article information

Jundishapur Journal of Natural Pharmaceutical Products: Vol.12, issue 3 (Supp); e64305
published online: August 31, 2017
article type: Review Article
received: July 20, 2016
revised: November 14, 2016
accepted: December 20, 2016
DOI: https://doi.org/10.5812/jjnpp.64305
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Are Melatonin and its Agonist the Natural Solution for Prevention of Delirium in Critically Ill Patients? A Review of Current Studies

authors:

avatar Maryam Aghakouchakzadeh 1 , avatar Mandana Izadpanah ORCID 1 , * , avatar Farhad Soltani ORCID 2 , avatar Mehrnoush Dianatkhah 3

Department of Clinical Pharmacy, School of Pharmacy, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran
Department of Anesthesiology and Critical Care, School of Medicine, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran
Department of Clinical Pharmacy, School of Pharmacy, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran

how to cite: Aghakouchakzadeh M, Izadpanah M, Soltani F, Dianatkhah M. Are Melatonin and its Agonist the Natural Solution for Prevention of Delirium in Critically Ill Patients? A Review of Current Studies. Jundishapur J Nat Pharm Prod. 2017;12(3 (Supp)):e64305. https://doi.org/10.5812/jjnpp.64305.

Abstract

Background:

Delirium is a neuropsychiatric syndrome, which is a common complication at the intensive care unit (ICU). Delirium is a risk factor for increased duration of mechanical ventilation and increased time of stay at the ICU and death. Melatonin is a hormone produced and secreted by the pineal gland, that regulates circadian rhythm. The aim of this investigation was to demonstrate the effect of melatonin in controlling and improving delirium.

Methods:

Available data from Pubmed, Scopus, Medline, EMBASE, the Cochrane central register of controlled trials, and Cochrane database systematic reviews were reviewed.

Results:

Pathogenic pathways of delirium are unclear, yet many risk factors have been identified, including patient’s history, acute illness, environment, administered drugs, and neuronal pathway. Several studies have suggested that delirium could be caused by decreased tryptophan as a precursor to the neurotransmitters, including serotonin and melatonin. On the other hand, a few studies have described that abnormal melatonin metabolism could be one of the mechanisms of delirium.

Conclusion:

Exogenous melatonin could improve circadian rhythm and prevent delirium, therefore melatonin supplementation could be used for improvement or control of delirium at the ICU.

1. Background

Delirium is a neuropsychiatric syndrome, which is a common complication at the intensive care unit (ICU), especially found in older patients, and it is a risk factor for morbidity and mortality in this population (1-3). Delirium, which is presented in approximately 20% of hospitalized patients (2), is defined as an acute onset, fluctuating change, in mental status characterized by a reduced awareness of the environment and disturbance of attention, according to the diagnostic and statistical manual of mental disorders IV (DSM-IV) (4). Delirium leads to an increase in the duration of mechanical ventilation, by interfering with weaning, increasing the time of stay at the ICU, and decrease of functional outcomes. It is also associated with disturbance in consciousness, change in cognition, disturbed psychomotor activity, and abnormal sleep-wake cycle (5-9).

The etiology of delirium remains unclear, yet many risk factors have been associated with delirium, including age, patient’s history, pre-existing cognitive impairment, disruption of the circadian rhythm, acute illness, experience of major surgery, environment, dehydration, malnutrition, hypoxemia, severe concomitant diseases attributing to acid-base imbalance, metabolic disturbances, sensory deprivation, and the administered drugs (1, 5, 10, 11) (Figure 1).

Pathophysiology of Delirium
1, Melatonin could affect delirium via two mechanism: 1-1, via secretion of the pineal gland; low levels of tryptophan, serotonin and melatonin are associated with an increased risk of delirium; and 1-2, via environmental factors at the ICU, such as light and noise, that with disturbance of circadian rhythm could lead to delirium. 2, Other effective causes on delirium include cholinergic deficiency, pre-exiting cognitive impairment, acute illness, experience of major surgery, dehydration, malnutrition, and hypoxemia.

1, Melatonin could affect delirium via two mechanism: 1-1, via secretion of the pineal gland; low levels of tryptophan, serotonin and melatonin are associated with an increased risk of delirium; and 1-2, via environmental factors at the ICU, such as light and noise, that with disturbance of circadian rhythm could lead to delirium. 2, Other effective causes on delirium include cholinergic deficiency, pre-exiting cognitive impairment, acute illness, experience of major surgery, dehydration, malnutrition, and hypoxemia.

