Letters to the Editor / Clinical Neurology and Neurosurgery 128 (2015) 130–133 [10] Mattingly T, Kole MK, Nicolle D, Boulton M, Pelz D, Lownie SP. Visual outcomes for surgical treatment of large and giant carotid ophthalmic segment aneurysms: a case series utilizing retrograde suction decompression (the Dallas technique). J Neurosurg 2013;118(5):937–46. [11] Ferrell AS, Lessne ML, Alexander MJ, Shah P, Golshani K, Zomorodi A, et al. Visual complications after stent-assisted endovascular embolization of paraophthalmic and suprasellar variant superior hypophyseal aneurysms: the Duke Cerebrovascular Center experience in 57 patients. World Neurosurg 2012;78(3–4):289–94. [12] Puffer RC, Kallmes DF, Cloft HJ, Lanzino G. Patency of the ophthalmic artery after flow diversion treatment of paraclinoid aneurysms. J Neurosurg 2012;116(4):892–6. [13] Ding D, Starke RM, Liu KC. Microsurgical strategies following failed endovascular treatment with the pipeline embolization device: case of a giant posterior cerebral artery aneurysm. J Cerebrovasc Endovasc Neurosurg 2014;16(1):26–31. [14] Ding D, Liu KC. Microsurgical extraction of a malfunctioned pipeline embolization device following complete deployment. J Cerebrovasc Endovasc Neurosurg 2013;15(3):241–5. [15] Ding D, Liu KC. Management strategies for intraprocedural coil migration during endovascular treatment of intracranial aneurysms. J Neurointerv Surg 2014;6(6):428–31. [16] Starke RM, Raper DM, Ding D, Chalouhi N, Owens GK, Hasan DM, et al. Tumor necrosis factor-alpha modulates cerebral aneurysm formation and rupture. Transl Stroke Res 2014;5(2):269–77. [17] Starke RM, Chalouhi N, Ding D, Raper DM, McKisic MS, Owens GK, et al. Vascular smooth muscle cells in cerebral aneurysm pathogenesis. Transl Stroke Res 2014;5(3):338–46.

Disclosures None.

Funding None.

Reference ˜ [1] Miró J, Fortuny R, Juncadella M, Aiguabella M, Veciana M, Castaner S, et al. Antithyroid antibodies as a potential marker of autoimmune-mediated late onset temporal lobe epilepsy. Clin Neurol Neurosurg 2014;121:46–50.

Nitin K. Sethi ∗ Department of Neurology, New York-Presbyterian Hospital, Weill Cornell Medical Center, New York, USA ∗ Correspondence

to: Comprehensive Epilepsy Center, New York-Presbyterian Hospital, Weill Cornell Medical Center, 525 East, 68th Street, New York 10065, USA. Tel.: +1 212 746 2346; fax: +1 212 746 8845. E-mail address: [email protected]

Dale Ding ∗ University of Virginia, Department of Neurosurgery, Charlottesville, 22908, USA

27 May 2014 Available online 25 November 2014

∗ Correspondence

to: University of Virginia, Department of Neurosurgery, P.O. Box 800212, Charlottesville, VA 22908, USA. Tel.: +1 434 924 2203; fax: +1 434 982 5753. E-mail address: [email protected] 8 October 2014 Available online 24 November 2014 http://dx.doi.org/10.1016/j.clineuro.2014.10.025

Anti-thyroid antibodies in temporal epilepsy-to check or not to check?

