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Europace Advance Access originally published online on June 4, 2007
Europace 2007 9(9):823-828; doi:10.1093/europace/eum104
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© The European Society of Cardiology 2007. All rights reserved. For Permissions, please e-mail: journals.permissions@oxfordjournals.org


SYNCOPE

Daily, weekly, monthly, and seasonal patterns in the occurrence of vasovagal syncope in an older population

Nynke van Dijk1,*, Mardi C. Boer2, Tiziana De Santo3, Nicoletta Grovale3, Arnaud J.J. Aerts4, Lucas Boersma5 and Wouter Wieling2

1 Department of Clinical Epidemiology, Biostatistics and Bioinformatics, Academic Medical Centre, PO Box 22700, 1100 DE Amsterdam, The Netherlands; 2 Department of Internal Medicine, Academic Medical Centre, Amsterdam, The Netherlands; 3 Medtronic Italia, S.p.A, Italy; 4 Department of Cardiology, Atrium Medical Centre, Heerlen, The Netherlands; 5 Cardiology Department, St Antonius Hospital, Heat Lung Centre, Utrecht, The Netherlands

Manuscript submitted 23 February 2007. Accepted after revision 26 April 2007.

* Corresponding author. Tel: +31 20 56668975; fax: +31 20 6912683. E-mail address: n.vandijk{at}amc.uva.nl


    Abstract
 Top
 Abstract
 Introduction
 Methods
 Results
 Discussion
 Acknowledgements
 References
 
Aims The aim of this study was to assess the frequency of vasovagal episodes over the day, week, month, and seasons.

Methods and results This study was part of the multi-centre International Study on Syncope of Uncertain Etiology-2 (ISSUE-2), which included patients, aged 30 years or older, with severe neurally mediated syncope between June 2002 and July 2004. The Implantable Loop Recorder (ILR) was used to document the syncope-related ECG periods. For this study patients with recorded syncopal episodes after ILR-implantation was selected. At least one episode was documented in 106 patients. A higher number of episodes were documented during the morning than during other periods of the day (P < 0.01). There was no difference between various days of the week, episodes per month, or between seasons. There was no difference between age and gender groups, although elderly patients seemed to be responsible for the peak in the morning.

Conclusion A circadian pattern in the frequency of vasovagal episodes exists, with a peak in the morning. This is in accordance with reports of diurnal variations in blood pressure and heart rate. No difference was observed in syncope distribution between days of the week, months, or seasons.

Key Words: Syncope, Vasovagal, Implantable loop recorder, Daily variation, Weekly variation, Seasonal variation


    Introduction
 Top
 Abstract
 Introduction
 Methods
 Results
 Discussion
 Acknowledgements
 References
 
Blood pressure (BP) and heart rate (HR) are regulated according to a circadian pattern.1Go,2Go BP and HR are significantly lower at night than during the daytime,1Go,3Go decline throughout the night and increase substantially at awaking.1Go Possible explanations for BP and HR diurnal patterns include differences in physical activity1Go and differences in activity of the autonomic nervous system between day and night.1Go–3Go A circadian distribution has also been demonstrated for cardiovascular ischaemic events, with a peak between 6 am and noon.4Go,5Go

Since BP and HR vary in a circadian pattern, it could be that a circadian pattern also exists for inappropriate low BP responses. In patients with orthostatic hypotension due to autonomic failure, an inverse of the normal 24-h BP profile was observed with high BP at night6Go,7Go and especially low BP in the morning, making patients more vulnerable to syncopal episodes in the morning. Whether this variation in the occurrence of syncopal episodes also exists in vasovagal patients is unknown, although one retrospective chart-study in young subjects, suggested a peak-occurrence in the morning.8Go

Although most vasovagal syncopal episodes are initiated by orthostatic stress, they can also occur in a supine position9Go,10Go or even during sleep.11Go,12Go Symptoms of these episodes include light-headedness, blurring of vision, and a feeling of generalized weakness. They are caused by systemic hypotension, leading to hypoperfusion of the brain due to a vasovagal response.10Go

But not only fluctuations in the frequency of vasovagal responses during the day, but also per day of the week, months, or even seasons have been suggested. In an earlier study a weekly pattern was suggested, while a slight predilection for the beginning of the week was recorded.13Go However, in this study no quantitative results were reported. Furthermore, a high ambient temperature and heat acclimatization may affect the incidence of vasovagal syncope14Go over the year.

