ABSTRACT
The objective of this study was to compare the rate of pneumonia resolution in obese (body mass index [BMI], ≥30 kg/m2) and nonobese (BMI, <30 kg/m2) patients treated with 1 gram ertapenem daily. In this retrospective cohort study, we evaluated patients treated at The Ohio State University Wexner Medical Center between 1 January 2015 and 31 August 2020. Patients were included if they were between 18 and 89 years old and received ertapenem for at least 48 hours for pneumonia treatment. Patients were excluded if they were pregnant, were incarcerated, had renal impairment, received antibiotics with Gram-negative activity for a significant period prior to or in addition to ertapenem, and had other concomitant deep-seated infections. The primary outcome of clinical resolution was defined as meeting any of the following three criteria in order of evaluations: discontinuation of antibiotics by day 8 of therapy, afebrile while on ertapenem in addition to a decrease in white blood cell count, or improvement on chest radiograph at day 7 of therapy. A multivariable logistic regression analysis was performed to examine the association between obesity and clinical resolution, while adjusting for proven confounders. There were 76 nonobese and 65 obese patients included. The median patient BMI was 23.7 kg/m2 (21.0 to 26.9) and 35.0 kg/m2 (32.8 to 39.8) for the nonobese and obese cohorts, respectively. Clinical resolution was achieved in 78% (59/76) of nonobese and 75% (49/65) of obese patients (P = 0.75) without an observed difference in the regression model. Outcomes were similar in obese and nonobese patients treated with 1 gram of ertapenem daily for pneumonia.
Subject(s)
Obesity , Pneumonia , Adolescent , Adult , Aged , Aged, 80 and over , Body Mass Index , Ertapenem/therapeutic use , Female , Humans , Middle Aged , Obesity/complications , Obesity/drug therapy , Pneumonia/complications , Pneumonia/drug therapy , Pregnancy , Retrospective Studies , Treatment Outcome , Young AdultABSTRACT
PURPOSE: The purpose of this study was to examine the ability of the YMCA submaximal exercise test protocol using a total body recumbent stepper to predict VËO(2peak). METHODS: Of 112 individuals initially screened, 110 individuals with low to moderate cardiovascular disease risk met the inclusion criteria for participation in the study. The maximal exercise test used a motorized treadmill and the Bruce or modified Bruce protocol. Oxygen uptake was measured and analyzed through collection of expired gases using a metabolic measurement system. The submaximal exercise test was performed at least 24 h later but no more than 5 d after maximal exercise testing. Participants were instructed to keep a pace of 100 steps per minute and the resistance increase every 3 min according to the protocol until fatigue, or until 85% of HR max was achieved. A cross-validation study was also performed to determine the accuracy of the prediction equation. RESULTS: Using a stepwise regression, we report that VËO(2peak) can be predicted using a five-element model including age, weight, sex, wattsend_submax, and HRend_submax (F5,69 = 70.31, P < 0.001). We report a strong correlation between the predicted VËO(2peak) to the actual VËO(2peak). CONCLUSIONS: These data suggest the YMCA submaximal exercise test can be used with the total body recumbent stepper to predict VËO(2peak) in healthy adults.