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Can Physical Activities Reduce Postoperative Pain in Adults

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Chiayi Christian Hospital

Märksõnad

Abstraktne

BACKGROUND:
Recommendation is strong on exercise and physical activity (PA) in the prehabilitation of Enhanced Recovery After Surgery (ERAS) for various types of surgeries. The evidence is however weak regarding ERAS protocols. Many studies have showed that exercise and PA have hypoalgesic effects on healthy individuals and they have better pain tolerance too. Here the investigators study changes in postoperative pain for various types of surgical patients after performing 6 to 8 weeks of preoperative PA at moderate or vigorous intensity Vs non-preoperative PA patients.

Kirjeldus

METHODS:

This is a single center, randomized prospective control trial (PA patients group vs control non-PA patients group). Information on the incidence and severity of pain and other sufferings of each patient were periodically recorded at time-points of 1, 4, 7, 10 and 24 hours after various types of surgical operations. Our study was aimed to determine beneficial effects on postoperative pain for patients after performing preoperative PA for 6 to 8 weeks vs non-PA patients. The investigators employed the recommendations of the American College of Sport Medicine and the World Health Organization for adults to divide our PA patients group into moderate-intensity as 30-60 min∙d-1 (≥150 min∙wk-1 ) and vigorous-intensity as 20-60 min∙d-1 (≥75 min∙wk-1). The severity of postoperative pain will be measured prospectively at 1, 4, 7, 10 and 24 hours after the surgical operations for the PA patients group and the control non-PA patients group. The operations were performed under general anesthesia (GA) with endotracheal intubation or inhalation through laryngeal mask.

The procedures of GA will be discussed and decided by one of our anesthesiologists of the Chia-Yi Christian Hospital together with patients/caregivers at the Pre-Anesthesia Consultation Clinic. The investigators used the American Society of Anesthesiologists physical status scoring system for risk stratification, the approaches of Apfel's preventive strategy of postoperative nausea and vomiting (PONV) prophylaxis, perioperative multi-modal pain management in addition to other appropriate elements in ERAS. PONV defined as nausea, vomiting or retching within 24 h of surgery.

Statistical Analysis:

Data will be analyzed using SPSS Version 22.0 and Mplus Version 8.2. Data on demographics, pain scores, PONV frequency and severity or sufferings were analyzed using descriptive statistics and frequency distributions.

Latent growth models are constructed through structural equation modeling using maximum likelihood estimations. The investigators will examine three unconditional growth models: (1) a linear model with the slope factor fixed at 0,1, 2, 3, and 4, (2) a quadratic model with the linear slope factor fixed at 0, 1, 2, 3, and 4, and the quadratic slope factor fixed at 0, 1, 4, 9, 16, and (3) an unspecified curve model with the slope factor loadings at the following settings: (a) wave 1 set to 0; (b) wave 2 set to 1; (c) wave 3, wave 4, and wave 5 allowed to be estimated freely.21 After choosing the model that had best fitted our data, the investigators introduce the predictive variable of PA, and the 9 time-invariant covariates and 15 time-varying covariates. The 9 time-invariant covariates are control variables of intercept and slope factors. The 15 time-varying covariates are repeated exogenous predictors of the pain scores. The pain scores in each waves are assigned three covariates. The investigators run the model including the predictor, 9 time-invariant variables and 15 time-variant covariates and all variables are allowed to correlate with one another.

The performance of model fitting are evaluated using goodness of fit indices, including the following: χ2 statistic, root mean square error of approximation (RMSEA), comparative fit index (CFI), standardized root mean square residual (SRMR), Akaike information criterion (AIC), and Bayesian information criterion (BIC). An RMSEA of 0.0 indicates a model with an exact fit and the investigators will adopte RMSEA of ≤0.08 and preferably ≤0.05 to indicate good fitting of models. CFI has a range from 0 to 1.00, the investigators will adopte CFI ≥0.90 or preferably ≥0.95 to indicate good fitting models. SRMR ≤0.05 indicated good-fitting model and values as high as 0.08 are considered acceptable. Although the investigators will perform the chi-square test in our results of model fit, its known sensitivity to sample size necessarily excludes its use as proper measure of goodness of fit.

