TY - JOUR
T1 - Neuromyelitis optica
T2 - Evaluation of 871 attacks and 1,153 treatment courses
AU - Kleiter, Ingo
AU - Gahlen, Anna
AU - Borisow, Nadja
AU - Fischer, Katrin
AU - Wernecke, Klaus Dieter
AU - Wegner, Brigitte
AU - Hellwig, Kerstin
AU - Pache, Florence
AU - Ruprecht, Klemens
AU - Havla, Joachim
AU - Krumbholz, Markus
AU - Kümpfel, Tania
AU - Aktas, Orhan
AU - Hartung, Hans Peter
AU - Ringelstein, Marius
AU - Geis, Christian
AU - Kleinschnitz, Christoph
AU - Berthele, Achim
AU - Hemmer, Bernhard
AU - Angstwurm, Klemens
AU - Stellmann, Jan Patrick
AU - Schuster, Simon
AU - Stangel, Martin
AU - Lauda, Florian
AU - Tumani, Hayrettin
AU - Mayer, Christoph
AU - Zeltner, Lena
AU - Ziemann, Ulf
AU - Linker, Ralf
AU - Schwab, Matthias
AU - Marziniak, Martin
AU - Then Bergh, Florian
AU - Hofstadt-Van Oy, Ulrich
AU - Neuhaus, Oliver
AU - Winkelmann, Alexander
AU - Marouf, Wael
AU - Faiss, Jürgen
AU - Wildemann, Brigitte
AU - Paul, Friedemann
AU - Jarius, Sven
AU - Trebst, Corinna
N1 - Publisher Copyright:
© 2015 American Neurological Association.
PY - 2016/2/1
Y1 - 2016/2/1
N2 - Objective Neuromyelitis optica (NMO) attacks often are severe, are difficult to treat, and leave residual deficits. Here, we analyzed the frequency, sequence, and efficacy of therapies used for NMO attacks. Methods A retrospective review was made of patient records to assess demographic/diagnostic data, attack characteristics, therapies, and the short-term remission status (complete remission [CR], partial remission [PR], no remission [NR]). Inclusion criteria were NMO according to Wingerchuk's 2006 criteria or aquaporin-4 antibody-positive NMO spectrum disorder (NMOSD). Remission status was analyzed with generalized estimating equations (GEEs), a patient-based statistical approach. Results A total of 871 attacks in 185 patients (142 NMO/43 NMOSD, 82% female) were analyzed. The 1,153 treatment courses comprised high-dose intravenous steroids (HD-S; n = 810), plasma exchange (PE; n = 192), immunoadsorption (IA; n = 38), other (n = 80), and unknown (n = 33) therapies. The first treatment course led to CR in 19.1%, PR in 64.5%, and NR in 16.4% of attacks. Second, third, fourth, and fifth treatment courses were given in 28.2%, 7.1%, 1.4%, and 0.5% of attacks, respectively. This escalation of attack therapy significantly improved outcome (p < 0.001, Bowker test). Remission rates were higher for isolated optic neuritis versus isolated myelitis (p < 0.001), and for unilateral versus bilateral optic neuritis (p = 0.020). Isolated myelitis responded better to PE/IA than to HD-S as first treatment course (p = 0.037). Predictors of CR in multivariate GEE analysis were age (odds ratio [OR] = 0.97, p = 0.011), presence of myelitis (OR = 0.38, p = 0.002), CR from previous attack (OR = 6.85, p < 0.001), and first-line PE/IA versus HD-S (OR = 4.38, p = 0.006). Interpretation Particularly myelitis and bilateral optic neuritis have poor remission rates. Escalation of attack therapy improves outcome. PE/IA may increase recovery in isolated myelitis.
AB - Objective Neuromyelitis optica (NMO) attacks often are severe, are difficult to treat, and leave residual deficits. Here, we analyzed the frequency, sequence, and efficacy of therapies used for NMO attacks. Methods A retrospective review was made of patient records to assess demographic/diagnostic data, attack characteristics, therapies, and the short-term remission status (complete remission [CR], partial remission [PR], no remission [NR]). Inclusion criteria were NMO according to Wingerchuk's 2006 criteria or aquaporin-4 antibody-positive NMO spectrum disorder (NMOSD). Remission status was analyzed with generalized estimating equations (GEEs), a patient-based statistical approach. Results A total of 871 attacks in 185 patients (142 NMO/43 NMOSD, 82% female) were analyzed. The 1,153 treatment courses comprised high-dose intravenous steroids (HD-S; n = 810), plasma exchange (PE; n = 192), immunoadsorption (IA; n = 38), other (n = 80), and unknown (n = 33) therapies. The first treatment course led to CR in 19.1%, PR in 64.5%, and NR in 16.4% of attacks. Second, third, fourth, and fifth treatment courses were given in 28.2%, 7.1%, 1.4%, and 0.5% of attacks, respectively. This escalation of attack therapy significantly improved outcome (p < 0.001, Bowker test). Remission rates were higher for isolated optic neuritis versus isolated myelitis (p < 0.001), and for unilateral versus bilateral optic neuritis (p = 0.020). Isolated myelitis responded better to PE/IA than to HD-S as first treatment course (p = 0.037). Predictors of CR in multivariate GEE analysis were age (odds ratio [OR] = 0.97, p = 0.011), presence of myelitis (OR = 0.38, p = 0.002), CR from previous attack (OR = 6.85, p < 0.001), and first-line PE/IA versus HD-S (OR = 4.38, p = 0.006). Interpretation Particularly myelitis and bilateral optic neuritis have poor remission rates. Escalation of attack therapy improves outcome. PE/IA may increase recovery in isolated myelitis.
UR - http://www.scopus.com/inward/record.url?scp=84958108237&partnerID=8YFLogxK
U2 - 10.1002/ana.24554
DO - 10.1002/ana.24554
M3 - Article
C2 - 26537743
AN - SCOPUS:84958108237
SN - 0364-5134
VL - 79
SP - 206
EP - 216
JO - Annals of Neurology
JF - Annals of Neurology
IS - 2
ER -