L'efficacité de l'imagerie guidée sur la douleur, l'anxiété, le coping et le retour aux activités d'adolescents ayant subi une chirurgie correctrice de scoliose

De nombreuses études ont démontré que les adolescents qui subissent une chirurgie correctrice de scoliose éprouvent des douleurs postopératoires intenses et cela pendant plusieurs jours après leur chirurgie. L’originalité de cette étude de type quasi-expérimental, consistait à réaliser un DVD sur une technique d’imagerie guidée et de relaxation combinée à une intervention éducative (gestion de la douleur) sur la douleur, l’anxiété, le coping et le retour aux activités d’adolescents ayant subi une chirurgie correctrice de scoliose. Prenant appui sur la théorie du portillon (Melzack & Casey, 1968) et sur la théorie transactionnelle du stress et coping (Lazarus & Folkman, 1984), quatre hypothèses ont été retenues en vue de vérifier l’effet de cette intervention. Trente et un adolescents, âgés entre 13 et 19 ans ont été répartis en deux groupes de façon aléatoire. Les participantes du groupe expérimental devaient visionner un DVD sur une technique d’imagerie guidée et de relaxation combinée à de l’information sur la gestion de la douleur en période préopératoire, au moment du congé de l’hôpital et ce, au moins trois fois par semaine sur une période d’un mois post congé. De plus, ce groupe continuait à recevoir les soins usuels. Les participants du groupe contrôle ne recevaient que les soins usuels. Les instruments de mesure utilisés furent le questionnaire concis de la douleur (QCD) (Larue F, Colleau, Brasseur, & Cleeland, 1995), l’inventaire d’anxiété situationnelle et de trait d’anxiété (IASTA-Y) (Gauthier & Bouchard, 1993) et l’inventaire du coping face à la douleur pédiatrique (Spicher, 2003). Quatre temps de mesure ont été planifiés, soit la journée avant la chirurgie, au congé de l’hôpital, au 14ième jour post congé et lors de la visite à la clinique d’orthopédie à un mois post congé. Les résultats montraient que les deux groupes étaient équivalents en ce qui concernait les caractéristiques sociodémographiques et les variables dépendantes. Les participants du groupe expérimental présentaient une douleur générale ressentie dans le dernier 24 heures plus basse au 14ième jour (p = 0,012) et un mois après leur congé de l’hôpital (p = 0,049). Certaines activités quotidiennes ont démontré une différence significative au 14ième jour soit : les activités scolaires ou de travail (p = 0,046), et les activités de soutien vital (manger, dormir) (p = 0,024), Par contre, nous n’avons pas observé de différence significative au niveau de l’anxiété situationnelle et des stratégies adaptatives de coping entre les deux groupes. L’auteur conclut que le niveau de douleur postopératoire des adolescents qui ont subi une chirurgie correctrice de scoliose peut être réduit par un visionnement d’un DVD sur une technique d’imagerie guidée et de relaxation combinée à une intervention éducative (information sur la douleur). De plus, ceci semble avoir un effet positif sur le retour plus rapide de certaines activités quotidiennes.

Análisis de las trayectorias de dolor posoperatorio, primera hora vs. 24 horas. Estudio observacional en 234 pacientes

Introducción: El dolor posoperatorio no controlado es un predictor de dolor severo. La trayectoria de dolor durante la primera hora podría predecir el curso del dolor durante las primeras 24 horas. El control temprano del dolor posoperatorio facilita el manejo analgésico durante el primer día y mejora la experiencia del paciente, facilitando su recuperación y rehabilitación. Objetivo: Determinar la relación entre la trayectoria del dolor en la primera hora y durante las 24 horas post-operatorias. Material y métodos: Estudio analítico observacional prospectivo de 234 pacientes llevados a procedimientos quirúrgicos bajo anestesia general. Se registraron 8 intesidades de dolor durante las 24 horas. Se calcularon las pendientes y se estableció la relación entre ellas. Resultados: El 31,3% de pacientes tenían dolor no controlado al ingreso a recuperación. La intensidad del dolor al inicio se correlaciona de forma negativa con la trayectoria de la primera hora P1 rS= -0,657 (p=0.000). La intensidad de dolor inicial tiene una asociación negativa con P2 de rS= -0.141 (p=0.032). Al compararse las pendientes P1 y P2 y se encontró una correlación negativa muy baja rS= -0.126 (p=0.056). Conclusiones: Uno de cada tres pacientes presenta dolor severo durante el posoperatorio agudo. La trayectoria del dolor en la primera hora no permite predecir el comportamiento de la trayectoria durante el primer día posoperatorio. El comportamiento del dolor está relacionado con la intensidad al final de la anestesia. Cuando el dolor inicial es severo alcanzar la meta analgésica tarda más tiempo.

