The Effects of the Exogenous Melatonin on Shift Work Sleep Disorder in Health Personnel: A Systematic Review.
Study Design
- نوع الدراسة
- systematic review
- التدخل
- The Effects of the Exogenous Melatonin on Shift Work Sleep Disorder in Health Personnel: A Systematic Review. 1–10 mg
- المقارن
- Placebo
- اتجاه التأثير
- Positive
- خطر التحيز
- Moderate
Abstract
(1) Background: To know the medical documentation related to exogenous melatonin in sleep disorders caused by shift work in health personnel; (2) Methods: Systematic and critical review. Data were obtained by looking up the bibliographic data base: MEDLINE (via Pubmed), Embase, Cochrane Library, Scopus, Web of Science, Latin American and Caribbean literature in Health Sciences (LILACS) and Medicine in Spanish (MEDES). The used terms, as descriptors and text in the title and abstract record fields, were "Health Personnel", "Melatonin" and "Sleep Disorders", Circadian Rhythm, by using the following filters: "Humans", "Adult: 19+ years" and "Clinical Trial". The search update was in December 2021. The documentary quality of the articles was assessed using the CONSORT questionnaire. (3) Results: Having applied the inclusion and exclusion criteria, 10 clinical essays were selected out of 98 retrieved references. CONSORT scores ranged from a minimum of 6.0 to a maximum of 13. 7 with a median of 10.2. According to the SIGN criteria, this review presented "1-"evidence with a grade of recommendation B. The intervention dose via administration of exogenous melatonin ranged between 1 and 10 mg. It was not mentioned whether the route of administration was by fast or slow absorption. The outcomes showed decreased daytime sleepiness, lessened sleep onset latency, diminished night-time awakenings, increased total sleep period and improved daytime attention in the melatonin-treated group; (4) Conclusions: Exogenously administered melatonin is effective in shift worker health personnel that are suffering from sleep disorders, and given its low adverse effects and tolerability, it might be recommended. A great disparity was evidenced in terms of dose, follow-up periods and type of melatonin, small participant population, same age ranges and young age. Therefore, new trials would be needed to amend these observations in order to have full evidence that is able to ensure the efficacy of exogenous melatonin in the studied population.
Full Text
Figures
Figure 1
PRISMA flowchart showing the systematic literature search and screening process for studies on exogenous melatonin supplementation in health personnel with shift work sleep disorder.
flowchart
Figure 2
Summary of included study characteristics and outcomes from the systematic review on melatonin's effectiveness for shift work sleep disorder among healthcare workers.
Tables
Table 1
| Author, Year | Studied Population | Country | Intervention Period | Intervention Type | Observed Result |
|---|---|---|---|---|---|
| Marqueze et al., | Population type: Nurses | Brazil | 24 weeks | Administration of 3 mg exogenous melatonin or placebo on nights when they were not working. | Significant 20% decrease in circadian misalignment ( |
| Farahmand et al., | Population type: emergency medicine residents | Iran | 4 weeks | Take 3 mg melatonin, versus placebo, 1 h before bedtime for 2 consecutive days. | Melatonin therapy meaningfully lessened daytime sleepiness in comparison with placebo from the second night onwards ( |
| Sadeghniiat-Haghighi et al., | Population type: | Iran | 3 nights’ treatment and 2 weeks washout period. | Take 3 mg melatonin, versus placebo, 30 min before bedtime. | Melatonin therapy improved sleep onset latency and decreased nocturnal awakenings, although there was no association when compared to the placebo group in relation to total sleep time and awakening after sleep onset ( |
| Sadeghniiat-Haghighi et al., | Population type: nurses with insomnia | Iran | 1 night treatment with melatonin and washing out for 4 days. | Oral intake of 5 mg melatonin taken 30 min before night-time sleep. | While the subjects were taking melatonin ( |
| Cavallo et al., | Population type: 2º year paediatric residents | USA | 2 Weeks | Taking melatonin (3 mg) vs. placebo before bedtime in the morning after the night shift. | There were no significant differences in measures of sleep and mood. |
| Yoon et al., | Population type: Night shift nurses | Korea | Follow-up for 9 days. | Three groups were set: placebo, melatonin, and melatonin with sunglasses. Melatonin (6 mg) was administered before bedtime for 2 days. Alertness, night-time sleep period and daytime sleep and mood were observed. | Total sleep period and total sleep times increased meaningfully with melatonin treatments ( |
