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Negative Impact of Vestibular Suppressant Drugs on Provocative Positional Tests of BPPV: A Study from the Western Part of India.
Gurumukhani, Jayanti K; Patel, Dhruvkumar M; Shah, Sudhir V; Patel, Mukundkumar V; Patel, Maitri M; Patel, Anand V.
Afiliación
  • Gurumukhani JK; Consultant Neurologist, Jay Neurology and Physiotherapy Clinic, Bhavnagar, Gujarat, India.
  • Patel DM; Junior Resident in Medicine, Zydus Medical College and Hospital, Ahmedabad, Gujarat, India.
  • Shah SV; Professor and Head, Department of Neurology, Smt. NHL Municipal Medical College, Ahmedabad, Gujarat, India.
  • Patel MV; Associate Professor of Medicine, Zydus Medical College and Hospital, Dahod, Gujarat, India.
  • Patel MM; GCS Medical College, Research Center and Hospital, Ahmedabad, Gujarat, India.
  • Patel AV; Assistant Professor of Neurology, University of Texas Medical Branch, Galveston, Texas, USA.
Ann Indian Acad Neurol ; 24(3): 367-371, 2021.
Article en En | MEDLINE | ID: mdl-34446999
ABSTRACT

AIMS:

To study the impact of vestibular suppressant drugs (VSD) on provocative positional tests (PPT) in patients with benign paroxysmal positional vertigo (BPPV). SETTINGS AND

DESIGN:

A prospective case-control observational study. MATERIALS AND

METHODS:

Patients with a history suggestive of BPPV were tested for PPT. Patients with vertiginous symptoms and with nystagmus on PPT were classified as objective BPPV (O-BPPV, control group), while those without nystagmus with no alternate diagnosis were classified as subjective BPPV (S-BPPV, case group). Details of VSD treatment were noted in all the patients. In both groups, patients were instructed to discontinue VSD and were further assigned as the VSD and non-VSD subgroups. Patients were followed for 2 months with PPT every week. PPT positive patients were treated by vestibular rehabilitation maneuvers. STATISTICS Student t-test with two-tailed, unpaired, was used for continuous scale and Chi-square test for categorical differences between the two groups.

RESULTS:

295 consecutive BPPV patients were enrolled in the study, 55 in the S-BPPV group and 240 in the O-BPPV group. Significantly higher proportion of patients in the S-BPPV group were on VSD at presentation, 80.00% vs. 53.75% (OR 2.52; 95% CI 1.30-4.86), P = 0.006. In an unadjusted analysis of the S-BPPV group following discontinuation of VSD, PPT became positive in 79.54% of patients as compared to 18.19% in the non-VSD group (OR 35.0; 95% CI 6.2-197.3), P < 0.001.

CONCLUSION:

A higher proportion of S-BPPV patients were receiving VSD in comparison to O-BPPV at the initial visit. The PPT converted positive four times higher after ceasing the VSD in S-BPPV patients. STUDY

DESIGN:

Prospective case-control observational study.
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Observational_studies Idioma: En Revista: Ann Indian Acad Neurol Año: 2021 Tipo del documento: Article País de afiliación: India

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Observational_studies Idioma: En Revista: Ann Indian Acad Neurol Año: 2021 Tipo del documento: Article País de afiliación: India