Effects of aspirin and heparin treatment on perioperative outcomes in patients with Moyamoya disease.


Journal

Acta neurochirurgica
ISSN: 0942-0940
Titre abrégé: Acta Neurochir (Wien)
Pays: Austria
ID NLM: 0151000

Informations de publication

Date de publication:
05 2021
Historique:
received: 04 09 2020
accepted: 01 12 2020
pubmed: 7 1 2021
medline: 9 7 2021
entrez: 6 1 2021
Statut: ppublish

Résumé

When superficial temporal artery-middle cerebral artery bypass is combined with indirect methods (e.g., revascularization surgery) to treat Moyamoya disease (MMD), antiplatelet treatment can impact bypass patency, infarction, or hemorrhage complications. Recently, heparin has been proposed as an anticoagulant treatment against white thrombus at the anastomosis site. The study aims to evaluate the effect of aspirin on the perioperative outcomes and investigate the results of heparin treatment for white thrombus. This retrospective study included 74 procedures of combined revascularization surgery for MMD patients who either received or did not receive aspirin. Perioperative outcomes were compared between the two groups. In addition, the effects of heparin treatment for white thrombus were evaluated. The rate of white thrombus at the anastomosis site was significantly higher in the non-aspirin medication group (univariate: p = 0.032, multivariate: p = 0.044) and, accordingly, initial bypass patency was lower in the non-aspirin medication group (p = 0.049). Of the 17 patients with white thrombus development, five received heparin injections, and all white thrombi disappeared; however, there was one case of epidural hematoma and another of subdural hematoma. The risk of hemorrhagic complications was significantly higher in the surgical procedures that received heparin injections (p = 0.021). In MMD patients who received combined revascularization surgery, aspirin medication lowered the occurrence of white thrombus. Heparin injections help to treat white thrombus but can enhance the risk of hemorrhagic complications.

Sections du résumé

BACKGROUND
When superficial temporal artery-middle cerebral artery bypass is combined with indirect methods (e.g., revascularization surgery) to treat Moyamoya disease (MMD), antiplatelet treatment can impact bypass patency, infarction, or hemorrhage complications. Recently, heparin has been proposed as an anticoagulant treatment against white thrombus at the anastomosis site. The study aims to evaluate the effect of aspirin on the perioperative outcomes and investigate the results of heparin treatment for white thrombus.
METHODS
This retrospective study included 74 procedures of combined revascularization surgery for MMD patients who either received or did not receive aspirin. Perioperative outcomes were compared between the two groups. In addition, the effects of heparin treatment for white thrombus were evaluated.
RESULTS
The rate of white thrombus at the anastomosis site was significantly higher in the non-aspirin medication group (univariate: p = 0.032, multivariate: p = 0.044) and, accordingly, initial bypass patency was lower in the non-aspirin medication group (p = 0.049). Of the 17 patients with white thrombus development, five received heparin injections, and all white thrombi disappeared; however, there was one case of epidural hematoma and another of subdural hematoma. The risk of hemorrhagic complications was significantly higher in the surgical procedures that received heparin injections (p = 0.021).
CONCLUSIONS
In MMD patients who received combined revascularization surgery, aspirin medication lowered the occurrence of white thrombus. Heparin injections help to treat white thrombus but can enhance the risk of hemorrhagic complications.

Identifiants

pubmed: 33404873
doi: 10.1007/s00701-020-04668-0
pii: 10.1007/s00701-020-04668-0
doi:

