Spinal Cord Stimulation and Pain Relief in Painful Diabetic Peripheral Neuropathy: A Prospective Two-Center Randomized Controlled Trial

被引:175
作者
Slangen, Rachel [1 ]
Schaper, Nicolaas C. [2 ]
Faber, Catharina G. [3 ]
Joosten, Elbert A. [1 ]
Dirksen, Carmen D. [4 ,5 ]
van Dongen, Robert T. [6 ]
Kessels, Alfons G. [4 ]
van Kleef, Maarten [1 ,7 ]
机构
[1] Maastricht Univ, Med Ctr, Dept Anesthesiol & Pain Med, Maastricht, Netherlands
[2] Maastricht Univ, Med Ctr, Dept Internal Med, Maastricht, Netherlands
[3] Maastricht Univ, Med Ctr, Dept Neurol, Maastricht, Netherlands
[4] Maastricht Univ, Med Ctr, Dept Clin Epidemiol & Med Technol Assessment, Maastricht, Netherlands
[5] Maastricht Univ, CAPHRI Sch Publ Hlth & Primary Care, Maastricht, Netherlands
[6] Radboud Univ Nijmegen, Med Ctr, Dept Anesthesiol Pain & Palliat Care, Nijmegen, Netherlands
[7] Free Univ Amsterdam, Dept Anesthesiol, Amsterdam, Netherlands
关键词
QUALITY-OF-LIFE; CLINICAL IMPORTANCE; HEALTH-STATUS; POPULATION; VALIDATION; MANAGEMENT; COMMUNITY; RECOMMENDATIONS; INVOLVEMENT; PREVALENCE;
D O I
10.2337/dc14-0684
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE Painful diabetic peripheral neuropathy (PDPN) is a common complication of diabetes mellitus. Unfortunately, pharmacological treatment is often partially effective or accompanied by unacceptable side effects, and new treatments are urgently needed. Small observational studies suggested that spinal cord stimulation (SCS) may have positive effects. RESEARCH DESIGN AND METHODS We performed a multicenter randomized clinical trial in 36 PDPN patients with severe lower limb pain not responding to conventional therapy. Twenty-two patients were randomly assigned to SCS in combination with the best medical treatment (BMT) (SCS group) and 14 to BMT only (BMT group). The SCS system was implanted only if trial stimulation was successful. Treatment success was defined as >= 50% pain relief during daytime or nighttime or "(very) much improved" for pain and sleep on the patient global impression of change (PGIC) scale at 6 months. RESULTS Trial stimulation was successful in 77% of the SCS patients. Treatment success was observed in 59% of the SCS and in 7% of the BMT patients (P < 0.01). Pain relief during daytime and during nighttime was reported by 41 and 36% in the SCS group and 0 and 7% in the BMT group, respectively (P < 0.05). Pain and sleep were "(very) much improved" in 55 and 36% in the SCS group, whereas no changes were seen in the BMT group, respectively (P < 0.001 and P < 0.05). One SCS patient died because of a subdural hematoma. CONCLUSIONS Treatment success was shown in 59% of patients with PDPN who were treated with SCS over a 6-month period, although this treatment is not without risks.
引用
收藏
页码:3016 / 3024
页数:9
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