三磷酸腺苷输注抗惊厥药对剧烈癌痛患者疗效的预后:一项前瞻性观察研究

A. Karelov, A. A. Ryazankina, V. A. Semkichev
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摘要

简介:疼痛是癌症患者的常见症状,即使给予止痛药。目的:评价静脉输注非选择性嘌呤受体激动剂三磷酸腺苷对加巴喷丁抗惊厥药在接受非选择性环氧化酶抑制剂联合弱阿片类曲马多治疗的中重度疼痛癌症患者的预后价值。材料与方法:34例伴有剧烈疼痛的癌症患者被纳入研究。静脉滴注三磷酸腺苷35-45 mg•kg-1•min-1,时间为100 ~ 160分钟。所有患者均服用加巴喷丁(900 mg,每日3次)。分别在输注前30分钟、输注后30分钟和服用加巴喷丁900 mg/d 4天后评估疼痛。此外,我们研究了三磷酸腺苷输注对加巴喷丁给药有效性的预后意义。结果:我们发现三磷酸腺苷输注后疼痛强度显著降低(Z = 4.0;< 0.0001 - Wilcoxon符号秩检验)。加巴喷丁给药4 d后结果相同(Z = 4.9;< 0.0001 - Wilcoxon符号秩检验)。此外,我们发现统计学上的中度相关(t(N - 2) = 3.94;密切相关= 0.57;三磷酸腺苷输注后疼痛强度值与服用加巴喷丁疼痛强度值的Spearman等级相关系数< 0.0004)。回归分析表明,模型的预测能力较好(R2 = 0.55,修正后R2 = 0.53);F = 38.74;< 0.0001)。结论:1。静脉输注三磷酸腺苷可能对非选择性环氧化酶抑制剂联合弱阿片类曲马多治疗的中重度疼痛癌症患者抗惊厥药加巴喷丁疗效的预后有重要意义。2. 静脉输注三磷酸腺苷或服用抗惊厥药加巴喷丁可显著减轻非选择性环氧化酶抑制剂加弱阿片类曲马多作用弱的癌症患者的疼痛强度。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prognosis of adenosine triphosphate infusion for anticonvulsants efficacy in patients with intensive cancer pain: a prospective observational study
INTRODUCTION: Pain is a common symptom in cancer patients even when analgesics were given. OBJECTIVE: To assess the prognostic value of intravenous infusion of non-selective purine receptors agonist adenosine triphosphate for effectiveness of anticonvulsant gabapentin in cancer patients with moderate and severe pain who received non-selective inhibitor of cyclooxygenase plus weak opioid tramadol. MATERIALS AND METHODS: Thirty-four cancer patients with intensive pain were scheduled for the study. The intravenous infusion of adenosine triphosphate 35-45 mg • kg-1 • min-1 was performed within the period from 100 to 160 minutes. Then all patients were taken gabapentin (900 mg in three times daily). Pain was estimated 30 minutes before infusion, 30 minutes after infusion, and after taking 900 mg/day gabapentin for 4 days. Moreover, we studied prognostic significance of adenosine triphosphate infusion for the effectiveness of gabapentin administration. RESULTS: We revealed significant reduction of pain intensity after adenosine triphosphate infusion (Z = 4.0; р < 0.0001 - Wilcoxon signed rank test). The same result was obtained after taking of gabapentin for 4 days (Z = 4.9; р < 0.0001 - Wilcoxon signed rank test). Moreover, we found statistically moderate correlation link (t(N - 2) = 3.94; closeness correlation = 0.57; р < 0.0004 - Spearman’s rank correlation coefficient) between pain intensity value after adenosine triphosphate infusion and taking of gabapentin. Regression analysis demonstrated satisfactory predictive ability of the resulting model (R2 = 0.55 (corrected R2 = 0.53); F = 38.74; р < 0.0001). CONCLUSIONS: 1. Intravenous infusion of adenosine triphosphate may has significance for prognosis of taking anticonvulsant gabapentin effectiveness in cancer patients with moderate and severe pain who received non-selective cyclooxygenase inhibitor plus weak opioid tramadol. 2. Intravenous infusion of adenosine triphosphate or taking anticonvulsant gabapentin may significantly reduce pain intensity in cancer patients who had weak effect of administration of non-selective inhibitor of cyclooxygenase plus weak opioid tramadol.
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