ADMINISTRAÇÃO EPIDURAL DE OPIÓIDES em CÃES

Os opióides têm sido utilizados em Medicina Veterinária há vários anos como alternativa para o alívio da dor pós-operatória ou traumática. Atualmente, tem-se dado maior valor ao controle da dor nos animais, visando a oferecer melhores condições de recuperação ao paciente traumatizado ou recém-operado. A morfina foi o primeiro opióide usado em animais. Mais recentemente, a administração dessa substância, por via epidural, vem sendo empregada no controle da dor com resultados promissores. Assim, nesta revisão, abordam-se vários aspectos referentes aos efeitos e às indicações da administração epidural de opióides em cães.

Avaliação e comparação da dor e da resposta inflamatória pós-cirúrgica em cadelas submetidas à ovário-histerectomia laparoscópica com único portal; realizada com pinça bipolar com corte e coagulação simultâneos ou por miniceliotomia com ganho de Snook

Pós-graduação em Cirurgia Veterinária - FCAV

Analgesia peridural com ropivacaína associada ao midazolam em cadelas submetidas a ovário-salpingo-histerectomia

Pós-graduação em Ciência Animal - FMVA

Estudo comparativo entre o bloqueio interescalênico do plexo branquial e o bloqueio seletivo dos nervos supraescapular e axilar nas cirurgias artroscópicas de ombro

Pós-graduação em Anestesiologia - FMB

Ovum pick-up technique in recently weaned ewe lambs subjected to ovarian stimulation

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Influência da aplicação de laser de baixa intensidade no recobrimento radicular associado à técnica de enxerto de tecido conjuntivo em indivíduos fumantes: ensaio clínico controlado randomizado

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Analgesia controlada pelo paciente comparada a analgesia padrão na função pulmonar, força muscular respiratória e dor no pós-operatório e revascularização do miocárdio: ensaio clínico randonizado

