The effects of LED emissions on sternotomy incision repair after myocardial revascularization: a randomized double-blind study with follow-up

2013 ◽  
Vol 29 (3) ◽  
pp. 1195-1202 ◽  
Author(s):  
Rauirys Alencar de Oliveira ◽  
Gilderlene Alves Fernandes ◽  
Andréa Conceição Gomes Lima ◽  
Antônio Dib Tajra Filho ◽  
Raimundo de Barros Araújo ◽  
...  
1984 ◽  
Vol 15 (3) ◽  
pp. 240-244 ◽  
Author(s):  
Gerhard H. Fromm ◽  
Christopher F. Terrence ◽  
Amrik S. Chattha

Blood ◽  
2021 ◽  
Vol 138 (Supplement 1) ◽  
pp. 2127-2127
Author(s):  
Jean philippe Galanaud ◽  
Genty Celine ◽  
Alexa Comte ◽  
Carole Rolland ◽  
Francois Verriere ◽  
...  

Abstract Introduction: Elastic compression stockings (ECS) are commonly used for the prevention of post-thrombotic syndrome (PTS) after deep venous thrombosis (DVT). However, their efficacy is controversial. While two open-label studies reported a 50% risk reduction of PTS in the ECS vs. no-ECS groups, a large double-blind study didn't find any benefit of ECS vs. placebo-ECS to prevent PTS. These opposite results could be explained either by a placebo effect in the open-label studies or to a lack of compliance to study ECS in the double-blind study. Additional data on the impact of compliance on ECS efficacy, obtained in a double-blind way, are therefore needed. Methods: We analyzed data from the French, CELEST, multicentre double-blind trial comparing 25mmHg ECS vs. 35mmHg ECS to prevent PTS at 2 years after a first symptomatic ipsilateral proximal DVT (NCT01578122). All CELEST patients who had complete data for primary outcome (i.e. PTS, defined as a Villalta score ≥5 on the DVT affected leg at the one- or 2-year follow up visit) were included. The objectives of this predefined analysis were to: i) compare the incidences of PTS at 2 years according to compliance to ECS (irrespective of allocated treatment group) during the first 3 months of treatment and during the 2-year follow-up; ii) assess independent predictors of PTS using a stepwise multivariable model including all of the following variables (baseline patients' and DVT characteristics, anticoagulant treatment and compliance to ECS) if they achieved a p value of 0.2 or less in univariate analysis as well as ECS strength allocation group; iii) build an induction tree algorithm to measure the impact in terms of incidence of PTS of each of the independent predictor of PTS. Compliance to ECS was defined as reasonable and optimal if the patient had worn the study ECS more than 50% and more than 80% of the time respectively and had a modified GIRERD score of 0-2. Results: 249 patients were eligible for this analysis. Mean baseline age was 57 years, 70% (n=174) were men, 20% (n=50) were obese, 21% (n=52) had previous VTE event, 7% (n=18) had a baseline Villalta score ≥5 and the most proximal extent of DVT was the iliac vein in 15% (n=37) of cases. In 80% (n=179) of cases patients were treated with anticoagulation for more than 6 months after DVT and a direct oral anticoagulant (DOAC) was used in 69% (n=164) of cases. 32 % (n=80) of patients developed PTS at 2 years. When patients wore study ECS>80% of the time (i.e optimal compliance), incidence of PTS over 2 years was 26.1% (n=31). Incidence of PTS was 25.0% (n=10) and 40.5% (n=34) in those patients who wore ECS 50-80% and <50% of the time, p=0.06. When comparing patients who never wore study ECS (compliance<50% during the whole study follow-up) to those who were reasonably compliant during the whole study follow-up, incidence of PTS was respectively 46.4% (n=13) vs. 25.3% (n=38), p=0.02. Results of the univariate and multivariate analyses are presented in Table 1 and induction tree algorithm is provided in Figure 1. Conclusions: In our double bling study assessing 25mmHg vs. 35mmHg ECS to prevent PTS, compliance to ECS was a significant independent predictor of PTS in our multivariable model. Impact of ECS use became apparent when patient used ECS at least 50% of the time without any strong benefit beyond. Wearing study ECS>50% of the time was associated with 2-fold decreased risk of developing PTS, which is consistent with the results from previous 'positive' open-label studies. It suggests that use of ECS influences the risk of developing PTS. Our induction tree algorithm evidences that being compliant with ECS seems particularly beneficial in - non-obese - patients with extensive DVT. Figure 1 Figure 1. Disclosures Verriere: Laboratoires Innothera: Current Employment.


2017 ◽  
Vol 35 (1) ◽  
pp. 24-31 ◽  
Author(s):  
Andréa Conceição Gomes Lima ◽  
Gilderlene Alves Fernandes ◽  
Raimundo de Barros Araújo ◽  
Isabel Clarisse Gonzaga ◽  
Rauirys Alencar de Oliveira ◽  
...  

AIDS ◽  
1994 ◽  
Vol 8 (Supplement 4) ◽  
pp. S25 ◽  
Author(s):  
M Wainberg ◽  
JSG Montaner ◽  
A Rachlis ◽  
J Gill ◽  
R Beaulieu ◽  
...  

1986 ◽  
Vol 95 (1) ◽  
pp. 32-35 ◽  
Author(s):  
Jens Thomsen ◽  
Mirko Tos ◽  
Poul Bretlau ◽  
Niels Jon Johnsen

The reason for the effectiveness of endolymphatic sac-mastoid shunt surgery in the treatment of patients with Meniere's disease is still open for debate. In a double-blind study, published in 1981, we could not demonstrate any difference between the effect of a simple mastoidectomy and a regular endolymphatic sac-mastoid Silastic sheet shunt. However, a significant reduction in symptoms could be demonstrated in both groups, and 70% of patients in both groups could be classified as successes. The patients were reexamined 3 years after surgery, and it was still not possible to demonstrate any differences between the sham and the active surgery. In this study, no significant differences between the two groups have been found at follow-up averaging 84 months, and success has been maintained in about 70% of patients. The only three failures, who have consistent vertiginous attacks, have been confined to the actual shunt group. Two patients in the active group have lost their hearing as compared with none in the sham group, and 35% of the patients have now developed bilateral disease. We believe that endolymphatic sac-mastoid shunt surgery is a nonspecific treatment modality, and we find no need for sac shunt surgery. The vast majority of the patients can be successfully treated by nonsurgical means, but we emphasize that above all the patient must be assured that in the event of persistent debilitating symptoms, a surgical solution to the problem is available.


Pain ◽  
1993 ◽  
Vol 53 (2) ◽  
pp. 223-227 ◽  
Author(s):  
K. Schmidt ◽  
P. H. Althoff ◽  
A. G. Harris ◽  
H. Prestele ◽  
P. M. Schumm-Draeger ◽  
...  

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