The aim of the present study was to assess circadian variation of syncope frequency in adults over the day, testing the hypothesis that vasovagal syncope shows a peak frequency in the morning. Second aim was to assess weekly, monthly, and seasonal patterns of the frequency of syncopal episodes.


    Methods
 Top
 Abstract
 Introduction
 Methods
 Results
 Discussion
 Acknowledgements
 References
 
This study was part of the International Study on Syncope of Uncertain Etiology-2 (ISSUE-2).15Go,16Go

Patients
All patients, aged 30 years or older, suspected of or diagnosed with neurally mediated syncope according to the guidelines published by the Task Force on Syncope of the European Society of Cardiology17Go were eligible for inclusion.15Go Only patients who had experienced three or more syncopal episodes in the last 2 years and had a severe clinical presentation of syncope requiring treatment initiation were included in this study. Patients with high likelihood of carotid sinus syndrome, cardiac syncope, symptomatic orthostatic hypotension, subclavian steal syndrome, or loss of consciousness different from syncope (such as epilepsy, psychiatric episodes of loss of consciousness) were not included.

Protocol
The ISSUE-2 was a multi-centre, prospective, observational study. The main objective was to verify the value of the implantable loop recorder (ILR) in assessing the mechanism of syncope and the efficacy of the ILR-guided therapy after syncope recurrence.15Go,16Go Patients were enrolled at 63 European and American centres, between June 2002 and July 2004. Data were collected by local investigators and sent to an independent clinical research organization (RDES SL, Barcelona, Spain) via a dedicated Internet website. This organization maintained the database, issued data-clarification forms, and assisted by Medtronic clinical monitors, verified source documents.

The study was approved by the institutional review boards and signed informed consent was obtained from each patient at the time of enrolment.15Go,16Go

The ILR was used to document, quantify, and classify the syncope-related ECG periods. Arrhythmias were automatically detected by the ILR and stored. In addition, patients could activate the ILR and store the heart rhythm in case of symptoms of (pre)syncope. Furthermore, time and date of all (pre)syncopal events were collected. Follow-up was performed every 3 months, for a maximum of 24 months or until study ending.

For this study, the recordings were used to assess diurnal, weekly, and seasonal patterns in the occurrence of vasovagal syncope. In many patients with a syncope-recurrence after implantation of the ILR, the recorder was removed to start ILR-guided therapy according to study protocol.16Go Registration and occurrence of further episodes were thus dependent on the treatment the patient received. Therefore, only the first documented syncopal episode after ILR implantation was used for the analysis of the distribution of episodes.

For this study only patients with one or more recorded syncopal episodes after ILR implantation were selected. Patient characteristics, time and date from the episodes, and type of syncopal events were retrieved from the database.

Analysis
All episodes were classified according to time of day (h), weekday, month of the year, and season.

Numerical data were graphically assessed for normality. Normal distributed data were expressed as mean (SD). Non-normal distributed data were expressed as median (quartiles). Categorical data were expressed as percentage of the total group of patients. Patients were divided into two age groups based on the median age, to assess the influence of age on the pattern of the episodes. Time of day was divided into hours and into four periods, morning (6 am to noon), afternoon (noon to 6 pm), evening (6 pm to midnight), and night (midnight to 6 am) and compared with uniform occurrence (expected count of 25% of all patients in each group) using a {chi}2Go test. Documented responses were divided into five possible categories by an endpoints committee: normal sinus rhythm, bradycardia, asystole, tachycardia, or other.15Go,16Go Differences in these responses per daily period were assessed using a {chi}2Go test. Dates of the episodes were recoded into months and seasons. The frequency distributions per daily period and seasons were compared between age groups and gender groups using a {chi}2Go test. Differences in time between implantation and first syncopal event between the seasons in which the ILR was implanted were calculated using a Kruskall–Wallis test.


    Results
 Top
 Abstract
 Introduction
 Methods
 Results
 Discussion
 Acknowledgements
 References
 
During the 2-year inclusion period 442 patients were eligible for inclusion in ISSUE-2.15Go,16Go An ILR was implanted in 417 patients, as 25 patients or their physicians refused the implant. Of these patients, 36% (n = 143) had at least one syncopal recurrence. This episode was documented by ECG in 106 patients. Twenty-five patients had normal sinus rhythm during the episode and five bradycardic, 56 asystolic (median duration 12 s; range 3–90), 16 tachycardic, and two other responses were recorded (Figure 1). These 106 patients were included for this analysis (Figure 1). Baseline characteristics of the included patients are shown in Table 1. Median age of the patients was 69 years. This age was used as a cut-off point to assess the influence of age on the pattern of episodes.


