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Pregnant and postpartum patients have a four- to five-fold increased risk of venous thromboembolism (VTE) compared to the general population, accounting for almost 10% of all maternal deaths. Therefore, it is important to screen all pregnant patients for risk factors in order to provide appropriate prophylaxis. When VTE is diagnosed, appropriate treatment with low molecular weight or unfractionated heparin is required. Anticoagulation should be paused prior to any planned labor induction or cesarean delivery to decrease risk of neuraxial anesthesia or intrapartum hemorrhage. Patients with VTE in pregnancy should be tested for acquired and inherited thrombophilias.
Despite previous observational studies suggesting that malnutrition could be involved in venous thromboembolism (VTE), definitive causality still lacks high-quality research evidence. This study aims to explore the genetic causal association between malnutrition and VTE. The study was performed using summary statistics from genome-wide association studies for VTE (cases = 23 367; controls = 430 366). SNP associated with exposure was selected based on quality control steps. The primary analysis employed the inverse variance weighted (IVW) method, with additional support from Mendelian randomisation (MR)-Egger, weighted median and weighted mode approaches. MR-Egger, leave-one-SNP-out analysis and MR pleiotropy residual sum and outlier (MR-PRESSO) were used for sensitivity analysis. Cochran’s Q test was used to assess heterogeneity between instrumental variables (IV). IVW suggested that overweight has a positive genetic causal effect on VTE (OR = 1·1344, 95 % CI = 1·056, 1·2186, P < 0·001). No genetic causal effect of malnutrition (IVW: OR = 0·9983, 95 % CI = 0·9593, 1·0388, P = 0·9333) was found on VTE. Cochran’s Q test suggests no possible heterogeneity in both related exposures. The results of the MR-Egger regression suggest that the analysis is not affected by horizontal pleiotropy. The results of the MR-PRESSO suggest that there are no outliers. The results revealed a statistical genetic association where overweight correlates with an increased risk of VTE. Meanwhile, no genetic causal link was observed between malnutrition and VTE. Further research is warranted to deepen our understanding of these associations.
Pediatric pulmonary embolism occurs in 8.6−57 per 100,000 hospitalised children. We report a novel case of bilateral pulmonary emboli in a child presenting with dyspnoea who was found to have large right ventricular myxoma and subsequent diagnosis of Carney complex. After resection of the right ventricular myxoma and bilateral pulmonary embolectomy, she had a full recovery and an excellent outcome.
The physiologic and hormonal stresses that occur during pregnancy and labor have the potential to worsen existing respiratory disease and can pose unique challenges in management for the obstetrician and obstetric anesthesiologist. Cases of respiratory disease in pregnancy require specific planning and management to optimize maternal and fetal outcome. This chapter discusses rare respiratory disorders that the obstetric anesthesiologist may encounter in practice: acute respiratory distress syndrome, cystic fibrosis, pneumothorax, status asthmaticus, thromboembolic disease, mediastinal mass, congenital central hypoventilation syndrome, pulmonary lymphangioleiomyomatosis, restrictive and interstitial lung disease, transfusion related acute lung injury, transfusion-associated circulatory overload and lung transplantation. The aim is to present relevant discussion in order provide the anesthesiologist with some background and evidence to support her/his decision-making when encountering these rare and challenging cases.
Acute pulmonary embolism (PE) carries a high risk of morbidity and mortality and has a wide spectrum of severity, from incidental diagnosis in an asymptomatic patient to sudden refractory shock and cardiovascular collapse. Although the exact incidence remains uncertain, it is estimated that approximately 600,000 patients are diagnosed with PE annually in the United States, with mortality rates as high as 30% for patients with hemodynamic instability at presentation. A high-risk PE is one associated with hypotension or bradycardia. An intermediate-risk PE has evidence of RV strain, either by imaging or biomarkers (troponin or BNP). All others are low-risk PEs. The diagnosis of PE is often complicated by presentations that can be subtle, atypical or confounded by another coexisting disease.
We describe a rare case of acute pulmonary artery thromboembolism in a 17-year-old male patient who presented to our emergency department following a syncopal episode. A chest radiograph showed a convex pulmonic cone and an increased cardiothoracic index, and two-dimensional echocardiogram suggested near-occlusion of both pulmonary arterial branches. Multi-slice pulmonary angio-tomography revealed massive thrombosis of the pulmonary artery. He was treated with systemic anticoagulation and subsequently required surgical thrombectomy, with favourable early outcome. Although the cause of the thromboembolism remains unproven, we discuss possible etiologies.
A 28-year-old nulligravida with known factor V Leiden mutation is referred by her primary care provider to your hospital center’s high-risk obstetrics unit for preconception counseling.