Venous thromboembolism in pregnant and puerperal women in Denmark 1995–2005

2011 ◽  
Vol 106 (08) ◽  
pp. 304-309 ◽  
Author(s):  
Rie Adser Virkus ◽  
Ellen Christine Leth Løkkegaard ◽  
Thomas Bergholt ◽  
Ulla Mogensen ◽  
Jens Langhoff-Roos ◽  
...  

SummaryVenous thromboembolism (VTE) is the leading cause of maternal death in the Western world, and the risk increases during pregnancy and puerperal period. It was the objective of the present study to estimate the absolute and the relative risk of VTE at different weeks of gestation and in the postnatal period as compared to non-pregnant women. This was a historical controlled national cohort study. The National Registry of Patients identified relevant diagnoses. These data were linked to The National Registry of Medical Products Statistics for information about current use of oral contraceptives. Danish women 15 to 49 years old during the period January 1995 through December 2005 were included in the study. In total 819,751 pregnant women were identified of whom 727 had a diagnosis of VTE. The absolute risk of VTE per 10,000 pregnancy-years increased from 4.1 (95% CI, 3.2 to 5.2) during week 1–11 up to 59.0 (95% CI: 46.1 to 76.4) in week 40 and decreased in the puerperal period from 60.0 (95% CI:47.2–76.4) during the first week after birth to 2.1 (95% CI:1.1 to 4.2) during week 9–12 after birth. Compared with non-pregnant women, the incidence rate ratio rose from 1.5 (95% CI:1.1 to1.9) in week 1–11, to 21.0 (95%CI16.7 to 27.4) in week 40 and 21.5 (95% CI:16.8 to 27.6) in the first week after delivery, declining to 3.8 (95% CI:2.5 to 5.8) 5–6 weeks after delivery. In conclusion, the risk of VTE increases almost exponentially through pregnancy and reaches maximum just after delivery and is no longer significantly increased six weeks after delivery.

2019 ◽  
Vol 27 (2) ◽  
Author(s):  
Divya J Karsanji ◽  
Shannon M Bates ◽  
Leslie Skeith

Abstract Background The average risk of venous thromboembolism (VTE) in long haul travellers is approximately 2.8 per 1000 travellers, which is increased in the presence of other VTE risk factors. In pregnant long-haul travellers, little is known in terms of the absolute risk of VTE in these women and, therefore, there is limited consensus on appropriate thromboprophylaxis in this setting. Objective This review will provide guidance to allow practitioners to safely minimize the risk of travel-related VTE in pregnant women. The suggestions provided are based on limited data, extrapolated risk estimates of VTE in pregnant travellers and recommendations from published guidelines. Results We found that the absolute VTE risk per flight appears to be <1% for the average pregnant or postpartum traveller. In pregnant travellers with a prior history of VTE, a potent thrombophilia or strong antepartum risk factors (e.g. combination of obesity and immobility), the risk of VTE with travel appears to be >1%. Postpartum, the risk of VTE with travel may be >1% for women with thrombophilias (particularly in those with a family history) and other transient risk factors and in women with a prior VTE. Conclusions Based on our findings, we recommend simple measures be taken by all pregnant travellers, such as frequent ambulation, hydration and calf exercises. In those at an intermediate risk, we suggest a consideration of 20–30 mmHg compression stockings. In the highest risk group, we suggest careful consideration for low-molecular-weight heparin thromboprophylaxis. If there are specific concerns, we advise consultation with a thrombosis expert at the nearest local centre.


Blood ◽  
2016 ◽  
Vol 128 (22) ◽  
pp. 2595-2595
Author(s):  
Leslie Skeith ◽  
Marc Carrier ◽  
Susan Robinson ◽  
Samah Alimam ◽  
Marc Rodger

