin-resistant S. aureus bacteraemia (MRSAB)

Fig. 6.

Forest plot of the risk ratio (RR) for all-cause mortality in patients with S. aureus endocarditis

Other factors that may affect the robustness of the outcome were also analysed by subgroups. The results of the subgroup analysis of the publication year showed that there was also no significant difference in mortality between the two groups (studies published before 2006, RR = 0.89; 95% CI 0.43–1.86; P = 0.76; I² = 4%; studies published in or after 2006, RR = 1.01; 95% CI 0.84–1.22; P = 0.93; I² = 0%). Similarly, the results of subgroup analysis to assess the size of the study population also yielded similar results (number of patients ≥ 200, RR = 1.05; 95% CI 0.85–1.30; P = 0.66; I² = 0%; number of patients < 200, RR = 0.87; 95% CI 0.61–1.25; P = 0.46; I² = 0%). The results of other subgroup analyses showed no significant difference in mortality between the two groups (Table 2).

Table 2.

Subgroup analysis of the effect on all-cause mortality

Subgroup	No. of studies	COMBO (events/total)	STAN (events/total)	Risk ratio (95% CI)	P value	I2%
Year of publication
Before 2006	6	14/143	13/139	0.89 (0.43–1.86)	0.76	4
In or after 2006	8	177/1022	185/1056	1.01 (0.84–1.22)	0.93	0
Number of patients
≥ 200	4	144/847	141/872	1.05 (0.85–1.30)	0.66	0
< 200	10	47/318	57/323	0.87 (0.61–1.25)	0.46	0
Adjuvant agents
BLs	2	40/201	34/203	1.19 (0.78–1.80)	0.42	0
Fosfomycin	1	18/74	22/81	0.90 (0.52–1.53)	0.69	–
Daptomycin	1	10/53	9/51	1.07 (0.47–2.41)	0.87	–
Ceftaroline	1	0/17	7/23	0.09 (0.01–1.46)	0.09	–
Rifampin	5	102/678	87/501	0.66 (0.37–1.19)	0.17	66
Levofloxacin	1	34/191	39/190	0.87 (0.57–1.31)	0.50	–
Gentamicin	4	27/216	21/212	1.24 (0.73–2.13)	0.43	0

STAN standard treatment, COMBO combination treatment, BLs β-lactam antibiotics

Safety Outcome

A meta-analysis of the three studies including 1154 patients suggested that there was no significant difference in the rate of any SAEs between the two groups (RR = 0.97, 95% CI 0.80–1.18; P = 0.78; I² = 19%) (Figure S2). A meta-analysis of 1450 patients in four studies suggested that the combination treatment group had a higher incidence of drug-related AEs than the monotherapy group (RR = 1.68; 95% CI 1.06–2.66; P = 0.03; I² = 67%) (Fig. 7). A meta-analysis of 500 patients in three studies suggested that there was no significant difference in the rate of any AEs leading to treatment discontinuation between the two groups (RR = 1.76; 95% CI 0.72–4.32; P = 0.21; I² = 36%) (Figure S3).

Fig. 7.

Forest plot of the risk ratio (RR) for drug-related adverse events in patients with S. aureus bacteraemia (SAB)

A meta-analysis of seven studies including 1580 patients suggested that combination therapy significantly increased the risk of nephrotoxicity compared with that for monotherapy (RR = 2.30; 95% CI 1.68–3.16; P < 0.00001; I² = 0%) (Fig. 8).

Fig. 8.

Forest plot of the risk ratio (RR) for nephrotoxicity in patients with S. aureus bacteraemia (SAB)

Publication Bias

A funnel chart for the main outcome indicator of all-cause mortality and the publication bias test revealed a basically symmetrical left and right side of the funnel chart, and combined with Egger’s test results (bias, − 0.39; 95% CI − 1.39 to 0.61; P = 0.411), these findings suggested a small possibility of publication bias (Fig. 9).

Fig. 9.

Funnel chart for all-cause mortality indicators by RevMan

Discussion

This meta-analysis summarizes the best available evidence of the administration of combination antibiotic therapy vs. monotherapy for treating SAB. Compared with monotherapy, the combination treatment, regardless of the resistance of the pathogenic bacteria resistance, did not significantly reduce the short- and long-term mortality of patients with SAB. The analysis of patients with S. aureus endocarditis and other evaluable subgroups was consistent with the main results. With respect to safety, although there was no significant difference in the incidence of SAEs or any AEs leading to treatment discontinuation between the two groups, the combination treatment group had more drug-related AEs and nephrotoxicity than monotherapy.

