Results
Description of cohort
226 patients were recruited into the cohort with complete data for 222 patients (refer Additional file
1). The population was predominantly male, Australian-born, and non-indigenous, with a median age of 62 years (interquartile range [IQR] 49-76) (Additional file
2: Table S1). Among the 51 patients (23.0%) who were admitted to the intensive care unit (ICU), the reason was directly related to SAB in 64% (32/50; 1 response not received). The main reasons for ICU transfer were haemodynamic support (10/51, 19.6%) and organ support for two or more systems (12/51, 23.5%).
Patient exposures, comorbidities and disease severity
The most common potential exposures for acquisition of
S. aureus prior to SAB onset included companion animal exposure, recent hospitalisation, recent healthcare attendance, and prior antibiotic therapy (Additional file
2: Table S1). Vancomycin accounted for almost one-quarter of antimicrobials used in those with prior antibiotic therapy (17/75, 22.7%; 2 responses not received). In patients where data were available, known prior colonisation with
S. aureus was also a potential exposure (34/75, 45.3%). The most frequent comorbidities were cardiovascular disease, diabetes mellitus and chronic kidney disease (Additional file
2: Table S1). Dialysis was required in 25/48 (52.1%) patients with pre-existing end-stage renal disease, of which 14 (56.0%) were through a native arteriovenous fistula.
Clinical and laboratory features
The most common clinical manifestations associated with SAB were: device-associated (81/222, 36.7%), osteoarticular (59/222, 26.6%), skin or soft tissue infection (46/222, 20.7%), uncomplicated bacteraemia (28/222, 12.6%), endocarditis (25/222, 11.3%), pneumonia (15/222, 6.8%), deep abscess (13/222, 5.9%), epidural abscess (10/222, 4.5%), severe sepsis including septic shock (7/222, 3.2%), central nervous system (1/222, 0.5%), and unknown foci (1/222, 0.5%); 22 patients (9.9%) had other manifestations not specified including intra-abdominal, urinary, septic thrombophlebitis, mediastinitis or ophthalmic foci. Echocardiography was performed in 91.9% (204/222) patients; the majority received transthoracic echocardiography alone (110/204, 53.9%). Endocarditis was mainly native valve (19/25, 76.0%) and left-sided (17/25, 68.0%). The most common device-associated infections were peripheral intravenous catheters (27/81, 33.3%), haemodialysis access (10/81, 12.3%), orthopaedic devices (10/81, 12.3%), and peripherally-inserted central venous catheters (7/81, 8.6%). Implanted devices were present in 69 patients (31.1%); 41/69 (59.4%) manifest as device-associated infection with SAB. In patients with device-associated infection, the device was removed in 75.3% (61/81) within a median of one day (IQR 0-2) of SAB onset.
Laboratory features included a median white cell count of 11.3 x10
9/L (IQR 8.1-16.9), median C-reactive protein (CRP) of 170.5 mg/L (IQR 100-277.6) [reference range <10 mg/L] and median albumin of 30 g/L (IQR 26-34). Acute renal failure at the onset of SAB [
9] was present in 22.1% (49/222).
Microbiologic features
MRSA accounted for 25.7% (57/222) of all episodes of SAB. The median duration of bacteraemia was one day (IQR 1-3 days), with the longest duration of 13 days in a patient with recurrent bioprosthetic aortic valve endocarditis and a chronic forearm wound with failed split skin grafting. Elevated vancomycin MIC ≥ 1.5 mg/L was present in 39.2% (87/222) using Etest® and 32.9% (73/222) using BMD.
Treatment
There was significant variability in antimicrobial treatment – antibiotics during a treatment course changed for a variety of reasons such as concurrent non-S. aureus infection requiring broader spectrum, toxicity, allergy or intolerance; thus the predominant definitive treatment received was flucloxacillin in 59.0% (131/222), vancomycin in 26.1% (58/222), and other antibiotics in 14.9% (33/222). Within the first seven days of therapy, the median flucloxacillin daily dose was 8 g (IQR 8-10.4 g) and the median vancomycin daily dose was 22.2 mg/kg (IQR 16.0-29.9 mg/kg). Nine patients with MSSA bacteraemia received vancomycin as the predominant antibiotic treatment; five of these had previous or new allergy or intolerance to β-lactams. Empiric treatment was adequate in 95.5% (212/222) of patients; in the 10 patients who received inappropriate empiric therapy, all had MRSA bacteraemia and received beta-lactams or aminoglycosides as initial therapy. In patients treated with definitive vancomycin, the median vancomycin trough concentration within 96 hours of treatment was 18 mg/L (IQR 14.2-22 mg/L).
One-third (74/222, 33.3%) of patients required surgical management as part of therapy; this included procedures to remove implanted devices such as prostheses and portacaths as well as aspiration, drainage or debridement.
