A case-controlled multicenter study of vasovagal reactions in blood donors: influence of sex, age, donation status, weight, blood pressure, and pulse

Transfusion ◽  
1999 ◽  
Vol 39 (3) ◽  
pp. 316-320 ◽  
Author(s):  
Jonathan J. Trouern-Trend ◽  
Ritchard G. Cable ◽  
Stanley J. Badon ◽  
Bruce H. Newman ◽  
Mark A. Popovsky
1999 ◽  
Vol 18 (4) ◽  
pp. 403-409 ◽  
Author(s):  
Lori A. Sauer ◽  
Christopher R. France

2003 ◽  
Vol 9 (5) ◽  
pp. 151-154
Author(s):  
Yu. N. Belenkov ◽  
I. Ye. Chazova

ROBIS is the first large multicenter study performed in Russia. The Objective of the study was to compare the efficiency, safely, and impact of two treatment policies (the application of an algorithm to the stepwise use of 4 classes of antihypertensive agents in an intensive care group and random antihypertensive therapy in a routine treatment group) on the incidence of cardiovascular events in patients with arterial hypertension. Design: This is a national multicenter open consecutive prospective study. The patients meeting the criteria of inclusion were randomly divided into two equal groups, one of them (an intensive care group) received therapy with a nifedipine retard in Fixed dose for 4 weeks. In patients who failed to achieve the target level of blood pressure (BP), the therapy was supplemented by enalapril, 20 mg, hydrochlorothiazide, 25 mg, and metoprolol, 50 mg, at a 4-week interval. After achieving the target BP level, the patients continued the treatment with which the level had been attained. If the antihypertensive effect of therapy was found to disappear, the above drugs were successively supplemented. The other group (a routine treatment group) continued to be treated with the antihypertensive drugs prescribed in the polyclinic (Fig. 1). BP and heart rate were monitored and the patients' complaints and adverse reactions were recorded on repeated visits 4, 8, 12, 16, 24, 52, 64, 70, 88, and 104 weeks after the initiation of therapy. Control blood and urine analyses and ECG studies were made 12, 16, 52, and 104 weeks after therapy.


Stroke ◽  
2019 ◽  
Vol 50 (Suppl_1) ◽  
Author(s):  
Mohammad Anadani ◽  
Yser Orabi ◽  
Ali Alawieh ◽  
Nitin Goyal ◽  
Abhi Pandhi ◽  
...  

2010 ◽  
Vol 30 (1) ◽  
pp. 29-34 ◽  
Author(s):  
Georgi Abraham ◽  
Vishnu Kumar ◽  
Karopadi Shivanand Nayak ◽  
Rajan Ravichandran ◽  
Geetha Srinivasan ◽  
...  

BackgroundLittle is known about survival on peritoneal dialysis (PD) in Indian patients since the initiation of continuous ambulatory PD (CAPD) in India in 1991. Survival data from single centers with small numbers have been published.ObjectiveA retrospective 4-center analysis for predictors of survival >3 years in south Indian chronic PD patients.MethodsA total of 309 patients were trained during the observation period (from 1999 to 2004) and were analyzed in a multicenter study (4 centers), including 150 patients (male:female 109:41) that survived ≥ 3 years and 59 patients that did not survive ≥ 3 years (nonsurvivors; male: female 43:16) that were taken as controls. The patients were on chronic PD, predominantly CAPD, using double-bag disconnect systems. They were supervised by 4 nephrologists. Mean age in the nonsurvival group was 56.6 ± 10.6 years. In the survival group, mean age was 50.9 ± 14.9 years; there were 92 (62%) nondiabetics and 58 (38%) diabetics; the majority were nonvegetarians; 148 patients were doing 6 – 8 L exchanges and 2 were doing >8 L exchanges daily; 93 of 102 patients were average transporters based on peritoneal equilibration testing. At the beginning, mean combined Kt/V was 2.31 and weekly creatinine clearance was 73 L. Patients making one lifetime payment were 46% and 21% belonged to the full reimbursement group.ResultsBody mass index (BMI) was normal in 114 patients (76%). Ultrafiltration volume was 1377 ± 452 at the start and 1400 ± 461 mL/day after 3 years. Anuric patients at the start were 12% and after 3 years 44%; urine output decreased from 527 ± 26 to 253 ± 14 mL/day from the start to after 3 years. Peritonitis rate was 1 episode/75 patient-months at the beginning and after 3 years it was 1 episode/30 patient-months. Exit-site care was done daily by 88% and 3 times weekly by 12%. Nonsmokers were 92% and smokers were 8%. Those that lived in the city were 62% and rural areas were 38%. Mean blood pressure was 143 ± 16/88 ± 10 and 136 ± 18/85 ± 9 mmHg, calcium × phosphorus product 44.6 ± 15.6 and 45.9 ± 15.7 mg2/dL2, albumin 3.33 ± 0.5 and 3.25 ± 0.4 g/dL, hemoglobin 9.18 ± 2 and 9.48 ± 1.8 g/dL at the beginning and after 3 years, respectively. Statistical analysis showed a significant fall in both systolic ( p ≤ 0.001) and diastolic blood pressure ( p ≤ 0.05), an increase in BMI ( p ≤ 0.01), and a decrease in blood urea ( p ≤ 0.001) in the survival group. Those with Hb ≥ 11 g/dL survived longer ( p ≤ 0.001), those with serum albumin ≥ 3 g/dL had better survival ( p = 0.001), and anuric patients survived longer ( p = 0.001).ConclusionThis multicenter cohort study of prevalent continuous PD patients in south India showed nondiabetics, average transporters, nonsmokers with reasonable nutritional status, with Hb 11 g/dL, with low peritonitis rate, with over 1 L ultrafiltration volume per day, the great majority that joined the once per lifetime payment scheme, and the reimbursement group survived for 3 years or longer.


