P. Christopher Parish
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
P. Christopher Parish has a total of 6 co-authors. Here are the top co-authors by number of shared publications:
- Alex D. Taylor
Atrium Health Wake Forest Baptist
1 shared publication Christopher A. Ohl
Wake Forest University School of Medicine
1 shared publication- James R. Beardsley
Department of Pharmacy, Atrium Health Wake Forest Baptist, Winston-Salem, North Carolina
1 shared publication - Michael E. DeWitt
Department of Medicine, Section on Infectious Diseases, Wake Forest University School of Medicine, Winston-Salem, North Carolina, USA
1 shared publication Tyler J. Stone
Atrium Health Wake Forest Baptist
1 shared publication- Vera P. Luther
Section on Infectious Diseases, Wake Forest University School of Medicine , Winston-Salem, North Carolina , USA
1 shared publication
Latest Publications
- Open Access
- 30 October 2025
- Published by Cambridge University Press (CUP) in Antimicrobial Stewardship & Healthcare Epidemiology
- Vol. 5 (1) , e291
Retrospective cohort study of the microbiology and clinical outcomes of spontaneous bacterial peritonitis (SBP) within a US academic health system
Objective: To determine the local applicability of 2021 American Academy for the Study of Liver Diseases spontaneous bacterial peritonitis (SBP) treatment guidelines by evaluating the microbiology and clinical outcomes of SBP cases in an academic health system. Design: Retrospective cohort study. Setting: Five-hospital academic health system. Patients: Hospitalized adult patients with SBP. Methods: This study involved 2 components. First, patients meeting inclusion criteria with peritoneal fluid cultures positive for a pathogen were included in the culture-positive group. Antibiotic susceptibilities were analyzed for these patients. Second, remaining culture-negative patients were randomly selected and sequentially evaluated until the culture-negative and culture-positive groups were approximately the same size. Clinical data for all patients were evaluated based on empiric antibiotics received. Results: Forty-nine patients with culture-positive SBP and 48 patients with culture-negative SBP were included. Eight (16%) positive cultures contained TGC-nonsusceptible organisms. Patients receiving empiric third-generation cephalosporin (TGC) monotherapy had similar clinical outcomes as patients receiving empiric broad-spectrum therapy, including similar 30-day mortality (36% vs 38%; P = 1.00), 90-day mortality (55% vs 55%; P = 1.00), and median duration of hospitalization (6.5 d vs 8 d; P = .25). ICU admission, recent hospitalization, and nosocomial infection were not associated with TGC-nonsusceptible pathogen isolation in a univariate logistic regression analysis. Conclusions: Within our health system, 16% of isolates in culture-positive SBP patients were nonsusceptible to TGCs. No statistically significant difference was detected in clinical outcomes in patients receiving TGC or broader-spectrum antimicrobial therapy.
- 30 October 2025
- Published by Cambridge University Press (CUP) in Antimicrobial Stewardship & Healthcare Epidemiology
- Vol. 5 (1) , e291
Open AccessRetrospective cohort study of the microbiology and clinical outcomes of spontaneous bacterial peritonitis (SBP) within a US academic health system
Objective: To determine the local applicability of 2021 American Academy for the Study of Liver Diseases spontaneous bacterial peritonitis (SBP) treatment guidelines by evaluating the microbiology and clinical outcomes of SBP cases in an academic health system. Design: Retrospective cohort study. Setting: Five-hospital academic health system. Patients: Hospitalized adult patients with SBP. Methods: This study involved 2 components. First, patients meeting inclusion criteria with peritoneal fluid cultures positive for a pathogen were included in the culture-positive group. Antibiotic susceptibilities were analyzed for these patients. Second, remaining culture-negative patients were randomly selected and sequentially evaluated until the culture-negative and culture-positive groups were approximately the same size. Clinical data for all patients were evaluated based on empiric antibiotics received. Results: Forty-nine patients with culture-positive SBP and 48 patients with culture-negative SBP were included. Eight (16%) positive cultures contained TGC-nonsusceptible organisms. Patients receiving empiric third-generation cephalosporin (TGC) monotherapy had similar clinical outcomes as patients receiving empiric broad-spectrum therapy, including similar 30-day mortality (36% vs 38%; P = 1.00), 90-day mortality (55% vs 55%; P = 1.00), and median duration of hospitalization (6.5 d vs 8 d; P = .25). ICU admission, recent hospitalization, and nosocomial infection were not associated with TGC-nonsusceptible pathogen isolation in a univariate logistic regression analysis. Conclusions: Within our health system, 16% of isolates in culture-positive SBP patients were nonsusceptible to TGCs. No statistically significant difference was detected in clinical outcomes in patients receiving TGC or broader-spectrum antimicrobial therapy.