A pilot randomized controlled trial of 7 versus 14 days of antibiotic treatment for bloodstream infection on non-intensive care versus intensive care wards
The optimal treatment duration for patients with bloodstream infection is understudied. The Bacteremia Antibiotic Length Actually Needed for Clinical Effectiveness (BALANCE) pilot randomized clinical trial (RCT) determined that it was feasible to enroll and randomize intensive care unit (ICU) patients with bloodstream infection to 7 versus 14 days of treatment, and served as the vanguard for the ongoing BALANCE main RCT. We performed this BALANCE-Ward pilot RCT to examine the feasibility and impact of potentially extending the BALANCE main RCT to include patients hospitalized on non-ICU wards.
We conducted an open pilot RCT among a subset of six sites participating in the ongoing BALANCE RCT, randomizing patients with positive non-Staphylococcus aureus blood cultures on non-ICU wards to 7 versus 14 days of antibiotic treatment. The co-primary feasibility outcomes were recruitment rate and adherence to treatment duration protocol. We compared feasibility outcomes, patient/pathogen characteristics, and overall outcomes among those enrolled in this BALANCE-Ward and prior BALANCE-ICU pilot RCTs. We estimated the sample size and non-inferiority margin impacts of expanding the BALANCE main RCT to include non-ICU patients.
A total of 134 patients were recruited over 47 site-months (mean 2.9 patients/site-month, median 1.0, range 0.1–4.4 patients/site-month). The overall recruitment rate exceeded the BALANCE-ICU pilot RCT (mean 1.10 patients/site-month, p < 0.0001). Overall protocol adherence also exceeded the adherence in the BALANCE-ICU pilot RCT (125/134, 93% vs 89/115, 77%, p = 0.0003). BALANCE-Ward patients were older, with lower Sequential Organ Failure Assessment scores, and higher proportions of infections caused by Escherichia coli and genito-urinary sources of bloodstream infection. The BALANCE-Ward pilot RCT patients had an overall 90-day mortality rate of 17/133 (12.8%), which was comparable to the 90-day mortality rate in the ICU pilot RCT (17/115, 14.8%) (p = 0.65). Simulation models indicated there would be minimal sample size and non-inferiority margin implications of expanding enrolment to increasing proportions of non-ICU versus ICU patients.
It is feasible to enroll non-ICU patients in a trial of 7 versus 14 days of antibiotics for bloodstream infection, and expanding the BALANCE RCT hospital-wide has the potential to improve the timeliness and generalizability of trial results.
Clinicaltrials.gov, NCT02917551. Registered on September 28, 2016.
KeywordsBacteremia Bloodstream infection Critical care Intensive care Duration of treatment
- ANZICS CTG
Australian & New Zealand Intensive Care Society Clinical Trials Group
Bacteremia Antibiotic Length Actually Needed for Clinical Effectiveness
Canadian Critical Care Trials Group
Intensive care unit
Randomized clinical trial
Sequential Organ Failure Assessment
The World Health Organization has declared antibiotic resistance a global public health threat, based on rising rates of resistant pathogens and diminishing rates of new antibiotic development . Antimicrobial stewardship is a cornerstone of efforts to counter this threat. However, evidence-informed stewardship treatment decisions for patients with life-threatening illnesses such as bloodstream infections are challenging because little evidence exists for the optimal duration of treatment. Among patients with suspected bloodstream infections, broad-spectrum antibiotics must be initiated empirically because early adequate empiric treatment is associated with improved survival [2, 3]. Due to the rising prevalence of resistant organisms, the tailoring or de-escalation of these empiric regimens is not possible even when blood culture and susceptibility results become available. Patients must then remain on broad-spectrum agents for their full treatment course . Therefore, shortening total treatment durations may be the most feasible approach to minimize patient-level and societal-level antimicrobial harms .
