PMID- 24996227 OWN - NLM STAT- MEDLINE DCOM- 20141209 LR - 20220311 IS - 1471-2377 (Electronic) IS - 1471-2377 (Linking) VI - 14 DP - 2014 Jul 5 TI - Quality of life in purely ocular myasthenia in Japan. PG - 142 LID - 10.1186/1471-2377-14-142 [doi] AB - BACKGROUND: Since there has been no conclusive evidence regarding the treatment of ocular myasthenia, treatment guidelines were recently issued by the European Federation of Neurological Societies/European Neurological Society (EFNS/ENS). However, the therapeutic outcomes concerning the quality-of-life (QOL) of patients with ocular myasthenia are not yet fully understood. METHODS: We investigated the therapeutic outcomes of patients with purely ocular myasthenia in a multicenter cross-sectional survey in Japan. To evaluate the severity of ocular symptoms, we used the ocular-quantitative MG (QMG) score advocated by Myasthenia Gravis Foundation of America. We used the Japanese translated version of the MG-QOL15, a self-appraised scoring system. RESULTS: Of 607 myasthenia gravis (MG) patients with an observation-duration of illness >/= 2 years, the cases of 123 patients (20%) were limited to ocular muscles (purely ocular myasthenia). During the entire clinical course, 81 patients experienced both ptosis and diplopia, 36 had ptosis alone, and six had diplopia alone. Acetyl-cholinesterase inhibitors and prednisolone were used in 98 and 52 patients, respectively. Treatment improved ocular symptoms, with the mean reduction in ocular-QMG score of 2.3 +/- 1.8 points. However, 47 patients (38%) failed to gain minimal manifestation or a better status. Patients with unfavorable outcomes also self-reported severe QOL impairment. Multivariate analyses showed that the pretreatment ocular-QMG score was associated with unfavorable outcomes, but not associated with the patient's QOL. CONCLUSION: A treatment strategy designed in accord with a patient's ocular presentation must be considered in order to improve ocular symptoms and the patient's QOL. FAU - Suzuki, Shigeaki AU - Suzuki S AD - Department of Neurology, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo 160-8582, Japan. sgsuzuki@z3.keio.jp. FAU - Murai, Hiroyuki AU - Murai H FAU - Imai, Tomihiro AU - Imai T FAU - Nagane, Yuriko AU - Nagane Y FAU - Masuda, Masayuki AU - Masuda M FAU - Tsuda, Emiko AU - Tsuda E FAU - Konno, Shingo AU - Konno S FAU - Oji, Satoru AU - Oji S FAU - Nakane, Shunya AU - Nakane S FAU - Motomura, Masakatsu AU - Motomura M FAU - Suzuki, Norihiro AU - Suzuki N FAU - Utsugisawa, Kimiaki AU - Utsugisawa K LA - eng PT - Journal Article PT - Multicenter Study PT - Research Support, Non-U.S. Gov't DEP - 20140705 PL - England TA - BMC Neurol JT - BMC neurology JID - 100968555 RN - 0 (Anti-Inflammatory Agents) RN - 0 (Cholinesterase Inhibitors) RN - 9PHQ9Y1OLM (Prednisolone) SB - IM MH - Anti-Inflammatory Agents/therapeutic use MH - Cholinesterase Inhibitors/therapeutic use MH - Cross-Sectional Studies MH - Female MH - Humans MH - Japan MH - Male MH - Middle Aged MH - Myasthenia Gravis/*complications/*drug therapy MH - Prednisolone/therapeutic use MH - *Quality of Life PMC - PMC4088302 EDAT- 2014/07/06 06:00 MHDA- 2014/12/15 06:00 PMCR- 2014/07/05 CRDT- 2014/07/06 06:00 PHST- 2014/04/14 00:00 [received] PHST- 2014/07/01 00:00 [accepted] PHST- 2014/07/06 06:00 [entrez] PHST- 2014/07/06 06:00 [pubmed] PHST- 2014/12/15 06:00 [medline] PHST- 2014/07/05 00:00 [pmc-release] AID - 1471-2377-14-142 [pii] AID - 10.1186/1471-2377-14-142 [doi] PST - epublish SO - BMC Neurol. 2014 Jul 5;14:142. doi: 10.1186/1471-2377-14-142.