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Addition of low-dose morphine to spinal anaesthesia improves analgesia with cFNB in TKA
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ARTHROPLASTY
Addition of low-dose morphine to spinal anaesthesia improves analgesia with cFNB in TKA .
Verified
This report has been verified by one or more authors of the original publication.

OrthoEvidence Journal (OE Journal) - ACE Report

OE Journal. 2016;4(20):3 BMC Anesthesiol. 2016 Jul 16;16(1):38

70 patients scheduled for total knee arthroplasty under spinal anesthesia and a continuous femoral nerve block were randomized to spinal anesthesia with or without the addition of mini-dose morphine (0.035mg). The purpose of this study was to evaluate if there was any significant difference between groups in pain scores and opioid consumption. Patients were monitored up to 48 hours postoperatively. Results demonstrated significantly lower pain scores and tramadol consumption in the group which received mini-dose spinal morphine. The incidence of postoperative nausea and vomiting was significantly greater within the first 6 hours in the group administered the mini-dose spinal morphine.


Detalhes do financiamento da publicação +
Financiamento:
Non-Industry funded
Patrocinador:
Faculty of Medicine Ramathibodi Hospital, Mahidol University
Conflitos:
None disclosed

Risco de viés

7/10

Critérios de notificação

14/20

Índice de Fragilidade

1

Was the allocation sequence adequately generated?

Was allocation adequately concealed?

Blinding Treatment Providers: Was knowledge of the allocated interventions adequately prevented?

Blinding Outcome Assessors: Was knowledge of the allocated interventions adequately prevented?

Blinding Patients: Was knowledge of the allocated interventions adequately prevented?

Was loss to follow-up (missing outcome data) infrequent?

Are reports of the study free of suggestion of selective outcome reporting?

Were outcomes objective, patient-important and assessed in a manner to limit bias (ie. duplicate assessors, Independent assessors)?

Was the sample size sufficiently large to assure a balance of prognosis and sufficiently large number of outcome events?

Was investigator expertise/experience with both treatment and control techniques likely the same (ie.were criteria for surgeon participation/expertise provided)?

Sim = 1

Incerto = 0,5

Não relevante = 0

Não = 0

A Avaliação dos Critérios de Relato avalia a transparência com que os autores relatam as caraterísticas metodológicas e do ensaio na publicação. A avaliação está dividida em cinco categorias que são apresentadas de seguida.

2/4

Randomization

3/4

Outcome Measurements

1/4

Inclusion / Exclusion

4/4

Therapy Description

4/4

Statistics

Detsky AS, Naylor CD, O'Rourke K, McGeer AJ, L'Abbé KA. J Clin Epidemiol. 1992;45:255-65

O Índice de Fragilidade é uma ferramenta que auxilia na interpretação de achados significativos, fornecendo uma medida de força para um resultado. O Índice de Fragilidade representa o número de eventos consecutivos que precisam de ser adicionados a um resultado dicotómico para que o resultado deixe de ser significativo. Um número pequeno representa um resultado mais fraco e um número grande representa um resultado mais forte.

Porque é que este estudo era necessário agora?

Severe knee pain following total knee arthroplasty is not uncommon and can delay physical therapy and recovery. Femoral nerve blocks are often used for postoperative analgesia after TKA, though mixed results regarding its efficacy have been reported. To improve the efficacy of a postoperative analgesia protocol involving FNB, use of mini-dose spinal morphine has been suggested as a possible supplementary method.

Qual era a principal questão de investigação?

In total knee arthroplasty with a continuous femoral nerve block, is there any significant difference in postoperative analgesia efficacy between spinal anesthesia with and without the addition of mini-dose morphine, assessed over 48 hours postoperatively?

Caraterísticas do estudo +
População:
70 patients, 40-80 years of age, scheduled for primary unilateral total knee arthroplasty. All patients received a femoral nerve block, under nerve stimulation guidance, with 20mL 0.25% levobupivacaine, followed by continuous infusion of 0.125% levobupivacaine at 7mL per hour (down to 5mL/hour at VAS < 3) for 48 hours. Tramadol 50mg IV was administered for breakthrough pain (VAS > 4).
Intervenção:
Mini-dose morphine group: Patients received spinal anaesthesia with 2.8mL levobupivacaine and morphine 0.035mg. (n=35; 35 analyzed) (Mean age: 69.60+/-7.39)
Comparação:
Control group: Patients received spinal anesthesia with 2.8mL levobupivacaine only. (n=35; 33 analyzed) (Mean age: 68.09+/-8.37)
Resultados:
The pain was assessed using a visual analog scale, and the incidence of severe postoperative pain (VAS 4-7) was documented. Cumulative tramadol consumption was also recorded. Adverse events were documented.
Métodos:
RCT; Assessor blind
Tempo:
Patients were assessed at 1, 6, 12, 24, 36, and 48 hours postoperatively.
Quais foram os resultados importantes?
  • Significant differences in median VAS pain scores were observed between groups, being significantly lower in the mini-dose morphine group compared to the control group at 12 hours (3 [0-7] vs. 6 [0-10]; p<0.01), 24 hours (3 [0-7] vs. 5 [0-10]; p<0.01), and 48 hours postoperatively (3 [0-7] vs. 4 [0-10]; p=0.03).
  • Groups also demonstrated a significant difference in the incidence of severe postoperative pain, being significantly lower in the mini-dose morphine group compared to the control group at 12 hours (15/35 vs. 23/33; p=0.03), 24 hours (16/35 vs. 22/33; p=0.03), and 48 hours (9/35 vs. 17/33; p=0.03).
  • Cumulative tramadol consumption over the first 48 hours postoperative was significantly lower in the mini-dose morphine group (125mg [50-400]) compared to the control group (200mg [50-500mg]) (p=0.01).
  • The incidence of postoperative nausea and vomiting (PONV) was significantly greater in the mini-dose morphine group (40%) compared to the control group (15%) at 6 hours postoperatively (p=0.05); differences between groups at 1, 12, 24, 36, and 48 hours postoperatively were not significant.
De que é que me devo lembrar mais?

In total knee arthroplasty, the addition of morphine 0.035mg to spinal anaesthesia with levobupivacaine, in combination with standardized continuous femoral nerve block, demonstrated significantly lower pain scores and incidences of severe pain within the first 48 hours postoperatively when compared to spinal anaesthesia without morphine, but also increased the incidence of PONV at 6 hours postoperatively.

Como é que isto afectará o tratamento dos meus doentes?

The results of this study suggest that the addition of low-dose morphine to spinal anesthesia may offer improved short-term analgesic efficacy of a multimodal regimen with continuous femoral nerve block in patients undergoing total knee arthroplasty. Nonetheless, even the low dose used in the current study was observed to increase the rate of postoperative nausea and vomiting to a significant degree. As such, there is a need for further study methods of potentially limiting the impact of the morphine-related side effects on patient outcome, or whether an even lower dose of morphine can demonstrate the same analgesic efficacy observed in this trial while avoiding an increase in the incidence of PONV.

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Como citar isto ACE Report

OrthoEvidence. Addition of low-dose morphine to spinal anaesthesia improves analgesia with cFNB in TKA. OE Journal. 2016;4(20):3. Available from: https://myorthoevidence.com/AceReport/Show/addition-of-low-dose-morphine-to-spinal-anaesthesia-improves-analgesia-with-cfnb-in-tka

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