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哌替啶在顽固性疼痛患者中的最小有效镇痛血药浓度。

The minimum effective analgetic blood concentration of pethidine in patients with intractable pain.

作者信息

Mather L E, Glynn C J

出版信息

Br J Clin Pharmacol. 1982 Sep;14(3):385-90. doi: 10.1111/j.1365-2125.1982.tb01995.x.

Abstract

1 Pethidine infusions were performed in 16 patients with intractable pain in order to define a minimum effective analgetic blood concentration (MEAC) range. 2 Pethidine blood concentrations at the return of pain following a period of analgesia were considered to provide a more useful estimation of the MEAC than that at the onset of analgesia. 3. The MEAC range found in 15 of the 16 patients was 0.10 mg/l to 0.82 mg/l (median 0.25 mg/l). The intravenous dose of pethidine used in this study did not provide analgesia in one patient. 4 If the MEAC was greater than 0.40 mg/l in any patient, then additional techniques were required to provide adequate long term analgesia, e.g. destructive neurolytic techniques or antidepressant therapy. 5 The pharmacokinetic properties of pethidine found in the majority of these patients were in the range considered to be normal. 6 The clinical pharmacokinetic properties of pethidine found in the majority of these patients were in the range considered to be normal. 6 The clinical pharmacokineticist has in important role to play in the investigation, diagnosis and treatment of patients with intractable pain by detecting those patients with atypical pharmacokinetic and/or pharmacodynamic characteristics towards analgesic drugs.

摘要
  1. 对16例顽固性疼痛患者进行了哌替啶输注,以确定最低有效镇痛血药浓度(MEAC)范围。

  2. 与镇痛开始时的血药浓度相比,镇痛一段时间后疼痛复发时的哌替啶血药浓度被认为能更有效地估计MEAC。

  3. 16例患者中有15例的MEAC范围为0.10mg/L至0.82mg/L(中位数为0.25mg/L)。本研究中使用的静脉注射哌替啶剂量对1例患者未产生镇痛效果。

  4. 如果任何患者的MEAC大于0.40mg/L,则需要采用其他技术来提供充分的长期镇痛,例如破坏性神经溶解技术或抗抑郁治疗。

  5. 大多数患者体内哌替啶的药代动力学特性在被认为是正常的范围内。

  6. 大多数患者体内哌替啶的临床药代动力学特性在被认为是正常的范围内。

  7. 临床药代动力学家在顽固性疼痛患者的调查、诊断和治疗中具有重要作用,通过检测那些对镇痛药具有非典型药代动力学和/或药效学特征的患者。

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引用本文的文献

本文引用的文献

1
Relief of pain in incurable cancer.缓解不治之症的疼痛。
Lancet. 1955 Jan 1;268(6853):18-20. doi: 10.1016/s0140-6736(55)93213-x.
2
Rate of formation of norpethidine from pethidine.哌替啶去甲哌替啶的生成速率。
Br J Anaesth. 1981 Mar;53(3):255-8. doi: 10.1093/bja/53.3.255.
3
Pharmacokinetics of morphine injected intravenously into the anesthetized dog.
Anesthesiology. 1981 Jan;54(1):38-47. doi: 10.1097/00000542-198101000-00008.
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The clinical assessment of analgesic drugs.镇痛药的临床评估。
Br J Clin Pharmacol. 1981 Apr;11(4):319-32. doi: 10.1111/j.1365-2125.1981.tb01128.x.
7
Meperidine and other basic drugs: general method for their determination in plasma.
J Pharm Sci. 1974 Feb;63(2):306-7. doi: 10.1002/jps.2600630232.
10
Clinical pharmacokinetics of pethidine.哌替啶的临床药代动力学。
Clin Pharmacokinet. 1978 Sep-Oct;3(5):352-68. doi: 10.2165/00003088-197803050-00002.

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