A prospective open label 2-8 year extension of the randomised controlled ICON trial on the long-term efficacy and safety of occipital nerve stimulation in medically intractable chronic cluster headache

被引:8
作者
Brandt, Roemer B. [1 ,8 ]
Wilbrink, Leopoldine A. [2 ]
Coo, Ilse F. de [1 ,3 ]
Haan, Joost [1 ,4 ]
Mulleners, Wim M. [5 ]
Huygen, Frank J. P. M. [6 ]
Zwet, Erik W. van [7 ]
Ferrari, Michel D. [1 ]
Fronczek, Rolf [1 ]
机构
[1] Leiden Univ, Med Ctr, Dept Neurol, Leiden, Netherlands
[2] Zuyderland Hosp, Dept Neurol, Heerlen, Netherlands
[3] Dept Med Rehabil, Treant, Emmen, Netherlands
[4] Alrijne Hosp, Dept Neurol, Alphen aan den Rijn, Netherlands
[5] Canisius Wilhelmina Hosp, Dept Neurol, Nijmegen, Netherlands
[6] Dept Anaesthesiol, Erasmus MC, Rotterdam, Netherlands
[7] Leiden Univ, Med Ctr, Dept Biomed Data Sci, Leiden, Netherlands
[8] Leiden Univ, Med Ctr, Dept Neurol, Albinusdreef 2, NL-2333 ZA Leiden, Netherlands
关键词
Cluster headache; Medically intractable chronic cluster headache; Occipital nerve stimulation; Neuromodulation; HEALTH SURVEY SF-36; CHRONIC MIGRAINE; DOUBLE-BLIND; MANAGEMENT; QUALITY; TESTS;
D O I
10.1016/j.ebiom.2023.104895
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background We demonstrated in the randomised controlled ICON study that 48-week treatment of medically intractable chronic cluster headache (MICCH) with occipital nerve stimulation (ONS) is safe and effective. In L-ICON we prospectively evaluate its long-term effectiveness and safety. Methods ICON participants were enrolled in L-ICON immediately after completing ICON. Therefore, earlier ICON participants could be followed longer than later ones. L-ICON inclusion was stopped after the last ICON participant was enrolled in L-ICON and followed for >= 2 years by completing six-monthly questionnaires on attack frequency, side effects, subjective improvement and whether they would recommend ONS to others. Primary outcome was the change in mean weekly attack frequency 2 years after completion of the ICON study compared to baseline. Missing values for log-transformed attack-frequency were imputed for up to 5 years of follow-up. Descriptive analyses are presented as (pooled) geometric or arithmetic means and 95% confidence intervals.Findings Of 103 eligible participants, 88 (85%) gave informed consent and 73 (83%) were followed for >= 2 year, 61 (69%) >= 3 year, 33 (38%) >= 5 years and 3 (3%) >= 8.5 years. Mean (+/- SD) follow-up was 4.2 +/- 2.2 years for a total of 370 person years (84% of potentially 442 years). The pooled geometric mean (95% CI) weekly attack frequency remained considerably lower after one (4.2; 2.8-6.3), two (5.1; 3.5-7.6) and five years (4.1; 3.0-5.5) compared to baseline (16.2; 14.4-18.3). Of the 49/88 (56%) ICON >= 50% responders, 35/49 (71%) retained this response and 15/39 (38%) ICON non-responders still became a >= 50% responder for at least half the follow-up period. Most participants (69/88; 78% [0.68-0.86]) reported a subjective improvement from baseline at last follow-up and 70/88 (81% [0.70-0.87]) would recommend ONS to others. Hardware-related surgery was required in 44/88 (50%) participants in 112/122 (92%) events (0.35 person-year(-1) [0.28-0.41]). We didn't find predictive factors for effectiveness.Interpretation ONS is a safe, well-tolerated and long-term effective treatment for MICCH.
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