2020 ◽  
Vol 87 (6) ◽  
pp. 830-839 ◽  
Author(s):  
Mohammad Anadani ◽  
Adam S. Arthur ◽  
Georgios Tsivgoulis ◽  
Kit N. Simpson ◽  
Ali Alawieh ◽  
...  

2005 ◽  
Vol 15 (5) ◽  
pp. 389-394 ◽  
Author(s):  
E. K. Zervou ◽  
K. Ziciadis ◽  
F. Karabini ◽  
E. Xanthi ◽  
E. Chrisostomou ◽  
...  

Transfusion ◽  
2011 ◽  
Vol 51 (10) ◽  
pp. 2061-2063 ◽  
Author(s):  
Bruce H. Newman ◽  
Barry A. Siegfried

Author(s):  
Vijayalakshmi Kuttath ◽  
Harikumaran Nair ◽  
Muraleedharan Nair

Introduction: A crucial component of the effort to meet the growing demand for blood is the recruitment and retention of young novice blood donors. Reducing postdonation syncopal reactions could have a beneficial impact on donor convenience, safety, and desire to donate again. Aim: To evaluate the effectiveness of predonation hydration over standard blood donation in the prevention or decrease in severity of postdonation Vasovagal Reactions (VVR) in hydrated blood donors in comparison with the non hydrated group. Materials and Methods: The randomised controlled trial was conducted on 953 first time voluntary blood donors. Donors in the intervention arm drank 250 mL water 30 minutes before blood donation, while those in the control group did not receive any intervention. Blood was collected by standard protocol. Outcome, VVR, if present was graded as mild, moderate, and severe. Analysis of results were done using Statistical Package for the Social Sciences (SPSS) version 16.0. A sensitivity analysis was also done to consider the dropouts from the study. Results: A total of 900 participants were included in the study, of which 443 were controls and 457 were cases. An effect size of 6.1%, a Relative Risk (RR) of 0.54 {95% Confidence Interval (CI)=0.36-0.81} and a risk reduction of 45% was arrived at, pointing to a protective role for predonation hydration in preventing VVR. There was a significant reduction in the severity of VVR in the predonation hydration group compared to the standard blood donation group (p-value=0.002). The protective effect of hydration on decreasing the occurrence and severity of VVR had statistical support in males in the moderate and severe grades (p-value=0.017). A similar statistical significance was not established in females (p-value=0.173). Sensitivity analysis did not reveal a difference in the statistical significance of variables between compared groups. Conclusion: Predonation hydration was found to be effective in preventing and decreasing the severity of VVR in novice blood donors.


2019 ◽  
Vol 15 (2) ◽  
pp. 253-260
Author(s):  
Karan Kumar ◽  
Suchet Sachdev ◽  
Neelam Marwaha ◽  
Ratti Ram Sharma

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