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Treatment of thoracic or lumbar spinal tuberculosis complicated by resultant listhesis at the involved segment Keywords:

lobe

Keywords: Temporal lobe epilepsy Autoimmune disorder Steroids

Dear Editor I read with interest Miro et al.’s study on detecting anti-thyroid antibodies (aTR-ab) in middle aged women with pharmacoresistant late onset temporal lobe epilepsy (TLE) [1]. The author’s advice testing aTR-ab in late onset TLE patients of unknown etiology and treatment with corticosteroids if antibodies are detected. The detection of autoantibodies increases with age. Many a times the titers are low and unclear whether the mere presence of these autoantibodies is indicative of an active disease process warranting immunosuppressive and immunomodulatory therapies. One should consider screening a TLE patient for aTR-ab if onset of TLE is late in life, seizures are medically refractory, faciobrachial dystonic seizures are documented, a personal or family history of autoimmune disease and cutaneous or end organ stigmata of autoimmune disease are present. Testing all late onset refractory TLE patients for aTR-ab risks a high rate of false positives and erroneous treatment with steroids with potential serious side-effects.

Spinal tuberculosis Pott’s disease Abscess

Dear Editor, We have read with great interest the published article by Zou et al. entitled “Treatment of thoracic or lumbar spinal tuberculosis complicated by resultant listhesis at the involved segment” [1]. At this paper, the authors said “Generally administered in pure spinal tuberculosis without listhesis, adjuvant antituberculous chemotherapy is essential for improving patient outcomes.” and “Surgery is generally indicated in Pott’s disease in cases of neurological compromise, painful vertebral lesions, progressive cold abscesses, kyphosis, and therapeutically refractory disease” in discussion section [1]. However, this good manuscript related to listhesis with spinal tuberculosis, we think that some more points should be discussed on therapy planning. Some scientists reported paradoxal responses are defined as worsening of existing symptoms or the appearance of new lesions in patients who initially responded well to antituberculous therapy [2,3]. If spinal lesion is limited in the vertebrae and if there are not any complications, triple-drug anti-tuberculous chemotherapy can play a main role to treat tuberculosis [4]. However, with proper indications, surgical procedures are superior in the prevention of neurological deterioration, maintenance of stability and early recovery [5,6].

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Letters to the Editor / Clinical Neurology and Neurosurgery 128 (2015) 130–133

Oguz et al. [7] reported total 76 cases with spinal tuberculosis have excellent recovery develops without any neurological deterioration. As a result, they developed an effective classification system named GATA. This classification system is based on seven clinical and radiological criteria (abscess formation, vertebral collapse, disc degeneration, sagittal index, kyphosis, instability and neurological problems). At this system, spinal tuberculosis is divided into three types (Type I A/B, Type II and Type III) by using as this criteria and it also recommends specific therapeutic techniques for each type. They emphasized if there is a cold abscess, only antibioticanalgesic therapy cannot prevent the extensive destruction of vertebral bone and disc material [7–9]. After cold abscess and two-level disc degeneration, immediate drainage along with medical therapy can protect the patient from vertebral collapse [7]. We believe that this classification system should be considered as a practical guide for spinal tuberculosis treatment planning in all countries.

Reference [1] Zou MX, Li J, Lv GH, Wang B, Deng YW. Treatment of thoracic or lumbar spinal tuberculosis complicated by resultant listhesis at the involved segment. Clin Neurol Neurosurg 2014;125:1–8. [2] Cheng VC, Ho PL, Lee RA, Chan KS, Chan KK, Woo PC, et al. Clinical spectrum of paradoxical deterioration during antituberculosis therapy in non-HIV-infected patients. Eur J Clin Microbiol Infect Dis 2002;21:803–9. [3] Park JH, Kim YH, Kwon CH, Shin HI. Paralysis developing as a paradoxical response during the treatment for tuberculous spondylitis: a case report. Ann Rehabil Med 2014;38(3):405–9. [4] Moon MS, Moon YW, Moon JL, Kim SS, Sun DH. Conservative treatment of tuberculosis of the lumbar and lumbosacral spine. Clin Orthop 2002;398:40–9. [5] Rezai AR, Lee M, Cooper PR. Modern management of spinal tuberculosis. Neurosurgery 1995;36:87–97. [6] Ghadouane M, Elmansari O, Bousalmame N, Lezrek K, Aouam H, Moulay I. Role of surgery in the treatment of Pott’s disease in adults: apropos of 29 cases. Rev Chir Orthop Repar Appar Mot 1996;82:620–8. [7] Oguz E, Sehirlioglu A, Altinmakas M, Ozturk C, Komurcu M, Solakoglu C. A new classification and guide for surgical treatment of spinal tuberculosis. Int Orthop 2008;32:127–33. [8] McLain RF, Isada C. Spinal tuberculosis deserves a place on radar screen. Clevel Clin J Med 2004;71:537–49. [9] Upadhyay SS, Sell P, Saji MS. Surgical management of spinal tuberculosis in adults. Clin Orthop 1994;302:173–82.

