Abstract
Introduction
Jet lag is a syndrome caused by disruption of the 'body clock', and affects most air travellers crossing five or more time zones; it is worse on eastward than on westward flights.
Methods and outcomes
We conducted a systematic review and aimed to answer the following clinical question: What are the effects of interventions to prevent or minimise jet lag? We searched: Medline, Embase, The Cochrane Library, and other important databases up to January 2014 (Clinical Evidence reviews are updated periodically; please check our website for the most up-to-date version of this review). We included harms alerts from relevant organisations such as the US Food and Drug Administration (FDA) and the UK Medicines and Healthcare products Regulatory Agency (MHRA).
Results
We found five studies that met our inclusion criteria. We performed a GRADE evaluation of the quality of evidence for interventions.
Conclusions
In this systematic review, we present information relating to the effectiveness and safety of the following interventions: hypnotics, lifestyle and environmental adaptations, and melatonin.
Key Points
Jet lag is a syndrome associated with long-haul flights across several time zones, characterised by sleep disturbances, daytime fatigue, reduced performance, gastrointestinal problems, and generalised malaise.
It is caused by a disruption of the 'body clock', which gradually adapts under the influence of light and dark, mediated by melatonin secreted by the pineal gland: darkness switches on melatonin secretion; exposure to strong light switches it off.
The incidence and severity of jet lag increase with the number of time zones crossed; it is worse on eastward than on westward flights.
Melatonin reduces subjective ratings of jet lag on eastward and on westward flights compared with placebo.
The adverse effects of melatonin have not been systematically studied, but people with epilepsy and people taking an oral anticoagulant should not use it without medical supervision.
There may be a risk of fixed drug eruption, an allergic manifestation, with melatonin.
Routine pharmaceutical quality control of melatonin products is necessary.
Hypnotics (zopiclone or zolpidem), taken before bedtime on the first few nights after flying, may reduce the effects of jet lag by improving sleep quality and duration but not other components of jet lag.
Hypnotics are associated with various adverse effects, including headache, dizziness, nausea, confusion, and amnesia, which can outweigh any short-term benefits.
We found no studies that examined the effectiveness of lifestyle or environmental adaptations (such as eating, avoiding alcohol or caffeine, sleeping, daylight exposure, or arousal).
After a westward flight, it is worth staying awake while it is daylight at the destination and trying to sleep when it gets dark. After an eastward flight, one should stay awake but avoid bright light in the morning, and be outdoors as much as possible in the afternoon. This will help to adjust the body clock and turn on the body's own melatonin secretion at the right time.
About this condition
Definition
Jet lag is a syndrome associated with long-haul flights across several time zones, characterised by sleep disturbances, daytime fatigue, reduced performance, gastrointestinal problems, and generalised malaise. As with most syndromes, not all of the components must be present in any one case. It is caused by the 'body clock' continuing to function in the day–night rhythm of the place of departure. The rhythm adapts gradually under the influence of light and dark, mediated by melatonin secreted by the pineal gland: darkness switches on melatonin secretion; exposure to strong light switches it off.
Incidence/ Prevalence
Jet lag affects most air travellers crossing five or more time zones. The incidence and severity of jet lag increase with the number of time zones crossed.
Aetiology/ Risk factors
Someone who has previously experienced jet lag is liable to do so again. Jet lag worsens with the more time zones crossed in one flight, or series of flights, within a few days. Westward travel causes less disruption than eastward travel as it is easier to lengthen, rather than to shorten, the natural circadian cycle.
Prognosis
Jet lag is worst immediately after travel and gradually resolves over 4 to 6 days as the person adjusts to the new local time. The more time zones crossed, the longer it takes to wear off.
Aims of intervention
To prevent or minimise jet lag, with minimal adverse effects.
Outcomes
Severity of jet lag, including subjective jet lag score and daytime alertness; Sleep quality and duration; Adverse effects of treatment.
Methods
Clinical Evidence search and appraisal January 2014. The following databases were used to identify studies for this systematic review: Medline 1966 to January 2014, Embase 1980 to January 2014, and The Cochrane Database of Systematic Reviews 2013, issue 12 (1966 to date of issue). Additional searches were carried out in the Database of Abstracts of Reviews of Effects (DARE) and the Health Technology Assessment (HTA) Database. We also searched for retractions of studies included in the review. Titles and abstracts identified by the initial search, run by an information specialist, were first assessed against predefined criteria by an evidence scanner. Full texts for potentially relevant studies were then assessed against predefined criteria by an evidence analyst. Studies selected for inclusion were discussed with an expert contributor. All data relevant to the review were then extracted by an evidence analyst. Study design criteria for inclusion in this review were: published systematic reviews and RCTs, at least single-blinded, and containing more than 20 individuals of whom more than 80% were followed up. There was no minimum follow-up. We excluded all studies described as 'open', 'open label', or not blinded unless blinding was impossible. We included RCTs and systematic reviews of RCTs where harms of an included intervention were assessed, applying the same study design criteria for inclusion as we did for benefits. In addition, we use a regular surveillance protocol to capture harms alerts from organisations such as the FDA and the MHRA, which are added to the reviews as required. To aid readability of the numerical data in our reviews, we round many percentages to the nearest whole number. Readers should be aware of this when relating percentages to summary statistics such as relative risks (RRs) and odds ratios (ORs). We have performed a GRADE evaluation of the quality of evidence for interventions included in this review (see table). The categorisation of the quality of the evidence (high, moderate, low, or very low) reflects the quality of evidence available for our chosen outcomes in our defined populations of interest. These categorisations are not necessarily a reflection of the overall methodological quality of any individual study, because the Clinical Evidence population and outcome of choice may represent only a small subset of the total outcomes reported, and population included, in any individual trial. For further details of how we perform the GRADE evaluation and the scoring system we use, please see our website (www.clinicalevidence.com).