In-hospital complications
Forty-five percent (100/222) of patients experienced at least one pre-defined complication during hospitalisation: persistent renal impairment not returning to baseline within 30 days after onset of SAB (35/222, 15.8%), requirement for inpatient rehabilitation (35/222, 15.8%), hospital-acquired infection other than SAB (30/222, 13.5%), persistent fevers ≥ 7 days (24/222, 10.8%), metastatic infection beyond the primary site of infection (17/222, 7.7%), venous thrombosis (7/222, 3.2%), and pressure (decubitus) ulcer (3/222, 1.4%).
Adverse drug reactions (ADR) attributed to antimicrobial therapy occurred in 13.6% (30/221). These were attributed mainly to flucloxacillin (20/30, 66.7%) and vancomycin (7/30, 23.3%) but also included linezolid (1/30, 3.3%) and piperacillin-tazobactam (1/30, 3.3%); in two cases it was difficult to determine which antimicrobial was implicated, and one patient experienced ADR with two antibiotics at different time points during treatment. Of these ADRs, eight (8/30, 26.7%) were considered serious [
13] such as sensorineural hearing loss (vancomycin), Stevens-Johnson syndrome (vancomycin), angioedema (flucloxacillin), and fevers requiring re-admission to hospital (vancomycin). Nephrotoxicity occurred in 19.5% (43/221) occurring in 14/58 (24.1%) patients receiving definitive vancomycin compared with definitive flucloxacillin (24/131, 18.5%) or other antimicrobials (5/33, 15.2%) (
p=0.526). No patients classified with nephrotoxicity underwent renal biopsy to confirm antibiotic-induced kidney injury. Many patients (65.6%, 145/221) also received concomitant potential nephrotoxins regardless of kidney injury; these included Angiotensin Converting Enzyme Inhibitors (ACEIs) or Angiotensin Receptor Blockers (ARBs) (19/145, 13.1%), loop diuretics (17/145, 11.7%), radiocontrast dye (16/145, 11.0%), and non-steroidal anti-inflammatory drugs (NSAIDs) (14/145, 9.7%). Concomitant aminoglycosides (except those used in empiric treatment) were only prescribed in 1.4% (2/145). Concomitant nephrotoxins were prescribed more frequently in vancomycin-treated patients (40/57, 70.2%) in association with higher nephrotoxicity rates compared with flucloxacillin-treated patients (79/131, 60.3%).
Clinical outcomes
The composite 30-day endpoint of persistent bacteraemia, recurrent bacteraemia or all-cause mortality was present in 14.4% (32/222). Thirty-day all-cause mortality was 9.5% (21/222), of which the majority were directly attributed to SAB (15/21, 71.4%). More than two thirds were still receiving anti-staphylococcal antibiotics (132/199, 66.3%) at 30 days. The median length of hospital stay after onset of SAB was 30 days (IQR 17-46 days); in some jurisdictions this included home parenteral antibiotic therapy. All-cause mortality at 6 months and 12 months was 19.1% (42/220) and 24.2% (53/219) respectively.
Factors associated with 30-day treatment failure
Many variables were identified as potentially significant (
p<0.2) for inclusion in the multivariable logistic regression model (Table
1). However with the low event rate, the number of candidate variables was restricted
post-hoc to variables with
p<0.1. Prior to model selection, we removed variables that were expected to be collinear or were directly related to outcome, eg. presence of DNR order is directly linked with mortality and was excluded. Age is part of APACHE II or SAPS II score however as these scores were validated in ICU populations, we elected to use age as the representative variable for inclusion. Patients with dementia are likely to reside in a long-term care facility, so we elected to use dementia rather than residence in a long-term care facility. Using backward stepwise elimination, variables that were associated with 30-day treatment failure were age > 70 years, Pitt bacteraemia score ≥ 2, CRP at onset of SAB > 250 mg/L, and persistent fevers after SAB onset. Elevated vancomycin MIC was not associated with treatment failure in this cohort. Higher serum albumin at onset of SAB, performing echocardiography, receipt of appropriate empiric therapy, and recent healthcare attendance prior to SAB onset were protective. Goodness of fit of the final model appeared to be satisfactory (Hosmer-Lemeshow statistic 4.82,
p=0.777).
