张广华, 李锦成. 奥施康定用于慢性癌性中重度疼痛的疗效观察[J]. 中国肿瘤临床, 2008, 35(13): 733-735.
引用本文: 张广华, 李锦成. 奥施康定用于慢性癌性中重度疼痛的疗效观察[J]. 中国肿瘤临床, 2008, 35(13): 733-735.
ZHANG Guanghua, LI Jincheng. Curative Effect of Oxycontin on Moderate and Severe Chronic Cancer Pain[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2008, 35(13): 733-735.
Citation: ZHANG Guanghua, LI Jincheng. Curative Effect of Oxycontin on Moderate and Severe Chronic Cancer Pain[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2008, 35(13): 733-735.

奥施康定用于慢性癌性中重度疼痛的疗效观察

Curative Effect of Oxycontin on Moderate and Severe Chronic Cancer Pain

  • 摘要: 目的 :观察奥施康定(盐酸羟考酮控释片)治疗慢性癌性中重度疼痛的疗效及不良反应。 方法 :对50例慢性癌性中重度疼痛患者进行治疗,其中男26例,女24例;平均年龄(54.21±12.26)岁。无重要并发症及肝肾损害,无药物滥用史。疼痛类型:主要为骨痛,其次为胸痛、腹痛、神经疼痛、髋骶部疼痛等。奥施康定剂型为10mg,由患者主诉疼痛明显时给药,且均为首次服用奥施康定。奥施康定必须整片吞服,不得掰开、咀嚼或研磨。初始剂量10mg·12h-1,服用24小时如疼痛分级下降不到1级,则第二天加量至20mg·12h-1。服用24小时如疼痛分级仍下降不到1级,第三天加量至30mg·12h-1,以此类推,最多至60mg·12h-1。在用药过程中根据疼痛缓解程度调整剂量,所有患者均连续用药4周。 结果 :50例慢性癌性中重度疼痛患者使用的奥施康定最小剂量10mg·12h-1,最大剂量60mg·12h-1。治疗效果:完全缓解19例(38.0%),部分缓解29例(58.0%),轻度缓解2例(4.0%)。其中中度疼痛患者的显效率为100.0%(7/7),重度疼痛患者的显效率为95.3%(41/43),全部患者总的显效率为96.0%(48/50)。不良反应有:便秘9例,恶心呕吐6例,腹胀3例,厌食2例,嗜睡2例,头晕1例。 结论 :奥施康定治疗慢性癌性中重度疼痛疗效确切,有效率高,不良反应轻,服用安全。

     

    Abstract: Objective : To observe the analgesic effect and adverse effects of Oxycontin (Oxycodone HydrochlorideControlled- release Tablets) on moderate and severe chronic cancer pain. Methods : A total of 50 patients withmoderate and severe chronic cancer pain were selected. There were 26 males and 24 females, with an average age of 54.21±12.26 years, and they had no major complications, liver or kidney damage or history of drugabuse. The most common type of pain was bone pain. Other types of pain included chest pain, abdominalpain, nerve pain and hip sacral pain. The dosage of Oxycodone Hydrochloride Controlled- release Tabletswas 10 mg, administered when the patients complained of pain. It was the first time for all of the patients totake Oxycodone Hydrochloride Controlled-release Tablets. This medicine must be swallowed whole and wasnot to be separated, chewed or ground. Oxycodone Hydrochloride Controlled-release Tablets were administered at an initial dose of 10 mg every 12 hours and the dose was increased to achieve pain relief. If the painwas decreased less than one grade after 24 hours, the dosage was increased to 20 mg·12 h-1 the next day.If the pain was still decreased less than one grade, the dosage on the third day was increased to 30 mg·12h-1. The maximum dosage was 60 mg·12 h-1. All patients received this therapy for 4 weeks. Results : The doses ranged between 10 mg·12 h-1 and 60 mg·12h-1. Among the 50 patients suffering moderate and severechronic cancer pain, 19 (38.0%) achieved complete remission, 29 (58.0%) achieved partial remission, and 2(4.0%) achieved minor remission. Pain relief provided by Oxycodone Hydrochloride Controlled-releaseTablets was 100% (7/7) in patients with moderate chronic cancer pain, 95.3% (41/43) in patients with severechronic cancer pain, and 96.0% (48/50) for all patients combined. The adverse reactions were constipation (9cases), nausea and vomiting (6 cases), abdominal distention (3 cases), anorexy (2 cases), lethargy (2 cases)and dizziness (1 case). Conclusion : Oxycodone Hydrochloride Controlled-release Tablets are safe and effective for moderate and severe chronic cancer pain. They work quickly with few side effects.

     

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