Department of Anesthesiology and Pain Medicine, University of Washington Medical Center, Seattle, WA 98195-6540, USA.
Clin J Pain. 2012 May;28(4):338-41. doi: 10.1097/AJP.0b013e31822ad94c.
Opioid-induced constipation persists as a challenge in the management of chronic pain treated with opioid therapy. Multiple opioid antagonists have been applied in attempt to combat the gastrointestinal side effects of opioid analgesia, however their lipid-soluble nature allows passage into the central nervous system and consequent antagonism of centrally mediated analgesia. In contrast, methylnaltrexone offers the advantage of peripheral receptor-specific opioid antagonism due to chemical alterations conferring greater polarity and less lipid solubility. We present use of enteral methylnatrexone to treat severe opioid-induced constipation in a young boy who had failed treatment with the non-specific opioid antagonist, naloxone. This case reports describes the safe transition from enteral naloxone to enteral methylnaltrexone and discusses the potential risk of relative opioid toxicity during the transition.
Though methylnaltrexone has approved for subcutaneous use, the characteristics of the patient s disease required enteral administration which had not been described in pediatric dosing. Based on conservative extrapolation of data from adult dosing, a methylnaltrexone dosing regimen was selected and the naloxone was weaned over two days in an effort to avoid a relative opioid overdose.
The patient was successfully transitioned to methylnaltrexone from naloxone over two days. He did experience increased sedation during this time however no severe respiratory depression occurred due to the cessation of chronic central opioid antagonism causing a relative opioid toxicity. Following the institution of methylnaltrexone, his opioid requirement significantly decreased and his gastrointestinal symptoms improved.
Our case report demonstrates safe transition from enteral naloxone to enteral methylnaltrexone in a pediatric patient, avoiding the serious consequences of relative opioid toxicity. This patient experienced significant improvement of opioid-induced constipation and reduction in opioid requirements and it is possible that other patients would benefit as well. The role of enteral methylnaltrexone deserves further investigation.
阿片类药物引起的便秘在接受阿片类药物治疗的慢性疼痛管理中仍然是一个挑战。已经应用了多种阿片类药物拮抗剂来对抗阿片类药物镇痛的胃肠道副作用,但是它们的脂溶性允许其进入中枢神经系统,并导致中枢介导的镇痛拮抗。相比之下,美沙纳曲酮由于化学修饰赋予了更大的极性和更少的脂溶性,从而提供了外周受体特异性阿片拮抗剂的优势。我们报告了使用肠内美沙纳曲酮治疗一名年轻男孩的严重阿片类药物引起的便秘,该男孩对非特异性阿片拮抗剂纳洛酮治疗无效。本病例报告描述了从肠内纳洛酮安全过渡到肠内美沙纳曲酮,并讨论了在过渡期间相对阿片类药物毒性的潜在风险。
尽管美沙纳曲酮已获准皮下使用,但患者疾病的特征需要肠内给药,这在儿科剂量中尚未描述。根据成人剂量数据的保守外推,选择了美沙纳曲酮的剂量方案,并在两天内逐渐减少纳洛酮的剂量,以避免相对阿片类药物过量。
该患者在两天内成功地从纳洛酮过渡到美沙纳曲酮。在此期间,他确实经历了镇静作用增加,但由于慢性中枢阿片类药物拮抗作用的停止导致相对阿片类药物毒性,并未发生严重的呼吸抑制。在开始使用美沙纳曲酮后,他的阿片类药物需求显著减少,胃肠道症状得到改善。
我们的病例报告表明,在儿科患者中,从肠内纳洛酮安全过渡到肠内美沙纳曲酮可避免相对阿片类药物毒性的严重后果。该患者经历了阿片类药物引起的便秘显著改善,阿片类药物需求减少,并且其他患者可能也会受益。肠内美沙纳曲酮的作用值得进一步研究。