| Jockovich et al., | Population type: emergency medicine residents | USA | 3 consecutive days after each night shift. | Melatonin (1 mg) administration or placebo, 30 to 60 min before the daytime sleep session, for 3 consecutive days after each night shift. | There was no difference in sleep efficiency, duration, or latency ( |
| Wright et al., | Population type: doctors | USA | 36 days (4 days for intervention, 28 days for washout and 4 days for intervention) | Melatonin (5 mg) administration or placebo for 3 consecutive nights after the night shift with crossover to the opposite agent after a subsequent block of night shifts. | No beneficial effect of melatonin was found for sleep quality, fatigue or cognitive function in emergency physicians after the night shift ( |
| Jorgensen et al., | Population type: resident doctors | USA | 5, 4, 3 and 2-night series | Administration of 10 mg sublingual melatonin or placebo every morning after the evening urgency. | Melatonin improved daytime sleep and night-time alertness ( |
| James et al., | Population type: night-shifts paramedics | USA | A total of 4 consecutive night shifts (2 melatonin, 2 placebo) | Administration of melatonin 6 mg one capsule orally 30 min before each consecutive day’s sleep. | No clinical benefits were observed in staff working rotating night shifts. |
Table 2
| 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 10 | 11 | 12 | 13 | 14 | 15 | 16 | 17 | 18 | 19 | 20 | 21 | 22 | 23 | 24 | 25 | Total | % | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Marqueze et al., | 0.5 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 0 | 0 | 1 | 1 | 1 | 0 | 1 | 1 | 1 | 0 | 1 | 1 | 1 | 1 | 1 | 1 | 20.5 | 13.71 |
| Farahmand et al., | 1 | 1 | 1 | 1 | 1 | 0.5 | 0.5 | 1 | 0 | 0 | 0 | 0.5 | 1 | 0.5 | 1 | 1 | 1 | 1 | 0 | 1 | 1 | 1 | 0 | 1 | 1 | 18 | 12.04 |
| Sadeghniiat-Haghighi et al., | 1 | 1 | 1 | 1 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 1 | 1 | 1 | 0 | 0 | 1 | 1 | 0 | 1 | 1 | 1 | 0 | 0 | 1 | 15 | 10.03 |
| Sadeghniiat-Haghighi et al., | 1 | 1 | 0 | 1 | 1 | 0 | 0 | 0.5 | 0 | 0 | 0 | 0.5 | 0.5 | 0 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 0 | 0 | 1 | 14.5 | 9.69 |
| Cavallo et al., | 0.5 | 1 | 1 | 1 | 1 | 1 | 1 | 0.5 | 0 | 1 | 0 | 1 | 1 | 0.5 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 0 | 0 | 1 | 19.5 | 13.04 |
| Yoon et al., | 0.5 | 0.5 | 0.5 | 1 | 1 | 0.5 | 0 | 0 | 0 | 0 | 0 | 1 | 0.5 | 0.5 | 1 | 1 | 1 | 1 | 0 | 1 | 0 | 1 | 0 | 0 | 0 | 12 | 8.02 |
| Jockovich et al., | 0.5 | 1 | 1 | 1 | 1 | 0.5 | 0.5 | 0 | 0 | 0 | 0 | 1 | 0.5 | 0.5 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | 1 | 0 | 0 | 0 | 9.5 | 6.35 |
| Wright et al., | 0.5 | 1 | 0.5 | 1 | 1 | 0.5 | 0 | 0 | 0 | 1 | 0.5 | 0.5 | 1 | 0.5 | 1 | 1 | 1 | 0 | 1 | 1 | 1 | 1 | 0 | 0 | 1 | 16 | 10.70 |
| Jorgensen et al., | 0.5 | 0.5 | 1 | 1 | 1 | 0 | 0 | 0.5 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 1 | 0.5 | 0 | 0 | 1 | 9 | 6.02 |
| James et al., | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 0.5 | 0 | 1 | 0 | 0.5 | 1 | 0 | 0 | 1 | 0.5 | 0 | 1 | 1 | 1 | 1 | 0 | 0 | 0 | 15.5 | 10.36 |
Table 3
| 1 | 2 | 3 | 4 | 5 | 6 | 7 | |
|---|---|---|---|---|---|---|---|
| Marqueze et al. [ | No | No | Yes | Yes | No | No | No |
| Farahmand et al. [ | No | No | No | Yes | Yes | No | No |
| Sadeghniiat-Haghighi et al. [ | No | No | Yes | Yes | Yes | No | No |
| Sadeghniiat-Haghighi et al. [ | No | No | No | No | Yes | No | No |
| Cavallo et al. [ | No | No | No | No | Yes | Yes | Yes |
| Yoon et al. [ | No | No | No | No | Yes | Yes | No |
| Jockovich et al. [ | No | No | No | No | Unclear | Yes | Yes |
| Wright et al. [ | No | Unclear | Unclear | Unclear | Yes | Yes | No |
| Jorgensen et al. [ | No | No | No | No | Yes | No | Yes |
| James et al. [ | No | No | Unclear | Yes | Yes | No | Yes |
|
Selection bias (Generation of random sequences) Selection bias (Concealment of allocation) Performance bias (Blinding of participants and staff) Detection bias (Blinding of outcome assessment) Attrition bias (Unfinished result data) Reporting bias (Selective reporting) Other biases (Description of other sources of bias) | |||||||
References
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
- Untitled
Used In Evidence Reviews
Similar Papers
Journal of sleep research · 2017
European guideline for the diagnosis and treatment of insomnia.
Chronobiology international · 2012
Circadian typology: a comprehensive review.
Journal of clinical sleep medicine : JCSM : official publication of the American Academy of Sleep Medicine · 2017
Clinical Practice Guideline for the Pharmacologic Treatment of Chronic Insomnia in Adults: An American Academy of Sleep Medicine Clinical Practice Guideline.
Movement disorders : official journal of the Movement Disorder Society · 2011
The Movement Disorder Society Evidence-Based Medicine Review Update: Treatments for the non-motor symptoms of Parkinson's disease.
Cell · 1981
Regulation of terminal differentiation of cultured human keratinocytes by vitamin A.
Journal of neuroendocrinology · 2003