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Efficacy of standardizing fibrinolytic therapy for parapneumonic effusion

BACKGROUND: While chest tube placement with pleural fibrinolytic medication is the established treatment of pediatric empyema, treatment failure is reported in up to 20% of these children. OBJECTIVE: Standardizing fibrinolytic administration among interventional radiology (IR) physicians to improve...

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Autores principales: James, Charles A., Lewis, P. Spencer, Moore, Mary B., Wong, Kevin, Rader, Emily K., Roberson, Paula K., Ghaleb, Nancy A., Jensen, Hanna K., Pezeshkmehr, Amir H., Stroud, Michael H., Ashton, Daniel J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9023697/
https://www.ncbi.nlm.nih.gov/pubmed/35451632
http://dx.doi.org/10.1007/s00247-022-05365-z
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author James, Charles A.
Lewis, P. Spencer
Moore, Mary B.
Wong, Kevin
Rader, Emily K.
Roberson, Paula K.
Ghaleb, Nancy A.
Jensen, Hanna K.
Pezeshkmehr, Amir H.
Stroud, Michael H.
Ashton, Daniel J.
author_facet James, Charles A.
Lewis, P. Spencer
Moore, Mary B.
Wong, Kevin
Rader, Emily K.
Roberson, Paula K.
Ghaleb, Nancy A.
Jensen, Hanna K.
Pezeshkmehr, Amir H.
Stroud, Michael H.
Ashton, Daniel J.
author_sort James, Charles A.
collection PubMed
description BACKGROUND: While chest tube placement with pleural fibrinolytic medication is the established treatment of pediatric empyema, treatment failure is reported in up to 20% of these children. OBJECTIVE: Standardizing fibrinolytic administration among interventional radiology (IR) physicians to improve patient outcomes in pediatric parapneumonic effusion. MATERIALS AND METHODS: We introduced a hospital-wide clinical pathway for parapneumonic effusion (1–2 mg tissue plasminogen activator [tPA] twice daily based on pleural US grade); we then collected prospective data for IR treatment May 2017 through February 2020. These data included demographics, co-morbidities, pediatric intensive care unit (PICU) admission, pleural US grade, culture results, daily tPA dose average, twice-daily dose days, skipped dose days, pleural therapy days, need for chest CT/a second IR procedure/surgical drainage, and length of stay. We compared the prospective data to historical controls with IR treatment from January 2013 to April 2017. RESULTS: Sixty-three children and young adults were treated after clinical pathway implementation. IR referrals increased (P = 0.02) and included higher co-morbidities (P = 0.005) and more PICU patients (P = 0.05). Mean doses per day increased from 1.5 to 1.9 (P < 0.001), twice-daily dose days increased from 38% to 79% (P < 0.001) and median pleural therapy days decreased from 3.5 days to 2.5 days (P = 0.001). No IR patients needed surgical intervention. No statistical differences were observed for gender/age/weight, US grade, need for a second IR procedure or length of stay. US grade correlated with greater positive cultures, need for chest CT/second IR procedure, and pleural therapy days. CONCLUSION: Interventional radiology physician standardization improved on a clinical pathway for fibrinolysis of parapneumonic effusion. Despite higher patient complexity, pleural therapy duration decreased. There were no chest tube failures needing surgical drainage.
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spelling pubmed-90236972022-04-22 Efficacy of standardizing fibrinolytic therapy for parapneumonic effusion James, Charles A. Lewis, P. Spencer Moore, Mary B. Wong, Kevin Rader, Emily K. Roberson, Paula K. Ghaleb, Nancy A. Jensen, Hanna K. Pezeshkmehr, Amir H. Stroud, Michael H. Ashton, Daniel J. Pediatr Radiol Original Article BACKGROUND: While chest tube placement with pleural fibrinolytic medication is the established treatment of pediatric empyema, treatment failure is reported in up to 20% of these children. OBJECTIVE: Standardizing fibrinolytic administration among interventional radiology (IR) physicians to improve patient outcomes in pediatric parapneumonic effusion. MATERIALS AND METHODS: We introduced a hospital-wide clinical pathway for parapneumonic effusion (1–2 mg tissue plasminogen activator [tPA] twice daily based on pleural US grade); we then collected prospective data for IR treatment May 2017 through February 2020. These data included demographics, co-morbidities, pediatric intensive care unit (PICU) admission, pleural US grade, culture results, daily tPA dose average, twice-daily dose days, skipped dose days, pleural therapy days, need for chest CT/a second IR procedure/surgical drainage, and length of stay. We compared the prospective data to historical controls with IR treatment from January 2013 to April 2017. RESULTS: Sixty-three children and young adults were treated after clinical pathway implementation. IR referrals increased (P = 0.02) and included higher co-morbidities (P = 0.005) and more PICU patients (P = 0.05). Mean doses per day increased from 1.5 to 1.9 (P < 0.001), twice-daily dose days increased from 38% to 79% (P < 0.001) and median pleural therapy days decreased from 3.5 days to 2.5 days (P = 0.001). No IR patients needed surgical intervention. No statistical differences were observed for gender/age/weight, US grade, need for a second IR procedure or length of stay. US grade correlated with greater positive cultures, need for chest CT/second IR procedure, and pleural therapy days. CONCLUSION: Interventional radiology physician standardization improved on a clinical pathway for fibrinolysis of parapneumonic effusion. Despite higher patient complexity, pleural therapy duration decreased. There were no chest tube failures needing surgical drainage. Springer Berlin Heidelberg 2022-04-22 2022 /pmc/articles/PMC9023697/ /pubmed/35451632 http://dx.doi.org/10.1007/s00247-022-05365-z Text en © The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2022 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Original Article
James, Charles A.
Lewis, P. Spencer
Moore, Mary B.
Wong, Kevin
Rader, Emily K.
Roberson, Paula K.
Ghaleb, Nancy A.
Jensen, Hanna K.
Pezeshkmehr, Amir H.
Stroud, Michael H.
Ashton, Daniel J.
Efficacy of standardizing fibrinolytic therapy for parapneumonic effusion
title Efficacy of standardizing fibrinolytic therapy for parapneumonic effusion
title_full Efficacy of standardizing fibrinolytic therapy for parapneumonic effusion
title_fullStr Efficacy of standardizing fibrinolytic therapy for parapneumonic effusion
title_full_unstemmed Efficacy of standardizing fibrinolytic therapy for parapneumonic effusion
title_short Efficacy of standardizing fibrinolytic therapy for parapneumonic effusion
title_sort efficacy of standardizing fibrinolytic therapy for parapneumonic effusion
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9023697/
https://www.ncbi.nlm.nih.gov/pubmed/35451632
http://dx.doi.org/10.1007/s00247-022-05365-z
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