Figure 1.

Pathophysiology of Delirium

Despite wide knowledge about delirium, its pathophysiology is still not fully understood (10). Cerebral metabolism dysfunction is one of its responsible mechanisms (12). Neurotransmission alternation and inflammation are influencing factors in the pathogenesis of delirium. Cholinergic deficiency appears to play a central role in the development of delirium. This hypothesis is supported by the effect of anticholinergic medication in increasing delirium symptoms while administration of acetylcholine esterase inhibitors have shown cognitive improvements (13, 14). Over-activity of the dopaminergic system is another mechanism in delirium pathophysiology (15). The increase in serotonergic activity and a relative deficiency of serotonin may also play an important role in the development of delirium (15-17). On the other hand, low levels of tryptophan may also lead to delirium. This amino acid acts as a precursor of some neurotransmitters, including serotonin and melatonin, therefore, low levels of tryptophan, serotonin, and melatonin are associated with increased risk of delirium (18, 19). Investigators have proposed that delirium may occur via 2 different mechanisms with alterations in tryptophan levels. This alternation may lead to the overproduction of neurotoxic metabolites or diversely in the production of melatonin (20, 21). In other words, the other effective mechanism might be the change in the circadian rhythms of the melatonin hormone, which is produced and secreted by the pineal gland (8, 10, 19).

Melatonin hormone is produced from serotonin by acetylation and methylation reaction in the pineal gland, and serotonin is produced from tryptophan by the hydroxylation reaction (22). Melatonin is the essential hormone for regulation of sleep cycle and it has other biological and physiological functions (23, 24). This process has been described in Figure 1.

Several causes could influence melatonin excretion rhythm, including systemic inflammatory response, hormone interactions, drugs, acuity of illness, mechanical ventilation, and environmental factors (25, 26).

Due to the high incidence of delirium in critically ill patients and a direct relationship between sleep disturbance, which may be caused by abnormal levels of melatonin and loss of circadian rhythms, several studies have been conducted to evaluate the level of melatonin and administration of exogenous melatonin or its agonists in this population (9, 17, 25, 27-31). The intention of this article was to review these conducted studies.

2. Methods

This review was designed to be applied across all types of research and evidence, including melatonin, melatonin agonist, delirium, pathophysiology f delirium, clinical trials of using melatonin at the ICU, effects of melatonin on delirium, and intensive care unit. Available data in Pubmed, Scopus, Medline, EMBASE, the Cochrane central register of controlled trials, and Cochrane databases were reviewed. Delirium is a common complication at the ICU and the current study only included studies on ICU patients that developed delirium.

The search retrieved 1023 articles, which were then filtered for articles using English language and human adult populations (18 years of age) using either descriptive or experimental study designs and using both melatonin and delirium as their key words. Review articles, case reports, and clinical studies were included. Ultimately, after the elimination of repetitive information, 58 articles were identified (Figure 2).

Diagram of the Process of Initiation and Selection of the Studies
Diagram of the Process of Initiation and Selection of the Studies
Figure 2.

Diagram of the Process of Initiation and Selection of the Studies

3. Results

3.1. Delirium

Delirium could be classified to 3 subtypes, including hyperactive, hypoactive, and mixed-type, based on the systematic clinical observation of hospitalized patients (32-34). In non-ICU patients, hyperactive delirium is recognized, while it is not observed in older patients (33, 35). In ICU patients, the most common types of delirium are mixed and hypoactive. Furthermore, hypoactive delirium is the major delirium witnessed in older patients (32, 33, 35). Melatonin degrades in the liver, and the metabolite of melatonin, 6-sulfatoxymelatonin (6-SMT), which is secreted in the kidney and could be directly measured (7). Given the known effects of melatonin, it appears that a relationship could exist between melatonin blood levels and/or a biochemical parameters (the urinary 6-SMT) and the subtypes of delirium, describing the low levels of urinary 6-SMT in hyperactive patients and the high levels of 6-SMT in hypoactive patients (7, 22, 25, 27).

Pharmacological and non-pharmacological approaches could be applied to prevent and control delirium in hospitalized patients (5, 36-38).

3.2. Melatonin in Delirium

Low levels of melatonin lead to an increase in the risk of delirium, therefore melatonin with a variety of doses has been used in studies that describe that the administration of melatonin could have beneficial effects, leading to prevention, management and improvement of delirium in critically ill patients with delirium (Table 1).

