Effect of mirtazapine on pruritus in patients on hemodialysis: a cross-over pilot study

被引:30
作者
Gholyaf, Mahmoud [1 ,2 ]
Sheikh, Vida [1 ,2 ]
Yasrebifar, Fatemeh [3 ]
Mohammadi, Younes [4 ]
Mirjalili, Mahtabalsadat [5 ]
Mehrpooya, Maryam [3 ]
机构
[1] Hamadan Univ Med Sci, Sch Med, Dept Internal Med, Hamadan, Hamadan, Iran
[2] Hamadan Univ Med Sci, Clin Res Dev Unit, Shahid Beheshti Hosp, Hamadan, Hamadan, Iran
[3] Hamadan Univ Med Sci, Sch Pharm, Dept Clin Pharm, Shahid Fahmideh Ave, Hamadan 6517838678, Hamadan, Iran
[4] Hamadan Univ Med Sci, Modeling Noncommunicable Dis Res Ctr, Sch Publ Hlth, Hamadan, Hamadan, Iran
[5] Shiraz Univ Med Sci, Sch Pharm, Dept Clin Pharm, Shiraz, Iran
关键词
Chronic kidney disease; Uremic pruritus; Mirtazapine; Gabapentin; UREMIC PRURITUS; ATOPIC-DERMATITIS; DOUBLE-BLIND; ONDANSETRON; MANAGEMENT; SEROTONIN; HISTAMINE; ITCH; ANTAGONISTS; GABAPENTIN;
D O I
10.1007/s11255-020-02473-3
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background Uremic pruritus (UP) is a highly prevalent and disturbing problem in patients with advanced chronic kidney disease (CKD); however, treatment of UP is largely unsatisfactory. The present study was designed to investigate the effectiveness of mirtazapine, an atypical antidepressant agent with potent antagonistic activity against serotonin (5HT2, 5HT3) and histamine (H1) receptors, in the treatment of pruritus in hemodialysis (HD) patients. Methods An 8-week long, prospective, open-label, and cross-over randomized clinical trial study was conducted on 77 HD patients with chronic pruritus. After a 2-week washout period, eligible patients were randomly assigned either to the mirtazapine (15 mg per day) or gabapentin (100 per day) for 2 weeks. Following 2 weeks washout period, subjects crossed over to the other treatment arm for 2 more weeks. The severity of pruritus was measured seven times during each treatment period using the visual analogue scale (VAS). Furthermore, at the end of the study, patients also were blindly asked which treatment (first or last in the sequential course of the study) they preferred. Results Sixty-one patients completed two treatment periods of the study. Although, compared to baseline, both gabapentin and mirtazapine treatment resulting in significant improvement in VAS scores, decreasing in pruritus severity was significantly greater in the mirtazapine treatment period compared with the gabapentin treatment period (P < 0.001). Furthermore, although side effects such as drowsiness and dry mouth more reported in the mirtazapine treatment period, overall higher percentage of the study patients preferred mirtazapine over gabapentin for the treatment of their pruritus symptoms. Conclusions Although preliminary, our study provides evidence that mirtazapine can be an effective therapy for UP in patients who are on maintenance HD. However, further studies would be necessary to confirm effectiveness as well as the safety of mirtazapine in the long-term management of chronic pruritus.
引用
收藏
页码:1155 / 1165
页数:11
相关论文
共 54 条
[1]  
Alam Abdulkader, 2013, Prim Care Companion CNS Disord, V15, DOI 10.4088/PCC.13r01525
[2]  
Anttila SAK, 2001, CNS DRUG REV, V7, P249
[3]  
Aramwit P., 2015, UPDATES HEMODIALYSIS, V9, P19, DOI DOI 10.5772/59352
[4]  
Asgari MR, 2017, J RENAL INJ PREV, V6, P49, DOI 10.15171/jrip.2017.09
[5]   Ondansetron therapy for uremic pruritus in hemodialysis patients [J].
Ashmore, SD ;
Jones, CH ;
Newstead, CG ;
Daly, MJ ;
Chrystyn, H .
AMERICAN JOURNAL OF KIDNEY DISEASES, 2000, 35 (05) :827-831
[6]  
Attia Enas A S, 2014, Arab J Nephrol Transplant, V7, P91
[7]   Histamine and serotonin in uremic pruritus: Effect of ondansetron in CAPD-pruritic patients [J].
Balaskas, EV ;
Bamihas, GI ;
Karamouzis, M ;
Voyiatzis, G ;
Tourkantonis, A .
NEPHRON, 1998, 78 (04) :395-402
[8]  
Bengtsson F, 1998, HUM PSYCHOPHARM CLIN, V13, P357, DOI 10.1002/(SICI)1099-1077(199807)13:5<357::AID-HUP8>3.0.CO
[9]  
2-K
[10]   EFFECTS OF NALOXONE INFUSIONS IN PATIENTS WITH THE PRURITUS OF CHOLESTASIS - A DOUBLE-BLIND, RANDOMIZED, CONTROLLED TRIAL [J].
BERGASA, NV ;
ALLING, DW ;
TALBOT, TL ;
SWAIN, MG ;
YURDAYDIN, C ;
TURNER, ML ;
SCHMITT, JM ;
WALKER, EC ;
JONES, EA .
ANNALS OF INTERNAL MEDICINE, 1995, 123 (03) :161-167