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Influence of a New “Call-Out Algorithm” for Management of Postoperative Pain and Its Side Effects on Length of Stay in Hospital: A Two-Centre Prospective Randomized Trial

BACKGROUND: We recently introduced the efficacy safety score (ESS) as a new “call-out algorithm” for management of postoperative pain and side effects. In this study, we report the influence of ESS recorded hourly during the first 8 hours after surgery on the mobility degree, postoperative nonsurgic...

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Autores principales: Dybvik, Lisa, Skraastad, Erlend, Yeltayeva, Aigerim, Konkayev, Aidos, Musaeva, Tatiana, Zabolotskikh, Igor, Bjertnaes, Lars, Dahl, Vegard, Raeder, Johan, Kuklin, Vladimir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5569639/
https://www.ncbi.nlm.nih.gov/pubmed/28855800
http://dx.doi.org/10.1155/2017/9431984
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author Dybvik, Lisa
Skraastad, Erlend
Yeltayeva, Aigerim
Konkayev, Aidos
Musaeva, Tatiana
Zabolotskikh, Igor
Bjertnaes, Lars
Dahl, Vegard
Raeder, Johan
Kuklin, Vladimir
author_facet Dybvik, Lisa
Skraastad, Erlend
Yeltayeva, Aigerim
Konkayev, Aidos
Musaeva, Tatiana
Zabolotskikh, Igor
Bjertnaes, Lars
Dahl, Vegard
Raeder, Johan
Kuklin, Vladimir
author_sort Dybvik, Lisa
collection PubMed
description BACKGROUND: We recently introduced the efficacy safety score (ESS) as a new “call-out algorithm” for management of postoperative pain and side effects. In this study, we report the influence of ESS recorded hourly during the first 8 hours after surgery on the mobility degree, postoperative nonsurgical complications, and length of hospital stay (LOS). METHODS: We randomized 1152 surgical patients into three groups for postoperative observation: (1) ESS group (n = 409), (2) Verbal Numeric Rate Scale (VNRS) for pain group (n = 417), and (3) an ordinary qualitative observation (Control) group (n = 326). An ESS > 10 or VNRS > 4 at rest or a nurse's observation of pain or adverse reaction to analgesic treatment in the Control group served as a “call-out alarm” for an anaesthesiologist. RESULTS: We found no significant differences in the mobility degree and number of postoperative nonsurgical complications between the groups. LOS was significantly shorter with 12.7 ± 6.3 days (mean ± SD) in the ESS group versus 14.2 ± 6.2 days in the Control group (P < 0.001). CONCLUSION: Postoperative ESS recording in combination with the possibility to call upon an anaesthesiologist when exceeding the threshold score might have contributed to the reductions of LOS in this two-centre study. This trial is registered with NCT02143128.
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spelling pubmed-55696392017-08-30 Influence of a New “Call-Out Algorithm” for Management of Postoperative Pain and Its Side Effects on Length of Stay in Hospital: A Two-Centre Prospective Randomized Trial Dybvik, Lisa Skraastad, Erlend Yeltayeva, Aigerim Konkayev, Aidos Musaeva, Tatiana Zabolotskikh, Igor Bjertnaes, Lars Dahl, Vegard Raeder, Johan Kuklin, Vladimir Pain Res Manag Clinical Study BACKGROUND: We recently introduced the efficacy safety score (ESS) as a new “call-out algorithm” for management of postoperative pain and side effects. In this study, we report the influence of ESS recorded hourly during the first 8 hours after surgery on the mobility degree, postoperative nonsurgical complications, and length of hospital stay (LOS). METHODS: We randomized 1152 surgical patients into three groups for postoperative observation: (1) ESS group (n = 409), (2) Verbal Numeric Rate Scale (VNRS) for pain group (n = 417), and (3) an ordinary qualitative observation (Control) group (n = 326). An ESS > 10 or VNRS > 4 at rest or a nurse's observation of pain or adverse reaction to analgesic treatment in the Control group served as a “call-out alarm” for an anaesthesiologist. RESULTS: We found no significant differences in the mobility degree and number of postoperative nonsurgical complications between the groups. LOS was significantly shorter with 12.7 ± 6.3 days (mean ± SD) in the ESS group versus 14.2 ± 6.2 days in the Control group (P < 0.001). CONCLUSION: Postoperative ESS recording in combination with the possibility to call upon an anaesthesiologist when exceeding the threshold score might have contributed to the reductions of LOS in this two-centre study. This trial is registered with NCT02143128. Hindawi 2017 2017-08-10 /pmc/articles/PMC5569639/ /pubmed/28855800 http://dx.doi.org/10.1155/2017/9431984 Text en Copyright © 2017 Lisa Dybvik et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Study
Dybvik, Lisa
Skraastad, Erlend
Yeltayeva, Aigerim
Konkayev, Aidos
Musaeva, Tatiana
Zabolotskikh, Igor
Bjertnaes, Lars
Dahl, Vegard
Raeder, Johan
Kuklin, Vladimir
Influence of a New “Call-Out Algorithm” for Management of Postoperative Pain and Its Side Effects on Length of Stay in Hospital: A Two-Centre Prospective Randomized Trial
title Influence of a New “Call-Out Algorithm” for Management of Postoperative Pain and Its Side Effects on Length of Stay in Hospital: A Two-Centre Prospective Randomized Trial
title_full Influence of a New “Call-Out Algorithm” for Management of Postoperative Pain and Its Side Effects on Length of Stay in Hospital: A Two-Centre Prospective Randomized Trial
title_fullStr Influence of a New “Call-Out Algorithm” for Management of Postoperative Pain and Its Side Effects on Length of Stay in Hospital: A Two-Centre Prospective Randomized Trial
title_full_unstemmed Influence of a New “Call-Out Algorithm” for Management of Postoperative Pain and Its Side Effects on Length of Stay in Hospital: A Two-Centre Prospective Randomized Trial
title_short Influence of a New “Call-Out Algorithm” for Management of Postoperative Pain and Its Side Effects on Length of Stay in Hospital: A Two-Centre Prospective Randomized Trial
title_sort influence of a new “call-out algorithm” for management of postoperative pain and its side effects on length of stay in hospital: a two-centre prospective randomized trial
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5569639/
https://www.ncbi.nlm.nih.gov/pubmed/28855800
http://dx.doi.org/10.1155/2017/9431984
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