Substances chimiques

Anticoagulants 0
Heparin 9005-49-6
Aspirin R16CO5Y76E

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1485-1491

Références

Furie B, Furie BC (2008) Mechanisms of thrombus formation. N Engl J Med 359(9):938–949
doi: 10.1056/NEJMra0801082
Golby AJ, Marks MP, Thompson RC, Steinberg GK (1999) Direct and combined revascularization in pediatric moyamoya disease. Neurosurgery 45(1):50–60
pubmed: 10414566
Gozdek M, Pawliszak W, Hagner W, Zalewski P, Kowalewski J, Paparella D, Carrel T, Anisimowicz L, Kowalewski M (2017) Systematic review and meta-analysis of randomized controlled trials assessing safety and efficacy of posterior pericardial drainage in patients undergoing heart surgery. J Thorac Cardiovasc Surg 153(4):865-875.e12
doi: 10.1016/j.jtcvs.2016.11.057
Houkin K, Nakayama N, Kuroda S, Nonaka T, Shonai T, Yoshimoto T (2005) Novel magnetic resonance angiography stage grading for Moyamoya disease. Cerebrovasc Dis 20(5):347–354
doi: 10.1159/000087935
Houlind K, Fenger-Grøn M, Holme SJ et al (2014) Graft patency after off-pump coronary artery bypass surgery is inferior even with identical heparinization protocols: results from the Danish On-pump Versus Off-pump Randomization Study (DOORS). J Thorac Cardiovasc Surg 148(5):1812-1819.e2
doi: 10.1016/j.jtcvs.2014.02.024
Kuroda S, Houkin K (2008) Moyamoya disease: current concepts and future perspectives. Lancet Neurol 7(11):1056–1066
doi: 10.1016/S1474-4422(08)70240-0
Martorell L, Martínez-González J, Rodríguez C, Gentile M, Calvayrac O, Badimon L (2008) Thrombin and protease-activated receptors (PARs) in atherothrombosis. Thromb Haemost 99(2):305–315
doi: 10.1160/TH07-08-0481
Mikami T, Suzuki H, Ukai R, Komatsu K, Akiyama Y, Wanibuchi M, Houkin K, Mikuni N (2019) Predictive factors for acute thrombogenesis occurring immediately after bypass procedure for moyamoya disease. Neurosurg Rev:609–617
Miyamoto S, Yoshimoto T, Hashimoto N et al (2014) Effects of extracranial-intracranial bypass for patients with hemorrhagic moyamoya disease: results of the Japan adult moyamoya trial. Stroke 45(5):1415–1421
doi: 10.1161/STROKEAHA.113.004386
Miyoshi K, Chida K, Kobayashi M, Kubo Y, Yoshida K, Terasaki K, Ogasawara K (2019) Two-year clinical, cerebral hemodynamic, and cognitive outcomes of adult patients undergoing medication alone for symptomatically ischemic Moyamoya disease without cerebral misery perfusion: a prospective cohort study. Clin Neurosurg 84(6):1233–1241
doi: 10.1093/neuros/nyy234
Onozuka D, Hagihara A, Nishimura K et al (2016) Prehospital antiplatelet use and functional status on admission of patients with non-haemorrhagic moyamoya disease: a nationwide retrospective cohort study ( J-ASPECT study). BMJ Open. https://doi.org/10.1136/bmjopen-2015-009942
Paparella D, Semeraro F, Scrascia G, Galeone A, Ammollo CT, Kounakis G, de Luca Tupputi Schinosa L, Semeraro N, Colucci M (2010) Coagulation-fibrinolysis changes during off-pump bypass: effect of two heparin doses. Ann Thorac Surg 89(2):421–427
Rashad S, Fujimura M, Niizuma K, Endo H, Tominaga T (2016) Long-term follow-up of pediatric moyamoya disease treated by combined direct–indirect revascularization surgery: single institute experience with surgical and perioperative management. Neurosurg Rev 39(4):615–623
doi: 10.1007/s10143-016-0734-7
Research Committee on the Pathology and Treatment of Spontaneous Occlusion of the Circle of Willis (2012) Guidelines for diagnosis and treatment of Moyamoya disease (spontaneous occlusion of the circle of willis). Neurol Med Chir (Tokyo) 52(5):245–266
doi: 10.2176/nmc.52.245
Roberts N, Boehm M, Bates M, Braidley PC, Cooper GJ, Spyt TJ (2006) Two-center prospective randomized controlled trial of Blake versus Portex drains after cardiac surgery. J Thorac Cardiovasc Surg 132(5):1042–1046
doi: 10.1016/j.jtcvs.2006.06.031
Zhao Y, Zhang Q, Zhang D, Zhao Y (2017) Effect of aspirin in postoperative management of adult ischemic Moyamoya disease. World Neurosurg 105:728–731
doi: 10.1016/j.wneu.2017.06.057

Auteurs

Fumiaki Kanamori (F)

Department of Neurosurgery, Nagoya University Graduate School of Medicine, 65 Tsurumai, Showa-ku, Nagoya, Aichi, 466-8550, Japan. kanamori.fumiaki@f.mbox.nagoya-u.ac.jp.

Yoshio Araki (Y)

Department of Neurosurgery, Nagoya University Graduate School of Medicine, 65 Tsurumai, Showa-ku, Nagoya, Aichi, 466-8550, Japan.

Kinya Yokoyama (K)

Department of Neurosurgery, Nagoya University Graduate School of Medicine, 65 Tsurumai, Showa-ku, Nagoya, Aichi, 466-8550, Japan.

Kenji Uda (K)

Department of Neurosurgery, Nagoya University Graduate School of Medicine, 65 Tsurumai, Showa-ku, Nagoya, Aichi, 466-8550, Japan.

Takashi Mamiya (T)

Department of Neurosurgery, Nagoya University Graduate School of Medicine, 65 Tsurumai, Showa-ku, Nagoya, Aichi, 466-8550, Japan.

Masahiro Nishihori (M)

Department of Neurosurgery, Nagoya University Graduate School of Medicine, 65 Tsurumai, Showa-ku, Nagoya, Aichi, 466-8550, Japan.

Takashi Izumi (T)

Department of Neurosurgery, Nagoya University Graduate School of Medicine, 65 Tsurumai, Showa-ku, Nagoya, Aichi, 466-8550, Japan.

Sho Okamoto (S)

Aichi Rehabilitation Hospital, Nishio, Japan.

Atsushi Natsume (A)

Department of Neurosurgery, Nagoya University Graduate School of Medicine, 65 Tsurumai, Showa-ku, Nagoya, Aichi, 466-8550, Japan.

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