In terms of both clinical burden and absolute number of patients, SAB remains a common and highly morbid infection [34, 35]. The emergence of antibiotic resistance and continued high failure rate, including unacceptable mortality, in patients receiving standard therapies for SAB demonstrate the need for new therapeutic agents and approaches to this disease.

Improved outcomes for patients with SAB have been sought through efforts to enhance antimicrobial efficacy by using combination antimicrobial therapy. In a previous meta-analysis of β-lactams combined with aminoglycosides, rifampicin combined with standard regimens for the treatment of SAB, β-lactams combined with vancomycin, or daptomycin in the treatment of MRSAB, it was suggested that combination therapy cannot significantly reduce the mortality of patients compared with that for monotherapy [17, 18, 36]. The above three meta-analyses are consistent with our results; however, owing to the poor quality and heterogeneity of the studies included in these meta-analyses, convincing clinical data are sparse. Compared with previously published works, this meta-analysis is not limited by the inclusion of non-randomized studies with heterogeneity and confounders. To our knowledge, this study included the largest number of patients from geographically diverse regions. Additionally, almost all the different combination therapies used in the clinic were included in our study.

We performed several sensitivity analyses focusing on more homogeneous subsets of patients, such as those with bacterial endocarditis, to further evaluate our main study question. The results of subgroup analysis also suggested that rifampicin or gentamicin as an adjuvant combined with standard agents did not significantly reduce mortality compared with that for the standard regimen alone, which is consistent with the recommendation of the Infectious Diseases Society of America (IDSA) in 2011 that rifampicin or gentamicin combined with vancomycin is not recommended for the treatment of MRSAB or natural valve endocarditis [34]. Therefore, our results further confirm that the evidence available from the trials analysed does not show any survival benefit for the addition of synergistic drugs to a standard treatment of patients with SAB. In contrast, such an addition can lead to increased nephrotoxicity and drug-related AEs.

At present, many clinical studies and several meta-analyses have suggested that combining antibacterial agents could reduce the risk of microbial failure, recurrence of bacteraemia, and persistent bacteraemia and shorten the duration of bacteraemia in patients with SAB [13–15, 18, 19, 25, 37–43]. However, translating clinical success to survival in critically ill patients with SAB may be difficult and requires in-depth knowledge of the mechanisms and possible confounders contributing to death.

First, combined antimicrobial therapy can synergize sterilization and prevent the emergence of drug resistance, but it also leads to an increase in AEs, which leads to the elimination of the clinical survival benefits provided by combination therapy. An international randomized trial included in our meta-analysis was stopped by the data and safety monitoring board because of apparent futility, as evidenced by the absence of an effect on the composite outcome of death or complications by day 90, together with an imbalance in acute kidney injury (AKI) [14]. In this study, AKI occurred in 23.4% of combination therapy recipients but in only 6.2% of subjects receiving monotherapy (risk difference 17.2%; 95% CI 9.3–25.3; P = 0.001); a greater proportion of the AKI in the combination therapy group was of a higher severity, and the 45-day all-cause mortality of the two groups of patients was 15% and 11%, respectively. In another large (744 participants) multicentre, randomized, double-blind placebo-controlled trial, the effort to harness the potent anti-staphylococcal activity of rifampicin by combining it with standard antibiotic therapy for SAB failed to reduce mortality or bacteriological failure compared to those for standard of care plus placebo (17% vs. 18%; absolute risk difference − 1·4%; 95% CI − 7.0 to 4.3; P = 0.81) [13]. In contrast, a trend towards increased occurrence of drug-modifying AEs (17% vs. 10%; P = 0.004) and renal grade 3–4 AEs (5% vs. 2%; P = 0.053) was noted among rifampicin recipients, as was a significant increase in the occurrence of drug–drug interactions in this study (6% vs. 2%; P = 0.0005). A recent systematic review involving > 2 million participants showed that individuals with AKI were at increased long-term risk for chronic kidney disease, end-stage kidney disease, and death [44]. In this meta-analysis, compared with monotherapy, combination therapy significantly increased the incidence of drug-related AEs and nephrotoxicity, which may explain why combination antibiotics did not provide survival benefits for SAB patients.

