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Status: Bibliographieeintrag

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Verfasst von:Antolovič, Dalibor [VerfasserIn]   i
 Rakow, Anastasia [VerfasserIn]   i
 Contin, Pietro [VerfasserIn]   i
 Ulrich, Alexis [VerfasserIn]   i
 Rahbari, Nuh Nabi [VerfasserIn]   i
 Büchler, Markus W. [VerfasserIn]   i
 Weitz, Jürgen [VerfasserIn]   i
 Koch, Moritz [VerfasserIn]   i
Titel:A randomised controlled pilot trial to evaluate and optimize the use of anti-platelet agents in the perioperative management in patients undergoing general and abdominal surgery
Titelzusatz:the APAP trial (ISRCTN45810007)
Verf.angabe:D. Antolovic, A. Rakow, P. Contin, A. Ulrich, N. N. Rahbari, M. W. Büchler, J. Weitz, M. Koch
Jahr:2012
Jahr des Originals:2011
Umfang:10 S.
Fussnoten:Published online: 3 November 2011 ; Gesehen am 20.06.2018
Titel Quelle:Enthalten in: Langenbeck's archives of surgery
Ort Quelle:Berlin : Springer, 1948
Jahr Quelle:2012
Band/Heft Quelle:397(2012), 2, Seite 297-306
ISSN Quelle:1435-2451
Abstract:PURPOSE: Surgeons are increasingly confronted by patients on long-term low-dose acetylsalicylic acid (ASA). However, owing to a lack of evidence-based data, a widely accepted consensus on the perioperative management of these patients in the setting of non-cardiac surgery has not yet been reached. Primary objective was to evaluate the safety of continuous versus discontinuous use of ASA in the perioperative period in elective general or abdominal surgery. METHODS: Fifty-two patients undergoing elective cholecystectomy, inguinal hernia repair or colonic/colorectal surgery were recruited to this pilot study. According to cardiological evaluation, non-high-risk patients who were on long-term treatment with low-dose ASA were eligible for inclusion. Patients were allocated randomly to continuous use of ASA or discontinuation of ASA intake for 5 days before until 5 days after surgery. The primary outcome was the incidence of major haemorrhagic and thromboembolic complications within 30 days after surgery. RESULTS: A total of 26 patients were allocated to each study group. One patient (3.8%) in the ASA continuation group required re-operation due to post-operative haemorrhage. In neither study group, further bleeding complications occurred. No clinically apparent thromboembolic events were reported in the ASA continuation and the ASA discontinuation group. Furthermore, there were no significant differences between both study groups in the secondary endpoints. CONCLUSIONS: Perioperative intake of ASA does not seem to influence the incidence of severe bleeding in non-high-risk patients undergoing elective general or abdominal surgery. Further, adequately powered trials are required to confirm the findings of this study.
DOI:doi:10.1007/s00423-011-0867-7
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext: http://dx.doi.org/10.1007/s00423-011-0867-7
 DOI: https://doi.org/10.1007/s00423-011-0867-7
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:Adult
 Aged
 Aspirin
 Blood Loss, Surgical
 Cholecystectomy
 Colorectal Surgery
 Dose-Response Relationship, Drug
 Drug Administration Schedule
 Elective Surgical Procedures
 Follow-Up Studies
 Herniorrhaphy
 Humans
 Perioperative Care
 Pilot Projects
 Platelet Aggregation Inhibitors
 Postoperative Hemorrhage
 Reference Values
 Risk Assessment
 Surgical Procedures, Operative
 Thromboembolism
 Treatment Outcome
K10plus-PPN:1576571394
Verknüpfungen:→ Zeitschrift

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