Table.
GRADE Evaluation of interventions for Jet lag.
| Important outcomes | Severity of jet lag, Sleep quality | ||||||||
| Studies (Participants) | Outcome | Comparison | Type of evidence | Quality | Consistency | Directness | Effect size | GRADE | Comment |
| What are the effects of interventions to prevent or minimise jet lag? | |||||||||
| At least 6 (at least 232) | Severity of jet lag | Melatonin versus placebo | 4 | 0 | 0 | –2 | 0 | Low | Directness points deducted for non-standardised formulation of melatonin and different regimens |
| 1 (234) | Sleep quality | Melatonin versus placebo | 4 | –1 | 0 | –1 | 0 | Low | Quality point deducted for incomplete reporting of results; directness point deducted for unclear outcome definition |
| 2 (170) | Severity of jet lag | Hypnotics versus placebo | 4 | –2 | –1 | 0 | 0 | Very low | Quality point deducted for sparse data and incomplete reporting of results; consistency point deducted for conflicting results |
| 3 (303) | Sleep quality | Hypnotics versus placebo | 4 | –1 | 0 | 0 | 0 | Moderate | Quality point deducted for incomplete reporting of results |
| 1 (137) | Severity of jet lag | Zolpidem plus melatonin versus placebo | 4 | –2 | 0 | 0 | 0 | Low | Quality point deducted for sparse data and incomplete reporting of results |
| 1 (137) | Sleep quality | Zolpidem plus melatonin versus placebo | 4 | –2 | 0 | 0 | 0 | Low | Quality point deducted for sparse data and incomplete reporting of results |
| 1 (137) | Sleep quality | Zolpidem plus melatonin versus zolpidem alone | 4 | –2 | 0 | 0 | 0 | Low | Quality point deducted for sparse data and incomplete reporting of results |
| 1 (20) | Severity of jet lag | Different types of artificial light exposure versus each other | 4 | –2 | 0 | 0 | 0 | Low | Quality point deducted for sparse data and incomplete reporting of results |
| 1 (20) | Sleep quality | Different types of artificial light exposure versus each other | 4 | –2 | 0 | 0 | 0 | Low | Quality point deducted for sparse data and incomplete reporting of results |
We initially allocate 4 points to evidence from RCTs, and 2 points to evidence from observational studies. To attain the final GRADE score for a given comparison, points are deducted or added from this initial score based on preset criteria relating to the categories of quality, directness, consistency, and effect size. Quality: based on issues affecting methodological rigour (e.g., incomplete reporting of results, quasi-randomisation, sparse data [<200 people in the analysis]). Consistency: based on similarity of results across studies. Directness: based on generalisability of population or outcomes. Effect size: based on magnitude of effect as measured by statistics such as relative risk, odds ratio, or hazard ratio.
Glossary
- Low-quality evidence
Further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate.
- Moderate-quality evidence
Further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate.
- Very low-quality evidence
Any estimate of effect is very uncertain.
Disclaimer
The information contained in this publication is intended for medical professionals. Categories presented in Clinical Evidence indicate a judgement about the strength of the evidence available to our contributors prior to publication and the relevant importance of benefit and harms. We rely on our contributors to confirm the accuracy of the information presented and to adhere to describe accepted practices. Readers should be aware that professionals in the field may have different opinions. Because of this and regular advances in medical research we strongly recommend that readers' independently verify specified treatments and drugs including manufacturers' guidance. Also, the categories do not indicate whether a particular treatment is generally appropriate or whether it is suitable for a particular individual. Ultimately it is the readers' responsibility to make their own professional judgements, so to appropriately advise and treat their patients. To the fullest extent permitted by law, BMJ Publishing Group Limited and its editors are not responsible for any losses, injury or damage caused to any person or property (including under contract, by negligence, products liability or otherwise) whether they be direct or indirect, special, incidental or consequential, resulting from the application of the information in this publication.
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