Our systematic review, national practice survey, and observational studies have documented a lack of evidence to guide optimal treatment durations for bloodstream infections, wide variation in clinical practice, and collective equipoise for a trial of 7 versus 14 days of antibiotic treatment for patients with bloodstream infections [6, 7, 8]. Through the Bacteremia Antibiotic Length Actually Needed For Clinical Effectiveness (BALANCE) pilot randomized controlled trial (ClinicalTrials.gov NCT02261506) we documented the feasibility of this trial design among 115 patients in intensive care units (ICUs) . These patients served as a vanguard for the BALANCE main trial (ClinicalTrials.gov NCT03005145), which has recruited more than 600 patients across a growing number of ICU sites and countries.
The Canadian Critical Care Trials Group (CCCTG) and Australian & New Zealand Intensive Care Society Clinical Trials Group (ANZICS CTG) began the BALANCE trial in the ICU setting. As the majority of patients with bacteremia are cared for on general medical and surgical wards, we began to explore hospital-wide expansion to the full population of hospitalized patients with bacteremia as a means to improve the generalizability and timeliness of the BALANCE RCT. We first conducted a distinct BALANCE pilot trial focused on patients admitted to general hospital wards at the BALANCE central study site. We then expanded this approach to several community and academic hospitals participating in the BALANCE trial (ClinicalTrials.gov NCT02917551).
The objectives of this multi-centre BALANCE-Ward pilot RCT were three-fold: (1) to test the feasibility of ward (non-ICU) recruitment into this trial; (2) to compare the patient, pathogen, and outcome characteristics among patients enrolled in the BALANCE-Ward pilot RCT to characteristics in the prior BALANCE-ICU pilot RCT; and (3) to estimate the sample size and non-inferiority margin impacts of merging the BALANCE-Ward pilot with the BALANCE main trial.
General study design
We conducted a pilot RCT of 7 versus 14 days of antibiotic treatment for patients with bloodstream infection, which was identical to our prior BALANCE-ICU pilot RCT [9, 10], except that it focused on patients admitted to general medical and surgical wards. In this BALANCE-Ward pilot trial, as per the prior BALANCE-ICU pilot trial focused on critically ill patients, randomization was determined through a central, web-based system (http://www.randomize.net) with variable block sizes of four to six patients, stratified by site. The intervention related only to the duration of treatment, with patients randomized 1:1 in parallel to 7 versus 14 days of treatment. All other aspects of care (antibiotic selection, doses, intervals, routes of delivery, and timing of hospital discharge) were at the discretion of the clinical team. Participant and clinician blinding and placebo controls were not used given the diversity of pathogens and underlying foci of infection, but allocation concealment was maintained until the seventh day of treatment to mitigate selection bias and differential treatment. The central study team and statistician were blinded to treatment group. The BALANCE-Ward pilot trial was registered separately on Clinicaltrials.gov (NCT02917551), with unique ethics approval at all participating sites, so that enrolled patients could be kept distinct from the main trial until completion of the pilot and evaluation of feasibility.
The BALANCE-Ward pilot trial was launched at Sunnybrook Health Sciences Centre (SHSC) in October 2016, and then after 1 year extended to five other active BALANCE sites, including The Ottawa Hospital (TOH), Kingston General Hospital (KGH), Hamilton General Hospital (HGH), St. Joseph’s Health Centre (SJHC) Toronto, and North York General Hospital (NYGH).
The inclusion criteria differed, by definition, from the prior BALANCE pilot RCT [9, 10] in that we considered all adult patients with a blood culture reported as positive with a pathogenic bacterium while on a non-ICU ward rather than reported as positive while in an ICU. However, the exclusion criteria were unchanged from the BALANCE pilot RCT: previously enrolled patients, those with neutropenia, organ transplantation, prosthetic valves, endovascular grafts, suspected or documented syndromes requiring prolonged treatment (endocarditis, osteomyelitis, undrained abscess, unremoved prosthetic infection), patients with a single positive culture of a common contaminant organism, or bloodstream infection with Staphylococcus aureus, Staphylococcus lugdunensis, or fungal organisms.
