Effects of Low Intensity Antithrombotic Regimes on the Haemoglobin Level

1994 ◽  
Vol 71 (03) ◽  
pp. 284-285 ◽  
Author(s):  
T W Meade ◽  
D J Howarth ◽  
P J Brennan

SummaryThe effects on the haemoglobin level of low dose aspirin and of low intensity oral anticoagulation with warfarin separately and in combination have been established in men aged between 45 and 69 at high risk of ischaemic heart disease. The findings confirm that combined treatment with warfarin and aspirin (WA) leads to a clear excess of minor bleeding episodes over warfarin alone (W) or aspirin alone (A). Each separate treatment on its own (either W or A) leads to an increase in these episodes compared with those on placebo (P) treatment. However, neither combined treatment (WA) nor the separate treatments (W or A) cause a fall in haemoglobin levels over a period of up to two years.

1992 ◽  
Vol 68 (01) ◽  
pp. 001-006 ◽  
Author(s):  
T W Meade ◽  
P J Roderick ◽  
P J Brennan ◽  
H C Wilkes ◽  
C C Kelleher

SummaryData from the early stages of the thrombosis prevention trial (TPT) have been used to establish and quantify the risk of extracranial bleeding due to low dose aspirin (75 mg) and low intensity oral anticoagulation with warfarin (international normalised ratio, INR, 1.5) singly or in combination, in men aged between 45 and 69 who are at high risk of ischaemic heart disease (IHD). The design of the trial is factorial, the four treatments being combined low dose aspirin and low intensity anticoagulation (WA), low intensity anticoagulation alone (W), low dose aspirin alone (A) and double placebo treatment (P). The trial is being carried out through the Medical Research Council’s General Practice Research Framework, with participating practices throughout the United Kingdom. Results are based on the first 3,667 men entered. The risk of major gastrointestinal bleeding due to active treatment is probably about 1 in 500 man-years of treatment, there currently being no difference between the three active regimes (WA, W, A). Intermediate and minor bleeding episodes occur more frequently with WA than with W or A on their own, the excess being mainly due to minor nose bleeds and bruises. In turn, both W and A on their own cause more such minor episodes than placebo treatment, P. There is no evidence that any of the three active regimes increases the risk of peptic ulceration, nor do they increase reports of indigestion. Aspirin increases reports of constipation and reduces reports of blurred vision. Minor bleeding occurs less frequently in smokers than in non-smokers but is not influenced by age. The antithrombotic regimes used are feasible and acceptable. So far, combined treatment and treatment with warfarin alone are not associated with more frequent serious hazards than low dose aspirin on its own, a regime that is increasingly used in clinical practice. The results provide a measure of reassurance for further trials of low intensity oral anticoagulation with warfarin alone or in combination with low dose aspirin.


2001 ◽  
Vol 85 (02) ◽  
pp. 221-225 ◽  
Author(s):  
Anetta Undas ◽  
Robert Undas ◽  
Jan Brożek ◽  
Andrzej Szczeklik ◽  
Jacek Musiał

SummaryAspirin and statins are beneficial in coronary heart disease across a broad range of cholesterol levels. We assessed the effects of low-dose aspirin (75 mg daily) on thrombin generation in patients with coronary heart disease and average blood cholesterol levels. We also investigated whether in patients with borderline-high cholesterol level who have been already taking aspirin, additional treatment with simvastatin would affect thrombin generation.Seven-day treatment with low-dose aspirin decreased thrombin generation ex vivo only in patients with total cholesterol 5.2 mmol/L. In patients with higher cholesterol levels aspirin had no effect. In these patients, already taking low-dose aspirin, additional three-month simvastatin treatment resulted in a reduction of thrombin generation. This demonstrates that low-dose aspirin depresses thrombin generation only in subjects with desirable blood cholesterol levels, while in others, with borderline-high cholesterol, thrombin formation is being reduced following the addition of simvastatin.


Blood ◽  
2008 ◽  
Vol 112 (11) ◽  
pp. 2806-2806
Author(s):  
Sabine Struve ◽  
Guido Finazzi ◽  
Konstanze Doehner ◽  
Stefanie Schauer ◽  
Eva Lengfelder ◽  
...  