Furthermore, combination therapy may have survival benefits for patients with complicated and metastatic bacteraemia with higher mortality, and only some specific combination therapy with less toxicity and more synergistic sterilization can reduce mortality [16, 45]. In contrast to other β-lactam antibacterial drugs, ceftaroline is active against MRSA by binding to PBP2A and inhibiting peptidoglycan transpeptidation. Similar to other β-lactams, ceftaroline enhances daptomycin cell membrane binding. Therefore, ceftaroline combined with vancomycin or daptomycin is theoretically a more effective combination than other combination regimens for patients with MRSAB. A randomized controlled open-label pilot study compared the primary treatment of MRSAB with daptomycin plus ceftaroline with vancomycin. This study was terminated early when an unanticipated mortality difference was noted between the groups: 0/17 in the combination arm vs. 6/23 among vancomycin recipients (P = 0.029). Moreover, there were minimal treatment-related AEs [16]. Another large retrospective matched cohort study (171 participants) compared patients with MRSA bacteraemia treated with standard of care (SOC) treatment versus daptomycin plus ceftaroline. Many of the combination patients were inherently high risk because the combination was used in a salvage role, but despite this consideration, daptomycin-ceftaroline resulted in a numerically lower 30-day mortality rate than SOC (8.3% vs. 14.2%) [46]. However, two recent retrospective cohort studies evaluated the efficacy of the combination of ceftaroline with vancomycin or daptomycin in the treatment of patients with complicated MRSAB. Disappointingly, compared with monotherapy, combination therapy failed to reduce mortality [47, 48]. It is worth noting that the small sample size and inherent biases in clinician choice for selecting combination treatment, whereby those receiving combination treatment are likely at higher risk of treatment failure, should be cautiously interpreted. At present, the contradictory survival benefit results, high cost, and unavailability in most areas necessitate careful implementation of the combination treatment regimen containing ceftaroline without the support of more powerful large-scale randomized controlled trials.

For the management of SAB, reasonable and timely administration of antibacterial drugs is very important, but it is only one important part of many measures. Comprehensive management of SAB involves timely identification of the infecting strain and source of infection, proper choice of antibiotic treatment, and robust prevention strategies [49]. The combination of antibiotics plus a comprehensive clinical approach to managing MRSAB may have a positive impact on patient outcomes. Recently, a 7-year retrospective, quasi-experimental study involving 813 adult MRSAB patients suggested that compared with prepathway (PRE) patients (n = 379), those treated postpathway (POST, n = 434) plus combination treatment (vancomycin or daptomycin combined with β-lactams) had a significant reduction in 30-day (9.7% vs. 15.6%, P = 0.011) and 90-day mortality (12.2% vs. 19.0%, P = 0.007) [50]. Moreover, compared with that in the PRE group, the incidence of AKI in the POST group was similar (9.6% vs. 7.2%, P = 0.282). Notably, most of the adjunctive agents in the combined treatment of this study were cefazolin or cefepime, which avoided the use of ASPs with higher nephrotoxicity [51, 52].

Several limitations should be taken into consideration when interpreting the results of this meta-analysis. These studies included patients with primary bacteraemia or bacteraemia secondary to different infection sites, so employing either monotherapy or combination therapy should be considered depending on the type of infection (e.g., pneumonia, catheter infection, and urinary tract infection). Moreover, we found that very few studies have analysed the impact of possible confounding factors on the mortality of patients in different treatment groups, including the SOFA score, Charlson comorbidity index, age groups, and origin of S. aureus infection (community associated or healthcare associated), and data were not available for meaningful comparisons in these subpopulations. Furthermore, although we performed subgroup analysis of adjuvant drugs in the combined treatment regimen, there were too few evaluable studies on adjuvant drugs other than gentamicin or rifampicin to further evaluate the efficacy and safety of specific adjuvant drugs. It should not be neglected that in this meta-analysis we included comparative trials to examine special patients with endocarditis. For the treatment of endocarditis, whether patients have value replacement surgery will affect the length of antimicrobial treatment and the prognosis of patients. However, due to the limited data, we cannot further evaluate its impact. Finally, only studies published in English were included. This choice could introduce language bias, which may reduce the accuracy of the combined estimates of the treatment effects.

Conclusion

In conclusion, this meta-analysis suggests that in patients with SAB, the choice between combination therapy and monotherapy does not affect mortality rates. In contrast, compared with monotherapy, combination treatment will significantly increase the occurrence of drug-related AEs and nephrotoxicity. Therefore, the results of our current meta-analysis do not support routine combination therapy in patients with SAB as further studies are warranted to evaluate specific antibiotic combinations.

Supplementary Information

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