Using a New Measurement to Evaluate Pain Relief Among Cancer Inpatients with Clinically Significant Pain Based on a Nursing Information System: A Three-Year Hospital-Based Study
Objective. Developing a new measurement index is the first step in evaluating pain relief outcomes. Although the percentage difference in pain intensity (%PID) is the most popular indicator, this indicator does not take into account the goal of pain relief. Therefore, the aims of this study were to...
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Published in | Pain medicine (Malden, Mass.) Vol. 17; no. 11; pp. 2067 - 2075 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
Oxford University Press
01.11.2016
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Subjects | |
Online Access | Get full text |
ISSN | 1526-2375 1526-4637 |
DOI | 10.1093/pm/pnw026 |
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Abstract | Objective. Developing a new measurement index is the first step in evaluating pain relief outcomes. Although the percentage difference in pain intensity (%PID) is the most popular indicator, this indicator does not take into account the goal of pain relief. Therefore, the aims of this study were to develop a pain relief index (PRI) for outcome evaluation and to examine the index using demographic characteristics of cancer inpatients with clinically significant pain.
Design. Retrospective cohort study.
Setting. A national hospital.
Subjects. All cancer inpatients.
Methods. Pain intensity was assessed using a numerical rating scale, a faces pain scale or the Face, Legs, Activity, Cry, Consolability (FLACC) Behavioral Tool. Using a nursing information system, a pain score database containing data from 2011 through 2013 was analyzed.
Results. Cancer patients representing 93,812 hospitalizations were considered in this study. We focused on cancer patients for whom the worst pain intensity (WPI) was ≥ 4 points. PRI values of −62.02% to −72.55% were observed in the WPI ≥ 7 and 4 ≤ WPI ≤ 6 groups. Significant (P < 0.05) effects on PRI values were observed among patients who were > 65 years old, those who were admitted to the medicine or gynecology and those who had a hospital stay > 30 days.
Conclusion. This hospital-based study demonstrated that the PRI is an effective and valid measure for evaluating outcome data using an electronic nursing information system. We will further define the meaningful range of percentage difference in PRI from various perspectives. |
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AbstractList | Developing a new measurement index is the first step in evaluating pain relief outcomes. Although the percentage difference in pain intensity (%PID) is the most popular indicator, this indicator does not take into account the goal of pain relief. Therefore, the aims of this study were to develop a pain relief index (PRI) for outcome evaluation and to examine the index using demographic characteristics of cancer inpatients with clinically significant pain.
Retrospective cohort study.
A national hospital.
All cancer inpatients.
Pain intensity was assessed using a numerical rating scale, a faces pain scale or the Face, Legs, Activity, Cry, Consolability (FLACC) Behavioral Tool. Using a nursing information system, a pain score database containing data from 2011 through 2013 was analyzed.
Cancer patients representing 93,812 hospitalizations were considered in this study. We focused on cancer patients for whom the worst pain intensity (WPI) was ≥ 4 points. PRI values of -62.02% to -72.55% were observed in the WPI ≥ 7 and 4 ≤ WPI ≤ 6 groups. Significant (P < 0.05) effects on PRI values were observed among patients who were > 65 years old, those who were admitted to the medicine or gynecology and those who had a hospital stay > 30 days.
This hospital-based study demonstrated that the PRI is an effective and valid measure for evaluating outcome data using an electronic nursing information system. We will further define the meaningful range of percentage difference in PRI from various perspectives. Objective. Developing a new measurement index is the first step in evaluating pain relief outcomes. Although the percentage difference in pain intensity (%PID) is the most popular indicator, this indicator does not take into account the goal of pain relief. Therefore, the aims of this study were to develop a pain relief index (PRI) for outcome evaluation and to examine the index using demographic characteristics of cancer inpatients with clinically significant pain. Design. Retrospective cohort study. Setting. A national hospital. Subjects. All cancer inpatients. Methods. Pain intensity was assessed using a numerical rating scale, a faces pain scale or the Face, Legs, Activity, Cry, Consolability (FLACC) Behavioral Tool. Using a nursing information system, a pain score database containing data from 2011 through 2013 was analyzed. Results. Cancer patients representing 93,812 hospitalizations were considered in this study. We focused on cancer patients for whom the worst pain intensity (WPI) was ≥ 4 points. PRI values of −62.02% to −72.55% were observed in the WPI ≥ 7 and 4 ≤ WPI ≤ 6 groups. Significant (P < 0.05) effects on PRI values were observed among patients who were > 65 years old, those who were admitted to the medicine or gynecology and those who had a hospital stay > 30 days. Conclusion. This hospital-based study demonstrated that the PRI is an effective and valid measure for evaluating outcome data using an electronic nursing information system. We will further define the meaningful range of percentage difference in PRI from various perspectives. Objective. Developing a new measurement index is the first step in evaluating pain relief outcomes. Although the percentage difference in pain intensity (%PID) is the most popular indicator, this indicator does not take into account the goal of pain relief. Therefore, the aims of this study were to develop a pain relief index (PRI) for outcome evaluation and to examine the index using demographic characteristics of cancer inpatients with clinically significant pain. Design. Retrospective cohort