Low-dose aspirin therapy to prevent preeclampsia

Objective: Our aim was to test the hypothesis that acetylsalicylate (aspirin) treatment reduces the incidence or severity of pregnancy-associated hypertension. Study Design: Patients were nulliparous, healthy, and with a singleton gestation at between 20 and 22 weeks' gestation. A sample size o...

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Veröffentlicht in:American journal of obstetrics and gynecology 1993-04, Vol.168 (4), p.1083-1093
Hauptverfasser: Hauth, John C., Goldenberg, Robert L., Parker, C. Richard, Philips, Joseph B., Copper, Rachel L., DuBard, Mary B., Cutter, Gary R.
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container_end_page 1093
container_issue 4
container_start_page 1083
container_title American journal of obstetrics and gynecology
container_volume 168
creator Hauth, John C.
Goldenberg, Robert L.
Parker, C. Richard
Philips, Joseph B.
Copper, Rachel L.
DuBard, Mary B.
Cutter, Gary R.
description Objective: Our aim was to test the hypothesis that acetylsalicylate (aspirin) treatment reduces the incidence or severity of pregnancy-associated hypertension. Study Design: Patients were nulliparous, healthy, and with a singleton gestation at between 20 and 22 weeks' gestation. A sample size of 600 patients was calculated on the basis of p ≤ 0.05 and 90% power of observation. A 2-week placebo-controlled “run-in” was used to select compliant patients. Randomization occurred at 24 weeks, with 60 mg of aspirin or placebo treatment from randomization to delivery. Results: Follow-up was maintained on 99% of the patients. The randomized patients had a 94% pill compliance index. At randomization, serum thromboxane medians were similar in both groups. Thromboxane B2 levels in the aspirin group decreased significantly from baseline at 29 to 31 weeks, 34 to 36 weeks, and at delivery as compared with an overall increase in the placebo group. Preeclampsia developed in five of 302 women (1.7%) who received aspirin versus 17 of 302 (5.6%) who received the placebo (p = 0.009). Preeclamspia was severe in one aspirin and in six placebo recipients (p = 0.06). Conclusion: Daily ingestion of 60 mg of aspirin beginning at 24 weeks' gestation significantly reduced the occurrence of preeclampsia.
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Richard ; Philips, Joseph B. ; Copper, Rachel L. ; DuBard, Mary B. ; Cutter, Gary R.</creator><creatorcontrib>Hauth, John C. ; Goldenberg, Robert L. ; Parker, C. Richard ; Philips, Joseph B. ; Copper, Rachel L. ; DuBard, Mary B. ; Cutter, Gary R.</creatorcontrib><description>Objective: Our aim was to test the hypothesis that acetylsalicylate (aspirin) treatment reduces the incidence or severity of pregnancy-associated hypertension. Study Design: Patients were nulliparous, healthy, and with a singleton gestation at between 20 and 22 weeks' gestation. A sample size of 600 patients was calculated on the basis of p ≤ 0.05 and 90% power of observation. A 2-week placebo-controlled “run-in” was used to select compliant patients. Randomization occurred at 24 weeks, with 60 mg of aspirin or placebo treatment from randomization to delivery. Results: Follow-up was maintained on 99% of the patients. The randomized patients had a 94% pill compliance index. At randomization, serum thromboxane medians were similar in both groups. Thromboxane B2 levels in the aspirin group decreased significantly from baseline at 29 to 31 weeks, 34 to 36 weeks, and at delivery as compared with an overall increase in the placebo group. Preeclampsia developed in five of 302 women (1.7%) who received aspirin versus 17 of 302 (5.6%) who received the placebo (p = 0.009). Preeclamspia was severe in one aspirin and in six placebo recipients (p = 0.06). 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Richard</creatorcontrib><creatorcontrib>Philips, Joseph B.</creatorcontrib><creatorcontrib>Copper, Rachel L.</creatorcontrib><creatorcontrib>DuBard, Mary B.</creatorcontrib><creatorcontrib>Cutter, Gary R.</creatorcontrib><title>Low-dose aspirin therapy to prevent preeclampsia</title><title>American journal of obstetrics and gynecology</title><addtitle>Am J Obstet Gynecol</addtitle><description>Objective: Our aim was to test the hypothesis that acetylsalicylate (aspirin) treatment reduces the incidence or severity of pregnancy-associated hypertension. Study Design: Patients were nulliparous, healthy, and with a singleton gestation at between 20 and 22 weeks' gestation. A sample size of 600 patients was calculated on the basis of p ≤ 0.05 and 90% power of observation. A 2-week placebo-controlled “run-in” was used to select compliant patients. Randomization occurred at 24 weeks, with 60 mg of aspirin or placebo treatment from randomization to delivery. Results: Follow-up was maintained on 99% of the patients. The randomized patients had a 94% pill compliance index. At randomization, serum thromboxane medians were similar in both groups. Thromboxane B2 levels in the aspirin group decreased significantly from baseline at 29 to 31 weeks, 34 to 36 weeks, and at delivery as compared with an overall increase in the placebo group. Preeclampsia developed in five of 302 women (1.7%) who received aspirin versus 17 of 302 (5.6%) who received the placebo (p = 0.009). Preeclamspia was severe in one aspirin and in six placebo recipients (p = 0.06). Conclusion: Daily ingestion of 60 mg of aspirin beginning at 24 weeks' gestation significantly reduced the occurrence of preeclampsia.