Pneumocystis jirovecii pneumonia in liver transplant recipients in an era of routine prophylaxis

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Standard

Pneumocystis jirovecii pneumonia in liver transplant recipients in an era of routine prophylaxis. / Andreasen, Philip B.; Rezahosseini, Omid; Møller, Dina L.; Wareham, Neval E.; Thomsen, Magda T.; Houmami, Ranya; Knudsen, Andreas D.; Knudsen, Jenny; Kurtzhals, Jørgen A.L.; Rostved, Andreas A.; Pedersen, Christian R.; Rasmussen, Allan; Nielsen, Susanne D.

I: Immunity, Inflammation and Disease, Bind 10, Nr. 1, 2022, s. 93-100.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Andreasen, PB, Rezahosseini, O, Møller, DL, Wareham, NE, Thomsen, MT, Houmami, R, Knudsen, AD, Knudsen, J, Kurtzhals, JAL, Rostved, AA, Pedersen, CR, Rasmussen, A & Nielsen, SD 2022, 'Pneumocystis jirovecii pneumonia in liver transplant recipients in an era of routine prophylaxis', Immunity, Inflammation and Disease, bind 10, nr. 1, s. 93-100. https://doi.org/10.1002/iid3.546

APA

Andreasen, P. B., Rezahosseini, O., Møller, D. L., Wareham, N. E., Thomsen, M. T., Houmami, R., Knudsen, A. D., Knudsen, J., Kurtzhals, J. A. L., Rostved, A. A., Pedersen, C. R., Rasmussen, A., & Nielsen, S. D. (2022). Pneumocystis jirovecii pneumonia in liver transplant recipients in an era of routine prophylaxis. Immunity, Inflammation and Disease, 10(1), 93-100. https://doi.org/10.1002/iid3.546

Vancouver

Andreasen PB, Rezahosseini O, Møller DL, Wareham NE, Thomsen MT, Houmami R o.a. Pneumocystis jirovecii pneumonia in liver transplant recipients in an era of routine prophylaxis. Immunity, Inflammation and Disease. 2022;10(1):93-100. https://doi.org/10.1002/iid3.546

Author

Andreasen, Philip B. ; Rezahosseini, Omid ; Møller, Dina L. ; Wareham, Neval E. ; Thomsen, Magda T. ; Houmami, Ranya ; Knudsen, Andreas D. ; Knudsen, Jenny ; Kurtzhals, Jørgen A.L. ; Rostved, Andreas A. ; Pedersen, Christian R. ; Rasmussen, Allan ; Nielsen, Susanne D. / Pneumocystis jirovecii pneumonia in liver transplant recipients in an era of routine prophylaxis. I: Immunity, Inflammation and Disease. 2022 ; Bind 10, Nr. 1. s. 93-100.

Bibtex

@article{ff7180eda96c422a8751e6dc9315293d,
title = "Pneumocystis jirovecii pneumonia in liver transplant recipients in an era of routine prophylaxis",
abstract = "Background: Pneumocystis jirovecii pneumonia (PCP) is an opportunistic infection in organ transplant recipients that may be prevented by antibiotic prophylaxis. We aimed to investigate the incidence rate (IR) of PCP and the related hospitalization and mortality rates in liver transplant recipients in an era of routine prophylaxis. Methods: We included all adult liver transplant recipients transplanted at Rigshospitalet between January 1, 2011 and October 1, 2019. Microbiology data were obtained from the Danish Microbiology Database (MiBa), a national database containing all data from all Departments of Clinical Microbiology in Denmark receiving samples from both hospitals and general practices. According to local guidelines, PCP prophylaxis was initiated 1 week posttransplantation and discontinued after 6 months or sooner in patients experiencing side effects. Results: We included 343 liver transplant recipients with 1153 person-years of follow-up (PYFU), of which 269 (78%) received PCP prophylaxis during the first 6 months posttransplantation. Seven (2%) recipients were diagnosed with PCP during follow-up. In the first 6 months posttransplantation and in 269 transplant recipients who received prophylaxis there were zero PCP events while the IR was 32 (95% confidence interval [CI] 2.9–148) per 1000 PYFU in 74 recipient who did not receive prophylaxis. During 7th to 12th month posttransplantation the IR was 20 (95% CI: 5.5–53) per 1000 PYFU. All seven (100%) recipients diagnosed with PCP were hospitalized, however none died. Conclusions: PCP was not detected in liver transplant recipients while on prophylaxis. Though, it worth mentioning that two out of the seven PCP patients received high-dose prednisolone before the PCP event. All liver transplant recipients with PCP were hospitalized, but none died. Randomized clinical trials to determine the optimal duration of prophylaxis are warranted.",
keywords = "incidence, liver transplantation, Pneumocystis jirovecii pneumonia, prophylaxis, trimethoprim sulfamethoxazole",
author = "Andreasen, {Philip B.} and Omid Rezahosseini and M{\o}ller, {Dina L.} and Wareham, {Neval E.} and Thomsen, {Magda T.} and Ranya Houmami and Knudsen, {Andreas D.} and Jenny Knudsen and Kurtzhals, {J{\o}rgen A.L.} and Rostved, {Andreas A.} and Pedersen, {Christian R.} and Allan Rasmussen and Nielsen, {Susanne D.}",
note = "Publisher Copyright: {\textcopyright} 2021 The Authors. Immunity, Inflammation and Disease published by John Wiley & Sons Ltd.",
year = "2022",
doi = "10.1002/iid3.546",
language = "English",
volume = "10",
pages = "93--100",
journal = "Immunity, inflammation and disease",
issn = "2050-4527",
publisher = "JohnWiley & Sons Ltd",
number = "1",

}

RIS

TY - JOUR

T1 - Pneumocystis jirovecii pneumonia in liver transplant recipients in an era of routine prophylaxis

AU - Andreasen, Philip B.