study. Setting. A national hospital. Subjects. All cancer inpatients. Methods. Pain intensity was assessed using a numerical rating scale, a faces pain scale or the Face, Legs, Activity, Cry, Consolability (FLACC) Behavioral Tool. Using a nursing information system, a pain score database containing data from 2011 through 2013 was analyzed. Results. Cancer patients representing 93,812 hospitalizations were considered in this study. We focused on cancer patients for whom the worst pain intensity (WPI) was ≥ 4 points. PRI values of -62.02% to -72.55% were observed in the WPI ≥ 7 and 4 ≤ WPI ≤ 6 groups. Significant (P < 0.05) effects on PRI values were observed among patients who were > 65 years old, those who were admitted to the medicine or gynecology and those who had a hospital stay > 30 days. Conclusion. This hospital-based study demonstrated that the PRI is an effective and valid measure for evaluating outcome data using an electronic nursing information system. We will further define the meaningful range of percentage difference in PRI from various perspectives. OBJECTIVEDeveloping a new measurement index is the first step in evaluating pain relief outcomes. Although the percentage difference in pain intensity (%PID) is the most popular indicator, this indicator does not take into account the goal of pain relief. Therefore, the aims of this study were to develop a pain relief index (PRI) for outcome evaluation and to examine the index using demographic characteristics of cancer inpatients with clinically significant pain.DESIGNRetrospective cohort study.SETTINGA national hospital.SUBJECTSAll cancer inpatients.METHODSPain intensity was assessed using a numerical rating scale, a faces pain scale or the Face, Legs, Activity, Cry, Consolability (FLACC) Behavioral Tool. Using a nursing information system, a pain score database containing data from 2011 through 2013 was analyzed.RESULTSCancer patients representing 93,812 hospitalizations were considered in this study. We focused on cancer patients for whom the worst pain intensity (WPI) was ≥ 4 points. PRI values of -62.02% to -72.55% were observed in the WPI ≥ 7 and 4 ≤ WPI ≤ 6 groups. Significant (P < 0.05) effects on PRI values were observed among patients who were > 65 years old, those who were admitted to the medicine or gynecology and those who had a hospital stay > 30 days.CONCLUSIONThis hospital-based study demonstrated that the PRI is an effective and valid measure for evaluating outcome data using an electronic nursing information system. We will further define the meaningful range of percentage difference in PRI from various perspectives. |
Author | Liang, Chun-Yu Wang, Kwua-Yun Chu, Chi-Ming Ho, Shung-Tai Wang, Wei-Yun Wu, Yi-Syuan Sung, Chun-Sung |
Author_xml | – sequence: 1 givenname: Wei-Yun surname: Wang fullname: Wang, Wei-Yun email: kywang7@vghtpe.gov.tw organization: Graduate Institute of Medical Sciences, National Defense Medical Center and Department of Nursing, Tri-Service General Hospital, Taipei, Taiwan – sequence: 2 givenname: Chi-Ming surname: Chu fullname: Chu, Chi-Ming organization: †School of Public Health, National Defense Medical Center, Taipei, Taiwan – sequence: 3 givenname: Chun-Sung surname: Sung fullname: Sung, Chun-Sung organization: ‡Department of Anesthesiology, Taipei Veterans General Hospital and School of Medicine, National Yang-Ming University, Taipei, Taiwan – sequence: 4 givenname: Shung-Tai surname: Ho fullname: Ho, Shung-Tai email: yu0716@hotmail.com organization: §Hospital Division, Taipei Veterans General Hospital, Taipei, Taiwan – sequence: 5 givenname: Yi-Syuan surname: Wu fullname: Wu, Yi-Syuan organization: †School of Public Health, National Defense Medical Center, Taipei, Taiwan – sequence: 6 givenname: Chun-Yu surname: Liang fullname: Liang, Chun-Yu organization: ¶Graduate Institute of Medical Sciences, and School of Nursing, National Defense Medical Center, Taipei, Taiwan – sequence: 7 givenname: Kwua-Yun surname: Wang fullname: Wang, Kwua-Yun email: kywang7@vghtpe.gov.tw organization: ||Department of Nursing, Taipei Veterans General Hospital and Graduate Institute of Medical Sciences, and School of Nursing, National Defense Medical Center, Taipei, Taiwan |
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Cites_doi | 10.1016/j.jpain.2007.09.005 10.1097/00002820-199704000-00002 10.1002/j.1532-2149.2013.00337.x 10.1007/s11739-012-0815-8 10.1111/pme.12643 10.1016/j.jpainsymman.2012.07.021 10.1038/nm.2249 10.1016/S0304-3959(00)00339-0 10.1016/S0304-3959(00)00344-4 10.4037/ajcc2010624 10.3109/02656736.2010.525588 10.1016/j.pain.2010.03.013 10.1111/jan.12301 10.1093/annonc/mdl314 10.1016/j.ejpain.2004.09.010 10.1007/s101940200019 10.1007/PL00012189 10.1097/SMJ.0b013e3182296f20 10.1111/pme.12578 10.1016/j.jpain.2009.06.007 10.1097/ALN.0b013e3181de0e6d 10.1016/S0885-3924(03)00162-3 10.1016/S0304-3959(01)00349-9 10.1093/annonc/mdm056 10.1111/pme.12753 10.1016/S0885-3924(00)00209-8 10.1111/pme.12588 10.1111/pme.12075 |
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Copyright | 2016 American Academy of Pain Medicine. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com 2016 2016 American Academy of Pain Medicine. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com. Copyright © 2016 American Academy of Pain Medicine |
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Snippet | Objective. Developing a new measurement index is the first step in evaluating pain relief outcomes. Although the percentage difference in pain intensity (%PID)... Developing a new measurement index is the first step in evaluating pain relief outcomes. Although the percentage difference in pain intensity (%PID) is the... OBJECTIVEDeveloping a new measurement index is the first step in evaluating pain relief outcomes. Although the percentage difference in pain intensity (%PID)... |
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Title | Using a New Measurement to Evaluate Pain Relief Among Cancer Inpatients with Clinically Significant Pain Based on a Nursing Information System: A Three-Year Hospital-Based Study |
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