Low-Dose Aspirin after ASPRE-More Questions Than Answers? Current International Approach after PE Screening in the First Trimester.
Piotr ToustyMagda Fraszczyk-ToustySylwia DzidekHanna Jasiak-JóźwikKaja MichalczykEwa KwiatkowskaAneta Cymbaluk-PłoskaAndrzej TorbéSebastian KwiatkowskiPublished in: Biomedicines (2023)
Preeclampsia (PE) is a multi-factorial disorder of pregnancy, and it continues to be one of the leading causes of fetal and maternal morbidity and mortality worldwide. Aspirin is universally recommended for high-risk women to reduce preeclampsia risk. The purpose of this review is to summarize the recommendations of various scientific societies on predicting preeclampsia and their indications for the inclusion of acetylsalicylic acid (ASA) prophylaxis. Fourteen guidelines were compared. The recommended dose, screening method, and gestational age at the start of the test vary depending on the recommendation. The societies are inclined to recommend using increasingly higher doses (>75 mg) of ASA, with many encouraging doses from 100 mg upward. Most societies indicate that the optimal time for implementing aspirin is prior to 16 weeks' gestation. Following the publication of the Aspirin for Evidence-Based Preeclampsia Prevention (ASPRE) trial results and other papers evaluating the Fetal Medicine Foundation (FMF) screening model, a large number of societies have changed their recommendations from those based on risk factors alone to the ones based on the risk assessment proposed by the FMF. This allows for the detection of a high-risk pregnancy population in whom aspirin will be remarkably effective in preventing preterm PE, thereby decreasing maternal and fetal morbidity.
Keyphrases
- low dose
- pregnancy outcomes
- gestational age
- birth weight
- preterm birth
- pregnant women
- early onset
- cardiovascular events
- high dose
- antiplatelet therapy
- risk assessment
- risk factors
- clinical trial
- low birth weight
- coronary artery disease
- randomized controlled trial
- clinical practice
- type diabetes
- anti inflammatory drugs
- cardiovascular disease
- polycystic ovary syndrome
- adipose tissue
- climate change
- physical activity
- phase iii
- human health
- real time pcr
- weight gain
- insulin resistance