Pós-graduação em Bases Gerais da Cirurgia - FMB

Interventions for the management of mandibular fractures

BACKGROUND Fractures of the mandible (lower jaw) are a common occurrence and usually related to interpersonal violence or road traffic accidents. Mandibular fractures may be treated using open (surgical) and closed (non-surgical) techniques. Fracture sites are immobilized with intermaxillary fixation (IMF) or other external or internal devices (i.e. plates and screws) to allow bone healing. Various techniques have been used, however uncertainty exists with respect to the specific indications for each approach. OBJECTIVES The objective of this review is to provide reliable evidence of the effects of any interventions either open (surgical) or closed (non-surgical) that can be used in the management of mandibular fractures, excluding the condyles, in adult patients. SEARCH METHODS We searched the following electronic databases: the Cochrane Oral Health Group's Trials Register (to 28 February 2013), the Cochrane Central Register of Controlled Trials (CENTRAL) (The Cochrane Library 2013, Issue 1), MEDLINE via OVID (1950 to 28 February 2013), EMBASE via OVID (1980 to 28 February 2013), metaRegister of Controlled Trials (to 7 April 2013), ClinicalTrials.gov (to 7 April 2013) and the WHO International Clinical Trials Registry Platform (to 7 April 2013). The reference lists of all trials identified were checked for further studies. There were no restrictions regarding language or date of publication. SELECTION CRITERIA Randomised controlled trials evaluating the management of mandibular fractures without condylar involvement. Any studies that compared different treatment approaches were included. DATA COLLECTION AND ANALYSIS At least two review authors independently assessed trial quality and extracted data. Results were to be expressed as random-effects models using mean differences for continuous outcomes and risk ratios for dichotomous outcomes with 95% confidence intervals. Heterogeneity was to be investigated to include both clinical and methodological factors. MAIN RESULTS Twelve studies, assessed as high (six) and unclear (six) risk of bias, comprising 689 participants (830 fractures), were included. Interventions examined different plate materials and morphology; use of one or two lag screws; microplate versus miniplate; early and delayed mobilization; eyelet wires versus Rapid IMF™ and the management of angle fractures with intraoral access alone or combined with a transbuccal approach. Patient-oriented outcomes were largely ignored and post-operative pain scores were inadequately reported. Unfortunately, only one or two trials with small sample sizes were conducted for each comparison and outcome. Our results and conclusions should therefore be interpreted with caution. We were able to pool the results for two comparisons assessing one outcome. Pooled data from two studies comparing two miniplates versus one miniplate revealed no significant difference in the risk of post-operative infection of surgical site (risk ratio (RR) 1.32, 95% CI 0.41 to 4.22, P = 0.64, I(2) = 0%). Similarly, no difference in post-operative infection between the use of two 3-dimensional (3D) and standard (2D) miniplates was determined (RR 1.26, 95% CI 0.19 to 8.13, P = 0.81, I(2) = 27%). The included studies involved a small number of participants with a low number of events. AUTHORS' CONCLUSIONS This review illustrates that there is currently inadequate evidence to support the effectiveness of a single approach in the management of mandibular fractures without condylar involvement. The lack of high quality evidence may be explained by clinical diversity, variability in assessment tools used and difficulty in grading outcomes with existing measurement tools. Until high level evidence is available, treatment decisions should continue to be based on the clinician's prior experience and the individual circumstances.

Ultrasound-guided pudendal nerve block in cats undergoing perineal urethrostomy: a prospective, randomised, investigator-blind, placebo-controlled clinical trial

The objective of this study was to evaluate the clinical usefulness, in terms of analgesic efficacy and safety, of ultrasound-guided pudendal nerve block performed with bupivacaine in cats undergoing perineal urethrostomy. Eighteen client-owned male cats scheduled for perineal urethrostomy were enrolled in the study and assigned to one of two treatment groups. The pudendal nerve block was performed under general anaesthesia as described elsewhere, with 0.3 ml/kg of either saline (group C) or 0.5% bupivacaine (group B) - the total injection volume being split equally on the two sites of injection (left and right). Intra-operatively, assessment of nociception was based on the rescue analgesics requirement, as well as on the evaluation of changes in physiological parameters in comparison with the baseline values. Post-operative pain assessment was performed using three different pain scales at recovery and then 1, 2 and 3 h after recovery. Cats in group B showed lower heart rates and required fewer analgesics during surgery than group C. Post-operatively, group B had lower pain scores and needed less rescue buprenorphine than group C. Iatrogenic block-related complications were not observed. In conclusion, the ultrasound-guided pudendal nerve block can be considered clinically useful in feline medicine as it provides reliable analgesia in cats undergoing perineal urethrostomy.

Minimally invasive approach to lumbosacral decompression in a cadaveric canine model

