ACE Report Cover
IV Dexamethasone offers postoperative pain reduction in femoral neck fracture fixation
Translate this  ACE Report Translate this  ACE Report Translate this  ACE Report
Idioma
Download Download Download
Descarregar
Cite this Report Cite this Report Cite this Report
Citar
Add to Favorites Add to Favorites Add to Favorites Remove from Favorites Remove from Favorites Remove from Favorites
+ Favoritos
Translate this  ACE Report Translate this  ACE Report Translate this  ACE Report
Idioma
Download Download Download
Descarregar
Cite this Report Cite this Report Cite this Report
Citar
Add to Favorites Add to Favorites Add to Favorites Remove from Favorites Remove from Favorites Remove from Favorites
+ Favoritos
BMC Anesthesiol
TRAUMA
IV Dexamethasone offers postoperative pain reduction in femoral neck fracture fixation .
Verified
This report has been verified by one or more authors of the original publication.

OrthoEvidence Journal (OE Journal) - ACE Report

OE Journal. 2021;9(16):29

BMC Anesthesiol. 2016 Sep 22;16(1):79

Autores contribuintes

S Szucs D Jessop G Iohom GD Shorten

37 patients, over the age of 65 years, with a femoral neck fracture who were scheduled for operative fixation, were randomized to a preoperative IV dose of either dexamethasone 0.1mh/kg or placebo. The purpose of this study was to determine if preoperative dexamethasone led to a significant reduction in pain and opioid consumption over the first 3 days and 1 week after surgery. Scores for pain at rest were significantly lower in the dexamethasone group compared to the placebo group at 6 hours, and morphine consumption within the first 24 hours was significantly lower in the dexamethasone group compared to the placebo group. The difference between groups in pain scores on movement did not reach significance, and no significant differences in either pain comparison were found at subsequent follow-up time points.


Detalhes do financiamento da publicação +
Financiamento:
Non-Industry funded
Patrocinador:
Department of Anaesthesia, Intensive Care and Pain Medicine, Cork University Hospital
Conflitos:
None disclosed

Risco de viés

8/10

Critérios de notificação

13/20

Índice de Fragilidade

N/A

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.

4/4

Randomization

3/4

Outcome Measurements

0/4

Inclusion / Exclusion

2/4

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?

Femoral neck fractures are common among elderly patients presenting with trauma, necessitating surgical fixation. Preoperative low-dose dexamethasone has been suggested as a possible addition to multimodal analgesia regimens to improve postoperative analgesic efficacy. However, there have been concerns expressed relating to a possible increase in adverse events, particularly in such an age group.

Qual era a principal questão de investigação?

In the fixation of femoral neck fractures, does a preoperative IV dose of dexamethasone 0.1mg/kg result in significantly lower pain scores at 6 hours postoperatively when compared to placebo saline?

Caraterísticas do estudo +
População:
37 patients, over the age of 65, with a femoral neck fracture who were scheduled for operative fixation. All procedures were performed under spinal anesthesia. Postoperative analgesia included intravenous paracetamol 1g every 6 hours, and intramuscular morphine 5-10mg for rescue analgesia.
Intervenção:
Dexamethasone group: Within the operating room prior to surgery, patients were administered intravenously, dexamethasone 0.1mg/kg.
Comparação:
Placebo group: Within the operating room prior to surgery, patients were administered intravenously, placebo saline.
Resultados:
The primary outcome measure was pain on a numeric rating scale (NRS; 0-10), both at rest and on movement. Secondary outcomes included analgesic consumption and incidence of nausea/vomiting, sedation, and pruritus.
Métodos:
RCT
Tempo:
Patients were assessed at 6h (primary endpoint), 12h, 24h, 48h, 72h, and 1 week postoperatively.
Quais foram os resultados importantes?
  • At 6 hours, NRS pain at rest scores was significantly lower in the dexamethasone group (0.8+/-1.3) compared to the placebo group (3.9+/-2.9) (p=0.0004). The difference in NRS pain on movement between the dexamethasone group (3.2+/-2.6) and placebo group (5.5+/-3.8) did not reach statistical significance (p=0.055).
  • No significant differences between groups in NRS pain at rest or on movement were reported from 12h to 1 week postoperatively.
  • Cumulative 24h morphine consumption was significantly lower in the dexamethasone group (7.7+/-8.3mg) compared to the placebo group (15.1+/-9.4mg) (p=0.04).
  • The incidence of postoperative nausea/vomiting, sedation, and pruritus were reported to not significantly differ between groups.
De que é que me devo lembrar mais?

