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1.
J Bone Joint Surg Am ; 95(21): 1935-41, 2013 Nov 06.
Article in English | MEDLINE | ID: mdl-24196463

ABSTRACT

BACKGROUND: We studied the efficacy of local infiltration analgesia in surgical wounds with 0.2% ropivacaine (50 mL), ketorolac (15 mg), and adrenaline (0.5 mg) compared with that of local infiltration analgesia combined with continuous infusion of 0.2% ropivacaine as a method of pain control after total hip arthroplasty. We hypothesized that as a component of multimodal analgesia, local infiltration analgesia followed by continuous infusion of ropivacaine would result in reduced postoperative opioid consumption and lower pain scores compared with infiltration alone, and that both of these techniques would be superior to placebo. METHODS: In this prospective, double-blind, placebo-controlled study, 105 patients were randomized into three groups: Group I, in which patients received infiltration with ropivacaine, ketorolac, and adrenaline followed by continuous infusion of 0.2% ropivacaine at 5 mL/hr; Group II, in which patients received infiltration with ropivacaine, ketorolac, and adrenaline followed by continuous infusion of saline solution at 5 mL/hr; and Group III, in which patients received infiltration with saline solution followed by continuous infusion of saline solution at 5 mL/hr.All patients received celecoxib, pregabalin, and acetaminophen perioperatively and patient-controlled analgesia; surgery was performed under general anesthesia. Before wound closure, the tissues and periarticular space were infiltrated with ropivacaine, ketorolac, and adrenaline or saline solution and a fenestrated catheter was placed. The catheter was attached to a pump prefilled with either 0.2% ropivacaine or saline solution set to infuse at 5 mL/hr.The primary outcome measure was postoperative opioid consumption and the secondary outcome measures were pain scores, adverse side effects, and patient satisfaction. RESULTS: There were no differences between groups in the administration of opioids in the operating room, in the recovery room, or on the surgical floor. The pain scores on recovery room admission and discharge and the floor were low and similar between groups. There were no differences in the incidence of adverse side effects among groups. Patient satisfaction with pain management was similar in all groups. CONCLUSIONS: Local infiltration analgesia alone or followed by continuous infusion of ropivacaine as part of multimodal analgesia provides no additional analgesic benefit or reduction in opioid consumption compared with placebo following total hip arthroplasty. LEVEL OF EVIDENCE: Therapeutic level I. See Instructions for Authors for a complete description of levels of evidence.


Subject(s)
Analgesia/methods , Anesthesia, Local/methods , Anesthetics, Local/therapeutic use , Arthroplasty, Replacement, Hip/methods , Adolescent , Adult , Aged , Aged, 80 and over , Amides/administration & dosage , Amides/therapeutic use , Analgesia, Patient-Controlled/methods , Anesthetics, Local/administration & dosage , Double-Blind Method , Drug Administration Routes , Epinephrine/administration & dosage , Epinephrine/therapeutic use , Female , Humans , Ketorolac/administration & dosage , Ketorolac/therapeutic use , Male , Middle Aged , Pain Management , Pain Measurement , Ropivacaine
2.
Clin Orthop Relat Res ; 471(6): 1865-72, 2013 Jun.
Article in English | MEDLINE | ID: mdl-23065331

ABSTRACT

BACKGROUND: The growth of consumer-directed health plans has sparked increased demand for information regarding the cost and quality of healthcare services, including total joint arthroplasty (TJA). However, the factors that influence patients' choice of provider when pursuing elective orthopaedic care, such as TJA, are poorly understood. QUESTIONS/PURPOSES: We evaluated the factors patients consider when selecting an orthopaedic surgeon and hospital for TJA. METHODS: Two hundred fifty-one patients who sought treatment from either an academic or community-based orthopaedic practice for primary TJA completed a 37-item survey using a 5-point Likert scale rating ("unimportant" to "very important") regarding seven established clinical and nonclinical dimensions of care patients considered when selecting a provider and hospital. RESULT: Patients rated physician manner (average Likert, 4.7) and physician quality (eg, outcomes) (average Likert, 4.6) as most important in their selection of surgeon and hospital for TJA. Despite the expressed importance of surgeon and hospital quality, only 46% of patients were able to find useful information to compare outcomes among surgeons, and 47% for hospitals that perform TJA. CONCLUSIONS: Our findings suggest physician manner and surgical outcomes are the most important considerations for patients when choosing a provider for elective TJA. Cost sharing is the least important criterion patients considered. Patients expressed high motivation to seek out provider quality information but indicated accessible and actionable sources of information are lacking. Future efforts should be directed at developing clinically relevant, easily interpretable, objective, risk-adjusted measures of physician and hospital quality.


Subject(s)
Arthroplasty, Replacement/psychology , Choice Behavior , Community Participation/psychology , Delivery of Health Care , Elective Surgical Procedures/psychology , Patient Acceptance of Health Care/psychology , Arthritis/surgery , Clinical Competence , Data Collection , Humans , Physician-Patient Relations , Quality of Health Care , Treatment Outcome
3.
Pain Manag Nurs ; 10(3): 124-33, 2009 Sep.
Article in English | MEDLINE | ID: mdl-19706349

ABSTRACT

The patient-controlled fentanyl HCl iontophoretic transdermal system (ITS) is a compact, self-contained, needle-free system that has been approved for acute postoperative pain management in hospitalized adults. The objective of the present analysis was to evaluate patients' assessment of fentanyl ITS and morphine intravenous patient-controlled analgesia (IV PCA) convenience on 7 different subscales, using a validated patient ease of care (EOC) questionnaire in 2 prospective, open-label, randomized, phase IIIb clinical trials. Patients received fentanyl ITS or morphine IV PCA (N = 1,305) for up to 72 h after total hip replacement surgery (THR study) or abdominal or pelvic surgery (APS study). For the majority of items on the patient EOC questionnaire, trends suggest that greater percentages of patients reported the most positive response for fentanyl ITS than they did for morphine IV PCA in both studies; differences were particularly noteworthy for items on the Movement subscale. In the THR study, more patients in the fentanyl ITS group were responders compared with those in the morphine IV PCA group for the subscales Confidence with Device, Pain Control, Knowledge/Understanding, and Satisfaction. In the APS study, responder rates for these subscales did not differ between treatment groups. These findings indicate that patients assessed the EOC associated with fentanyl ITS higher compared with morphine IV PCA for the management of acute postoperative pain and suggest that fentanyl ITS has the potential to improve acute postoperative pain care for patients and nurses.


Subject(s)
Analgesia, Patient-Controlled/psychology , Analgesics, Opioid/administration & dosage , Iontophoresis/psychology , Pain, Postoperative/drug therapy , Patient Satisfaction , Administration, Cutaneous , Adult , Analgesia, Patient-Controlled/methods , Analysis of Variance , Chi-Square Distribution , Fentanyl/administration & dosage , Humans , Infusions, Intravenous/psychology , Iontophoresis/methods , Morphine/administration & dosage , Nursing Methodology Research , Pain Measurement , Pain, Postoperative/psychology , Prospective Studies , Surveys and Questionnaires , Treatment Outcome
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