Figure 1
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Figure 1 Flow of patients through ISSUE-2.

 


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Table 1 Baseline characteristics

 
Figure 2 shows the frequency distribution of syncope-episodes over the day, with striking peaks during the morning. Comparison of daily periods with expected uniform occurrence showed a statistical significant difference (P < 0.01) between the morning and other daily periods. The frequency of episodes in daily periods between age and gender groups was not statistically different (P = 0.332 and P = 0.727, respectively), although elderly patients seem to be mainly responsible for the peak in the morning (Figure 3). There was no difference in the type of syncopal responses over the day (P = 0.813).


Figure 2
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Figure 2 Circadian distribution of vasovagal episodes.

 


Figure 3
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Figure 3 Circadian distribution of syncopal episodes per age group.

 
As shown in Figure 2, syncopal episodes occurred at night as well. We recorded eight nocturnal (midnight to 6 am) episodes; five asystolic responses, and three times normal sinus rhythm. These episodes occurred in three women and five men with ages ranging from 46 to 87. Nocturnal episodes were most frequent (n = 3) between 5 and 6 am.

Figure 4 shows syncope distribution during the week. There is no difference between the days of the week, or between weekdays and weekend days. Weekly distribution is not different between age (P = 0.646) and gender groups (P = 0.120).


Figure 4
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Figure 4 Distribution of syncopal episodes over the week.

 
The distribution of syncopal episodes per month (Figure 5) shows no differences between the various months or seasons. Seasonal frequency distributions were not significantly different between age (P = 0.763) and gender groups (P = 0.624). Median time between implantation and the event was 83 days (quartiles 25–217). Time until event did not differ per season in which the ILR was implanted (P = 0.461).


Figure 5
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Figure 5 Distribution of syncopal episodes over the year.

 

    Discussion
 Top
 Abstract
 Introduction
 Methods
 Results
 Discussion
 Acknowledgements
 References
 
This study shows that a clear circadian variation in the frequency of syncopal episodes exists, with a striking peak in the morning, while there is no variation over days of the week, months of the year, seasons, or between older and younger patients or men and women.

Evidence of a day–night pattern in BP and HR is abundant.1Go–5Go,18Go,19Go The results of this study confirm our hypothesis that diurnal variation exists in syncopal episodes, based on these variations in BP and HR. These results confirm the retrospective results of Mineda et al.8Go in a younger patient group (mean age 37 years), who demonstrated a circadian pattern of vasovagal syncope, with two thirds of the total episodes occurring between 6 am and noon. In other studies, Head-Up Tilt (HUT)-positive paediatric syncope patients showed significantly more syncopal episodes in the morning, compared with HUT-negative syncope patients.20Go

Although there are important differences in autonomic BP and HR regulation between young and elderly patients, these differences did not result in a different pattern between age groups in our study.21Go Autonomic responses of elderly subjects to orthostatic stresses are reduced, which could result in more syncopal episodes.21Go In addition in patients with orthostatic hypotension due to autonomic failure, an inverse of the normal 24-h BP profile was observed with high BP at night6,7—and especially low BP in the morning. Both nocturnal polyuria and a redistribution of body fluid are mechanisms underlying the pronounced decreases in BP after prolonged recumbency at night.6Go Although we observed a trend towards more episodes of elderly patients in the morning this did not reach statistical significance when comparing periods of the day.

Another remarkable feature is the occurrence of syncope at night. Although vasovagal syncopal episodes seem unlikely to happen in a supine position, cases of vasovagal episodes at night or even during sleep have been reported.11Go,12Go In these cases the patient usually wakes up because of feeling faint, often with abdominal discomfort, and loses consciousness in bed or immediately upon standing. Some patients reported having nightmares before the episode.

Proposed mechanisms for syncope interrupting sleep included asymmetrical slow wave activity in the cortex, changes between stages of sleep and nightmares, inhibiting sympathetic outflow.11Go However, in case of transient loss of consciousness at night, causes such as epilepsy22Go–24Go and cardiac syncope (Stokes Adams attack,25Go Brugada,26Go,27Go long QT-syndrome28Go) should be excluded first. Especially, LQTS3 patients are more likely to have events during rest or sleep than during exercise.29Go Other diagnostic possibilities include sleep apnoea, panic attacks, sleep paralysis, and hypoglycaemia.