In the operative fixation of a femoral neck fracture in those 65 years of age or older, the use of a preoperative dose of dexamethasone 0.1mg/kg demonstrated significantly reduced pain at rest for the first 6 hours after surgery, and significantly lower opioid consumption for the first 24 hours after surgery. Differences between groups at subsequent time points were not significant, nor was pain during movement at any time point.

Como é que isto afectará o tratamento dos meus doentes?

The results of this study suggest that an IV dose (0.1mg/kg) of dexamethasone prior to fixation of a femoral neck fracture may be beneficial for early pain management in older patients. Nevertheless, pain rebounded beyond 6 hours and was similar to placebo for the remainder of the follow-up period. Therefore, the use of a postoperative dexamethasone dose in multimodal analgesia regimens should be considered for investigation in future trials. Additionally, the sample size of the current study was quite small, limiting the strength of the obtained results. Larger trials are needed to confirm the findings of the current study.

AVISO LEGAL

O conteúdo desta página destina-se apenas a fins informativos e não pretende substituir o aconselhamento, diagnóstico ou tratamento médico profissional. Se necessitar de tratamento médico, procure sempre o conselho do seu médico ou dirija-se ao serviço de urgência mais próximo. As opiniões, crenças e pontos de vista expressos pelos indivíduos no conteúdo encontrado nesta página não reflectem as opiniões, crenças e pontos de vista da OrthoEvidence.

0 de 4 artigos mensais GRATUITOS desbloqueados
Atingiu o seu limite de 4 visualizações de artigos gratuitos este mês

Aceda à OrthoEvidence por apenas $1,99 por semana.

Mantenha-se ligado às últimas evidências. Cancele a qualquer altura.
  • Avaliações críticas dos mais recentes ensaios clínicos aleatórios de alto impacto e revisões sistemáticas em ortopedia
  • Acesso ao conteúdo do podcast OrthoEvidence, incluindo colaborações com o Journal of Bone and Joint Surgery, entrevistas com cirurgiões reconhecidos internacionalmente e discussões em mesa redonda sobre notícias e tópicos ortopédicos
  • Subscrição do The Pulse, um boletim informativo duas vezes por semana baseado em evidências, concebido para o ajudar a tomar melhores decisões clínicas
Upgrade
Close Dialog
Bem-vindo de volta!
Esqueceu-se da palavra-passe?
Comece hoje o seu teste GRATUITO!

A sua conta será afiliada a
e inclui acesso gratuito ao OrthoEvidence


OU
Esqueceu-se da palavra-passe?

OU
Verifique o seu e-mail

Se existir uma conta com o endereço de e-mail fornecido, ser-lhe-á enviado um e-mail de reposição da palavra-passe. Se não vir uma mensagem de correio eletrónico, verifique a sua pasta de spam ou de lixo eletrónico.

Para obter mais assistência, contacte a nossa equipa de apoio.

Inicie sessão para ativar esta funcionalidade

Para aceder a esta funcionalidade, tem de iniciar sessão numa conta OrthoEvidence ativa. Inicie a sessão ou crie uma conta de avaliação GRATUITA.

Traduzir o Relatório ACE

A OrthoEvidence utiliza um serviço de tradução de terceiros para tornar o conteúdo acessível em vários idiomas. Tenha em atenção que, embora sejam feitos todos os esforços para garantir a exatidão, as traduções podem nem sempre ser perfeitas.

Como citar isto ACE Report

OrthoEvidence. IV Dexamethasone offers postoperative pain reduction in femoral neck fracture fixation. OE Journal. 2021;9(16):29. Available from: https://myorthoevidence.com/AceReport/Show/iv-dexamethasone-offers-postoperative-pain-reduction-in-femoral-neck-fracture-fixation

Copie a citação
Inicie sessão para ativar esta funcionalidade

Para aceder a esta funcionalidade, tem de iniciar sessão numa conta OrthoEvidence ativa. Inicie a sessão ou crie uma conta de avaliação GRATUITA.

Funcionalidade de Membro Premium

Para aceder a esta funcionalidade, tem de ter sessão iniciada numa conta Premium da OrthoEvidence.

Partilhe isto ACE Report