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Assessment of venous thromboembolism risk and initiation of appropriate prophylaxis in psychiatric patients
INTRODUCTION: Venous thromboembolism (VTE) prophylaxis is not included among the measures for the Inpatient Psychiatric Facilities Quality Reporting Program. Evidence suggests that antipsychotic agents may be an independent risk factor for the development of VTE; therefore, development of a VTE risk...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
College of Psychiatric & Neurologic Pharmacists
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6007734/ https://www.ncbi.nlm.nih.gov/pubmed/29955548 http://dx.doi.org/10.9740/mhc.2018.03.068 |
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author | Ruhe, Ann Marie Hebbard, Amy Hayes, Genevieve |
author_facet | Ruhe, Ann Marie Hebbard, Amy Hayes, Genevieve |
author_sort | Ruhe, Ann Marie |
collection | PubMed |
description | INTRODUCTION: Venous thromboembolism (VTE) prophylaxis is not included among the measures for the Inpatient Psychiatric Facilities Quality Reporting Program. Evidence suggests that antipsychotic agents may be an independent risk factor for the development of VTE; therefore, development of a VTE risk stratification tool would improve the quality and safety of care for the psychiatric inpatient population. This study aims to develop clinically relevant criteria to assess VTE risk upon admission to an inpatient psychiatric hospital. METHODS: This retrospective, single-center cohort study enrolled patients in 2 cohorts from an inpatient psychiatric hospital. Patients in cohort I with new-onset VTE diagnosis during admission were identified through international classification of diseases 9 and 10 coding. Cohort II consisted of a random sample of 100 patients in a 3-month period. The percentage meeting criteria for prophylaxis in each cohort was assessed utilizing both the Padua Prediction Score and a modified score. RESULTS: In cohorts I and II, 66.7% and 14% of patients, respectively, met criteria for VTE prophylaxis utilizing the modified Padua Prediction Score. One patient received VTE prophylaxis in each cohort, and the median time to VTE diagnosis in cohort I was 42 days. In cohort I, the rate of VTE was 0.08% based on estimated discharges in the 26-month period. This is less than the annual rate of 1% to 2.4% for nursing homes or postacute rehabilitation facilities. DISCUSSION: We recommend the implementation of clinical decision support to prompt individualized reassessment of VTE risk when length of stay exceeds 30 days. |
format | Online Article Text |
id | pubmed-6007734 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | College of Psychiatric & Neurologic Pharmacists |
record_format | MEDLINE/PubMed |
spelling | pubmed-60077342018-06-28 Assessment of venous thromboembolism risk and initiation of appropriate prophylaxis in psychiatric patients Ruhe, Ann Marie Hebbard, Amy Hayes, Genevieve Ment Health Clin Original Research INTRODUCTION: Venous thromboembolism (VTE) prophylaxis is not included among the measures for the Inpatient Psychiatric Facilities Quality Reporting Program. Evidence suggests that antipsychotic agents may be an independent risk factor for the development of VTE; therefore, development of a VTE risk stratification tool would improve the quality and safety of care for the psychiatric inpatient population. This study aims to develop clinically relevant criteria to assess VTE risk upon admission to an inpatient psychiatric hospital. METHODS: This retrospective, single-center cohort study enrolled patients in 2 cohorts from an inpatient psychiatric hospital. Patients in cohort I with new-onset VTE diagnosis during admission were identified through international classification of diseases 9 and 10 coding. Cohort II consisted of a random sample of 100 patients in a 3-month period. The percentage meeting criteria for prophylaxis in each cohort was assessed utilizing both the Padua Prediction Score and a modified score. RESULTS: In cohorts I and II, 66.7% and 14% of patients, respectively, met criteria for VTE prophylaxis utilizing the modified Padua Prediction Score. One patient received VTE prophylaxis in each cohort, and the median time to VTE diagnosis in cohort I was 42 days. In cohort I, the rate of VTE was 0.08% based on estimated discharges in the 26-month period. This is less than the annual rate of 1% to 2.4% for nursing homes or postacute rehabilitation facilities. DISCUSSION: We recommend the implementation of clinical decision support to prompt individualized reassessment of VTE risk when length of stay exceeds 30 days. College of Psychiatric & Neurologic Pharmacists 2018-03-26 /pmc/articles/PMC6007734/ /pubmed/29955548 http://dx.doi.org/10.9740/mhc.2018.03.068 Text en © 2018 CPNP. http://creativecommons.org/licenses/by-nc/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial 3.0 License, which permits non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Ruhe, Ann Marie Hebbard, Amy Hayes, Genevieve Assessment of venous thromboembolism risk and initiation of appropriate prophylaxis in psychiatric patients |
title | Assessment of venous thromboembolism risk and initiation of appropriate prophylaxis in psychiatric patients |
title_full | Assessment of venous thromboembolism risk and initiation of appropriate prophylaxis in psychiatric patients |
title_fullStr | Assessment of venous thromboembolism risk and initiation of appropriate prophylaxis in psychiatric patients |
title_full_unstemmed | Assessment of venous thromboembolism risk and initiation of appropriate prophylaxis in psychiatric patients |
title_short | Assessment of venous thromboembolism risk and initiation of appropriate prophylaxis in psychiatric patients |
title_sort | assessment of venous thromboembolism risk and initiation of appropriate prophylaxis in psychiatric patients |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6007734/ https://www.ncbi.nlm.nih.gov/pubmed/29955548 http://dx.doi.org/10.9740/mhc.2018.03.068 |
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