Table 1.

Characteristics of the Studies Using Melatonin at the Intensive Care Unit for Delirium

StudyType of StudyDose of Melatonin, mgOther InterventionDuration of StudyConclusion
Hanania et al. (29)Case reports: 2 cases2-3 daysPrevention and management of delirium
Sultan (39)RCT, N = 3005The control group, 7.5 mg midazolam, 100 µg clonidinePreoperative for 2 doses and postoperatively for 3 nights to those with postoperative deliriumA significant decrease in the percentage of post-operative delirium (9.43% vs. 32.65%)
Al-Aama et al. (40)RCT, N = 1450.5Placebo14 days or until dischargeA lower risk of delirium with melatonin (12.0% vs. 31.0%, P value = 0.014)
Lammers et al. (41)Case reports2, twice per day-14 daysSignificant improvement in behavior
Jonghe et al. (42)RCT, N= 3783Placebo5 daysNo effect of melatonin on the incidence of delirium, but led to long-lasting episode of delirium (> 2 days) (25.5% v. 46.9%; P = 0.02)
Chen et al. (6)RCT, N = 6690.5 - 5Surgical wards3 - 5 daysDecreased incidence of delirium
Medical wards7 - 14 days
Clayton-Chubb et al. (43)RCT, N = 365Placebo5 days or until dischargeLed to significant outcome benefits for delirious inpatients

Hanania et al. (2002) described 2 cases; case 1 was a 53-year-old male with a history of Crohn’s disease, and had a hip pinning procedure and experienced postoperative delirium. His delirium ultimately improved with a daily intake of 2 mg of melatonin for 4 days. Case 2 was a 78-year-old male with a history of coronary artery disease and transient ischemic attacks, who had undergone a hip pinning procedure and experienced confusion, mild agitation, and sleep disturbance after the procedure. He was visited 3 years later for open debridement of an infected knee joint. He received 2 mg of melatonin before the operation and the same amount for 3 nights, postoperatively; therefore, he slept well and remained alert and oriented without confusion (29). Sherif S Sultan (2010) performed a controlled, randomized, double-blind study with 300 patients aged > 65 years old undergoing hip arthroplasty under spinal anesthesia. Patients were categorized to 4 groups, including the control group, 5 mg melatonin, 7.5 mg midazolam, and 100 µg clonidine. They received one dose at sleep time on the night of the operation and another dose 90 minutes pre-operatively. The results revealed a statistically significant decrease in the percentage of post-operative delirium to 9.43% (5 out of 53 patients) in the melatonin group versus 32.65% (16 out of 49 patients) in the control group. Finally, melatonin could decrease after the operation and played a successful role in treating more than half of the patients when administered postoperatively for 3 nights (39). Al-Aama et al. (2010) randomly assigned 145 acutely ill medical inpatients aged 65 years old. In this controlled, randomized, double-blind study, the patients were classified to 2 groups and received either 0.5 mg of melatonin or placebo every night for 14 days or until discharge. The results demonstrated that melatonin was associated with a lower risk of delirium (12.0% vs. 31.0%, P value = 0.014), with an odds ratio (OR) adjusted for dementia and comorbidities of 0.19 (95% confidence intervals (CI): 0.06 - 0.62). These differences remained statistically significant when the patients with prevalent delirium on admission were excluded. Thus, the nightly administration of low-dose melatonin to elderly patients admitted to the acute care unit could be a potential protective agent for delirium (40). Lammers et al. (2013) described a case, who was an 81-year-old male diagnosed with Alzheimer’s disease 4 years prior to the study and delirium one month before admission. Moreover, haloperidol was not effective for him. Subsequently, 2 mg of melatonin was administrated twice per day and improved his sleep quality, significantly ameliorating his behavior (41). Jonghe et al. (2014) conducted a controlled, randomized, double-blind clinical trial of 378 hip surgery patients aged 65 years or older. The patients received 3 mg of melatonin or placebo in the evenings for 5 days, starting within 24 hours after admission. The results did not show any effects for melatonin on the incidence of delirium between the melatonin (55/ out of 186, 29.6%) and placebo (49 out of 192, 25.5%) groups when a smaller proportion of participants in the melatonin group experienced a long-lasting episode of delirium (> 2 days) (42). Chen et al. (2015) carried out controlled clinical, randomized trials of 669 elderly patients. The data indicated that melatonin supplementation induced a significant 75% decrease in the incidence of delirium in elderly patients, who were presented to medical wards; however, no effect on sleep-wake disturbances was observed (6). Clayton-Chubb et al. (2016) undertook placebo-controlled, double-blind, randomized trials of 36 elderly patients with delirium, who were hospitalized (≥ 70 years old). The patients were divided to 2 groups and received either 5 mg of melatonin or placebo per night for 5 nights or until discharge. The results demonstrated that the administration of melatonin to elderly inpatients with delirium could lead to considerable outcome benefits for delirious inpatients (43).

