Abstract
Purpose
We aimed to demonstrate the patient demographics, etiologies and apraclonidine test results in adult Horner's syndrome.
Methods
This retrospective study was performed by the analysis of medical data of patients who were given 0.5% apraclonidine test. Patients' past medical history, demographic data, etiologies, accompanying neurological findings and pharmacological test results were assessed.
Results
Forty patients (21 females and 19 males) with a mean age of 50.3 ± 11.6 years were evaluated. Apraclonidine 0.5% test was positive in 37 patients (92.5%). An etiology could be identified in 20 patients (central [9 patients, 45%], preganglionic [9 patients, 45%] and postganglionic [2 patients, 10%]). Neurological findings accompanying Horner’s syndrome were present in 8 patients.
Conclusion
Despite detailed investigations, in a significant number of patients with Horner's syndrome an underlying cause may not be detected. Among the identifiable lesions, central and preganglionic involvements are still the first leading causes of Horner's syndrome. In addition, apraclonidine test may not be positive in all patients and a negative response does not exclude Horner's syndrome.
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All data obtained during the study process were used in the study.
References
Martin TJ (2018) Horner syndrome: a clinical review. ACS Chem Neurosci 9:177–186
Kanagalingam S, Miller NR (2015) Horner syndrome: clinical perspectives. Eye Brain 7:35–46
Bremner F (2019) Apraclonidine is better than cocaine for detection of Horner syndrome. Front Neurol 10:55
Karti DT, Karti O, Celebisoy N (2019) A rare cause of Horner’s syndrome: cervicothoracic spinal root cysts. Neurol Sci 40:1311–1314
Khan Z, Bollu PC. Horner Syndrome. 2021 May 4. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2021 Jan–. PMID: 29763176.
Han J, Park SY, Lee JY (2021) Nationwide population-based incidence and etiologies of pediatric and adult Horner syndrome. J Neurol 268:1276–1283
Trobe JD (2010) The evaluation of Horner syndrome. J Neuroophthalmol 30(1):1–2
Gamaleldin OA, Donia MM, Elsebaie NA, Abdelkhalek Abdelrazek A, Rayan T, Khalifa MH (2020) Role of fused three-dimensional time-of-flight magnetic resonance angiography and 3-dimensional t2-weighted imaging sequences in neurovascular compression. World Neurosurg 133:e180–e186
Razek AAKA, Maher H, Kasem MA, Helmy E (2021) Imaging of congenital cranial dysinnervation disorders: what radiologist wants to know? Clin Imaging 71:106–116
Abdel Razek AAK, Gamaleldin OA, Elsebaie NA (2020) Peripheral nerve sheath tumors of head and neck: imaging-based review of world health organization classification. J Comput Assist Tomogr 44:928–940
Wilhelm H, Ochsner H, Kopycziok E, Trauzettel-Klosinski S, Schiefer U, Zrenner E (1992) Horner’s syndrome: a retrospective analysis of 90 cases and recommendations for clinical handling. Ger J Ophthalmol 1:96–102
Sabbagh MA, De Lott LB, Trobe JD (2020) Causes of Horner syndrome: a study of 318 patients. J Neuroophthalmol 40:362–369
Maloney WF, Younge BR, Moyer NJ (1980) Evaluation of the causes and accuracy of pharmacologic localization in Horner’s syndrome. Am J Ophthalmol 90:394–402
Thompson H, Maxner C, Corbett J. Horner’s syndrome due to damage to the preganglionic neuron of the oculosympathetic pathway. In: Huber A, editor. Symphathetics and the Eye [English Translation]. Stuttgart, Germany: Ferdinand Enke; 1990
Top Karti D, Karti O, Koc AM, Esen O, Celebisoy N (2019) Unilateral Abducens nerve palsy with ipsilateral Horner’s syndrome as an initial manifestation of recurrent nasopharyngeal carcinoma. Neuroophthalmology 44:379–383
