The Effectiveness of Intravenous Parecoxib on the Incidence of Ipsilateral Shoulder Pain After Thoracotomy: A Randomized, Double-Blind, Placebo-Controlled Trial
© 2018 Elsevier Inc. Objectives: To determine the incidence of ipsilateral shoulder pain (ISP) with the therapeutic use of parecoxib compared with a placebo after thoracotomy. Design: A prospective, randomized, double-blind, placebo-controlled trial. Setting: A tertiary-care university hospital. Par...
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th-cmuir.6653943832-589952018-09-05T04:36:07Z The Effectiveness of Intravenous Parecoxib on the Incidence of Ipsilateral Shoulder Pain After Thoracotomy: A Randomized, Double-Blind, Placebo-Controlled Trial Tanyong Pipanmekaporn Yodying Punjasawadwong Somrat Charuluxananan Worawut Lapisatepun Pavena Bunburaphong Settapong Boonsri Apichat Tantraworasin Nutchanart Bunchungmongkol Medicine © 2018 Elsevier Inc. Objectives: To determine the incidence of ipsilateral shoulder pain (ISP) with the therapeutic use of parecoxib compared with a placebo after thoracotomy. Design: A prospective, randomized, double-blind, placebo-controlled trial. Setting: A tertiary-care university hospital. Participants: Adult patients undergoing an elective thoracotomy between June 2011 and February 2015. Interventions: Patients were allocated randomly into the parecoxib group (n = 80) and the control group (n = 80). In the parecoxib group, 40 mg of parecoxib was diluted into 2 mL and given intravenously 30 minutes before surgery and then every 12 hours postoperatively for 48 hours. In the control group, 2 mL of normal saline was given to the patients at the same intervals. Measurements and Main Results: A numerical rating scale was used to assess the intensity of ISP at 2, 6, 12, 24, 48, 72, and 96 hours after surgery. Intravenous morphine (0.05 mg/kg) was used as the rescue medication for ISP during the 96-hour period. Baseline characteristics of patients in both groups were comparable. Patients in the parecoxib group had a significantly lower incidence of ISP, both overall (42.5% v 62.0%, p = 0.014) and of moderate-to-severe ISP when compared with the control group (26.2% v 49.4%, p = 0.003). Parecoxib reduced the risk of ISP by a statistically significant 32% (risk ratio, 0.68; 95% confidence interval, 0.50-0.93, p = 0.016). There were no significant differences in the occurrence of adverse effects between the groups. Conclusions: Intravenous parecoxib significantly can reduce the incidence and severity of ISP after thoracotomy. 2018-09-05T04:36:07Z 2018-09-05T04:36:07Z 2018-02-01 Journal 15328422 10530770 2-s2.0-85041410863 10.1053/j.jvca.2017.05.048 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85041410863&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/58995 |
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Medicine Tanyong Pipanmekaporn Yodying Punjasawadwong Somrat Charuluxananan Worawut Lapisatepun Pavena Bunburaphong Settapong Boonsri Apichat Tantraworasin Nutchanart Bunchungmongkol The Effectiveness of Intravenous Parecoxib on the Incidence of Ipsilateral Shoulder Pain After Thoracotomy: A Randomized, Double-Blind, Placebo-Controlled Trial |
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© 2018 Elsevier Inc. Objectives: To determine the incidence of ipsilateral shoulder pain (ISP) with the therapeutic use of parecoxib compared with a placebo after thoracotomy. Design: A prospective, randomized, double-blind, placebo-controlled trial. Setting: A tertiary-care university hospital. Participants: Adult patients undergoing an elective thoracotomy between June 2011 and February 2015. Interventions: Patients were allocated randomly into the parecoxib group (n = 80) and the control group (n = 80). In the parecoxib group, 40 mg of parecoxib was diluted into 2 mL and given intravenously 30 minutes before surgery and then every 12 hours postoperatively for 48 hours. In the control group, 2 mL of normal saline was given to the patients at the same intervals. Measurements and Main Results: A numerical rating scale was used to assess the intensity of ISP at 2, 6, 12, 24, 48, 72, and 96 hours after surgery. Intravenous morphine (0.05 mg/kg) was used as the rescue medication for ISP during the 96-hour period. Baseline characteristics of patients in both groups were comparable. Patients in the parecoxib group had a significantly lower incidence of ISP, both overall (42.5% v 62.0%, p = 0.014) and of moderate-to-severe ISP when compared with the control group (26.2% v 49.4%, p = 0.003). Parecoxib reduced the risk of ISP by a statistically significant 32% (risk ratio, 0.68; 95% confidence interval, 0.50-0.93, p = 0.016). There were no significant differences in the occurrence of adverse effects between the groups. Conclusions: Intravenous parecoxib significantly can reduce the incidence and severity of ISP after thoracotomy. |
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Tanyong Pipanmekaporn Yodying Punjasawadwong Somrat Charuluxananan Worawut Lapisatepun Pavena Bunburaphong Settapong Boonsri Apichat Tantraworasin Nutchanart Bunchungmongkol |
author_facet |
Tanyong Pipanmekaporn Yodying Punjasawadwong Somrat Charuluxananan Worawut Lapisatepun Pavena Bunburaphong Settapong Boonsri Apichat Tantraworasin Nutchanart Bunchungmongkol |
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Tanyong Pipanmekaporn |
title |
The Effectiveness of Intravenous Parecoxib on the Incidence of Ipsilateral Shoulder Pain After Thoracotomy: A Randomized, Double-Blind, Placebo-Controlled Trial |
title_short |
The Effectiveness of Intravenous Parecoxib on the Incidence of Ipsilateral Shoulder Pain After Thoracotomy: A Randomized, Double-Blind, Placebo-Controlled Trial |
title_full |
The Effectiveness of Intravenous Parecoxib on the Incidence of Ipsilateral Shoulder Pain After Thoracotomy: A Randomized, Double-Blind, Placebo-Controlled Trial |
title_fullStr |
The Effectiveness of Intravenous Parecoxib on the Incidence of Ipsilateral Shoulder Pain After Thoracotomy: A Randomized, Double-Blind, Placebo-Controlled Trial |
title_full_unstemmed |
The Effectiveness of Intravenous Parecoxib on the Incidence of Ipsilateral Shoulder Pain After Thoracotomy: A Randomized, Double-Blind, Placebo-Controlled Trial |
title_sort |
effectiveness of intravenous parecoxib on the incidence of ipsilateral shoulder pain after thoracotomy: a randomized, double-blind, placebo-controlled trial |
publishDate |
2018 |
url |
https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85041410863&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/58995 |
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