Recruitment and consent
Potentially eligible patients were identified through microbiology laboratory reports of positive blood cultures. The site research coordinator screened the medical records of these patients to confirm that they met all inclusion criteria, and no exclusion criteria, and then provided patients with study information materials. Consenting patients could be enrolled any time up to the seventh day of adequate antibiotic treatment .
Primary feasibility outcomes and secondary clinical outcomes
As per the original BALANCE-ICU pilot RCT, the co-primary feasibility outcomes were (1) recruitment rates and (2) adherence to treatment protocol. Protocol adherence was defined as receipt of 7 ± 2 days of antibiotics or 14 ± 2 days of antibiotics for patients randomized to shorter versus longer duration treatment, respectively. We did not target a specific protocol adherence rate to consider the trial feasible, but sought to determine whether the protocol adherence rate would exceed the rate seen in the BALANCE ICU pilot RCT (77%) . As with the BALANCE ICU pilot RCT, we expected that there would be some patients for whom clinicians would continue antibiotic treatment beyond the assigned duration because of concerns of new infection, persistent infection, or previously unrecognized deep-seated infection. These were counted as protocol deviations. The target recruitment rate was an average of one patient per site per month to consider including ward enrolments in the BALANCE main trial. The panel of secondary clinical outcomes (e.g., length of stay, mortality, antibiotic-free days, Clostridiodes difficile, and antibiotic resistant organisms) were identical to those collected in the original BALANCE pilot RCT [9, 10]. Included among these secondary outcomes was the planned primary outcome from the main BALANCE RCT, 90-day mortality. Antibiotic-free days were calculated as the number of days alive and not on any antibiotics in the time period from collection of the index blood culture to 28 days after this date; patients that died prior to day 28 were assigned 0 antibiotic-free days. Treatment adherence and clinical outcomes were recorded by the site research coordinator, via chart review and discussion with the clinical team if needed.
Data collection and follow-up
Patients were followed throughout the hospital stay to a 90-day maximum, with capture of baseline characteristics and outcome information on the same electronic case report form used for the BALANCE main trial. Ninety-day mortality was collected via follow-up phone call 90 days from the index bacteremia.
There were no interim analyses or stopping rules within this pilot RCT. As with our initial BALANCE pilot RCT, we planned a priori to maintain blinding of treatment assignment in the BALANCE-Ward pilot RCT . A feasibility pilot RCT is not powered to identify clinically important differences in safety or efficacy endpoints, but rather this is the goal of the BALANCE main RCT. We analyzed the BALANCE-Ward pilot RCT results as a single cohort, describing overall rates of recruitment per site per month and overall protocol adherence as the co-primary feasibility outcomes of interest.
Next, we compared these feasibility outcomes to those achieved during our initial BALANCE-ICU pilot RCT . Poisson regression was used to compare recruitment rates per month in the ICU versus non-ICU pilots; chi-square test was used to compare protocol adherence. To further evaluate the difference between the two pilot RCTs we compared baseline patient characteristics, pathogens, foci of infection, and clinical outcomes among ward and ICU patients; the chi-square test or Fischer’s exact test were used to compare categorical variables, while a t-test or the Wilcoxon rank sum test were used to compare continuous variables. The Wilson Score method was used to determine 95% confidence intervals. P values were not adjusted for multiple comparisons.
If the BALANCE-Ward pilot demonstrated feasibility, we planned to consider merging the ward-based protocol with the ICU-based protocol of the BALANCE main trial. Therefore, we estimated the percentage of recruited patients that would be enrolled from ICU versus non-ICU wards as a function of the percentage of sites expanding to hospital-wide enrolments. Next, we estimated the impact on overall trial sample size and non-inferiority margins as a function of the proportion of anticipated ICU versus ward enrolments at the time of trial completion. For these calculations we estimated the 90-day mortality for ward patients using outcome data from this ward pilot RCT, and we estimated the mortality for ICU patients from up-to-date data from the ongoing BALANCE main RCT. At the time the ward pilot was completed, 600 patients had been enrolled and reached the 90-day endpoint in the BALANCE main trial.