Table 1
Final multivariable logistic regression model of risk factors for treatment failure at 30 days in patients with SAB
Age > 70 years | <0.001 | 4.13 | 1.54-11.07 | 0.005 |
Albumin (g/L) | <0.001 | 0.88 | 0.80-0.96 | 0.003 |
CRP > 250 mg/L | 0.002 | 5.41 | 1.93-15.19 | 0.001 |
Persistent fevers | 0.029 | 6.65 | 1.73-25.62 | 0.006 |
Healthcare attendance | 0.003 | 0.13 | 0.03-0.59 | 0.008 |
Pitt bacteraemia score ≥ 2a | 0.04 | 2.94 | 1.03-8.39 | 0.044 |
Echocardiogram performed | 0.092 | 0.23 | 0.06-0.94 | 0.041 |
Appropriate empiric treatment | 0.018 | 0.14 | 0.02-0.85 | 0.032 |
DNR orderb | <0.001 | | | - |
WCC (x 109/L) | 0.048 | | | - |
ICU admission | 0.003 | | | - |
APACHE II score > 11.5b | 0.003 | | | - |
Combination treatment > 7 days | 0.026 | | | - |
Severe sepsis | 0.029 | | | - |
Body mass index (kg/m2) | 0.037 | | | - |
Directed vancomycin treatment | 0.044 | | | - |
Dementia | 0.055 | | | - |
Directed flucloxacillin treatment | 0.058 | | | - |
Nephrotoxicity | 0.068 | | | - |
ARF at onset of SAB | 0.07 | | | - |
Residence in LTCFb | 0.09 | | | - |
Female sex | 0.091 | | | - |
MRSA | 0.098 | | | - |
Discussion
Results from this cohort have generated new insights about clinical features, treatment, and complications of SAB, and reinforced data from previous studies. The major findings from this study include lower than expected 30-day treatment failure and all-cause mortality, persistently high longer-term mortality, and morbidity from significant in-hospital treatment complications in patients with SAB in Australia. Whilst a number of strategies have undoubtedly impacted on short-term mortality rates, future research and interventions need to be directed at reducing other morbidity associated with treatment and hospitalisation for SAB.
Community-onset MSSA is still the predominant cause of SAB in Australia and tends to affect older males [
14]. Among the multiple potential risk factors for acquisition of
S. aureus analysed, the most frequent was animal exposure; however no sampling or testing of animal isolates was performed to determine any similarities between human-animal pairs. International travel has also been implicated in the spread of MRSA clones [
15] however this was not a common risk factor for
S. aureus acquisition in our cohort; this may be in part due to the presence of more MSSA in our study, and the relationship between travel and spread of MSSA clones is less well established. In addition, higher BMI was associated with treatment failure on univariate analysis, and obesity has been associated with an increased risk of colonisation with
S. aureus [
16], antibiotic treatment failure and mortality [
17,
18].
In-hospital complications associated with SAB can be attributed to underlying host factors and complications related to the disease, hospitalisation, and treatment administered. Here we see a significant burden of persistent renal impairment after SAB, nosocomial infections, persistent fevers and vascular thrombosis during hospitalisation, and that almost one in six patients experienced an adverse event attributed to antimicrobial therapy. Although not statistically significant, nephrotoxicity was numerically more frequent in patients receiving definitive vancomycin compared with flucloxacillin, although concomitant nephrotoxins were also prescribed more frequently in vancomycin-treated patients. Whilst risk factors for vancomycin-associated nephrotoxicity have been established, such as higher steady state concentrations [
11,
19], higher daily dosage [
10], longer duration of exposure [
19], and ACEI or ARBs [
20], it is difficult to determine causality due to concomitant nephrotoxins and changing renal function and haemodynamics as a consequence of the infection itself [
21]. Although infrequent, renal toxicity also occurs in anti-staphylococcal penicillins (ASP) [
22,
23] and can occur early in therapy [
24]; multiple studies have reported higher rates of adverse events including acute kidney injury in patients receiving ASP compared with cefazolin [
25‐
29]. However little is known about predictors of nephrotoxicity in flucloxacillin-treated patients, and this should be a focus of future research. Venous thrombosis is a recognised common complication of short- and long-term central venous catheter-related SAB [
30], and it is possible that the effects of
S. aureus surface proteins and exotoxins on the coagulation pathway may also contribute to vascular thrombosis in the absence of venous catheters [
31].