AU - Rezahosseini, Omid

AU - Møller, Dina L.

AU - Wareham, Neval E.

AU - Thomsen, Magda T.

AU - Houmami, Ranya

AU - Knudsen, Andreas D.

AU - Knudsen, Jenny

AU - Kurtzhals, Jørgen A.L.

AU - Rostved, Andreas A.

AU - Pedersen, Christian R.

AU - Rasmussen, Allan

AU - Nielsen, Susanne D.

N1 - Publisher Copyright: © 2021 The Authors. Immunity, Inflammation and Disease published by John Wiley & Sons Ltd.

PY - 2022

Y1 - 2022

N2 - Background: Pneumocystis jirovecii pneumonia (PCP) is an opportunistic infection in organ transplant recipients that may be prevented by antibiotic prophylaxis. We aimed to investigate the incidence rate (IR) of PCP and the related hospitalization and mortality rates in liver transplant recipients in an era of routine prophylaxis. Methods: We included all adult liver transplant recipients transplanted at Rigshospitalet between January 1, 2011 and October 1, 2019. Microbiology data were obtained from the Danish Microbiology Database (MiBa), a national database containing all data from all Departments of Clinical Microbiology in Denmark receiving samples from both hospitals and general practices. According to local guidelines, PCP prophylaxis was initiated 1 week posttransplantation and discontinued after 6 months or sooner in patients experiencing side effects. Results: We included 343 liver transplant recipients with 1153 person-years of follow-up (PYFU), of which 269 (78%) received PCP prophylaxis during the first 6 months posttransplantation. Seven (2%) recipients were diagnosed with PCP during follow-up. In the first 6 months posttransplantation and in 269 transplant recipients who received prophylaxis there were zero PCP events while the IR was 32 (95% confidence interval [CI] 2.9–148) per 1000 PYFU in 74 recipient who did not receive prophylaxis. During 7th to 12th month posttransplantation the IR was 20 (95% CI: 5.5–53) per 1000 PYFU. All seven (100%) recipients diagnosed with PCP were hospitalized, however none died. Conclusions: PCP was not detected in liver transplant recipients while on prophylaxis. Though, it worth mentioning that two out of the seven PCP patients received high-dose prednisolone before the PCP event. All liver transplant recipients with PCP were hospitalized, but none died. Randomized clinical trials to determine the optimal duration of prophylaxis are warranted.

AB - Background: Pneumocystis jirovecii pneumonia (PCP) is an opportunistic infection in organ transplant recipients that may be prevented by antibiotic prophylaxis. We aimed to investigate the incidence rate (IR) of PCP and the related hospitalization and mortality rates in liver transplant recipients in an era of routine prophylaxis. Methods: We included all adult liver transplant recipients transplanted at Rigshospitalet between January 1, 2011 and October 1, 2019. Microbiology data were obtained from the Danish Microbiology Database (MiBa), a national database containing all data from all Departments of Clinical Microbiology in Denmark receiving samples from both hospitals and general practices. According to local guidelines, PCP prophylaxis was initiated 1 week posttransplantation and discontinued after 6 months or sooner in patients experiencing side effects. Results: We included 343 liver transplant recipients with 1153 person-years of follow-up (PYFU), of which 269 (78%) received PCP prophylaxis during the first 6 months posttransplantation. Seven (2%) recipients were diagnosed with PCP during follow-up. In the first 6 months posttransplantation and in 269 transplant recipients who received prophylaxis there were zero PCP events while the IR was 32 (95% confidence interval [CI] 2.9–148) per 1000 PYFU in 74 recipient who did not receive prophylaxis. During 7th to 12th month posttransplantation the IR was 20 (95% CI: 5.5–53) per 1000 PYFU. All seven (100%) recipients diagnosed with PCP were hospitalized, however none died. Conclusions: PCP was not detected in liver transplant recipients while on prophylaxis. Though, it worth mentioning that two out of the seven PCP patients received high-dose prednisolone before the PCP event. All liver transplant recipients with PCP were hospitalized, but none died. Randomized clinical trials to determine the optimal duration of prophylaxis are warranted.

KW - incidence

KW - liver transplantation

KW - Pneumocystis jirovecii pneumonia

KW - prophylaxis

KW - trimethoprim sulfamethoxazole

U2 - 10.1002/iid3.546

DO - 10.1002/iid3.546

M3 - Journal article

C2 - 34713963

AN - SCOPUS:85118213589

VL - 10

SP - 93

EP - 100

JO - Immunity, inflammation and disease

JF - Immunity, inflammation and disease

SN - 2050-4527

IS - 1

ER -

ID: 320003013