Anticipated Versus Actual Patient and Caregiver Burden Following Ambulatory Orthopedic Surgery

Overview

In 2011, 38.6 million hospital stays occurred in the United States at a cost of $387.2 billion. 47.9 percent involved hospitalizations during which surgical procedures were performed. Orthopedic procedures constituted the most frequently performed and most costly of operating room procedures. As the healthcare climate in the United States continues to change, there is a trend towards providing effective care in a fiscally conservative manner. Central to this strategy is the shift towards increasing ambulatory surgical procedures from surgeries requiring post-operative admission for patients. While savings to hospitals and third-party payers are implied, there may be an unrecognized increase in financial, physical, and psychosocial post-operative costs to patients undergoing ambulatory surgery and to their caregivers. Rawal et al., and McGarth and colleagues have found that patients undergoing orthopedic procedures had moderate to severe post-operative pain. We propose to present a survey to patients and their caregivers before surgery and at multiple timepoints post-operatively to acquire information on the impacts of ambulatory orthopedic surgery. In addition to assessing post-operative pain, this study serves to examine various other possible burdens to patients that have not been previously evaluated in this patient population. REFERENCES McGarth B, Elgendy H, Chung F, Kamming D, Curti B, King S. Thirty percent of patients have a moderate to severe pain 24 hr after ambulatory surgery: a survey of 5,703 patients. Can J Anesth. 2004; 51:886-891. Rawal N, Hylander J, Nydahl P, Olofsson I, Gupta A. Survey of postoperative analgesia following ambulatory surgery. Acta Anesthesiol Scand. 1997; 41:1017-1022.

Study Type

  • Study Type: Observational
  • Study Design
    • Time Perspective: Prospective
  • Study Primary Completion Date: March 2016

Interventions

  • Other: Survey
    • Patients and their caregivers will be asked to complete surveys about their expected and actual time taken off from work. They will also answer questions about the patient’s recovery, as well as the patient/caregiver relationship.

Arms, Groups and Cohorts

  • Patient/Caregiver Dyad

Clinical Trial Outcome Measures

Primary Measures

  • Time taken off from work–specifically, the number of extra days taken off from work by patients and their caregivers after surgery
    • Time Frame: Holding area before surgery, post-operative day 1 (POD 1), POD 7, biweekly thereafter until patient returns to baseline level of work, and two weeks after patient returns to baseline level of work
    • Patients and caregivers will be considered able to return to their baseline level of work once they can fulfill all responsibilities at their current occupation with no restrictions.

Secondary Measures

  • Expected Burden of Recovery
    • Time Frame: Holding area before surgery, post-operative day 1 (POD 1), POD 7, biweekly thereafter until patient returns to baseline level of work, and two weeks after patient returns to baseline level of work
    • Patient: pain, nausea, vomiting, doctor appointments/hospital visits, days to return to daily activities, days to achieve recovery, days missed from work, emotional duress Caregiver: days missed from work; days to return to daily activities; emotional duress; productivity, sleep, work and personal adjustments
  • Excess (Actual Beyond Expected) Burden of Recovery
    • Time Frame: Holding area before surgery, post-operative day 1 (POD 1), POD 7, biweekly thereafter until patient returns to baseline level of work, and two weeks after patient returns to baseline level of work
    • Patient: pain, nausea, vomiting, doctor appointments/hospital visits, days to return to daily activities, days to achieve recovery beyond expected, days missed from work, emotional duress Caregiver: days missed from work; days to return to daily activities; emotional duress; productivity, sleep, work and personal adjustments

Participating in This Clinical Trial

Inclusion Criteria

  • Patients undergoing outpatient arthroscopic knee debridement or meniscectomy surgery – Age 18-85 – Primary caregiver available during preoperative period who is employed full-time or part-time – English speaking – Patients who are employed full-time or part-time Exclusion Criteria:

  • Patients on disability or worker's compensation – Patients undergoing concurrent procedures – Patients who are self-employed – Caregivers who are self-employed – Surgeons: Dr. Altchek, Dr. Warren, Dr. O'Brien

Gender Eligibility: All

Minimum Age: 18 Years

Maximum Age: 85 Years

Are Healthy Volunteers Accepted: No

Investigator Details

  • Lead Sponsor
    • Hospital for Special Surgery, New York
  • Provider of Information About this Clinical Study
    • Sponsor
  • Overall Official(s)
    • Kanupriya Kumar, MD, Principal Investigator, Hospital for Special Surgery, New York

References

McGrath B, Elgendy H, Chung F, Kamming D, Curti B, King S. Thirty percent of patients have moderate to severe pain 24 hr after ambulatory surgery: a survey of 5,703 patients. Can J Anaesth. 2004 Nov;51(9):886-91. doi: 10.1007/BF03018885.

Rawal N, Hylander J, Nydahl PA, Olofsson I, Gupta A. Survey of postoperative analgesia following ambulatory surgery. Acta Anaesthesiol Scand. 1997 Sep;41(8):1017-22. doi: 10.1111/j.1399-6576.1997.tb04829.x.

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