Rose E H, Aledort L M
Mount Sinai School of Medicine, New York, New York.
Ann Intern Med. 1991 Apr 1;114(7):563-8. doi: 10.7326/0003-4819-114-7-563.
To evaluate the effect of a nasal spray preparation of desmopressin (DDAVP) on levels of factor VIII activity, ristocetin cofactor activity, and von Willebrand antigen as well as the length of bleeding time in patients with mild hemophilia A and von Willebrand disease; to determine whether effective hemostatic levels can be attained; and to compare the effect of this spray with that of standard intravenous desmopressin treatment.
Before-and-after trial in patients known to respond to intravenous desmopressin.
Regional, comprehensive, hemophilia diagnosis and treatment center.
A total of 22 patients, including 11 patients with von Willebrand disease, 8 patients with mild hemophilia A, and 3 symptomatic hemophilia carriers.
Patients were infused with desmopressin, 0.3 micrograms/kg body weight. At least 1 week later, they were taught to self-administer desmopressin nasal spray, 150 micrograms to each nostril.
In patients with hemophilia, the level of factor VIII activity was measured; in patients with von Willebrand disease, levels of factor VIII activity, ristocetin cofactor activity, and von Willebrand antigen as well as bleeding time were measured before and after each administration of desmopressin.
Desmopressin, when administered intravenously or intranasally, elevated levels of factor VIII, ristocetin cofactor, and von Willebrand antigen in both mildly hemophiliac patients and patients with von Willebrand disease when compared with baseline measures (P less than 0.05). Factor VIII levels adequate for hemostasis were achieved by 82% of the hemophiliac patients. An abnormal bleeding time was corrected in the majority (62%) of patients with von Willebrand disease.
A nasal spray preparation of desmopressin apparently was effective both in treating bleeding episodes and when used prophylactically for minor surgical procedures in several patients.
评估去氨加压素(DDAVP)鼻喷雾剂对轻度甲型血友病和血管性血友病患者的凝血因子Ⅷ活性、瑞斯托霉素辅因子活性、血管性血友病因子抗原水平以及出血时间的影响;确定是否能达到有效的止血水平;并比较这种喷雾剂与标准静脉注射去氨加压素治疗的效果。
对已知对静脉注射去氨加压素有反应的患者进行前后对照试验。
地区性综合血友病诊断和治疗中心。
共22例患者,包括11例血管性血友病患者、8例轻度甲型血友病患者和3例有症状的血友病携带者。
患者静脉输注0.3微克/千克体重的去氨加压素。至少1周后,指导他们自行使用去氨加压素鼻喷雾剂,每侧鼻孔喷150微克。
对血友病患者测量凝血因子Ⅷ活性水平;对血管性血友病患者,在每次给予去氨加压素前后测量凝血因子Ⅷ活性、瑞斯托霉素辅因子活性、血管性血友病因子抗原水平以及出血时间。
与基线测量值相比,静脉注射或鼻内给予去氨加压素后,轻度血友病患者和血管性血友病患者的凝血因子Ⅷ、瑞斯托霉素辅因子和血管性血友病因子抗原水平均升高(P<0.05)。82%的血友病患者达到了足以止血的凝血因子Ⅷ水平。大多数(62%)血管性血友病患者的异常出血时间得到了纠正。
去氨加压素鼻喷雾剂在治疗出血发作以及对部分患者进行小型外科手术预防性用药时显然均有效。