» Articles » PMID: 7906809

CLASP: a Randomised Trial of Low-dose Aspirin for the Prevention and Treatment of Pre-eclampsia Among 9364 Pregnant Women. CLASP (Collaborative Low-dose Aspirin Study in Pregnancy) Collaborative Group

Overview
Journal Lancet
Publisher Elsevier
Specialty General Medicine
Date 1994 Mar 12
PMID 7906809
Citations 122
Affiliations
Soon will be listed here.
Abstract

Pre-eclampsia is a common and serious complication of pregnancy that affects both mother and child. Review of previous small trials of antiplatelet therapy, particularly low-dose aspirin, suggested reductions of about three-quarters in the incidence of pre-eclampsia and some avoidance of intrauterine growth retardation (IUGR), but larger trials have not confirmed these results. In our multicentre study 9364 women were randomly assigned 60 mg aspirin daily or matching placebo. 74% were entered for prophylaxis of pre-eclampsia, 12% for prophylaxis of IUGR, 12% for treatment of pre-eclampsia, and 3% for treatment of IUGR. Overall, the use of aspirin was associated with a reduction of only 12% in the incidence of proteinuric pre-eclampsia, which was not significant. Nor was there any significant effect on the incidence of IUGR or of stillbirth and neonatal death. Aspirin did, however, significantly reduce the likelihood of preterm delivery (19.7% aspirin vs 22.2% control; absolute reduction of 2.5 [SD 0.9] per 100 women treated; 2p = 0.003). There was a significant trend (p = 0.004) towards progressively greater reductions in proteinuric pre-eclampsia the more preterm the delivery. Aspirin was not associated with a significant increase in placental haemorrhages or in bleeding during preparation for epidural anaesthesia, but there was a slight increase in use of blood transfusion after delivery. Low-dose aspirin was generally safe for the fetus and newborn infant, with no evidence of an increased likelihood of bleeding. Our findings do not support routine prophylactic or therapeutic administration of antiplatelet therapy in pregnancy to all women at increased risk of pre-eclampsia or IUGR. Low-dose aspirin may be justified in women judged to be especially liable to early-onset pre-eclampsia severe enough to need very preterm delivery. In such women it seems appropriate to start low-dose aspirin prophylactically early in the second trimester.

Citing Articles

Secondary prevention of preeclampsia.

Akbar M, Rosaudyn R, Gumilar K, Shanmugalingam R, Dekker G Front Cell Dev Biol. 2025; 13:1520218.

PMID: 39989985 PMC: 11842342. DOI: 10.3389/fcell.2025.1520218.


Influence of aspirin on obstetric outcomes in women with pre-gestational diabetes mellitus: a South-Western Sydney cohort study.

Jeyaruban A, Shanmugalingam R, Wu P, Cao R, Wong V, Wong T Obstet Med. 2024; 18(1):18-23.

PMID: 39553192 PMC: 11563550. DOI: 10.1177/1753495X241230719.


How to undertake procedures while on antiplatelet agents: a hematologist's view.

Swan D, Turner R, Douketis J, Thachil J Res Pract Thromb Haemost. 2024; 8(6):102539.

PMID: 39318772 PMC: 11419924. DOI: 10.1016/j.rpth.2024.102539.


Aspirin resistance in pregnancy is associated with reduced interleukin-2 (IL-2) concentrations in maternal serum: Implications for aspirin prophylaxis for preeclampsia.

Hernandez F, Chavez H, Goemans S, Kirakosyan Y, Luevano C, Canfield D Pregnancy Hypertens. 2024; 37:101131.

PMID: 38851168 PMC: 11610477. DOI: 10.1016/j.preghy.2024.101131.


Barriers and facilitators of adherence to low-dose aspirin during pregnancy: A co-produced systematic review and COM-B framework synthesis of qualitative evidence.

Vinogradov R, Holden E, Patel M, Grigg R, Errington L, Araujo-Soares V PLoS One. 2024; 19(5):e0302720.

PMID: 38701053 PMC: 11068207. DOI: 10.1371/journal.pone.0302720.