Safak Ekinci ∗ Department of Orthopaedic Surgery, Agri Military Hospital, Agri, Turkey Mehmet Agilli Department of Biochemistry, Agri Military Hospital, Agri, Turkey Gulbanu Horzum Ekinci Department of Pulmonology, Sureyyapasa Center for Chest Diseases and Thoracic Surgery Training and Investigation Hospital, Istanbul, Turkey Omer Ersen Department of Orthopaedic Surgery, Erzurum Military Hospital, Erzurum, Turkey ∗ Corresponding

author. Tel.: +90 5327339850; fax: +90 472 215 27 47. E-mail address: [email protected] (S. Ekinci) 29 October 2014 Available online 29 November 2014 http://dx.doi.org/10.1016/j.clineuro.2014.11.016

Reply to editorial – Neurophobia: A global and under-recognized phenomenon We thank McGee and colleagues for their interesting editorial commentary [1] on our paper [2]. We wish to clarify some of the highlighted issues to help advance discussion of this important topic. Our study included only general practitioner (GP) trainees during their postgraduate training; substantive GPs were not included. An evaluation from GP trainees in their second and third year of specialist training facilitated an up-to-date appraisal of their neurology training by examining the primary and secondary care components of their neurology education. As postgraduate training offers an opportunity to compensate for any fear of the neural sciences, we specifically studied GP trainees. We targeted this group of doctors as educational interventions at early stages of a career may enhance long-term motivation. In a recent study Danish GPs have highlighted the importance of motivation (and therefore interest) to promote continuous professional development and self-directed learning [3]. McGee and colleagues [1] suggest that we barely scraped the surface of the wealth of information, which could be obtained from GP trainees. We have however explored some of the issues in further detail in a focus group study [4]. We then applied triangulation to our mixed methods approach (questionnaire and focus group) to look for emerging themes [4]. This is increasingly acknowledged as an important way of identifying robust findings. Partial or full agreement for improving neurology teaching was identified in areas such as direct communication with a neurologist, more teaching for postgraduate GP trainees and a desire for experiential learning and formative feedback. We believe these are robust findings, which along with our recently published systematic review of educational interventions in neurology [5] represent the beginning of an evidence base “to improve teaching of the various components of neurology in the future”. Our study population called for emphasis on structured, yet simplified education in the area of neurology. In the UK and Ireland neurologists have only been based in district general hospitals within the last 15 years; indeed one of the authors of our paper was the first neurologist appointed in a general hospital in Northern Ireland (in 2003). Most GP training involves 50% district general hospital training and 50% primary care in the UK and Ireland. Even in 2014 neurologists are rarely involved in postgraduate neurology training for GP trainees. This prevents trainees from “assessing different effective instructional approaches” in neurology. Our study is the first published evidence that GP trainees desire experiential learning in neurology. Future research should not be just a summary of trainees’ reactions to a teaching experience, but rather an opportunity to achieve increasingly robust outcomes such as the Kirkpatrick levels of professional development [6] or fulfillment of Guskey’s five critical levels of professional development [7]: participant reaction; participant learning; organization support and change; participant use of new knowledge and skills; and learning outcomes. McGee and colleagues [1] suggested that other survey questions may have better addressed the presence of neurophobia or the “fear of neural sciences due to an inability to apply knowledge of neurology to clinical situations”. They also expressed concern that response bias may have affected our results. Although our emailed information sheet for the survey entitled Deficits and potential in postgraduate neurology education for GP trainees – a questionnaire study may have risked response bias, a systematic review of questionnaire responses from the questions used by Schon et al. [8] has shown the global nature of neurophobia [9]. We used the questionnaire designed by Schon et al. [8] not only because these survey questions have been repeatedly used

