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1.
Anesth Analg ; 109(2): 586-91, 2009 Aug.
Article in English | MEDLINE | ID: mdl-19608835

ABSTRACT

BACKGROUND: We previously reported that extending an overnight continuous posterior lumbar plexus nerve block to 4 days after hip arthroplasty provides clear benefits during the perineural infusion in the immediate postoperative period. However, it remains unknown whether the extended infusion improves subsequent health-related quality of life. METHODS: Patients undergoing hip arthroplasty received a posterior lumbar plexus perineural infusion of ropivacaine 0.2% from surgery until the following morning, at which time patients were randomized to continue either perineural ropivacaine (n = 24) or normal saline (n = 23) in a double-masked fashion. Patients were discharged with their catheter and a portable infusion pump, and catheters were removed on postoperative Day 4. Health-related quality of life was measured using the Western Ontario and McMaster Universities Osteoarthritis (WOMAC) Index preoperatively and then at 7 days and 1, 2, 3, 6, and 12 mo after surgery. The WOMAC evaluates three dimensions of health-related quality of life, such as pain, stiffness, and physical functional disability (global score of 0-96, lower scores indicate lower levels of symptoms or physical disability). For inclusion in the primary analysis, we required a minimum of three of the six timepoints, including Day 7 and at least two of Months 3, 6, and 12. RESULTS: The two treatment groups had similar global WOMAC scores for the mean area under the curve calculations (point estimate for the difference in mean area under the curve for the two groups [extended infusion group-overnight infusion group] = 0.8, 95% confidence interval: -5.3 to + 6.8 [-5.5% to + 7.1%]; P = 0.80) and at all individual timepoints (P > 0.05). CONCLUSIONS: This investigation found no evidence that extending an overnight continuous posterior lumbar plexus nerve block to 4 days improves (or worsens) subsequent health-related quality of life between 7 days and 12 mo after hip arthroplasty.


Subject(s)
Arthroplasty, Replacement, Hip/psychology , Lumbosacral Plexus , Nerve Block , Quality of Life , Adolescent , Adult , Aged , Aged, 80 and over , Amides , Anesthetics, Local , Area Under Curve , Disability Evaluation , Double-Blind Method , Female , Follow-Up Studies , Humans , Male , Middle Aged , Nerve Block/adverse effects , Osteoarthritis/psychology , Osteoarthritis/surgery , Postoperative Period , Prospective Studies , Ropivacaine , Treatment Outcome , Young Adult
2.
Anesth Analg ; 108(4): 1320-5, 2009 Apr.
Article in English | MEDLINE | ID: mdl-19299806

ABSTRACT

BACKGROUND: We previously provided evidence that extending an overnight continuous femoral nerve block to 4 days after tricompartment knee arthroplasty (TKA) provides clear benefits during the perineural infusion in the immediate postoperative period. However, it remains unknown if the extended infusion improves subsequent health-related quality of life between 7 days and 12 mo. METHODS: Patients undergoing TKA received a femoral perineural infusion of ropivacaine 0.2% from surgery until the following morning, at which time patients were randomized to either continue perineural ropivacaine (n = 25) or normal saline (n = 25) in a double-masked fashion. Patients were discharged with their catheter and a portable infusion pump, and catheters were removed on postoperative day 4. Health-related quality of life was measured using the Western Ontario and McMaster Universities Osteoarthritis (WOMAC) Index preoperatively and then at 7 days, as well as 1, 2, 3, 6, and 12 mo after surgery. The WOMAC evaluates three dimensions of health-related quality of life: pain, stiffness, and physical functional disability. For inclusion in the analysis, we required a minimum of 4 of the 6 time points, including day 7 and at least 2 of mo 3, 6, and 12. RESULTS: The two treatment groups had similar WOMAC scores for the mean area under the curve calculations (point estimate for the difference in mean area under the curve for the two groups [overnight infusion group-extended infusion group] = 1.2, 95% confidence interval: -5.6 to +8.0; P = 0.72) and at all individual time points (P > 0.05). CONCLUSIONS: We found no evidence that extending an overnight continuous femoral nerve block to 4 days improves (or worsens) subsequent health-related quality of life between 7 days and 12 mo after TKA. (ClinicalTrials.gov number, NCT00135889.).