Abstract Background: Philadelphia negative chronic myeloproliferative disorders (CMPDs) frequently present in women of childbearing age. Due to the high incidence of thromboembolic and hemorrhagic complications management of pregnancy is difficult in these patients. In order to document the course and outcome of pregnancies in CMPDs a registry has been implemented within the European LeukemiaNet project (work package 9). Case report forms are available via internet (http://www.uniklinik-ulm.de/struktur/kliniken/innere-medizin/klinik-fuer-innere-medizin-iii/home/studienzentrale/therapiestudien/cmps.html). A management strategy for pregnancy in CMPDs is proposed according to the experience of the authors and the available data in the literature [Griesshammer M. et al. Semin Thromb Hemost2006; 32: 422–9]. Results: From 01/2004 until 08/2008 we have registered 104 pregnancies in 52 patients including 43 patients with essential thrombocythemia (ET), 8 with polycythemia vera (PV) and 1 with primary myelofibrosis (PMF). Patients have been recruited by 7 centers from 6 countries (Austria, Czech Republic, Germany, Italy, Slovakia, Switzerland). The median age was 31,5 years (range 20,5 – 42,5 years). Seven of the 104 pregnancies are still ongoing, 8 have been terminated by elective abortion. The remaining 89 pregnancies had a life birth rate of 72% (64/89). A full-term normal delivery was observed in 86% (55/64). Spontaneous abortion was the most frequent complication occurring in 25% (22/89), mostly during the first trimester of pregnancy. Other complications such as stillbirth, premature delivery and intrauterine growth retardation occurred in 14% (12/89). The cumulative incidence of severe maternal complications was 9% (8/89), i.e. 2 cases of preeclampsia, 2 major thromboembolic events and 4 major bleeding episodes; furthermore 4 cases of microcirculatory disturbances and 2 minor bleeding episodes, i.e. recurrent epistaxis, were reported. Major thromboembolic events included a splenic vein thrombosis and a thrombotic occlusion of the vertebral artery. All major bleeding episodes were associated with obstetrical complications such as preterm detachment of the placenta, metratonia and peripartal injuries such as perineal and vaginal laceration. About half of our patients (50%) received no treatment during pregnancy, 20% had low-dose aspirin alone, 14% had low-dose aspirin plus low molecular weight heparin and the remaining patients (3%) had interferon alpha plus low-dose aspirin with or without low molecular weight heparin. In 13% information concerning treatment is still lacking. Interestingly, patients with the Jak2 mutation showed a significantly lower life birth rate compared to patients without (p = 0,0354). Conclusions: Pregnancies in CMPDs, especially ET, go along with a live birth rate around 72%. Spontaneous abortion is the most frequent fetal complication. Maternal complications are relatively rare, nevertheless severe thromboembolic and hemorrhagic events do occur, the latter especially in context with obstetrical complications. The Jak2 mutation seems to be a significant risk factor for adverse pregnancy outcome.


2020 ◽  
Vol 2 (2) ◽  
pp. 44
Author(s):  
Anak Agung Indah Astrijayanti ◽  
Made Krisna Adi Jaya ◽  
Ida Ayu Manik Partha Sutema ◽  
Ni Putu Wulanda Evayanti ◽  
Ni Ketut Tria Purnamisari

Introduction: Coronary heart disease (CHD) is a disorder of heart function due to a lack of blood in the heart muscle due to narrowing of the coronary arteries. Antiplatelet in patients with CHD is a therapy that must be obtained by patients throughout their lives to prevent recurrent attacks and deaths from CHD. In the Province of Bali, especially in Denpasar, there is a lack of information about the type of side effects that occur on antiplatelet medication, so it is necessary to do a related study. Objective: The aim of this study is to identify the type of side effects that occur on antiplatelet medication in patients with CHD. Methods: A cross-sectional study involving 97 patients was done by observed the CHD patients treated with antiplatelet medication. Side effects were evaluate using Naranjo Algorithm. Patients were divided into three groups, including a low dose aspirin user group, clopidogrel user group, and aspirin-clopidogrel combination user group. Results: Antiplatelet side effects that occur in patients include headache (2.06%), diarrhea (1.03%), cyanosis (1.03%), gastrointestinal bleeding (8.25%), heartburn (11.34%), and nausea (6.19%). These side effects only occurred in 31.96% of the total subjects. The incidence of aspirin side effects was significantly greater than clopidogrel as well as aspirin-clopidogrel in combination (p <0.05). Conclusion: Patients with CHD who use antiplatelet agents in the long term to be more aware of the potential side effects that will occur, especially heartburn in chronic low-dose aspirin users. Keywords: Coronary Heart Disease, Side Effects, Antiplatelet, Aspirin, Clopidogrel


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