Data

Evidence-based Processes and Outcomes of Care (EPOC): Improving services and outcomes for joint replacement patients

University of New South Wales
Badge, Helen ; Timothy, Churches ; Xuan, Wei ; Armstrong, Elizabeth ; Harris, Ian ; Naylor, Justine
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ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Adc&rfr_id=info%3Asid%2FANDS&rft_id=info:doi10.26190/c46r-ne05&rft.title=Evidence-based Processes and Outcomes of Care (EPOC): Improving services and outcomes for joint replacement patients &rft.identifier=https://doi.org/10.26190/c46r-ne05&rft.publisher=UNSW&rft.description=The data includes 1013 variables: participant demographic information, comorbid health conditions, acute care and surgical data (total primary joint replacement), patient-reported outcomes measures (Oxford Hip or Knee Score and EQ-5D) at baseline, 35, 90 and 365 days post-surgery, patient-reported satisfaction and perception of success of surgery, details of VTE and antimicrobial prophylaxis, rehabilitation and health service utilisation and any money spent in recovery. ANy identifying information (names, dates and sites have been removed) Methodology The data were collected as part of a large prospective observational study involving 19 high volume total joint replacement sites from five Australian states. Participants include adults (over 18 years) undergoing primary total hip or knee joint replacement, able to give informed consent, participate in follow-up in English for one-year post-surgery, without cognitive impairment affecting the ability to participate in interviews. Data were collected from patients prior to surgery (after consenting). SItes provided acute care data. Follow up was completed by researchers via telephone at approximately 35, 90 and 365 days post-surgery. Compliance with clinical guidelines for preventing venous thromboembolism and surgical site infection was calculated based on agreed criteria and taking patient appropriate variations into account (as compliant).&rft.creator=Badge, Helen &rft.creator=Timothy, Churches &rft.creator=Xuan, Wei &rft.creator=Armstrong, Elizabeth &rft.creator=Harris, Ian &rft.creator=Naylor, Justine &rft.date=2021&rft.relation=https://doi.org/10.1177/2309499018802493&rft.relation=https://doi.org/10.1371/journal.pone.0180090&rft.relation=https://doi.org/10.1371/journal.pone.0159799&rft.relation=https://doi.org/10.1177/2309499021992605&rft.relation=https://doi.org/10.1371/journal.pone.0179820&rft.coverage=Australia&rft_rights=Whitlam Orthopaedic Research Centre, 2021&rft_rights=Creative Commons Attribution 4.0 International (CC BY 4.0)&rft_subject=total joint replacement&rft_subject=arthroplasty&rft_subject=clinical guidelines&rft_subject=venous thromboembolism&rft_subject=surgical site infection&rft_subject=prophylaxis&rft_subject=surgical complications&rft_subject=patient reported outcomes&rft_subject=CLINICAL SCIENCES,&rft.type=dataset&rft.language=English Access the data

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Creative Commons Attribution 4.0 International (CC BY 4.0)

Whitlam Orthopaedic Research Centre, 2021

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Contact Information

Orthopaedic Department, Ingham Institute

Brief description

The data includes 1013 variables: participant demographic information, comorbid health conditions, acute care and surgical data (total primary joint replacement), patient-reported outcomes measures (Oxford Hip or Knee Score and EQ-5D) at baseline, 35, 90 and 365 days post-surgery, patient-reported satisfaction and perception of success of surgery, details of VTE and antimicrobial prophylaxis, rehabilitation and health service utilisation and any money spent in recovery. ANy identifying information (names, dates and sites have been removed)

Methodology

The data were collected as part of a large prospective observational study involving 19 high volume total joint replacement sites from five Australian states. Participants include adults (over 18 years) undergoing primary total hip or knee joint replacement, able to give informed consent, participate in follow-up in English for one-year post-surgery, without cognitive impairment affecting the ability to participate in interviews. Data were collected from patients prior to surgery (after consenting). SItes provided acute care data. Follow up was completed by researchers via telephone at approximately 35, 90 and 365 days post-surgery. Compliance with clinical guidelines for preventing venous thromboembolism and surgical site infection was calculated based on agreed criteria and taking patient appropriate variations into account (as compliant).

Spatial Coverage And Location

text: Australia

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