</description><subject>Adult</subject><subject>aspirin</subject><subject>Aspirin - administration &amp; dosage</subject><subject>Biological and medical sciences</subject><subject>Eclampsia - prevention &amp; control</subject><subject>Female</subject><subject>Genital system. Reproduction</subject><subject>Humans</subject><subject>Hypertension - prevention &amp; control</subject><subject>Medical sciences</subject><subject>Parity</subject><subject>Pharmacology. Drug treatments</subject><subject>Pre-Eclampsia - prevention &amp; control</subject><subject>Preeclampsia prevention</subject><subject>Pregnancy</subject><subject>Pregnancy Complications, Cardiovascular - prevention &amp; control</subject><subject>Pregnancy Outcome</subject><subject>Prospective Studies</subject><subject>serum thromboxane</subject><subject>Thromboxane B2 - blood</subject><issn>0002-9378</issn><issn>1097-6868</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1993</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kEtLxDAQgIMo67r6DxR6ENFDNUmbJrkIsvhYWPCi55AmU4z0ZdJd8d-bumWPXmYY5pth5kPonOBbgklxhzGmqcy4uJbZjcQZI-nqAM0JljwtRCEO0XyPHKOTED7Hkko6QzORcyYZmyO87r5T2wVIdOidd20yfIDX_U8ydEnvYQvtMGYwtW764PQpOqp0HeBsygv0_vT4tnxJ16_Pq-XDOjWZKIaUUW0sy63WJVQ03is0EQLTIiOWGUIFo6XIQTBOrTA55AykIYUtOZeU8ipboKvd3t53XxsIg2pcMFDXuoVuExRnhaSMiQjmO9D4LgQPleq9a7T_UQSrUZQa31ajhRjUnyi1imMX0_5N2YDdD01mYv9y6utgdF153RoX9ljOeRH_idj9DoPoYuvAq2ActAas82AGZTv3_x2_F5GDBg</recordid><startdate>19930401</startdate><enddate>19930401</enddate><creator>Hauth, John C.</creator><creator>Goldenberg, Robert L.</creator><creator>Parker, C. 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Richard ; Philips, Joseph B. ; Copper, Rachel L. ; DuBard, Mary B. ; Cutter, Gary R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c386t-52acd54daabef21018a18802631d5c12852b84e8572d8c4e45e9c16db779227f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1993</creationdate><topic>Adult</topic><topic>aspirin</topic><topic>Aspirin - administration &amp; dosage</topic><topic>Biological and medical sciences</topic><topic>Eclampsia - prevention &amp; control</topic><topic>Female</topic><topic>Genital system. Reproduction</topic><topic>Humans</topic><topic>Hypertension - prevention &amp; control</topic><topic>Medical sciences</topic><topic>Parity</topic><topic>Pharmacology. Drug treatments</topic><topic>Pre-Eclampsia - prevention &amp; control</topic><topic>Preeclampsia prevention</topic><topic>Pregnancy</topic><topic>Pregnancy Complications, Cardiovascular - prevention &amp; control</topic><topic>Pregnancy Outcome</topic><topic>Prospective Studies</topic><topic>serum thromboxane</topic><topic>Thromboxane B2 - blood</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hauth, John C.</creatorcontrib><creatorcontrib>Goldenberg, Robert L.</creatorcontrib><creatorcontrib>Parker, C. Richard</creatorcontrib><creatorcontrib>Philips, Joseph B.</creatorcontrib><creatorcontrib>Copper, Rachel L.</creatorcontrib><creatorcontrib>DuBard, Mary B.</creatorcontrib><creatorcontrib>Cutter, Gary R.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>American journal of obstetrics and gynecology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hauth, John C.</au><au>Goldenberg, Robert L.</au><au>Parker, C. Richard</au><au>Philips, Joseph B.</au><au>Copper, Rachel L.</au><au>DuBard, Mary B.</au><au>Cutter, Gary R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Low-dose aspirin therapy to prevent preeclampsia</atitle><jtitle>American journal of obstetrics and gynecology</jtitle><addtitle>Am J Obstet Gynecol</addtitle><date>1993-04-01</date><risdate>1993</risdate><volume>168</volume><issue>4</issue><spage>1083</spage><epage>1093</epage><pages>1083-1093</pages><issn>0002-9378</issn><eissn>1097-6868</eissn><coden>AJOGAH</coden><abstract>Objective: Our aim was to test the hypothesis that acetylsalicylate (aspirin) treatment reduces the incidence or severity of pregnancy-associated hypertension. Study Design: Patients were nulliparous, healthy, and with a singleton gestation at between 20 and 22 weeks' gestation. A sample size of 600 patients was calculated on the basis of p ≤ 0.05 and 90% power of observation. A 2-week placebo-controlled “run-in” was used to select compliant patients. Randomization occurred at 24 weeks, with 60 mg of aspirin or placebo treatment from randomization to delivery. Results: Follow-up was maintained on 99% of the patients. The randomized patients had a 94% pill compliance index. At randomization, serum thromboxane medians were similar in both groups. Thromboxane B2 levels in the aspirin group decreased significantly from baseline at 29 to 31 weeks, 34 to 36 weeks, and at delivery as compared with an overall increase in the placebo group. Preeclampsia developed in five of 302 women (1.7%) who received aspirin versus 17 of 302 (5.6%) who received the placebo (p = 0.009). Preeclamspia was severe in one aspirin and in six placebo recipients (p = 0.06). 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identifier ISSN: 0002-9378
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subjects Adult
aspirin
Aspirin - administration & dosage
Biological and medical sciences
Eclampsia - prevention & control
Female
Genital system. Reproduction
Humans
Hypertension - prevention & control
Medical sciences
Parity
Pharmacology. Drug treatments
Pre-Eclampsia - prevention & control
Preeclampsia prevention
Pregnancy
Pregnancy Complications, Cardiovascular - prevention & control
Pregnancy Outcome
Prospective Studies
serum thromboxane
Thromboxane B2 - blood
title Low-dose aspirin therapy to prevent preeclampsia
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