Philipp K. Agyeman (Switzerland)

Inselspital, Bern University Hospital Pediatrics
I work as a consultant in paediatric infectious diseases at the Children's University Hospital Bern in Switzerland and I am a board certified paediatrician and infectious diseases specialist. After my training in Switzerland, I spent one year in the UK working in the bone marrow transplant unit of the Great North Children's Hospital in Newcastle. I am a clinician researcher and my main research interests are sepsis, invasive bacterial and fungal infections in children with cancer, diagnostics of infections, and epidemiology of viral respiratory diseases in children. I like R programming and statistical analyses.

Author Of 2 Presentations

Expert

Date
Thu, 12.05.2022
Session Time
07:00 - 07:50
Session Type
Meet The Experts
Room
NIKOS SKALKOTAS HALL
Lecture Time
07:00 - 07:00

VALIDATION OF PEDIATRIC ORGAN DYSFUNCTION SCORES IN CHILDREN WITH BLOOD CULTURE-PROVEN INFECTION – A NATIONAL PROSPECTIVE COHORT STUDY

Date
Fri, 13.05.2022
Session Time
10:00 - 11:30
Session Type
Oral Presentations Session
Room
DIMITRIS MITROPOULOS HALL
Lecture Time
10:42 - 10:52

Abstract

Backgrounds:

Previous studies applying Sepsis-3 criteria to pediatric sepsis were based on retrospective analyses of pediatric intensive care unit (PICU) cohorts. We aimed to validate organ dysfunction criteria in a population-based cohort of children with blood culture-proven infection, including emergency department, PICU, and ward patients.

Methods

National multi-center prospective cohort study of children <17 years with blood culture-proven sepsis between 1.9.2011 and 31.12.2015. We excluded preterm infants and neonates ≤7 days. We compared the 2005 International Pediatric Sepsis Consensus Conference (IPSCC), Pediatric Logistic Organ Dysfunction (PELOD)-2, pediatric Sequential Organ Failure Assessment (pSOFA), and Pediatric Organ Dysfunction Information Update Mandate (PODIUM) scores measured on day of blood culture sampling to predict 30-day mortality using area under the receiver-operating characteristic curves (AUC). Conditional random forest analyses and generalized linear mixed model prediction were used.

Results:

We analyzed 877 sepsis episodes in 807 children, with a 30-day mortality of 4.3%. Presence of any organ dysfunction ranged from 32.7% (2005 IPSCC) to 55.3% (pSOFA). In adjusted analyses, the accuracy to predict mortality was highest for 2005 IPSCC (AUC 0.871, 95%CI: 0.819−0.924), followed by pSOFA (0.852; 95%CI: 0.784−0.92), PODIUM (0.852; 95%CI: 0.791−0.912), and PELOD-2 (0.827; 95%CI: 0.761−0.892). Neurologic, respiratory, and cardiovascular dysfunction were most predictive of 30-day mortality. Considering only these three organs adjusted AUC was 0.784 (0.70 - 0.868) for 2005 IPSCC and 0.771 (0.684-0.857) for PODIUM, while pSOFA (0.734; 0.641-0.828) and PELOD-2 (0.724; 0.627-0.822) had lower performances.

Conclusions/Learning Points:

When comparing scores for organ dysfunction, 2005 IPSCC performed best, followed by pSOFA and PODIUM criteria. Although the accuracy between scores was comparable, we observed major differences in terms of classification of individual organ dysfunctions. Our findings confirm the importance of neurologic, respiratory, and cardiovascular dysfunction.

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Presenter of 2 Presentations

Expert

Date
Thu, 12.05.2022
Session Time
07:00 - 07:50
Session Type
Meet The Experts
Room
NIKOS SKALKOTAS HALL
Lecture Time
07:00 - 07:00

VALIDATION OF PEDIATRIC ORGAN DYSFUNCTION SCORES IN CHILDREN WITH BLOOD CULTURE-PROVEN INFECTION – A NATIONAL PROSPECTIVE COHORT STUDY

Date
Fri, 13.05.2022
Session Time
10:00 - 11:30
Session Type
Oral Presentations Session
Room
DIMITRIS MITROPOULOS HALL
Lecture Time
10:42 - 10:52

Abstract

Backgrounds:

Previous studies applying Sepsis-3 criteria to pediatric sepsis were based on retrospective analyses of pediatric intensive care unit (PICU) cohorts. We aimed to validate organ dysfunction criteria in a population-based cohort of children with blood culture-proven infection, including emergency department, PICU, and ward patients.

Methods

National multi-center prospective cohort study of children <17 years with blood culture-proven sepsis between 1.9.2011 and 31.12.2015. We excluded preterm infants and neonates ≤7 days. We compared the 2005 International Pediatric Sepsis Consensus Conference (IPSCC), Pediatric Logistic Organ Dysfunction (PELOD)-2, pediatric Sequential Organ Failure Assessment (pSOFA), and Pediatric Organ Dysfunction Information Update Mandate (PODIUM) scores measured on day of blood culture sampling to predict 30-day mortality using area under the receiver-operating characteristic curves (AUC). Conditional random forest analyses and generalized linear mixed model prediction were used.

Results:

We analyzed 877 sepsis episodes in 807 children, with a 30-day mortality of 4.3%. Presence of any organ dysfunction ranged from 32.7% (2005 IPSCC) to 55.3% (pSOFA). In adjusted analyses, the accuracy to predict mortality was highest for 2005 IPSCC (AUC 0.871, 95%CI: 0.819−0.924), followed by pSOFA (0.852; 95%CI: 0.784−0.92), PODIUM (0.852; 95%CI: 0.791−0.912), and PELOD-2 (0.827; 95%CI: 0.761−0.892). Neurologic, respiratory, and cardiovascular dysfunction were most predictive of 30-day mortality. Considering only these three organs adjusted AUC was 0.784 (0.70 - 0.868) for 2005 IPSCC and 0.771 (0.684-0.857) for PODIUM, while pSOFA (0.734; 0.641-0.828) and PELOD-2 (0.724; 0.627-0.822) had lower performances.

Conclusions/Learning Points:

When comparing scores for organ dysfunction, 2005 IPSCC performed best, followed by pSOFA and PODIUM criteria. Although the accuracy between scores was comparable, we observed major differences in terms of classification of individual organ dysfunctions. Our findings confirm the importance of neurologic, respiratory, and cardiovascular dysfunction.

Hide