Abstract Introduction: There is an increased risk of venous thromboembolism (VTE) in patients with essential thrombocythemia (ET), however, what the absolute VTE risk is during pregnancy is largely unknown and is based on small cohort or registry studies. Recommendation for the use of low-molecular-weight heparin (LMWH) prophylaxis in the antepartum and/or postpartum setting is based on the absolute VTE and bleeding risk in other patient populations, for example, in women with inherited thrombophilia. A better estimate of absolute VTE risk will provide guidance for the use of LMWH in pregnant women with ET, as well as other treatments such as interferon. Objective: The aim of our meta-analysis is to quantify the absolute risk of VTE with or without LMWH prophylaxis in women with ET during pregnancy and in the postpartum setting. Methods: A systematic literature search was conducted on MEDLINE, EMBASE and EBM reviews. The primary outcome was VTE and the secondary outcomes were bleeding events and arterial thromboembolism (ATE). Studies were excluded if less than 5 pregnancies were reported, or if there was any duplication in publication, then only the most recent study was included. Using a standardized form, data was extracted independently by two investigators with disagreements resolved by consensus (L.S. and M.A.R.). Data on the use of LMWH, aspirin (ASA) and interferon was collected. Primary and secondary outcomes were reported per pregnancy in the antepartum and postpartum setting using pooled proportions, with 95% confidence intervals reported. Pregnancies ending in first trimester loss were excluded from the postpartum VTE analysis. Peripartum bleeding (delivery to 24 hours) was excluded. Placental abruptions were included as bleeding events. Results: There were 21 studies included that reported outcomes of interest in 504 patients and 756 pregnancies (1991-2016). Ten authors provided additional data. Among 756 pregnancies, there were 8 VTE events in the antepartum setting (1.06%, 95% CI, 0.54-2.07). Among 607 pregnancies (excluding first trimester losses), there were 8 VTE events in the postpartum setting (1.32%, 95% CI, 0.67-2.58). Of the 18 studies that reported VTE with respect to antepartum LMWH prophylaxis use, there were 0 antepartum VTE events among 82 pregnancies with LMWH use (0%, 95% CI, 0.0-4.48), and 8 antepartum VTE events among 407 pregnancies without LMWH use (1.97%, 95% CI, 1.00-3.83). Of the 14 studies that reported VTE with respect to postpartum LMWH prophylaxis use in pregnancies that excluded first trimester losses, there were 0 postpartum VTE events among 96 pregnancies with LMWH use (0%, 95% CI, 0.0-3.85), and 6 postpartum VTE events among 229 pregnancies without LMWH use (2.62%, 95% CI, 1.21-5.60) (Table 1). There were 12 antepartum bleeds reported in 756 pregnancies (1.59%, 95% CI, 0.91-2.75), 9 of which were placental abruptions (1.19%, 95% CI, 0.63-2.25). There were 11 postpartum bleeds reported in 756 pregnancies (1.46%, 95% CI 0.81-2.59). Bleeding according to LMWH prophylaxis use in the antepartum and postpartum setting is presented in Table 1. Among 756 pregnancies, there were 4 possible ATE events described in the antepartum setting: transient visual loss after ASA was held for 1 week, an ocular TIA at 6 weeks gestation while on ASA, and 2 patients who described both visual disturbance and dizziness with unknown ASA use. No patient with possible ATE received LMWH prophylaxis. Conclusion: Women with ET who are pregnant have an increased risk of VTE in both the antepartum and postpartum setting compared to the general pregnant population. The absolute risk of VTE in the antepartum and postpartum setting is not above a threshold where LMWH is clearly indicated or below a threshold where LMWH should be withheld. The role of thromboprophylaxis in this setting requires a shared decision-making process, taking into account patient values and preferences and the risks and benefits of LMWH. Disclosures Carrier: BMS: Research Funding; Leo Pharma: Research Funding. Robinson:Novartis: Honoraria; Pharmacosmos: Honoraria; Amgen: Honoraria. Rodger:Boehringer Ingelheim: Research Funding; Canadian Agency for Drugs and Technologies in Health: Consultancy.


Blood ◽  
2006 ◽  
Vol 108 (11) ◽  
pp. 1485-1485
Author(s):  
Nienke Folkeringa ◽  
Jan-Leendert P. Brouwer ◽  
Fleurisca J. Korteweg ◽  
Nic J.G.M Veeger ◽  
Jan Jaap H.M. Erwich ◽  
...  