Sample size calculation
We sought to enroll a minimum of 115 patients (to equal the sample size of our BALANCE-ICU pilot) , but to improve generalizability of the BALANCE-Ward pilot trial we planned to continue enrolment until successful enrolment of at least one patient at all five additional non-central study sites. Recruitment extended from 17 October 2016 to 12 December 2018.
Screened, eligible, and randomized patients
BALANCE-Ward pilot randomized clinical trial feasibility outcomes, overall and by site
Hospital type (bed size)
Number (%) enrolled
Recruitment rate (/month)
Protocol adherence (%)
A total of 134 patients were recruited over 47 site-months (mean 2.9 patients/site-month; Table 1). The recruitment rate varied across the six participating sites: hospital A (4.1 patients per month, over 26.9 months), hospital B (4.4 patients/month, over 3.6 months), hospital C (1.1 patient/month, over 3.7 months), hospital D (0.1 patients per month, over 6.7 months), hospital E (1.0 patients/month, over 1 month), and hospital F (0.4 patients/month, over 5.1 months) (Table 1). The overall recruitment rate significantly exceeded the recruitment rate in the BALANCE-ICU pilot RCT (2.9 patients/site-month vs 1.1 patients/site-month, p < 0.0001).
The overall adherence to treatment duration protocol was 125/134 (93%), with minimal variation across study sites: SHSC 103/110, SJHC 15/16, TOH 1/1, KGH 1/2, NYGH 4/4, HGH 1/1 (Table 1). Overall protocol adherence significantly exceeded the adherence achieved in the BALANCE-ICU pilot RCT (125/134, 93% vs 89/115, 77%, p = 0.0003).
Patient, infection, and pathogen characteristics
Patient, pathogen, and infection characteristics in the BALANCE-Ward pilot RCT compared to the BALANCE-ICU pilot RCT
n = 134
n = 115
Age in years
SOFA score on day 0
Coronary artery disease
Congestive heart failure
Peripheral vascular disease
Chronic obstructive pulmonary disease
Acquisition of bacteremia
Source of bacteremia
Skin and/or soft tissue
Most commonly isolated pathogens in blood culturesb
Coagulase negative staphylococci
Streptococcus anginosus group
Clinical outcomes in the BALANCE-Ward pilot RCT compared to the BALANCE-ICU pilot RCT and updated data from the BALANCE main RCT
BALANCE Ward Pilot
n = 134
BALANCE ICU pilot
n = 115
BALANCE Main RCTa
n = 600
P value Ward pilot vs ICU pilot
P value Ward pilot vs main RCT
At 90 daysb
Length of stay in hospital (in days)
Relapse of bacteremia
Antibiotic-free days (by day 28)
Antimicrobial-related adverse outcomes
Acute kidney injury
Clostridiodes difficile infection
Secondary infection with resistant microorganisms
Modeling the final proportion of patients that would be enrolled in ICU versus non-ICU settings
Modeling sample size and non-inferiority margin implications of merging non-ICU ward patients into the BALANCE main RCT
In the prior BALANCE-ICU pilot RCT we demonstrated that it was feasible to enroll ICU patients into a trial of 7 versus 14 days of treatment for bloodstream infection , thereby providing the vanguard patients for the multinational, multicentre BALANCE main RCT. In this subsequent BALANCE-Ward pilot RCT, we have confirmed that it is feasible to enroll patients cared for on general hospital wards and have clarified the viability and implications of expanding the BALANCE main RCT to include hospital-wide patients with bacteremia.