3.3. Melatonin Agonist, Ramelteon, in Delirium

Ramelteon, a melatonin receptor agonist, has a high affinity for the melatonin receptors (44). Previous case reports indicated that the administration of melatonin agonist, Ramelteon, has some beneficial effects leading to prevention and management of delirium without showing any adverse effects (Table 2).

Table 2.

Ramelteon Administration at the Intensive Care Unit, an Overview of Studies and Characteristics

StudyType of StudyDose of Ramelteon, mgOther InterventionDuration of the StudyConclusion
Kimura et al. (2011)Case reports: 3 cases8-7 daysA significant improvement in delirium
Furuya et al. (2012)Case reports: 5cases8-During 24 hManagement of delirium
Tsuda et al. (2013)Case reports80.5 mg risperidone5 daysImproved delirium without over sedation
Ohta et al. (2013)RCT, N = 288Other drug such as brotizolam, zopiclone, and haloperidol7 daysA significant improvement in delirium
Hatta et al. (2015)RCT, N = 678Placebo7 daysA lower risk of incidence of delirium with ramelteon (12.0% vs. 31.0%, P value = 0.014)

Kimura et al. (2011) described 3 case reports that were 3 females admitted to the hospital, who illustrated symptoms of delirium during hospitalization and were administrated 8 mg of Ramelteon per day for the treatment of delirium (45). Furuya et al. (2012) described 5 cases, 3 of which had a primary neurological disease such as Alzheimer’s disease. In addition, one of these 5 cases had no previous psychiatric history, but he did have a medical history of asthma, Hashimoto’s disease. He later had steroid-induced psychosis and illustrated symptoms of delirium during hospitalization. At the end, they were all successfully treated by receiving 8 mg of Ramelteon per day (46). Tsuda et al. (2013) described a case, who was a 100-year-old male with severe pneumonia admitted to the ICU. He had a surgical history and no history of neuropsychiatric problems or dementia. After moving to a general ward from the ICU, he was diagnosed as having delirium. Subsequently, he received a single dose of 0.5 mg of risperidone at 18:00 on the sixth day. He showed over-sedation all day for 2 days and had severe psychomotor excitement after 9 days. The administration of 8 mg of Ramelteon improved delirium without having any adverse effects, such as over-sedation (47). Ohta et al. (2013) performed a study on elderly patients with delirium and insomnia after acute stroke. Seven patients were treated with Ramelteon and 21 patients with the other drugs. The results confirmed that all the patients treated with Ramelteon showed significant improvement within a week (48). Hatta et al. (2015) conducted a multi-center, rater-blinded, randomized, placebo-controlled trial of 67 patients aged between 65 and 89 years old, who were recently admitted for serious medical problems to the ICU. The patients received melatonin agonist, Ramelteon, (8 mg/d; 33 patients) or placebo (34 patients) every night for 7 days. The results confirmed that Ramelteon was associated with a lower risk of incidence of delirium (12.0% vs. 31.0%, P value = 0.014). Therefore, described melatonin neurotransmission could have a possible pathogenic role in delirium (49).

4. Discussion

Despite considerable advances in the understanding of the delirium mechanisms and its effects on critically ill patient outcomes, its prevention and management is still a significant issue. According to the association between delirium and irregular patterns of melatonin secretion, which has been described by several studies, irregular melatonin secretion could be one of the mechanisms of delirium (10, 23, 30, 31, 50-52) as well as the presence of sleep deprivation in hospitalized delirious patients at the ICU, as it has been indicated that melatonin and its agonists could be an effective supplement for prevention and management of delirium (38, 53, 54). Furthermore, several studies have reported the marked improvement of delirium in delirious patients without side effects due to the use of melatonin and ramelteon (6, 45, 46). According to the literature, pharmacological methods are not yet recommended for prevention of delirium in critically ill patients, based on reviewed studies, especially because melatonin could improve patients’ sleep; further trials could be performed to evaluate the efficacy of melatonin on prevention of delirium.