Abstract Venous thromboembolism (VTE)during pregnancy is still an important cause of maternal morbidity and mortality in the Western world. The risk VTE in pregnant women is five times higher than in non-pregnant women of the same age. This risk is increased by thrombophilic defects. In a family cohort study we assessed the risk of VTE during pregnancy/puerperium and the contribution of concomitant thrombophilic defects in women with hereditary antithrombin, protein C or protein S deficiencies. Women were recruited from a previous large family cohort study, which was designed to estimate the risk of VTE in first degree relatives from probands with documented VTE and a deficiency of antithrombin, protein C or protein S. Probands were excluded from analysis. Blood samples of female relatives were tested on the index deficiencies and prothrombin G20210A, factor V Leiden, hyperhomocysteinemia and increased levels of VIII:C, IX:C and XI:C. Observation time was defined as the fertile period (from age 15–45 years), or until the first VTE, or until end of study period. The cohort contained 222 female relatives, of whom 101 women were deficient and 121 non-deficient. The absolute risk of venous thromboembolism in deficient women was 1.76 per 100 person-years versus 0.19 per 100 person-years in non-deficient women (Relative Risk (RR) 9.2; 95% CI 3.8–26.7). Concomitance of none, one and more than one thrombophilic defect increased the risk in deficient (1.55, 2.14 and 2.92 per 100 person-years, respectively) and non-deficient women (0.16, 0.09 and 0.54 per 100 person -years, respectively). Annual incidences (AI) were lower in ever pregnant than never pregnant deficient women, 1.37 per 100 person-years versus 2.96 per 100 person-years (RR 0.5; 95% CI 0.2–0.99)(Table). These were 0.09 per 100 person-years versus 0.70 per 100 person-years in non-deficient women (RR 0.1; 95% CI 0.02–0.9). In ever pregnant deficient women 71% of VTE episodes were pregnancy related. A majority (75%) of never pregnant deficient women revealed VTE associated with oral contraceptives. Women with hereditary antithrombin, protein C or protein S deficiencies are at high risk of VTE. Concomitance of other thrombophilic defects increased this risk. In fertile women most episodes of VTE are associated with either pregnancy or oral contraceptives. Deficient Non-deficient Ever pregnant (n=54) Never Pregnant (n=47) Ever pregnant (n=79) Never pregnant (n=42) Women with VTE, n 17 12 2 3 Observation period, yr 1241 405 2169 430 AI, % (95% CI) 1.37 (0.80–2.19) 2.96 (1.53–5.18) 0.09 (0.01–0.33) 0.70 (0.14–2.04) RR (95% CI) 0.5 (0.2–0.99) P=0.05 0.1 (0.02–0.9) P=0.04 Pregnancy related VTE, n (%) 12 (71) 0 1 (50) 0 Oral contraceptive related VTE, n (%) 2 (12) 9 (75) 0 3 (100)


Blood ◽  
2017 ◽  
Vol 129 (8) ◽  
pp. 934-939 ◽  
Author(s):  
Leslie Skeith ◽  
Marc Carrier ◽  
Susan E. Robinson ◽  
Samah Alimam ◽  
Marc A. Rodger

Abstract We performed a meta-analysis to evaluate the risk of venous thromboembolism (VTE) in pregnant women with essential thrombocythemia. Twenty-one trials and 756 pregnancies met inclusion criteria. The absolute VTE risk in the antepartum period is not above a threshold where low-molecular-weight heparin (LMWH) prophylaxis is clearly indicated or below a threshold where LMWH should be withheld (2.5%; 95% CI, 1.3-4.3). Postpartum, the absolute VTE risk is above a threshold where postpartum LMWH prophylaxis should be considered (4.4%; 95% CI, 1.2-9.5).


2010 ◽  
Vol 63 (5-6) ◽  
pp. 376-379 ◽  
Author(s):  
Milena Veljkovic ◽  
Jasmina Popovic

Introduction. Because of their safety and efficacy, oral contraceptives are available without prescription in many countries. Monophasic combined oral contraceptives are a combination of estrogen and progestin taken in constant amounts. Venous thromboembolism. Combined oral contraceptives slightly increase the risk of venous thromboemolism, but this event is very rare among non-pregnant women of reproductive age. The absolute risk rises with age, obesity, recent surgery and certain forms of thrombophilia. The estrogen component of combined oral contraceptives increases the synthesis of several coagulation factors in a dose-dependent manner. Changes of most of these parameters are very small and there is no evidence that they have any effect upon the clinical risk of developing venous thrombosis. If a woman has an inherited coagulation disorder that increases her risk of developing thrombosis, the risk is increased several fold if she ingests estrogen containing oral contraception. Conclusion. The increased risk of venous thromboembolism associated with combined oral contraceptives should have little impact on healthy women, but may have substantial impact on women with a history of thromboembolism. Combined oral contraceptive use increases the risk of venous thromboembolosm in a dose-dependent manner. The absolute risk of venous thromboembolism rises with age, obesity, recent surgery and certain forms of thrombophilia, as well.


Cancers ◽  
2021 ◽  
Vol 13 (18) ◽  
pp. 4603
Author(s):  
Michael Saerens ◽  
Emiel A. De Jaeghere ◽  
Heini Kanervo ◽  
Nele Vandemaele ◽  
Hannelore Denys ◽  
...  