The BALANCE-Ward pilot RCT documented feasibility with respect to both co-primary outcomes of recruitment rate and protocol adherence. We achieved mean recruitment rates of 2.9 patients per site-month; the median recruitment rate per site per month was lower (1.0) but still met our feasibility target. Similarly, we achieved protocol adherence rates of 93%, which exceeded the 77% adherence rates in the ICU population. On the basis of these co-primary outcomes it appears feasible that the BALANCE RCT could be extended from ICUs to include non-ICU patients. The increased recruitment rate on the wards can be attributed to the larger number of bacteremic patients than those who are in the ICU. The superior protocol adherence rates on the general wards may be due to the lower severity of illness and lower risk of secondary nosocomial infections among these patients with shorter lengths of hospital stay and fewer indwelling devices such as endotracheal tubes and central venous catheters.
As expected, there were some measurable differences in critically ill patients with bacteremia enrolled in the initial BALANCE pilot compared to the patients on the wards who were enrolled in this pilot. The latter were older, had lower severity of illness at baseline, and more commonly had community-acquired bacteremia, genito-urinary sources of infection, and E. coli as a causative pathogen. On the one hand, merging non-ICU patients with ICU patients into a single trial could be viewed as mixing two heterogeneous populations together. On the other hand, combining these patients together could be considered as reflecting a broader population of patients with bloodstream infection, yielding more generalizable trial results. The ICU and non-ICU pilot trial patients were both infected with a diverse range of Gram negative and Gram positive bacterial pathogens, and each included patients with a diverse range of host comorbidities. Typically a trial based on a specific diagnosis (e.g., pulmonary embolism, myocardial infarction) would be conducted across the full spectrum of severity, including those patients admitted to ICU and non-ICU wards. Conceptually, enrolling both non-ICU and ICU patients captures the full spectrum of bacteremic illness, and the patients are only dichotomized by the location of care within the hospital.
The 90-day mortality rate in this pilot RCT (12.8%) was similar to the mortality rate seen in a recently published RCT of 604 patients allocated to 7 versus 14 days of antibiotics for patients with Gram negative bacteremia conducted on non-ICU wards in three centers in Israel and Italy . As expected, the 90-day mortality rate was lower than that seen in our prior BALANCE-ICU pilot RCT (15%) . The mortality difference between non-ICU and ICU patients is even wider than the ICU pilot data suggest, because a more updated mortality estimate from the BALANCE main trial suggests that the mortality has risen to 17.3%. At a fixed non-inferiority margin of 4%, adding non-ICU ward patients in the study would decrease our total sample size requirement (Fig. 3); maintaining our sample size target would enable us to reduce the achievable absolute non-inferiority margin (Fig. 4). It is important to note that our 4% non-inferiority margin is already much smaller than the non-inferiority margins used in recent trials of antibiotic treatment duration in patients with serious bacterial infections [12, 13, 14, 15], and is also much lower than the US Federal Drug Administration recommendation of non-inferiority margins for ventilator-associated pneumonia . Therefore, we have opted to maintain our current overall sample size target (n = 3626) for the BALANCE main trial.
Our BALANCE-Ward pilot RCT enrolled patients in six sites, and so we cannot be certain that the recruitment and adherence results would be generalizable to all of the sites involved in the BALANCE main RCT. However, the generalizability is bolstered by inclusion of a mix of both community and academic hospitals, as well as sites with long-standing versus recent involvement in the CCCTG. Another limitation is that we cannot predict whether expansion to include non-ICU enrolment will lead to a compensatory decrease in ICU recruitments by diluting study teams’ efforts across broader clinical units. In our six pilot RCT sites, though, we did not see reductions in ICU recruitments. As BALANCE is expanded hospital-wide, we will assess the interplay of ICU and non-ICU recruitment rates over time. The low rate of enrolment of eligible ward patients, and wide variation across sites, suggests that further efforts may be necessary to foster enrolments, including educating ward clinicians about the pre-RCT work which has documented practice heterogeneity and collective clinical equipoise. The BALANCE-Ward pilot RCT experience suggests that sites with infectious diseases engagement on the study team achieve much higher recruitment rates and percent enrolment of eligible patients, and so this will be crucial for future sites considering hospital-wide recruitment. We will also need to track eligible non-enrolled patients, along with recruitment rates and protocol adherence, as a site-specific metric throughout the conduct of the trial.