Subject(s)
Amides/administration & dosage , Anesthetics, Local/administration & dosage , Arthroplasty, Replacement, Knee , Femoral Nerve , Nerve Block , Osteoarthritis, Knee/surgery , Pain, Postoperative/prevention & control , Quality of Life , Amides/adverse effects , Analgesics/therapeutic use , Anesthetics, Local/adverse effects , Catheterization , Disability Evaluation , Drug Administration Schedule , Follow-Up Studies , Humans , Infusion Pumps , Osteoarthritis, Knee/physiopathology , Pain Measurement , Prospective Studies , Recovery of Function , Ropivacaine , Time Factors , Treatment Outcome
3.
Anesthesiology ; 109(3): 491-501, 2008 Sep.
Article in English | MEDLINE | ID: mdl-18719448

ABSTRACT

BACKGROUND: The authors tested the hypotheses that after hip arthroplasty, ambulation distance is increased and the time required to reach three specific readiness-for-discharge criteria is shorter with a 4-day ambulatory continuous lumbar plexus block (cLPB) than with an overnight cLPB. METHODS: A cLPB consisting of 0.2% ropivacaine was provided from surgery until the following morning. Patients were then randomly assigned either to continue ropivacaine or to be switched to normal saline. Primary endpoints included (1) time to attain three discharge criteria (adequate analgesia, independence from intravenous analgesics, and ambulation > or = 30 m) and (2) ambulatory distance in 6 min the afternoon after surgery. Patients were discharged with their cLPB and a portable infusion pump, and catheters were removed on the fourth postoperative day. RESULTS: Patients given 4 days of perineural ropivacaine (n = 24) attained all three discharge criteria in a median (25th-75th percentiles) of 29 (24-45) h, compared with 51 (42-73) h for those of the control group (n = 23; estimated ratio = 0.62; 95% confidence interval, 0.45-0.92; P = 0.011). Patients assigned to receive ropivacaine ambulated a median of 34 (9-55) m the afternoon after surgery, compared with 20 (6-46) m for those receiving normal saline (estimated ratio = 1.3; 95% confidence interval, 0.6-3.0; P = 0.42). Three falls occurred in subjects receiving ropivacaine (13%), versus none in subjects receiving normal saline. CONCLUSIONS: Compared with an overnight cLPB, a 4-day ambulatory cLPB decreases the time to reach three predefined discharge criteria by an estimated 38% after hip arthroplasty. However, the extended infusion did not increase ambulation distance to a statistically significant degree.


Subject(s)
Ambulatory Care/methods , Amides/therapeutic use , Arthroplasty, Replacement, Hip/adverse effects , Lumbosacral Plexus/drug effects , Nerve Block/methods , Pain, Postoperative/drug therapy , Aged , Amides/administration & dosage , Anesthetics, Local/administration & dosage , Anesthetics, Local/therapeutic use , Female , Humans , Infusion Pumps , Infusions, Intravenous , Male , Middle Aged , Ropivacaine , Sodium Chloride/administration & dosage , Time Factors , Treatment Outcome
4.
Anesthesiology ; 108(4): 703-13, 2008 Apr.
Article in English | MEDLINE | ID: mdl-18362603

ABSTRACT

BACKGROUND: The authors tested the hypotheses that, compared with an overnight continuous femoral nerve block (cFNB), a 4-day ambulatory cFNB increases ambulation distance and decreases the time until three specific readiness-for-discharge criteria are met after tricompartment total knee arthroplasty. METHODS: Preoperatively, all patients received a cFNB (n = 50) and perineural ropivacaine 0.2% from surgery until the following morning, at which time they were randomly assigned to either continue perineural ropivacaine or switch to perineural normal saline. Primary endpoints included (1) time to attain three discharge criteria (adequate analgesia, independence from intravenous analgesics, and ambulation of at least 30 m) and (2) ambulatory distance in 6 min the afternoon after surgery. Patients were discharged with their cFNB and a portable infusion pump, and catheters were removed on postoperative day 4. RESULTS: Patients given 4 days of perineural ropivacaine attained all three discharge criteria in a median (25th-75th percentiles) of 25 (21-47) h, compared with 71 (46-89) h for those of the control group (estimated ratio, 0.47; 95% confidence interval, 0.32-0.67; P <0.001). Patients assigned to receive ropivacaine ambulated a median of 32 (17-47) m the afternoon after surgery, compared with 26 (13-35) m for those receiving normal saline (estimated ratio, 1.21; 95% confidence interval, 0.71-1.85; P = 0.42). CONCLUSIONS: Compared with an overnight cFNB, a 4-day ambulatory cFNB decreases the time to reach three important discharge criteria by an estimated 53% after tricompartment total knee arthroplasty. However, the extended infusion did not increase ambulation distance the afternoon after surgery. (ClinicalTrials.gov No. NCT00135889.).