4.1. Conclusion

Exogenous melatonin and melatonin agonist, ramelteon, could improve circadian rhythm, therefore, the use of melatonin supplementation leads to prevention, improvement and control of delirium at the ICU.

References

  • 1.

    Ceriana P, Fanfulla F, Mazzacane F, Santoro C, Nava S. Delirium in patients admitted to a step-down unit: analysis of incidence and risk factors. J Crit Care. 2010;25(1):136-43. [PubMed ID: 19781903]. https://doi.org/10.1016/j.jcrc.2009.07.004.

  • 2.

    Meagher D, O'Regan N, Ryan D, Connolly W, Boland E, O'Caoimhe R, et al. Frequency of delirium and subsyndromal delirium in an adult acute hospital population. Br J Psychiatry. 2014;205(6):478-85. [PubMed ID: 25359923]. https://doi.org/10.1192/bjp.bp.113.139865.

  • 3.

    American Geriatrics Society Expert Panel on Postoperative Delirium in Older A. American Geriatrics Society abstracted clinical practice guideline for postoperative delirium in older adults. J Am Geriatr Soc. 2015;63(1):142-50. [PubMed ID: 25495432]. https://doi.org/10.1111/jgs.13281.

  • 4.

    Lloyd DG, Ma D, Vizcaychipi MP. Cognitive decline after anaesthesia and critical care. Cont Educ Anaesth Crit Care Pain. 2012;12(3):105-9. https://doi.org/10.1093/bjaceaccp/mks004.

  • 5.

    Ford AH, Almeida OP. Pharmacological interventions for preventing delirium in the elderly. Maturitas. 2015;81(2):287-92. [PubMed ID: 25890587]. https://doi.org/10.1016/j.maturitas.2015.03.024.

  • 6.

    Chen S, Shi L, Liang F, Xu L, Desislava D, Wu Q, et al. Exogenous Melatonin for Delirium Prevention: a Meta-analysis of Randomized Controlled Trials. Mol Neurobiol. 2016;53(6):4046-53. [PubMed ID: 26189834]. https://doi.org/10.1007/s12035-015-9350-8.

  • 7.

    Dessap AM, Roche-Campo F, Launay JM, Charles-Nelson A, Katsahian S, Brun-Buisson C, et al. Delirium and Circadian Rhythm of Melatonin During Weaning From Mechanical Ventilation: An Ancillary Study of a Weaning Trial. Chest. 2015;148(5):1231-41. [PubMed ID: 26158245]. https://doi.org/10.1378/chest.15-0525.

  • 8.

    Mistraletti G, Carloni E, Cigada M, Zambrelli E, Taverna M, Sabbatici G, et al. Sleep and delirium in the intensive care unit. Minerva Anestesiol. 2008;74(6):329-33. [PubMed ID: 18500209].

  • 9.

    Weinhouse GL. Delirium and sleep disturbances in the intensive care unit: can we do better? Curr Opin Anaesthesiol. 2014;27(4):403-8. [PubMed ID: 24824827]. https://doi.org/10.1097/ACO.0000000000000093.

  • 10.

    Piotrowicz K, Klich-Raczka A, Pac A, Zdzienicka A, Grodzicki T. The diurnal profile of melatonin during delirium in elderly patients--preliminary results. Exp Gerontol. 2015;72:45-9. [PubMed ID: 26368540]. https://doi.org/10.1016/j.exger.2015.09.007.

  • 11.

    Van Rompaey B, Elseviers MM, Van Drom W, Fromont V, Jorens PG. The effect of earplugs during the night on the onset of delirium and sleep perception: a randomized controlled trial in intensive care patients. Crit Care. 2012;16(3):R73. [PubMed ID: 22559080]. https://doi.org/10.1186/cc11330.

  • 12.

    Engel GL, Romano J. Delirium, a syndrome of cerebral insufficiency. J Chronic Dis. 1959;9(3):260-77. [PubMed ID: 13631039]. https://doi.org/10.1016/0021-9681(59)90165-1.

  • 13.

    Hshieh TT, Fong TG, Marcantonio ER, Inouye SK. Cholinergic deficiency hypothesis in delirium: a synthesis of current evidence. J Gerontol A Biol Sci Med Sci. 2008;63(7):764-72. [PubMed ID: 18693233]. https://doi.org/10.1093/gerona/63.7.764.

  • 14.