The BALANCE steering committee and CCCTG have guided us in conducting step-wise pilots of the BALANCE RCT protocol in the initial ICU population, and now in this non-ICU population, once again confirming the feasibility of the BALANCE trial design on general hospital wards. We have carefully reviewed the one-group findings (maintaining allocation concealment) with the CCCTG and the BALANCE international steering committee, both of which have strongly endorsed the option for participating BALANCE sites to extend enrolments hospital-wide. Given the success of this non-ICU pilot, no other protocol changes are required to facilitate inclusion of non-ICU patients in the BALANCE main trial. A detailed statistical analysis plan involving the entire cohort will be published before the trial is completed; randomization will be stratified by ICU and non-ICU ward location, and a subgroup analysis will be conducted. The subgroup analyses, by definition, will not be powered to achieve the same non-inferiority margin as the overall BALANCE trial population. However, the achievable non-inferiority margins within the ICU and non-ICU subgroups will still be less than the non-inferiority margins used in recent landmark antimicrobial minimization studies involving patients with serious bacterial infections [4, 13, 14, 15]. We anticipate that the final BALANCE trial results will be more generalizable to the full population of patients admitted to hospital with bloodstream infections, and yet will include a majority of critically ill patients, ensuring that the data are relevant to our sickest of patients. In doing so, we hope that BALANCE will provide an evidence foundation for the treatment of a broad range of patients with non-S. aureus bacteremia, and allow us to maximize the benefits while minimizing the harms of antimicrobial treatments for bloodstream infections.
We would like to acknowledge the extraordinary efforts of the research coordinators at each participating site in screening and enrolling eligible patients, including Kanthi Kavikondala, Miranda Hunt, Shelley Acres, Rebecca Porteous, Irene Watpool, Alexandra Sabev, Nevena Savija, Katrina Fimiani, Alexandra Lostun, and Rizani Ravindran. We also like to acknowledge the crucial contributions of Lisa Buckingham and Nicole Zytaruk at the CLARITY methods centre in helping to develop the electronic case report form and database. We thank Allan Garland and Kirsten Feist for providing internal manuscript review within the CCCTG.
ND and RAF conceived and designed the study, obtained funding, developed the statistical analysis plan, database development, drafted the manuscript, and are responsible for overall management and supervision. AHR participated in the study design, helped develop paper and electronic CRF and web randomization and drafting of the manuscript. RP contributed to the study design, provided statistical and methodological expertise, and helped draft the manuscript. YA, EPBC, RC, MD, DJC, RH, SM, LM, JM, RP, SR, BR, YS, PS, and RW participated in the study design, contributed to writing grant applications, and helped in reviewing and revising the manuscript for intellectual content. All the authors have reviewed and approved the manuscript for publication.
Supported by grants from Ontario Ministry of Health and Long-Term Care Academic Health Sciences Centre Alternative Funding Plan (AFP) Innovation Fund Awards, Canadian Frailty Network (CFN) and Canadian Institute of Health research (CIHR).
Ethics approval and consent to participate
Ethics approval was granted by the Clinical Trials Ontario, provincial REB. Informed consent was obtained from all study participants.
Consent for publication
Dr. Rob Fowler is supported by a personnel award from the Heart and Stroke Foundation, Ontario Provincial Office. Dr. Deborah Cook holds a Canada Research Chair of Research Transfer in Intensive Care.
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