Letters to the Editor / Clinical Neurology and Neurosurgery 128 (2015) 130–133

in other populations, but also because one of the major objectives of our paper was to employ a novel statistical approach to determine whether parametric statistics (t-tests) employed in previous publications were appropriate. Although other “straightforward questions” may have less inherent bias, we believe that future research in neurology education should really be directed at assessing interventions in neurology education specific for GP trainees. The suggestions of McGee and colleagues [1] along with further involvement of neurologists in GP training are required to adequately address neurology educational needs of tomorrow’s GPs, who ultimately make up the main referral source for neurology services. However, only improved outcomes from educational interventions in neurology for GP trainees will herald an opportunity for an effective prevention strategy for neurophobia. Improving the neurological skills of clinicians has potential economic, medico legal, patient safety as well as patient and doctor satisfaction benefits [10]. Reference [1] McGee J, Maghzi AH, Minagar A. Neurophobia: a global and under-recognized phenomenon. Clin Neurol Neurosurg 2014;122:iii–v. [2] McCarron MO, Stevenson M, Loftus AM, McKeown PP. Neurophobia among general practice trainees: the evidence, perceived causes and solutions. Clin Neurol Neurosurg 2014;122:124–8. [3] Kjaer NK, Steenstrup AP, Pedersen LB, Halling A. Continuous professional development for GPs: experience from Denmark. Postgrad Med J. doi:10.1136/postgradmedj-2012-131679. [4] McCarron MO [Dissertation] Neurology training for general practice trainees: deficits and potential for improvement. Belfast: Queen’s University; 2011. [5] McColgan P, McKeown PP, Doherty-Allan R, Selai C, McCarron MO. Educational interventions in neurology: a comprehensive systematic review. Eur J Neurol 2013;20:1006–16. [6] Kirkpatrick DL, Kirkpatrick JD. Evaluating training programs. 3rd ed. San Francisco: Berret-Koehler Publishers Inc.; 2008.

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[7] Guskey TR. Evaluating professional development. 1st ed. California/London/New Delhi: Corwin Press Inc.; 2000. [8] Schon F, Hart P, Fernandez C. Is clinical neurology really so difficult? J Neurol Neurosurg 2002;72:557–9. [9] McCarron MO. A systematic review of neurophobia and perceived causes among medical students and junior doctors. J Neurol Neurosurg 2012;83:e1 [abstract]. [10] Nicholl DJ, Appleton JA. Clinical neurology: why this still matters in the 21st century. J Neurol Neurosurg Psychiatry. doi:10.1136/jnnp-2013-306881.

Mark O. McCarron ∗ Department of Neurology, Altnagelvin Hospital, Derry BT47 6SB, Northern Ireland, UK Michael Stevenson Department of Medical Statistics, Queen’s University of Belfast, Belfast, Northern Ireland, UK Angela M. Loftus Aberfoyle Medical Practice, Derry, Northern Ireland, UK Pascal McKeown The Queen’s University of Belfast Centre for Medical Education, School of Medicine, Dentistry & Biomedical Sciences, Whitla Medical Building, Lisburn Road, Belfast BT9 7BL, Northern Ireland, UK ∗ Corresponding

author. Tel.: +44 28 71345171. E-mail address: [email protected] (M.O. McCarron) 22 June 2014 Available online 29 November 2014

http://dx.doi.org/10.1016/j.clineuro.2014.11.017

©2015 Elsevier

Treatment of thoracic or lumbar spinal tuberculosis complicated by resultant listhesis at the involved segment.

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