Morales J, Brown SM, Abdul-Rahim AS, Crosson CE (2000) Ocular effects of apraclonidine in Horner syndrome. Arch Ophthalmol 118:951–954
Kong YX, Wright G, Pesudovs K, O’Day J, Wainer Z, Weisinger HS (2007) Horner syndrome. Clin Exp Optom 90:336–344
Koc F, Kavuncu S, Kansu T, Acaroglu G, Firat E (2005) The sensitivity and specificity of 0.5% apraclonidine in the diagnosis of oculosympathetic paresis. Br J Ophthalmol 89:1442–1444
Watts P, Satterfuekd D, Lim MK (2007) Adverse effects of apraclonidine used in the diagnosis of Horner syndrome in infants. J AAPOS 11:282–283
Enyedi LB, Freedman SF (2001) Safety and efficacy of brimonidine in children with glaucoma. J JAAPOS 5:281–284
Carlson J, Zabriskie N, Known T, Barbe ME, Scott WE (1999) Apparent central nervous system depression in infants after the use of topical brimonidine. Am J Ophthalmol 128:255–256
Chen PL, Chen JT, Lu DW, Chen YC, Hsiao CH (2006) Comparing efficacies of 0.5% apraclonidine with 4% cocaine in the diagnosis of horner syndrome in pediatric patients. J Ocul Pharmacol Ther 22:182–187
Mahoney NR, Liu GT, Menacker SJ, Wilson MC, Hogarty MD, Maris JM (2006) Pediatric Horner syndrome: etiologies and roles of imaging and urine studies to detect neuroblastoma and other responsible mass lesions. Am J Ophthalmol 142:651–659
Kardon R (2005) Are we ready to replace cocaine with apraclonidine in the pharmacologic diagnosis of Horner syndrome? J Neuroophthalmol 25:69–70
Bohnsack BL, Parker JW (2008) Positive apraclonidine test within two weeks of onset of Horner syndrome caused by carotid artery dissection. J Neuroophthalmol 28:235–236
Bacal D, Levy SR (2004) The use of apraclonidine in the diagnosis of Horner syndrome in pediatric patients. Arch Ophthalmol 122(276–9):5
Brown SM, Aouchiche R, Freedman KA (2003) The utility of 0.5% apraclonidine in the diagnosis of Horner syndrome. Arch Ophthalmol 121:1201–1203
Chen PL, Hsiao CH, Chen JT, Lu DW, Chen WY (2006) Efficacy of apraclonidine 0.5% in the diagnosis of Horner syndrome in pediatric patients under low or high illumination. Am J Ophthalmol 142:469–474
Chu EA, Byrne PJ (2007) Pharmacologic reversal of Horner’s syndrome related ptosis with apraclonidine. Ear Nose Throat J 86:270–273
Freedman KA, Brown SM (2005) Topical apraclonidine in the diagnosis of suspected Horner syndrome. J Neuroophthalmol 25:83–85
Garibaldi DC, Hindman HB, Grant MP, Iliff NT, Merbs SL (2006) Effect of 0.5% apraclonidine on ptosis in Horner syndrome. Ophthalmic Plast Reconstr Surg 22:53–55
Acknowledgements
This work was supported by Scientific Research Project Coordination Unit of İzmir Democracy University. Project number:TPF-20H04.
Funding
This work was supported by Scientific Research Project Coordination Unit of İzmir Democracy University. Project number: TPF-20H04.
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All co-authors have contributed to the study, and all have read and approved the final version of the manuscript. O.K. and D.T.K had contributed to the concept. O.K., D.T.K., N.C. and F.G. were involved in the designing. F.G., N.C., O.K., D.T.K. and G.S.D participated in data collection or processing, analysis or interpretation, literature search and writing.
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Top Karti, D., Karti, O., Saruhan Durmaz, G. et al. The evaluation of patient demographics, etiologies and apraclonidine test results in adult Horner's syndrome. Int Ophthalmol 42, 1233–1239 (2022). https://doi.org/10.1007/s10792-021-02109-0
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DOI: https://doi.org/10.1007/s10792-021-02109-0