    Han L, McCusker J, Cole M, Abrahamowicz M, Primeau F, Elie M. Use of medications with anticholinergic effect predicts clinical severity of delirium symptoms in older medical inpatients. Arch Intern Med. 2001;161(8):1099-105. [PubMed ID: 11322844]. https://doi.org/10.1001/archinte.161.8.1099.

  • 15.

    Flacker JM, Lipsitz LA. Neural mechanisms of delirium: current hypotheses and evolving concepts. J Gerontol A Biol Sci Med Sci. 1999;54(6):B239-46. [PubMed ID: 10411009]. https://doi.org/10.1093/gerona/54.6.B239.

  • 16.

    Robinson TN, Raeburn CD, Angles EM, Moss M. Low tryptophan levels are associated with postoperative delirium in the elderly. Am J Surg. 2008;196(5):670-4. [PubMed ID: 18789427]. https://doi.org/10.1016/j.amjsurg.2008.07.007.

  • 17.

    Balan S, Leibovitz A, Zila SO, Ruth M, Chana W, Yassica B, et al. The relation between the clinical subtypes of delirium and the urinary level of 6-SMT. J Neuropsychiatry Clin Neurosci. 2003;15(3):363-6. [PubMed ID: 12928514]. https://doi.org/10.1176/jnp.15.3.363.

  • 18.

    van der Mast RC, van den Broek WW, Fekkes D, Pepplinkhuizen L, Habbema JD. Is delirium after cardiac surgery related to plasma amino acids and physical condition? J Neuropsychiatry Clin Neurosci. 2000;12(1):57-63. [PubMed ID: 10678514]. https://doi.org/10.1176/jnp.12.1.57.

  • 19.

    Marcantonio ER, Rudolph JL, Culley D, Crosby G, Alsop D, Inouye SK. Serum biomarkers for delirium. J Gerontol A Biol Sci Med Sci. 2006;61(12):1281-6. [PubMed ID: 17234821]. https://doi.org/10.1093/gerona/61.12.1281.

  • 20.

    Shim JJ, Leung JM. An update on delirium in the postoperative setting: prevention, diagnosis and management. Best Pract Res Clin Anaesthesiol. 2012;26(3):327-43. [PubMed ID: 23040284]. https://doi.org/10.1016/j.bpa.2012.08.003.

  • 21.

    Pandharipande PP, Morandi A, Adams JR, Girard TD, Thompson JL, Shintani AK, et al. Plasma tryptophan and tyrosine levels are independent risk factors for delirium in critically ill patients. Intensive Care Med. 2009;35(11):1886-92. [PubMed ID: 19588122]. https://doi.org/10.1007/s00134-009-1573-6.

  • 22.

    Di WL, Djahanbakhch O, Kadva A, Street C, Silman R. The pineal and extra-pineal origins of 5-sulphatoxy N-acetyl-serotonin in humans. J Pineal Res. 1999;26(4):221-6. [PubMed ID: 10340724]. https://doi.org/10.1111/j.1600-079X.1999.tb00587.x.

  • 23.

    Olofsson K, Alling C, Lundberg D, Malmros C. Abolished circadian rhythm of melatonin secretion in sedated and artificially ventilated intensive care patients. Acta Anaesthesiol Scand. 2004;48(6):679-84. [PubMed ID: 15196098]. https://doi.org/10.1111/j.0001-5172.2004.00401.x.

  • 24.

    Wade A, Downie S. Prolonged-release melatonin for the treatment of insomnia in patients over 55 years. Expert Opin Investig Drugs. 2008;17(10):1567-72. [PubMed ID: 18808316]. https://doi.org/10.1517/13543784.17.10.1567.

  • 25.

    Figueroa-Ramos MI, Arroyo-Novoa CM, Lee KA, Padilla G, Puntillo KA. Sleep and delirium in ICU patients: a review of mechanisms and manifestations. Intensive Care Med. 2009;35(5):781-95. [PubMed ID: 19165463]. https://doi.org/10.1007/s00134-009-1397-4.

  • 26.

    Huang HW, Zheng BL, Jiang L, Lin ZT, Zhang GB, Shen L, et al. Effect of oral melatonin and wearing earplugs and eye masks on nocturnal sleep in healthy subjects in a simulated intensive care unit environment: which might be a more promising strategy for ICU sleep deprivation? Crit Care. 2015;19:124. [PubMed ID: 25887528]. https://doi.org/10.1186/s13054-015-0842-8.

  • 27.