An unexpected finding was the low rate of 30-day treatment failure (14.4%) in the cohort, predominantly driven by very low all-cause mortality (9.5%). Recent but not contemporaneous studies in Australia and New Zealand reported 30-day mortality rates of 17-20% [
1,
32,
33] and although mortality rates have been reported as low as 6.8-13% in studies from Finland, Iceland and Taiwan, the vast majority of patients in these cohorts had MSSA bacteraemia [
34‐
36]. In a pooled analysis of over 3300 patients from 5 large multi-centre international studies [
14] 30-day mortality was 21% - much higher than the current study. There may be multiple reasons for this. First, identification of an infective focus was determined in 99.5% of our patients; the absence of an identified focus has been strongly associated with mortality [
14]. Second, more than 95% of our patients received adequate empiric therapy, ensuring appropriate coverage in the first few critical days of therapy, and serum vancomycin levels were therapeutic early in therapy in those treated with vancomycin. Third, there was attention to focus eradication and source control as this is crucial in SAB management [
37]; more than one-third of our patients required formal surgical management, three-quarters had their device removed within a median of 24 hours after the onset of SAB, and more than 91% underwent echocardiography. Fourth, there were fewer isolates with elevated vancomycin MIC (compared with our previous work [
1]) which has been associated with treatment failure and mortality [
38]. This may be due to different
S. aureus genotypes in this cohort, and typing is underway. Fifth, mortality rates in critically ill patients with severe sepsis in Australia and New Zealand have fallen from 2000 to 2012 [
39]; this secular trend is contemporaneous with our current study and suggests that supportive care and management of these patients have improved over this time and led to the favourable clinical outcomes found in our cohort. Although we did not specifically record formal ID consultation, all the participating hospitals had guidelines for ID consultation in patients with SAB. Furthermore 30-day mortality rates in patients with SAB have also fallen in our region from 20.6% in 2007-2008 [
32] to 14.4% in 2013 [
40]. Sixth, bias may have been introduced as time dependent variables will have changed the number of patients at risk for the outcome assessment and are not captured in a logistic regression analysis. Finally, there may have been an unintended bias from our enrolment strategy towards less critically ill patients or towards patients where treatment success was more likely. As informed consent was required to participate it was not appropriate to consent patients where death was imminent; some patients with severe disease and early death from or with SAB were therefore not included.
All-cause mortality continues to increase in patients following an episode of SAB, and this has also been noted in the literature [
41‐
43]. Although we did not determine attributable mortality at 6-months and 12-months, the increased mortality seen is likely to reflect patient age and comorbidities as well as the consequences of complications that occur after an episode of SAB; our study demonstrates that in-hospital complications are frequent and cause morbidity that persist beyond 30 days and may contribute to overall increased mortality in the medium term.
Elevated vancomycin MIC was detected in approximately one-third of our isolates, yet interestingly there was no association with increased mortality or treatment failure. We have previously observed inferior clinical outcomes such as mortality or complicated infection in patients whose isolates have an elevated vancomycin MIC [
1], and others have also reported similar findings even among patients with MSSA bacteraemia [
44‐
46]. However the association between vancomycin MIC and poor clinical outcomes has been contentious. In the systematic review and meta-analysis performed by van Hal
et al. [
38] elevated vancomycin MIC was associated with a higher mortality rate in patients with MRSA infections, regardless of the source of infection or MIC methodology. In contrast Kalil
et al. [
47] found no statistically significant difference in mortality in patients with SAB. Even when assessing vancomycin MIC by the Microscan method, there was no difference in 90-day mortality, readmission or recurrence in a prospective single centre cohort [
48]. Moreover there are also problems with the definition of elevated vancomycin MIC and differences in MIC methodology, so currently there are limited data to support changing clinical practice as a result of vancomycin MIC testing in order to improve clinical outcomes [
49‐
51].
Predictors associated with treatment failure in this study, notwithstanding the low event rate of 30-day treatment failure, comprised clinical and biochemical variables that are easily obtained during the initial evaluation of a patient with SAB such as age, Pitt bacteraemia score, serum albumin and CRP. Significant elevations in CRP have also been associated with mortality in bacteraemic patients [
52] and treatment failure in MRSA bacteraemia [
53]. Recent healthcare exposure was associated with lower treatment failure; possible explanations may include higher incidence of uncomplicated line-associated bacteraemia, earlier hospital presentation when unwell, or earlier appropriate MRSA therapy in patients known to be colonised. Persistent fevers and performing echocardiography were also predictors of treatment response and this is presumably related to underlying source identification and focus eradication as important adjuncts in SAB management. Appropriate empiric therapy was also associated with lower treatment failure, consistent with the literature that delays in appropriate therapy are associated with inferior outcomes [
54,
55], although confounding by indication has also been observed when evaluating appropriate antibiotic therapy [
56]. The wide confidence intervals for the odds ratios in the multivariable analysis reflect the low event rate of treatment failure and are another potential limitation of the study.
Acknowledgements
The authors would like to acknowledge Yuen Su (Liverpool Hospital), Paul M. Griffin (Princess Alexandra Hospital), Mohammad Bagherirad, Sarah C. Boyd, Anthony Kwan Fu Htin (Barwon Health), Ainsley Swanson, and Sze K. Lim (Monash Health) who assisted with data collection and initial manuscript revision. The authors would also like to acknowledge Janine Trevillyan, Bradley Gardiner and James Pollard for additional data clarification, Wei Gao for being the second observer for reading minimum inhibitory concentrations for all tested blood culture isolates, and the microbiology laboratory and phlebotomy staff at all participating hospitals.