Subject(s)
Ambulatory Care/methods , Arthroplasty, Replacement, Knee/trends , Femoral Nerve/physiology , Nerve Block/methods , Nerve Block/trends , Patient Discharge/trends , Aged , Female , Humans , Infusion Pumps , Infusions, Intravenous , Male , Middle Aged
5.
Reg Anesth Pain Med ; 31(2): 113-8, 2006.
Article in English | MEDLINE | ID: mdl-16543096

ABSTRACT

OBJECTIVE: Total hip arthroplasty (THA) results in severe postoperative pain requiring hospitalization to provide potent analgesia. Consequently, the average duration of hospitalization after THA in the United States is 4 to 5 days. This prospective study investigated the feasibility of converting THA into an overnight-stay procedure using a continuous psoas compartment nerve block provided at home with a portable infusion pump. CASE REPORT: Preoperatively, patients undergoing THA had a psoas compartment perineural catheter placed. Postoperatively, perineural ropivacaine 0.2% was delivered through postoperative day (POD) 4. Patients were discharged home when they met specific, prospectively defined criteria, as early as POD 3 for the first phase and POD 1 for the second phase. Of the patients in the first phase (n = 7) who remained hospitalized for at least 3 postoperative nights, 5 met discharge criteria on POD 1 and the remainder on POD 2. Of the patients in phase 2 (n = 5), all but 1 met discharge criteria on POD 1 and 3 were discharged directly home on POD 1. Postoperative pain was well controlled, opioid requirements and sleep disturbances were minimal, and patient satisfaction high. CONCLUSIONS: These results suggest that for a subset of patients without major comorbidities, it is feasible to convert THA into an overnight-stay procedure using an ambulatory continuous psoas compartment nerve block as part of a multimodal analgesic regimen provided at home. Additional research is required to replicate these results in a controlled trial, define the appropriate subset of patients, and assess the incidence of complications associated with this practice before its mainstream use.


Subject(s)
Ambulatory Care , Analgesia, Patient-Controlled , Arthroplasty, Replacement, Hip , Nerve Block , Pain, Postoperative/epidemiology , Aged , Ambulatory Care/methods , Analgesia, Patient-Controlled/methods , Arthroplasty, Replacement, Hip/methods , Feasibility Studies , Female , Hospitalization , Humans , Male , Middle Aged , Nerve Block/methods , Pain, Postoperative/therapy , Prospective Studies , Psoas Muscles
6.
Anesth Analg ; 102(1): 87-90, 2006 Jan.
Article in English | MEDLINE | ID: mdl-16368810

ABSTRACT

The average duration of hospitalization after total knee arthroplasty (TKA) in the United States is 4-5 days. In this two-phase study we investigated the feasibility of converting TKA into an overnight-stay procedure using a continuous femoral nerve block provided at home through postoperative day 4. Nine of 10 patients met discharge criteria and were discharged home the day after surgery. Pain was well controlled, opioid requirements and sleep disturbances were minimal, and patient satisfaction was high. Additional research is required to replicate these results in a controlled trial, define the appropriate subset of patients, and assess the incidence of complications associated with this practice before its mainstream use.


Subject(s)
Ambulatory Care/methods , Analgesia, Patient-Controlled/methods , Arthroplasty, Replacement, Knee/methods , Femoral Nerve , Nerve Block/methods , Adolescent , Adult , Aged , Aged, 80 and over , Amides/administration & dosage , Feasibility Studies , Female , Humans , Male , Middle Aged , Pain Measurement/methods , Pain, Postoperative/drug therapy , Pain, Postoperative/epidemiology , Prospective Studies , Ropivacaine , Time Factors
7.
J Arthroplasty ; 18(6): 792-8, 2003 Sep.
Article in English | MEDLINE | ID: mdl-14513456

ABSTRACT

We reviewed the performance of 22 shoulder implant arthroplasties in 19 patients age 50 or younger at surgery. Patients were evaluated by telephone interview, written questionnaire, and radiographic examination. The average age at surgery was 38.6 years, and the average follow-up was 5.6 years. Patients were grouped by disease process (rheumatoid arthritis [RA], avascular necrosis [AVN], trauma, and hemophilic arthropathy [HA]) and type of prosthesis (total vs. hemiarthroplasty). The highest scores (best shoulder function) were seen in patients with hemiarthroplasty for HA. Patients with hemiarthroplasty for trauma and AVN scored similarly, whereas those with a hemiarthroplasty for RA scored lowest. Patients with RA who had a total shoulder arthroplasty scored higher than patients with hemiarthroplasty. When patients in our population with longer follow-up were compared with those with a shorter follow-up, no downward trends in shoulder function were seen. Accelerated deterioration of function of shoulder arthroplasties was not observed in our young patient population.


Subject(s)
Arthroplasty, Replacement , Shoulder Joint/surgery , Activities of Daily Living , Adult , Female , Humans , Interviews as Topic , Male , Middle Aged , Radiography , Shoulder Joint/diagnostic imaging , Shoulder Joint/physiopathology , Surveys and Questionnaires , Treatment Outcome
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