    Bourne RS, Mills GH. Melatonin: possible implications for the postoperative and critically ill patient. Intensive Care Med. 2006;32(3):371-9. [PubMed ID: 16477412]. https://doi.org/10.1007/s00134-005-0061-x.

  • 28.

    Lewis MC, Barnett SR. Postoperative delirium: the tryptophan dyregulation model. Med Hypotheses. 2004;63(3):402-6. [PubMed ID: 15288356]. https://doi.org/10.1016/j.mehy.2004.01.033.

  • 29.

    Hanania M, Kitain E. Melatonin for treatment and prevention of postoperative delirium. Anesth Analg. 2002;94(2):338-9. table of contents. [PubMed ID: 11812694]. https://doi.org/10.1213/00000539-200202000-00019.

  • 30.

    Cronin AJ, Keifer JC, Davies MF, King TS, Bixler EO. Melatonin secretion after surgery. Lancet. 2000;356(9237):1244-5. [PubMed ID: 11072950]. https://doi.org/10.1016/S0140-6736(00)02795-1.

  • 31.

    Shigeta H, Yasui A, Nimura Y, Machida N, Kageyama M, Miura M, et al. Postoperative delirium and melatonin levels in elderly patients. Am J Surg. 2001;182(5):449-54. [PubMed ID: 11754849]. https://doi.org/10.1016/S0002-9610(01)00761-9.

  • 32.

    Cavallazzi R, Saad M, Marik PE. Delirium in the ICU: an overview. Ann Intensive Care. 2012;2(1):49. [PubMed ID: 23270646]. https://doi.org/10.1186/2110-5820-2-49.

  • 33.

    Meagher D. Motor subtypes of delirium: past, present and future. Int Rev Psychiatry. 2009;21(1):59-73. [PubMed ID: 19219713]. https://doi.org/10.1080/09540260802675460.

  • 34.

    Liptzin B, Levkoff SE. An empirical study of delirium subtypes. Br J Psychiatry. 1992;161:843-5. [PubMed ID: 1483173]. https://doi.org/10.1192/bjp.161.6.843.

  • 35.

    Peterson JF, Pun BT, Dittus RS, Thomason JW, Jackson JC, Shintani AK, et al. Delirium and its motoric subtypes: a study of 614 critically ill patients. J Am Geriatr Soc. 2006;54(3):479-84. [PubMed ID: 16551316]. https://doi.org/10.1111/j.1532-5415.2005.00621.x.

  • 36.

    Inouye SK, Bogardus SJ, Charpentier PA, Leo-Summers L, Acampora D, Holford TR, et al. A multicomponent intervention to prevent delirium in hospitalized older patients. N Engl J Med. 1999;340(9):669-76. [PubMed ID: 10053175]. https://doi.org/10.1056/NEJM199903043400901.

  • 37.

    Wenham T, Pittard A. Intensive care unit environment. Contin Educ Anaesth Critical Care Pain. 2009;9(6):178-83. https://doi.org/10.1093/bjaceaccp/mkp036.

  • 38.

    Bellapart J, Boots R. Potential use of melatonin in sleep and delirium in the critically ill. Br J Anaesth. 2012;108(4):572-80. [PubMed ID: 22419624]. https://doi.org/10.1093/bja/aes035.

  • 39.

    Sultan SS. Assessment of role of perioperative melatonin in prevention and treatment of postoperative delirium after hip arthroplasty under spinal anesthesia in the elderly. Saudi J Anaesth. 2010;4(3):169-73. [PubMed ID: 21189854]. https://doi.org/10.4103/1658-354X.71132.

  • 40.

    Al-Aama T, Brymer C, Gutmanis I, Woolmore-Goodwin SM, Esbaugh J, Dasgupta M. Melatonin decreases delirium in elderly patients: a randomized, placebo-controlled trial. Int J Geriatr Psychiatry. 2011;26(7):687-94. [PubMed ID: 20845391]. https://doi.org/10.1002/gps.2582.

  • 41.

    Lammers M, Ahmed AI. Melatonin for sundown syndrome and delirium in dementia: is it effective? J Am Geriatr Soc. 2013;61(6):1045-6. [PubMed ID: 23772740]. https://doi.org/10.1111/jgs.12296.

  • 42.

    de Jonghe A, van Munster BC, Goslings JC, Kloen P, van Rees C, Wolvius R, et al. Effect of melatonin on incidence of delirium among patients with hip fracture: a multicentre, double-blind randomized controlled trial. CMAJ. 2014;186(14):E547-56. [PubMed ID: 25183726]. https://doi.org/10.1503/cmaj.140495.

