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December 08, 2015; 85 (23) Article

Tilt-induced vasovagal syncope and psychogenic pseudosyncope

Overlapping clinical entities

Helene Blad, Robert Jan Lamberts, J. Gert van Dijk, Roland D. Thijs
First published November 11, 2015, DOI: https://doi.org/10.1212/WNL.0000000000002184
Helene Blad
From Stichting Epilepsie Instellingen Nederland (SEIN) (H.B., R.J.L., R.D.T.), Heemstede; and the Department of Neurology (J.G.v.D., R.D.T.), Leiden University Medical Centre, the Netherlands.
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Robert Jan Lamberts
From Stichting Epilepsie Instellingen Nederland (SEIN) (H.B., R.J.L., R.D.T.), Heemstede; and the Department of Neurology (J.G.v.D., R.D.T.), Leiden University Medical Centre, the Netherlands.
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J. Gert van Dijk
From Stichting Epilepsie Instellingen Nederland (SEIN) (H.B., R.J.L., R.D.T.), Heemstede; and the Department of Neurology (J.G.v.D., R.D.T.), Leiden University Medical Centre, the Netherlands.
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Roland D. Thijs
From Stichting Epilepsie Instellingen Nederland (SEIN) (H.B., R.J.L., R.D.T.), Heemstede; and the Department of Neurology (J.G.v.D., R.D.T.), Leiden University Medical Centre, the Netherlands.
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Citation
Tilt-induced vasovagal syncope and psychogenic pseudosyncope
Overlapping clinical entities
Helene Blad, Robert Jan Lamberts, J. Gert van Dijk, Roland D. Thijs
Neurology Dec 2015, 85 (23) 2006-2010; DOI: 10.1212/WNL.0000000000002184

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This article has a correction. Please see:

  • Tilt-induced vasovagal syncope and psychogenic pseudosyncope: Overlapping clinical entities - January 17, 2017
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Abstract

Objective: To describe the combination of tilt-induced vasovagal syncope (VVS) and psychogenic pseudosyncope (PPS) and aid its clinical recognition.

Methods: We identified people with tilt-induced VVS/PPS from 2 tertiary syncope referral centers. For each case, 3 controls with tilt-induced VVS were selected at random from the same center. Clinical characteristics were compared between both groups adjusting for multiple comparisons.

Results: Of 1,164 tilt-table tests, 23 (2%) resulted in VVS/PPS; these 23 cases were compared with 69 VVS controls. VVS and PPS coincided more often than chance would predict: 2% vs 0.6%, p < 0.001. Typical VVS prodromes and triggers were reported in all people with VVS/PPS and in controls with VVS. Attack frequency was significantly higher in the VVS/PPS (2 per month, range 0.1–60) than in the VVS group (0.25 per month, range 0.02–4; p < 0.001). Delayed recovery of consciousness was more frequently reported in the VVS/PPS group (likelihood ratio [+LR] 8.14, 95% confidence interval [CI] 3.94–16.84), as well as episodes without prodromes (+LR 5.57, 95% CI 2.53–12.26), atypical triggers (+LR 5.00, 95% CI 2.04–12.24), eye closure (+LR 3.75, 95% CI 1.68–8.35), and apparent loss of consciousness >1 minute (+LR 2.86, 95% CI 1.98–4.13).

Conclusions: VVS/PPS presents with a complex phenotype. High attack frequency, delayed recovery of consciousness, apparent loss of consciousness >1 minute, ictal eye closure, atypical triggers, and the absence of prodromes may serve as indicators that PPS coincides with VVS.

GLOSSARY

AED=
antiepileptic drug;
BP=
blood pressure;
CI=
confidence interval;
HR=
heart rate;
LR=
likelihood ratio;
LUMC=
Leiden University Medical Centre;
PNES=
psychogenic epileptic seizure;
PPS=
psychogenic pseudosyncope;
SEIN=
Stichting Epilepsie Instellingen Nederland;
TLOC=
transient loss of consciousness;
VVS=
vasovagal syncope

Footnotes

  • ↵* These authors contributed equally to this work.

  • Go to Neurology.org for full disclosures. Funding information and disclosures deemed relevant by the authors, if any, are provided at the end of the article.

  • Supplemental data at Neurology.org

  • Editorial, page 2000

  • Received April 1, 2015.
  • Accepted in final form July 20, 2015.
  • © 2015 American Academy of Neurology
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