Clinical Evaluation of a Novel Technology for Oral Patient-Controlled Analgesia, the PCoA® Acute Device, for Hospitalized Patients with Postoperative Pain, in Pilot Feasibility Study

Background. Acute postoperative pain delays recovery and increases morbidity and mortality. Traditional administration of postoperative analgesics by nurses is often inefficient. The present study evaluated the safety, efficacy, and usability of a novel, patient-controlled analgesic dispenser, the P...

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Main Authors: Stefan Wirz, Stefan Conrad, Ronit Shtrichman, Kai Schimo, Eva Hoffmann
Format: Article
Language:English
Published: Hindawi Limited 2017-01-01
Series:Pain Research and Management
Online Access:http://dx.doi.org/10.1155/2017/7962135
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spelling doaj-a9bd9ddd8b0a497f85e74fbe3a39f0c62020-11-24T23:02:12ZengHindawi LimitedPain Research and Management1203-67651918-15232017-01-01201710.1155/2017/79621357962135Clinical Evaluation of a Novel Technology for Oral Patient-Controlled Analgesia, the PCoA® Acute Device, for Hospitalized Patients with Postoperative Pain, in Pilot Feasibility StudyStefan Wirz0Stefan Conrad1Ronit Shtrichman2Kai Schimo3Eva Hoffmann4Department of Anesthesia, Intensive Medicine, Pain Medicine/Palliative Medicine, Center for Pain Medicine, CURA Hospital GFO, Bad Honnef, GermanyDosentRx Ltd., 2 Hahar St., Har Tuv Industrial Zone A, 9980101 Har Tuv, IsraelDosentRx Ltd., 2 Hahar St., Har Tuv Industrial Zone A, 9980101 Har Tuv, IsraelDosentRx Ltd., 2 Hahar St., Har Tuv Industrial Zone A, 9980101 Har Tuv, IsraelDepartment of Anesthesia, Interdisciplinary Intensive Care, Emergency Medicine and Pain Medicine, EvK-Protestant Hospital Herne, Herne, GermanyBackground. Acute postoperative pain delays recovery and increases morbidity and mortality. Traditional administration of postoperative analgesics by nurses is often inefficient. The present study evaluated the safety, efficacy, and usability of a novel, patient-controlled analgesic dispenser, the PCoA Acute. Methods. A controlled pilot study was conducted at three medical centers. Patients scheduled for elective surgery were enrolled into two groups, both taking oral analgesics: a control group (n=43), opioids dispensed by nurses, and a test group (n=27), opioids dispensed via the PCoA Acute. Pill intake data were recorded. Pain ratings at rest and during movement were surveyed. Results. No severe adverse events were recorded. Average pill intake time was reduced from 8 : 58 minutes in the control group to 1 : 17 minutes in the test group (P value < 0.05). The test group took 67% more pills than the control group, indicating enhanced compliance. Pain scores were significantly lower for patients in the test group (P value < 0.05). Over 90% of PCoA Acute users were satisfied with its use. Conclusions. The study confirmed that PCoA Acute is safe and effective. It is well accepted by patients and medical staff. Its use can optimize pain medication administration.http://dx.doi.org/10.1155/2017/7962135
collection DOAJ
language English
format Article
sources DOAJ
author Stefan Wirz
Stefan Conrad
Ronit Shtrichman
Kai Schimo
Eva Hoffmann
spellingShingle Stefan Wirz
Stefan Conrad
Ronit Shtrichman
Kai Schimo
Eva Hoffmann
Clinical Evaluation of a Novel Technology for Oral Patient-Controlled Analgesia, the PCoA® Acute Device, for Hospitalized Patients with Postoperative Pain, in Pilot Feasibility Study
Pain Research and Management
author_facet Stefan Wirz
Stefan Conrad
Ronit Shtrichman
Kai Schimo
Eva Hoffmann
author_sort Stefan Wirz
title Clinical Evaluation of a Novel Technology for Oral Patient-Controlled Analgesia, the PCoA® Acute Device, for Hospitalized Patients with Postoperative Pain, in Pilot Feasibility Study
title_short Clinical Evaluation of a Novel Technology for Oral Patient-Controlled Analgesia, the PCoA® Acute Device, for Hospitalized Patients with Postoperative Pain, in Pilot Feasibility Study
title_full Clinical Evaluation of a Novel Technology for Oral Patient-Controlled Analgesia, the PCoA® Acute Device, for Hospitalized Patients with Postoperative Pain, in Pilot Feasibility Study
title_fullStr Clinical Evaluation of a Novel Technology for Oral Patient-Controlled Analgesia, the PCoA® Acute Device, for Hospitalized Patients with Postoperative Pain, in Pilot Feasibility Study
title_full_unstemmed Clinical Evaluation of a Novel Technology for Oral Patient-Controlled Analgesia, the PCoA® Acute Device, for Hospitalized Patients with Postoperative Pain, in Pilot Feasibility Study
title_sort clinical evaluation of a novel technology for oral patient-controlled analgesia, the pcoa® acute device, for hospitalized patients with postoperative pain, in pilot feasibility study
publisher Hindawi Limited
series Pain Research and Management
issn 1203-6765
1918-1523
publishDate 2017-01-01
description Background. Acute postoperative pain delays recovery and increases morbidity and mortality. Traditional administration of postoperative analgesics by nurses is often inefficient. The present study evaluated the safety, efficacy, and usability of a novel, patient-controlled analgesic dispenser, the PCoA Acute. Methods. A controlled pilot study was conducted at three medical centers. Patients scheduled for elective surgery were enrolled into two groups, both taking oral analgesics: a control group (n=43), opioids dispensed by nurses, and a test group (n=27), opioids dispensed via the PCoA Acute. Pill intake data were recorded. Pain ratings at rest and during movement were surveyed. Results. No severe adverse events were recorded. Average pill intake time was reduced from 8 : 58 minutes in the control group to 1 : 17 minutes in the test group (P value < 0.05). The test group took 67% more pills than the control group, indicating enhanced compliance. Pain scores were significantly lower for patients in the test group (P value < 0.05). Over 90% of PCoA Acute users were satisfied with its use. Conclusions. The study confirmed that PCoA Acute is safe and effective. It is well accepted by patients and medical staff. Its use can optimize pain medication administration.
url http://dx.doi.org/10.1155/2017/7962135
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