  • 43.

    Clayton-Chubb DI, Lange PW. Moderate dose melatonin for the abatement and treatment of delirium in elderly general medical inpatients: study protocol of a placebo controlled, randomised, double blind trial. BMC Geriatr. 2016;16:54. [PubMed ID: 26928392]. https://doi.org/10.1186/s12877-016-0230-5.

  • 44.

    Kato K, Hirai K, Nishiyama K, Uchikawa O, Fukatsu K, Ohkawa S, et al. Neurochemical properties of ramelteon (TAK-375), a selective MT1/MT2 receptor agonist. Neuropharmacology. 2005;48(2):301-10. [PubMed ID: 15695169]. https://doi.org/10.1016/j.neuropharm.2004.09.007.

  • 45.

    Kimura R, Mori K, Kumazaki H, Yanagida M, Taguchi S, Matsunaga H. Treatment of delirium with ramelteon: initial experience in three patients. Gen Hosp Psychiatry. 2011;33(4):407-9. [PubMed ID: 21762839]. https://doi.org/10.1016/j.genhosppsych.2011.03.013.

  • 46.

    Furuya M, Miyaoka T, Yasuda H, Yamashita S, Tanaka I, Otsuka S, et al. Marked improvement in delirium with ramelteon: five case reports. Psychogeriatrics. 2012;12(4):259-62. [PubMed ID: 23279149]. https://doi.org/10.1111/j.1479-8301.2012.00422.x.

  • 47.

    Tsuda A, Nishimura K, Naganawa E, Otsubo T, Ishigooka J. Successfully treated delirium in an extremely elderly patient by switching from risperidone to ramelteon. Psychiatry Clin Neurosci. 2013;67(2):130. [PubMed ID: 23438172]. https://doi.org/10.1111/pcn.12016.

  • 48.

    Ohta T, Murao K, Miyake K, Takemoto K. Melatonin receptor agonists for treating delirium in elderly patients with acute stroke. J Stroke Cerebrovasc Dis. 2013;22(7):1107-10. [PubMed ID: 23017429]. https://doi.org/10.1016/j.jstrokecerebrovasdis.2012.08.012.

  • 49.

    Hatta K, Kishi Y, Wada K, Takeuchi T, Odawara T, Usui C, et al. Preventive effects of ramelteon on delirium: a randomized placebo-controlled trial. JAMA Psychiatry. 2014;71(4):397-403. [PubMed ID: 24554232]. https://doi.org/10.1001/jamapsychiatry.2013.3320.

  • 50.

    Miyazaki T, Kuwano H, Kato H, Ando H, Kimura H, Inose T, et al. Correlation between serum melatonin circadian rhythm and intensive care unit psychosis after thoracic esophagectomy. Surgery. 2003;133(6):662-8. [PubMed ID: 12796735]. https://doi.org/10.1067/msy.2003.149.

  • 51.

    Yoshitaka S, Egi M, Morimatsu H, Kanazawa T, Toda Y, Morita K. Perioperative plasma melatonin concentration in postoperative critically ill patients: its association with delirium. J Crit Care. 2013;28(3):236-42. [PubMed ID: 23312124]. https://doi.org/10.1016/j.jcrc.2012.11.004.

  • 52.

    Mundigler G, Delle-Karth G, Koreny M, Zehetgruber M, Steindl-Munda P, Marktl W, et al. Impaired circadian rhythm of melatonin secretion in sedated critically ill patients with severe sepsis. Crit Care Med. 2002;30(3):536-40. [PubMed ID: 11990911]. https://doi.org/10.1097/00003246-200203000-00007.

  • 53.

    Devlin JW, Al-Qadhee NS, Skrobik Y. Pharmacologic prevention and treatment of delirium in critically ill and non-critically ill hospitalised patients: a review of data from prospective, randomised studies. Best Pract Res Clin Anaesthesiol. 2012;26(3):289-309. [PubMed ID: 23040282]. https://doi.org/10.1016/j.bpa.2012.07.005.

  • 54.

    Shilo L, Dagan Y, Smorjik Y, Weinberg U, Dolev S, Komptel B, et al. Patients in the intensive care unit suffer from severe lack of sleep associated with loss of normal melatonin secretion pattern. Am J Med Sci. 1999;317(5):278-81. [PubMed ID: 10334113]. https://doi.org/10.1097/00000441-199905000-00002.