TY - JOUR
T1 - External Validity of a Randomized Controlled Trial on Duration of Antibiotics for the Treatment of Gram-Negative Bacteremia
AU - Turjeman, Adi
AU - Koppel, Fidi
AU - Franceschini, Erica
AU - Yahav, Dafna
AU - Dolci, Giovanni
AU - Bacca, Erica
AU - Babich, Tanya
AU - Khazem, Ebtehal
AU - Baum, Eyal
AU - Nassar, Rima
AU - Bitterman, Roni
AU - Dishon-Benatta, Yael
AU - Hassoun-Kheir, Nasreen
AU - Santoro, Antonella
AU - Eliakim-Raz, Noa
AU - Poran, Itamar
AU - Pertzov, Barak
AU - Stern, Anat
AU - Dickstein, Yaakov
AU - Maroun, Elias
AU - Raines, Marina
AU - Meschiari, Marianna
AU - Bishara, Jihad
AU - Goldberg, Elad
AU - Venturelli, Claudia
AU - Sarti, Mario
AU - Mussini, Cristina
AU - Paul, Mical
AU - Leibovici, Leonard
N1 - Publisher Copyright:
© 2022 S. Karger AG, Basel. Copyright: All rights reserved.
PY - 2023/3/1
Y1 - 2023/3/1
N2 - Introduction: Reports regarding the external validity of randomized controlled trials (RCTs) are scarce. We aimed to assess the population external validity of an investigator-initiated RCT on the duration of antibiotics for the treatment of Gram-negative bacteremia by comparing patients included in the RCT to patients that were not included in the trial. Methods: Hospitalized patients with Gram-negative bacteremia were recruited into an RCT and randomized to receive 7 or 14 days of covering antibiotic therapy in Israel and Italy from 2013 to 2017. In a concomitant observational study, RCT participants were compared with patients who fulfilled the inclusion criteria but were not included in the trial due to participation in other trials, discharge before approached by researchers, refusal to participate, or unwillingness of the treating physician to allow participants' recruitment. Results: Six hundred and four RCT patients were compared with 613 nonincluded patients. Almost 50% of nonincluded patients (288/613) were dependent on others for activities of daily living at baseline compared to 37.7% of RCT participants (228/604). Dementia was nearly 2-fold more frequent in nonincluded patients than those included (5.9% [36/613] versus 3.6% [22/604], p = 0.07). Patients who were not included in the RCT were more likely to acquire their infection in the hospital (53.3% [327/613] versus 29.1% [176/604], p < 0.001). The primary composite outcome of mortality, clinical failure, readmissions, or extended hospitalization at 90 days occurred in 353 of 613 nonincluded patients (57.6%) compared to 299 of 604 RCT participants (49.6%), p = 0.005. However, on multivariate analysis noninclusion in the RCT was not an independent risk factor for clinical failure and mortality. Conclusions: RCTs, even with broad eligibility criteria, do not represent the whole spectrum of patients and leave out a population with more severe illness for whom the evidence is lacking.
AB - Introduction: Reports regarding the external validity of randomized controlled trials (RCTs) are scarce. We aimed to assess the population external validity of an investigator-initiated RCT on the duration of antibiotics for the treatment of Gram-negative bacteremia by comparing patients included in the RCT to patients that were not included in the trial. Methods: Hospitalized patients with Gram-negative bacteremia were recruited into an RCT and randomized to receive 7 or 14 days of covering antibiotic therapy in Israel and Italy from 2013 to 2017. In a concomitant observational study, RCT participants were compared with patients who fulfilled the inclusion criteria but were not included in the trial due to participation in other trials, discharge before approached by researchers, refusal to participate, or unwillingness of the treating physician to allow participants' recruitment. Results: Six hundred and four RCT patients were compared with 613 nonincluded patients. Almost 50% of nonincluded patients (288/613) were dependent on others for activities of daily living at baseline compared to 37.7% of RCT participants (228/604). Dementia was nearly 2-fold more frequent in nonincluded patients than those included (5.9% [36/613] versus 3.6% [22/604], p = 0.07). Patients who were not included in the RCT were more likely to acquire their infection in the hospital (53.3% [327/613] versus 29.1% [176/604], p < 0.001). The primary composite outcome of mortality, clinical failure, readmissions, or extended hospitalization at 90 days occurred in 353 of 613 nonincluded patients (57.6%) compared to 299 of 604 RCT participants (49.6%), p = 0.005. However, on multivariate analysis noninclusion in the RCT was not an independent risk factor for clinical failure and mortality. Conclusions: RCTs, even with broad eligibility criteria, do not represent the whole spectrum of patients and leave out a population with more severe illness for whom the evidence is lacking.
KW - Dementia
KW - External validity
KW - Gram-negative bacteremia
KW - Mobility
KW - Randomized controlled trial
UR - http://www.scopus.com/inward/record.url?scp=85141260232&partnerID=8YFLogxK
U2 - 10.1159/000526480
DO - 10.1159/000526480
M3 - ???researchoutput.researchoutputtypes.contributiontojournal.article???
C2 - 36273449
AN - SCOPUS:85141260232
SN - 0304-324X
VL - 69
SP - 312
EP - 320
JO - Gerontology
JF - Gerontology
IS - 3
ER -