AIC and BIC are useful for model selection, but do not provide absolute measurement of model fitting. The best-fitted model are those with smallest AIC and BIC values.

Kuupäevad

Viimati kinnitatud: 01/31/2020
Esmalt esitatud: 01/29/2020
Hinnanguline registreerumine on esitatud: 02/27/2020
Esmalt postitatud: 03/02/2020
Viimane värskendus on esitatud: 02/27/2020
Viimati värskendus postitatud: 03/02/2020
Õppe tegelik alguskuupäev: 06/30/2015
Eeldatav esmane lõpetamise kuupäev: 06/29/2016
Eeldatav uuringu lõpetamise kuupäev: 12/30/2017

Seisund või haigus

Postoperative Pain
Physical Activity

Sekkumine / ravi

Procedure: Compare the severity of postoperative pain of the physical activity group Vs non-physical activity group

Faas

-

Käerühmad

ArmSekkumine / ravi
Experimental: Physical activity group
Investigators employ the recommendations of the American College of Sport Medicine and the World Health Organization for adults to divide our enrolled patients having moderate-intensity as 30-60 min∙d-1 (≥150 min∙wk-1 ) or vigorous-intensity as 20-60 min∙d-1 (≥75 min∙wk-1) for 6-8 weeks preoperatively. The severity of postoperative pain are measured prospectively at 1, 4, 7, 10 and 24 hours after the surgical operations. The operations are performed under inhalation general anesthesia with endotracheal intubation or through laryngeal mask.
Experimental: non-physical activity group
No any moderate-intensity or vigorous-intensity physical activity for our enrolled patients preoperatively. The severity of postoperative pain are measured prospectively at 1, 4, 7, 10 and 24 hours after the surgical operations. Various types of operations are performed under inhalation general anesthesia with endotracheal intubation or through laryngeal mask.

Abikõlblikkuse kriteeriumid

Õppimiseks sobivad vanused 18 Years To 18 Years
Uuringuks kõlblikud soodAll
Võtab vastu tervislikke vabatahtlikkeJah
Kriteeriumid

Inclusion Criteria:

1. aged ≥18 y/o

2. Enrolled in-patients

3. Patients are scheduled to undergo various operations.

4. The surgeries are expected to last ≥60 minutes

5. Endotracheal intubation or laryngeal mask inhalation general anesthesia.

Exclusion Criteria:

1. Patients will transferred to the intensive care unit after operations.

2. American Society of Anesthesiology physical status ≥4

3. poorly controlled diabetic mellitus (HA1c ≥9)

4. prolonged corrected QT interval (male ≥0.45 sec, female ≥0.47 sec)

5. Allergy to any opioids (i.e., morphine, fentanyl, pethidine and others) and nonopioids (i.e., selective or nonselective NSAIDs and acetaminophen)

6. Allergy to dexamethasone, granisetron, droperidol, metoclopramide used for prevention of postoperative nausea and vomiting

7. Deaf or unable to speak/understand Taiwanese or Mandarin

8. Failed to recall or uncertain on how many days/times they had spent doing moderate or vigorous physical activity on recent 6 to 8 weeks before receiving surgery.

Tulemus

Esmased tulemusnäitajad

1. The beneficial effect of physical activity on postoperative pain after various types of surgeries [2 years and 6 months]

The pain scores different of the physical activity (PA) Vs non-physical activity (non-PA) groups are using the numeric pain rating scale (NRS) with 1 represent no pain and 5 represent the worst possible pain. The severity of postoperative pain will be measured prospectively by using NRS at different postoperative time points (i.e. 1, 4, 7, 10, and 24 hour) for comparing the postoperative pain different between PA and non-PA patients.

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