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Reducing Opioid Use Following Posterior Spinal Fusion Procedures: A Pilot Project
Reducing Opioid Use Following Posterior Spinal Fusion Procedures: A Pilot Project
Reducing Opioid Use Following Posterior Spinal Fusion Procedures: A Pilot Project

상세정보

자료유형  
 학위논문 서양
최종처리일시  
20260202103512
ISBN  
9798288806421
DDC  
610.73
저자명  
Cornett, Kevin.
서명/저자  
Reducing Opioid Use Following Posterior Spinal Fusion Procedures: A Pilot Project
발행사항  
[Sl] : Yale University, 2025
발행사항  
Ann Arbor : ProQuest Dissertations & Theses, 2025
형태사항  
61 p
주기사항  
Source: Dissertations Abstracts International, Volume: 87-01, Section: B.
주기사항  
Advisor: Feder, Shelli.
학위논문주기  
Thesis (D.N.P.)--Yale University, 2025.
초록/해제  
요약Importance: Opioid misuse and mortality remain a prevalent problem in the United States and there is a high rate of chronic opioid-use after spinal fusions. Current guidelines recommend the optimization of non-opioid analgesics as a primary pain control strategy with opioids acting as a secondary agent.Objective: To pilot an analgesic decision tree (ADT) featuring non-opioid analgesics to reduce postoperative pain, opioid consumption, and the incidence of adverse events during the first 48 hours after patients undergo a posterior spinal fusion.Methods: A literature review of opioid-sparing analgesics was conducted and a protocol developed as an interdisciplinary collaboration. The ADT was piloted in an intensive care unit for 10 weeks. Pain control, opioid consumption, and the incidence of adverse events were compared to historical controls from a previous 10-week period.Results: In total, 12 historical control charts were reviewed and 17 patients enrolled in the ADT group. There was no significant difference in groups. The ADT did not affect NRS scores, CPOT scores, MME consumption, or ORAE in a statistically significant way. Power analyses indicate that a minimum of 9894 patients are required to detect significance.Conclusions: The ADT may be non-inferior in pain control and opioid consumption, but future testing is required. Further pilots should control confounding influences to optimize power analyses. Subsequent projects should utilize these power analyses to determine the ADT's influence on pain control, opioid consumption, and adverse event incidence.
일반주제명  
Nursing
일반주제명  
Pharmacology
일반주제명  
Medicine
일반주제명  
Surgery
키워드  
Opioid misuse
키워드  
Posterior spinal fusion
키워드  
Analgesic decision tree
키워드  
Pain control
키워드  
Opioid consumption
기타저자  
Yale University Yale University School of Nursing
기본자료저록  
Dissertations Abstracts International. 87-01B.
전자적 위치 및 접속  
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MARC

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■040    ▼aMiAaPQ▼cMiAaPQ
■0820  ▼a610.73
■1001  ▼aCornett,  Kevin.
■24510▼aReducing  Opioid  Use  Following  Posterior  Spinal  Fusion  Procedures:  A  Pilot  Project
■260    ▼a[Sl]▼bYale  University▼c2025
■260  1▼aAnn  Arbor▼bProQuest  Dissertations  &  Theses▼c2025
■300    ▼a61  p
■500    ▼aSource:  Dissertations  Abstracts  International,  Volume:  87-01,  Section:  B.
■500    ▼aAdvisor:  Feder,  Shelli.
■5021  ▼aThesis  (D.N.P.)--Yale  University,  2025.
■520    ▼aImportance:  Opioid  misuse  and  mortality  remain  a  prevalent  problem  in  the  United  States  and  there  is  a  high  rate  of  chronic  opioid-use  after  spinal  fusions.  Current  guidelines  recommend  the  optimization  of  non-opioid  analgesics  as  a  primary  pain  control  strategy  with  opioids  acting  as  a  secondary  agent.Objective:  To  pilot  an  analgesic  decision  tree  (ADT)  featuring  non-opioid  analgesics  to  reduce  postoperative  pain,  opioid  consumption,  and  the  incidence  of  adverse  events  during  the  first  48  hours  after  patients  undergo  a  posterior  spinal  fusion.Methods:  A  literature  review  of  opioid-sparing  analgesics  was  conducted  and  a  protocol  developed  as  an  interdisciplinary  collaboration.  The  ADT  was  piloted  in  an  intensive  care  unit  for  10  weeks.  Pain  control,  opioid  consumption,  and  the  incidence  of  adverse  events  were  compared  to  historical  controls  from  a  previous  10-week  period.Results:  In  total,  12  historical  control  charts  were  reviewed  and  17  patients  enrolled  in  the  ADT  group.  There  was  no  significant  difference  in  groups.  The  ADT  did  not  affect  NRS  scores,  CPOT  scores,  MME  consumption,  or  ORAE  in  a  statistically  significant  way.  Power  analyses  indicate  that  a  minimum  of  9894  patients  are  required  to  detect  significance.Conclusions:  The  ADT  may  be  non-inferior  in  pain  control  and  opioid  consumption,  but  future  testing  is  required.  Further  pilots  should  control  confounding  influences  to  optimize  power  analyses.  Subsequent  projects  should  utilize  these  power  analyses  to  determine  the  ADT's  influence  on  pain  control,  opioid  consumption,  and  adverse  event  incidence.
■590    ▼aSchool  code:  0265.
■650  4▼aNursing
■650  4▼aPharmacology
■650  4▼aMedicine
■650  4▼aSurgery
■653    ▼aOpioid  misuse
■653    ▼aPosterior  spinal  fusion
■653    ▼aAnalgesic  decision  tree
■653    ▼aPain  control
■653    ▼aOpioid  consumption
■690    ▼a0569
■690    ▼a0576
■690    ▼a0564
■690    ▼a0419
■71020▼aYale  University▼bYale  University  School  of  Nursing.
■7730  ▼tDissertations  Abstracts  International▼g87-01B.
■790    ▼a0265
■791    ▼aD.N.P.
■792    ▼a2025
■793    ▼aEnglish
■85640▼uhttp://www.riss.kr/pdu/ddodLink.do?id=T17357438▼nKERIS▼z이  자료의  원문은  한국교육학술정보원에서  제공합니다.

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