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            <header>
                <identifier>oai:data.mendeley.com/6k3w5zyj7m.1</identifier>
                <datestamp>2020-08-22T22:05:17Z</datestamp>
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            <metadata><oai_dc:dc xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
    <dc:creator>Hetta, Helal</dc:creator>
    <dc:title>Data for : Preoperative Duloxetine to Improve acute pain and quality of recovery in  patients undergoing modified radical mastectomy: A dose-ranging randomized controlled trial </dc:title>
    <dc:publisher>Mendeley Data</dc:publisher>
    <dc:description>Preoperative Duloxetine to Improve acute pain and quality of recovery in  patients undergoing modified radical mastectomy: A dose-ranging randomized controlled trial 
Objective: Duloxetine has been recently used as a part of multimodal analgesia in perioperative settings, yet the optimal dose of Duloxetine is not determined.
Design: A parallel, randomized, placebo-controlled trial.
Setting: Tertiary level oncology center 
Patients: 88 female patients with breast cancer were subjected to modified radical mastectomy (MRM) with ASA class I and II were recruited.
Intervention: Participants were randomly allocated into 4 equal groups received 2 hours preoperatively, placebo (D0, N=22), Duloxetine 30 mg (D30, N=22), Duloxetine 60 mg (D60, N=22) and Duloxetine 90 mg (D90, N=22) tablet.
Measurements: The primary outcome; 24 h cumulative postoperative morphine consumption and the secondary outcomes; VAS score of pain intensity, quality of recovery (QoR-40), time to Aldrete 9, and side effects (sedation and vomiting) were measured.
Results: The median (IQR) consumption of morphine (mg) in the first postoperative 24 hours was significantly decreased in both (D60 and D90) groups compared to (D0 and D30) groups, P &lt; 0.001(Bonferroni corrected), however, a non-significant reduction was observed between D90 group vs. D60 group and D30 group vs. D0 group, P= 0.595 and P = 0.462 respectively, D60 vs. D0; 0(0-6) vs. 10(9-12), D60 vs. D30; 0(0-6) vs. 9(8-11), D90 vs. D0; 0(0-5) vs. 10(9-12), D90 vs. D30; 0(0-5) vs. 9(8-11), D90 vs. D60; 0(0-5) vs. 0(0-6), D30 vs. D0; 9(8-11) vs. 10(9-12), patients in D90 group took longer time to recover from anesthesia &quot; time to Aldrete 9&quot; and showed an increased level of sedation in comparison with other groups, vomiting was more frequent in the D90 group.
Conclusion: Preoperative oral Duloxetine of 60 mg, for patients subjected to MRM is the optimal dose considering its analgesic efficacy and side effects.
</dc:description>
    <dc:subject>Randomized Controlled Trial</dc:subject>
    <dc:contributor>hetta, diab</dc:contributor>
    <dc:contributor>Elgalaly, Nourhan</dc:contributor>
    <dc:contributor>Mohamed, Montaser</dc:contributor>
    <dc:type>Dataset</dc:type>
    <dc:identifier>doi:10.17632/6k3w5zyj7m.1</dc:identifier>
    <dc:identifier>oai:data.mendeley.com/6k3w5zyj7m.1</dc:identifier>
    <dc:rights>Creative Commons Attribution 4.0 International</dc:rights>
    <dc:rights>http://creativecommons.org/licenses/by/4.0</dc:rights>
    <dc:relation>https://data.mendeley.com/datasets/6k3w5zyj7m</dc:relation>
    <dc:date>2020-08-22T22:05:17Z</dc:date>
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