Thromboembolic events are the second cause of death in cancer patients. In ovarian cancer, 3–10% of patients present with venous thromboembolism (VTE), but the incidence may rise to 36% along the disease course. Bevacizumab is a monoclonal antibody directed against vascular endothelial-derived growth factor, and in in vitro studies it showed a predisposition to hemostasis perturbation, including thrombosis. However, in vivo and clinical studies have shown conflicting results for its use as a treatment for ovarian cancer, so we conducted a systematic review and meta-analysis on the risk of arterial thromboembolism (ATE) and VTE in ovarian cancer patients treated with bevacizumab. The review comprised 14 trials with 6221 patients: ATE incidence was reported in 5 (4811 patients) where the absolute risk was 2.4% with bevacizumab vs. 1.1% without (RR 2.45; 95% CI 1.27–4.27, p = 0.008). VTE incidence was reported in 9 trials (5121 patients) where the absolute risk was 5.4% with bevacizumab vs. 3.7% without (RR 1.32; 95% CI 1.02–1.79, p = 0.04). Our analysis showed that the risk of arterial and venous thromboembolism increased in patients treated with bevacizumab. Thrombolic events (TEs) are probably underreported, and studies should discriminate between ATE and VTE. Bevacizumab can be considered as an additional risk factor when selecting patients for primary prophylaxis with anticoagulants.


Author(s):  
Willian Sales ◽  
Iramar Nascimento ◽  
Guilherme Dienstmann ◽  
Matheus Souza ◽  
Grazielle Silva ◽  
...  

Objective To assess the effectiveness of metformin in the incidence of gestational diabetes mellitus (GDM) in obese pregnant women attending a public maternity hospital in Joinville, Santa Catarina, Brazil. Methods Randomized clinical trial including obese pregnant women with a body mass index (BMI) ≥ 30 kg/m2, divided into two groups (control and metformin). Both groups received guidance regarding diet and physical exercise. The participants were assessed at two moments, the first at enrollment (gestational age ≤ 20) and the second at gestational weeks 24–28. The outcomes assessed were BMI and gestational diabetes mellitus (GDM) diagnosis. The data distribution was assessed with the Friedman test. For all the analytical models, the p-values were considered significant when lower than 0.05. The absolute risk reduction was also estimated. Results Overall, 164 pregnant women were assessed and further divided into 82 participants per group. No significant difference was observed in BMI variation between the control and metformin groups (0.9 ± 1.2 versus 1.0 ± 0.9, respectively, p = 0.63). Gestational diabetes mellitus was diagnosed in 15.9% (n = 13) of the patients allocated to the metformin group and 19.5% (n = 16) of those in the control group (p = 0.683). The absolute risk reduction was 3.6 (95% confidence interval 8.0–15.32) in the group treated with metformin, which was not significant. Conclusion Metformin was not effective in reducing BMI and preventing GDM in obese pregnant women.


2021 ◽  
Vol 10 (7) ◽  
pp. 1487
Author(s):  
Isabel Añón-Oñate ◽  
Rafael Cáliz-Cáliz ◽  
Carmen Rosa-Garrido ◽  
María José Pérez-Galán ◽  
Susana Quirosa-Flores ◽  
...  

Rheumatic diseases (RD) and hereditary thrombophilias (HT) can be associated with high-risk pregnancies. This study describes obstetric outcomes after receiving medical care at a multidisciplinary consultation (MC) and compares adverse neonatal outcomes (ANOs) before and after medical care at an MC. This study is a retrospective observational study among pregnant women with RD and HT treated at an MC of a university hospital (southern Spain) from 2012 to 2018. Absolute risk reduction (ARR) and number needed to treat (NNT) were calculated. A total of 198 pregnancies were registered in 143 women (112 with RD, 31 with HT), with 191 (96.5%) pregnancies without ANOs and seven (3.5%) pregnancies with some ANOs (five miscarriages and two foetal deaths). Results previous to the MC showed 60.8% of women had more than one miscarriage, with 4.2% experiencing foetal death. MC reduced the ANO rate by AAR = 60.1% (95%CI: 51.6−68.7%). The NNT to avoid one miscarriage was 1.74 (95%CI: 1.5–2.1) and to avoid one foetal death NNT = 35.75 (95CI%: 15.2–90.9). A total of 84.8% of newborns and 93.2% of women did not experience any complication. As a conclusion, the follow-up of RD or HT pregnant women in the MC drastically reduced the risk of ANOs in this population with a previous high risk.


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