血液透析患者慢性肾病相关瘙痒症的诊断和治疗

Nephrologie & therapeutique Pub Date : 2024-02-28 Epub Date: 2024-01-31 DOI:10.1684/ndt.2024.60
Antoine Lanot, Laurent Misery, Guy Rostoker, Angelo Testa, Philippe Chauveau, Maxime Touzot, Nans Florens, Pierre Bataille
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摘要

慢性肾脏病相关性瘙痒症(CKD-aP)是一种常见的致残性症状,常常被低估。Pa-MRC对生活质量有负面影响,经常伴有睡眠障碍和抑郁。要批准卡巴阿片受体激动剂地匹法林用于这一适应症,就必须更新相关建议。首先,必须排除引起无皮损瘙痒的继发性原因,并采取一般性措施(润肤剂、心理支持、优化透析、将血清钙、磷酸盐和 PTH 恢复到 KGIDO 指南建议的范围内、治疗缺铁)。可建议使用非镇静剂口服抗组胺药进行治疗试验。如果测试结果呈阴性,则必须强烈怀疑 Pa-MRC,并评估其强度(WI-NRS 量表)和对生活质量的影响。如果是轻度 Pa-MRC(WI-NRS≤3),只需采取一般措施。如果 Pa-MRC 为中度至重度(WI-NRS ≥ 4),除了采取一般措施外,还可开始使用地匹法林进行为期 6 个月的特殊治疗。3 个月时,如果反应完全(WI-NRS 评分≤ 1 分)或部分反应(下降≥ 3 分),则继续治疗。6 个月时,如果反应完全,经患者同意可停止治疗;如果反应部分,则继续治疗。3 个月或 6 个月时,如果反应不充分(降幅< 3 分)和/或出现不耐受的情况,则停止治疗,并可在咨询皮肤科医生后考虑其他治疗方法(如加巴喷丁类药物、UVB)。
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Diagnosis and management of pruritus associated with chronic kidney disease in hemodialyzed patients

Chronic kidney disease-associated pruritus (CKD-aP) is a disabling symptom which is frequent and often underestimated. Pa-MRC has a negative impact on quality of life, and is frequently accompanied by sleep disorders and depression. The approval of difelikefalin – a kappa opioid receptor agonist – in this indication requires updated recommendations. As a first step, secondary causes of pruritus without skin lesions must be ruled out, and general measures taken (emollients, psychological support, optimization of dialysis, normalization of serum calcium, phosphate and PTH in the range proposed by the KGIDO guidelines, treatment of iron deficiency). A therapeutic test with a non-sedating oral antihistamine may be proposed. If this test is negative, Pa-MRC must be strongly suspected, and its intensity (WI-NRS scale) and impact on quality of life assessed. In the case of mild Pa-MRC (WI-NRS ≤ 3), only general measures are implemented. If Pa-MRC is moderate to severe (WI-NRS ≥ 4), specific treatment with difelikefaline can be initiated for 6 months in addition to general measures. At 3 months, if the response is complete (WI-NRS score ≤ 1) or partial (decline ≥ 3 points), treatment is continued. At 6 months, if the response is complete, treatment may be discontinued with the patient’s agreement; treatment is maintained if the response is partial. At 3 or 6 months, if response is insufficient (decline < 3 points) and/or in the event of intolerance, treatment is discontinued and an alternative treatment (e.g., gabapentinoids, UVB) may be considered after dermatological consultation.

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