AIMS To determine efficacy of a minimally invasive (MI) surgical approach using a human MI lumbar retractor for canine lumbosacral dorsal laminectomy and partial discectomy and to compare this technique to the standard open surgical (OS) approach. METHODS Lumbosacral dorsal laminectomy and partial discectomy was performed on 16 large-breed canine cadavers using either a standard OS (n=8) or MI (n=8) approach. Skin and fascial incision length, procedure time, and intraoperative complications were recorded. Postoperatively specimens were evaluated for laminectomy and discectomy dimensions, and visible damage to the cauda equina and exiting nerve roots. RESULTS Median length of skin and fascial incisions in the OS group were longer than in the MI group (p<0.001). Median laminectomy length was similar between both approaches (p=0.234) but width was greater for the MI than OS approach (p=0.002). Both approaches achieved similar partial discectomy width (p=0.279). Overall surgical time was longer for MI approaches compared to OS, with a median of 18.5 (min 15.5, max 21.8) minutes for MI compared to 14.6 (min 13.1, max 16.9) minutes for OS (p=0.001). CONCLUSIONS The MI approach reduced incision lengths while retaining comparable laminectomy and discectomy dimensions. For this in vitro model the MI approach required more time to complete, but this difference may not be relevant in clinical cases. CLINICAL RELEVANCE Dogs undergoing lumbosacral dorsal laminectomy are commonly large-breed dogs. The traditional open approach requires a large skin incision and soft tissue dissection, especially in overweight animals. A MI approach accomplishing the same surgical result while minimising soft tissue trauma could reduce post-operative pain and recovery time, and may lower wound-related complications. Clinical studies are needed to confirm postoperative benefit and assess operating times in vivo.

Prolonged Duration of Sciatic Nerve Blockade in the Elderly after Foot and Ankle Surgery

1.1 Background and Objectives: Perioperative morbidity related to anesthesia renders elderly patients vulnerable because age related factors affect medication effects, clearance and metabolism. Regional anesthesia within a multimodal regimen reduces opioid adverse effects in the elderly and improves immediate analgesia but not long term recovery and prolonged nerve blockade has been reported. The purpose of this study was to assess analgesic effects of sciatic nerve blockade in the elderly. 1.2 Methods: Postoperative sciatic nerve blockade was administered for foot and ankle surgery to patients over age 18 years. Preoperative, post-anesthesia unit and 24 hour postoperative pain scores and opioid doses for these same intervals were recorded. 1.3 Results: 47 patients enrolled and 12 (25.5%) were over age 70. Preoperative, immediate and 24 post-operative pain scores and total intraoperative and immediate postoperative opioid doses were lower in the elderly. The total 24 hour postoperative opioid doses in the elderly were lower compared to the younger group. 1.4 Conclusions: Total 24 hour postoperative cumulative opioid doses after sciatic nerve blockade in patients over 70 are lower than in younger patients. Further observations in greater numbers of patients and improved ultrasound to assess sciatic nerve structure in the elderly are warranted to study this effect.

Postoperative analgesic requirements - total laparoscopic hysterectomy versus vaginal hysterectomy

Background: There is limited information available on the requirement for postoperative analgesic drugs in patients submitted to total laparoscopic hysterectomy (TLH) compared with patients undergoing vaginal hysterectomy (VH). Aim: To compare the postoperative analgesic requirements in patients who underwent a TLH with patients who had a VH. Methods: Chart review of 53 patients who had TLH and 47 who had VH and were seen postoperatively by an acute pain management service in order to assess postoperative analgesic requirements. Patient controlled analgesia (PCA) was part of the standard protocol for postoperative pain management. Analgesic requirement was recorded as the mean doses of morphine and number of days that patients used non-steroidal anti-inflammatory drugs (NSAIDs), oxycodone and tramadol. Results: The requirement for total morphine was approximately half the dose in patients who had a TLH (10.8 +/- 12.6 mg) compared with patients who had a VH (19.4 +/- 21.9 mg) (P 0.017). The length of use of NSAIDs was significantly reduced in patients who had undergone a TLH (2.0 +/- 0.95 days) as compared with patients who had a VH (2.85 +/- 1.1 days) (P < 0.0001). Conclusions: Patients submitted to TLH require less postoperative analgesic drugs when compared with patients who had VH. Prospective randomised trials are warranted to compare analgesic requirements between patients submitted to TLH and VH.

Dexamethasone reduces pain, vomiting and overall complications following tonsillectomy in adults: a systematic review and meta-analysis of randomised controlled trials

Background: Tonsillectomy is one of the most common surgical procedures, but there is debate whether systemic steroids should be used to reduce pain and post-operative complications.