In this study, there was no difference between weekdays. This is in concordance with one previous publication.13Go Although work-related stressors might affect the susceptibility to vasovagal syncope, this was not found in this population. In a younger population, with more working subjects, differences between week and weekend days might however be present.

Heat acclimatization appears to have a remarkable influence on tilt tolerance14Go and warm environments are mentioned as one of the most common triggers for vasovagal episodes.30Go,31Go In this study, no significant difference in distribution of syncope was found between months or seasons of the year. Adaptations to lifestyle by subjects in warmer periods, and the limited variation in temperature in some countries between seasons, could be explanations for this lack of difference. Furthermore, it might be that only more acute changes in temperature, like entering a warm space or sauna, instead of more continuous high temperature levels to which subjects can adapt, are triggers for vasovagal episodes.

This study has several limitations. For the analysis only the first recurrent episode was used for analysis. Although the inclusion period consisted of two full years, a variation in inclusion frequency over the year could have influenced the number of patients at risk per month of the year and thereby the seasonal pattern. Furthermore, the episodes were not documented by ECG in 37 subjects. Since exact time and dates of the episodes in these subjects were not available, they were left out of the analysis. Since their episodes were not automatically registered by the ILR, their responses probably were different (no bradycardia or asystole) from the included group of patients. The results of this study might have been different in this group. Secondly, data were collected in a group of severely affected older group of patients with presumed vasovagal syncope. Whether these results are also applicable to less severely affected younger patients, needs to be studied.

This study shows a distinct circadian pattern in the frequency of vasovagal syncope. There is a striking peak in frequency of vasovagal episodes in the morning, which consists mainly of elderly patients. This is in accordance with reports of diurnal variations in BP, HR, and diurnal shifts in cardiac autonomic balance. There is no difference in syncope distribution between days of the week, months, or seasons.


    Acknowledgements
 Top
 Abstract
 Introduction
 Methods
 Results
 Discussion
 Acknowledgements
 References
 
ISSUE-2 was officially endorsed by the European Heart Rhythm Association and supported by a grant from Medtronic Europe. Nynke van Dijk is sponsored by a grant from the Netherlands Heart Foundation (grant 2003B156).

The following persons participated in the ISSUE-2 study. Steering Committee: M. Brignole (Chair), R. Sutton, C. Menozzi, A. Moya, R. Garcia-Civera, D.G. Benditt, P. Vardas, W. Wieling, D. Andresen, R. Migliorini, D. Hollinworth; Endpoints Committee: M. Brignole, C. Menozzi, R. Sutton, A. Moya; Database electronic management: RDES SL, Barcelona, Spain; Study management: M. Brignole, N. Grovale, F. Zanna; Clinical monitors: N. Grovale (Chair), F. Zanna, M.P. Lopez; S. Mohammad, A. Guthmann, M. Manders, D. Van Aggel, D. Erckens, V. Andersen, E. Sousani, C. Eppacher, J. St Ores; Statistical analysis: T. De Santo.

Conflict of interest: N. G. and T. D. S. are employees of Medtronic Italia, S.P.A., Italy.


    References
 Top
 Abstract
 Introduction
 Methods
 Results
 Discussion
 Acknowledgements
 References
 
[1] Veerman DP, Imholz BP, Wieling W, Wesseling KH, van Montfrans GA. Circadian profile of systemic hemodynamics. Hypertension (1995) 26:55–9.[Abstract/Free Full Text]

[2] Millar-Craig MW, Bishop CN, Raftery EB. Circadian variation of blood-pressure. Lancet (1978) 1:795–7.[Medline]

[3] Mancia G, Ferrari A, Gregorini L, Parati G, Pomidossi G, Bertinieri G, et al. Blood pressure and heart rate variabilities in normotensive and hypertensive human beings. Circ Res (1983) 53:96–104.[Free Full Text]

[4] Mulcahy D, Keegan J, Cunningham D, Quyyumi A, Crean P, Park A, et al. Circadian variation of total ischaemic burden and its alteration with anti-anginal agents. Lancet (1988) 2:755–9.[CrossRef][Web of Science][Medline]

[5] Cohen MC, Rohtla KM, Lavery CE, Muller JE, Mittleman MA. Meta-analysis of the morning excess of acute myocardial infarction and sudden cardiac death. Am J Cardiol (1997) 79:1512–6.[CrossRef][Web of Science][Medline]

[6] Omboni S, Smit AA, van Lieshout JJ, Settels JJ, Langewouters GJ, Wieling W. Mechanisms underlying the impairment in orthostatic tolerance after nocturnal recumbency in patients with autonomic failure. Clin Sci Lond (2001) 101:609–18.[Medline]

[7] Mathias CJ. A sound night's rest may do no good in autonomic failure. Clin Sci Lond (2001) 101:619–20.[Medline]

[8] Mineda Y, Sumiyoshi M, Tokano T, Yasuda M, Nakazato K, Nakazato Y, et al. Circadian variation of vasovagal syncope. J Cardiovasc Electrophysiol (2000) 11:1078–80.[CrossRef][Web of Science][Medline]

[9] Accurso V, Winnicki M, Shamsuzzaman AS, Wenzel A, Johnson AK, Somers VK. Predisposition to vasovagal syncope in subjects with blood/injury phobia. Circulation (2001) 104:903–7.[Abstract/Free Full Text]

[10] van Lieshout JJ, Wieling W, Karemaker JM, Eckberg DL. The vasovagal response. Clin Sci Lond (1991) 81:575–86.[Medline]

[11] Krediet CT, Jardine DL, Cortelli P, Visman AG, Wieling W. Vasovagal syncope interrupting sleep? Heart (2004) 90:e25.[Abstract/Free Full Text]

[12] Jardine DL, Krediet CT, Cortelli P, Wieling W. Fainting in your sleep? Clin Auton Res (2006) 16:76–8.[CrossRef][Web of Science][Medline]

[13] Clark G, Watt B. Does syncope occur more often on Sunday? Minn Med (1999) 82:6–7.[Medline]

[14] Shvartz E, Meyerstein N. Effect of heat and natural acclimatization to heat on tilt tolerance of men and women. J Appl Physiol (1970) 28:428–32.[Free Full Text]

[15] International Study on Syncope of Uncertain Etiology 2. The management of patients with suspected or certain neurally mediated syncope after the initial evaluation rationale and study design. Europace (2003) 5:317–21.[Abstract/Free Full Text]

[16] Brignole M, Sutton R, Menozzi C, Garcia-Civera R, Moya A, Wieling W, et al. Early application of an implantable loop recorder allows effective specific therapy in patients with recurrent suspected neurally-mediated syncope. Eur Heart J (2006) 27:1085–92.[Abstract/Free Full Text]

[17] Brignole M, Alboni P, Benditt DG, Bergfeldt L, Blanc JJ, Bloch Thomsen PE, et al. Guidelines on management (diagnosis and treatment) of syncope—update. Europace (2004) 6:467–537.[Free Full Text]

[18] Mancia G. Autonomic modulation of the cardiovascular system during sleep. N Engl J Med (1993) 328:347–9.[Free Full Text]

[19] Somers VK, Dyken ME, Mark AL, Abboud FM. Sympathetic-nerve activity during sleep in normal subjects. N Engl J Med (1993) 328:303–7.[Abstract/Free Full Text]

[20] Kula S, Olgunturk R, Tunaoglu FS, Saygili A. Distribution of syncopal episodes in children and adolescents with neurally mediated cardiac syncope through the day. Europace (2005) 7:634–7.[Abstract/Free Full Text]

[21] Wieling W, Karemaker JM. Measurement of heart rate: blood pressure to evaluate disturbances in neurocardiovascular control. In: Autonomic Failure: A Textbook of Clinical Disorders of the Autonomic Nervous System—Bannister R, Mathias CJ, eds. (1992) Oxford: Oxford University Press. p196–210.

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[26] Brugada P, Brugada J. Right bundle branch block, persistent ST segment elevation and sudden cardiac death: a distinct clinical and electrocardiographic syndrome. A multicenter report. J Am Coll Cardiol (1992) 20:1391–6.[Abstract]

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[30] Ganzeboom KS, Colman N, Reitsma JB, Shen WK, Wieling W. Prevalence and triggers of syncope in medical students. Am J Cardiol (2003) 91:1006–8.[CrossRef][Web of Science][Medline]

[31] Ganzeboom KS, Mairuhu G, Reitsma J, Linzer M, Wieling W, van Dijk N. Lifetime cumulative incidence of syncope in the general population: a study of 549 Dutch subjects aged 35–60 years. J Cardiovasc Electrophysiol (2006) 17:1172–6.[CrossRef][Web of Science][Medline]


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