Delirium Clinical Trial
Official title:
Melatonin Use in the Intensive Care Elderly Population
The investigators are studying the use of Melatonin in non-ventilated patients over the age of 65. Primary endpoint will be assesments of delirium, with secondary endpoints to include length of stay, use of anti-psychotic medications, and mortality
Summary Melatonin is a naturally produced hormone involved in the synchronization of
circadian rhythms and the sleep-wake cycle in humans. It is often given as a sleep aid and is
generally well tolerated, with very few drug-drug interactions. Recent studies have shown
marginal benefit in increasing amount of sleep, but have proven benefit in decreasing
delirium in elderly patients on medical wards.
Delirium is a serious problem in hospitals and Intensive-Care Units (ICUs), contributing to
longer hospital stays as well as morbidity and mortality. Studies have shown that each
additional day of delirium increases mortality by 10%1. It is estimated that delirium costs
the US healthcare system $38-$152 billion annually, and the cost of treating a delirious
patient is 2.5 times higher than treating one without delirium. It is estimated that up to
one third of cases of delirium are preventable. Additionally, many of the medications given
in the ICU can worsen delirium, including narcotics, antipsychotics, and benzodiazepines.
Treatment of delirium consists mostly of prevention, by frequently re-orienting the
individual, letting in as much natural light as possible, frequent touching, and providing a
quiet place for rest. Pharmacological treatment consists mostly of antipsychotics, which
often have adverse effects and can worsen delirium.
Incidents of delirium are much higher in elderly patients, up to 80% in some cohorts, as well
as ICU patients. Multiple theories for this exist, including the lack of a true rest time at
night, multiple sedatives that can affect sleep-wake cycle, and large amounts of noise. It is
also known that elderly patients have less total sleep and more nighttime arousals, and that
ICUs in particular are quite loud, especially at night. The increase in ambient noise paired
with frequent interruptions in sleep for monitoring and blood draws exacerbates this problem
and likely leads to a delirious state.
To our knowledge, no study has looked at melatonin's effect on elderly, non-ventilated
patients in the ICU, which is the group most at risk for developing delirium. Recent studies
have indicated that delirium is decreased with melatonin use in a simulated ICU environment.2
This randomized, controlled study would aim to confirm these results in an actual ICU
environment.
Additionally, it is unknown what doses are most effective for treatment of delirium.
Literature has shown improvement with both 3 mg and 5 mg, but recent meta-analysis have not
shown benefit of one over the other. 3 Participants Multiple studies done on critically ill,
non-ventilated patients in the ICU show an incidence of delirium of at least 60%, and in some
cases up to 80%4. At Parkview, the highest incidence recorded was 55%, but this was with all
patients. It is likely that this percentage is much higher in the elderly. Assuming an
average incidence of 70%, and assuming the investigators would want to be able to detect a
20% decrease in this incidence with our intervention, the investigators would aim to enroll
600 patients (200 in each arm), with an interim analysis to be done at 300 patients to asses
for harm or efficacy. This will be done by analyzing the primary outcome for a P-value of
<0.05.
Exclusion Criteria Patients with head trauma or Neurosurgical intervention Patients <65 years
of age Patients with an expected life expectancy <48 hours Blind patients Patients with a
seizure history Patients with uncontrolled hypertension Patients with a supratheraputic
(>3.0) INR Patients on strong CYP1A2 inhibitors: ciprofloxacin, fluvoxamine, methoxsalen,
ofloxacin, primaquine Patients who do not speak English or Spanish
Design Upon admission to the ICU, all consecutive, eligible patients or their POA will be
presented with an informed consent describing the trial (Appendix A). All patients over 65
will be screened. Attending physicians as well as Critical Care Fellows will be allowed to
consent the patients. At the point of deciding to join the trial, an order will be put in the
computer for "melatonin protocol". At this point, pharmacy will assign that patient to either
the placebo, 3mg, or 5mg arm of the study in a 1:1:1 fashion. Physicians, pharmacists, and
nursing staff will be blinded to the protocol. Melatonin dosages of 3 and 5mg will be used
for the study, as recent work with higher doses has been shown to have a "carryover" effect
into the following day. The placebo pill will be a small white tablet of similar size to the
3 and 5mg tablets of melatonin. It is sucrose and is regulated by the FDA as safe for human
consumption. Either placebo or melatonin will be administered at 9pm with evening
medications.
The treatment group will be given either the assigned dose or placebo nightly. Either PO or
PT would be acceptable. The protocol will run until the patient is discharged from the
hospital. Delirium will be assessed using the CAM-ICU evaluation tool in the ICU and bCAM on
the floor according to pre-existing protocols. These will be assessed every 12 hours per a
protocol already in place. These tools are the most widely used in the US, with multiple
studies showing reliable detection of delirium. The CAM scale is attached for reference.
If a patient deteriorates while in the ICU and requires intubation, they will be continued on
the protocol.
Melatonin is generally well-tolerated5, but the two most common side effects are headaches
and confusion. We hope to mitigate the confusion by using a lower dose of melatonin.
Incidence of headache will be tracked, and if deemed necessary by the attending physician,
melatonin therapy can be stopped. Melatonin has minor interactions with Warfarin and
dihydropyridine calcium channel blockers, but patient's INR (if they are on Warfarin) and BP
will be tracked routinely. Melatonin is metabolized by the CYP1A2 system, and so patients on
medications that are potent inhibitors of this enzyme will also be excluded from the study.
There is an interaction between Melatonin and Olanzipine, which is sometimes used for
treatment of delirium. There is the potential for increased sedation with this combination,
but patients will be monitored in an ICU setting while receiving these medications.
Primary outcome will be incidence of delirium (using the CAM-ICU and bCAM scores) in the
study population
Secondary outcomes will be:
ICU days Total Hospital days 30 and 90-day mortality Use of anti-psychotic medications for
treatment of delirium (Haloperidol, Ziprasidone, Olanzapine, Quetiapine) Average Richmond
Agitation and Sedation Scale (RASS) scores when delirium assessed
Hypothesis The investigators' hypothesis is that the use of melatonin will significantly
decrease the incidence of delirium in the elderly, non-ventilated patient. The investigators
will use an accepted P-value of < 0.05 to determine significance. If the p-value doesn't meet
significance, the null hypothesis that melatonin does not decrease the incidence of delirium
in the elderly non-ventilated patient will be accepted.
Collection/Retention of information:
Patients' CAM-ICU scores are already documented in Meditech. Other variables (when patient
moves to floor, when the patient is discharged) are already routinely documented. Following
completion, these variables will be placed in a database and de-identified. The data will be
kept for an additional 3 years to allow for further analysis if required.
Nursing staff as well as house staff will undergo a brief in-service on the study principles
as well as a reminder of how to use the CAM-ICU scores.
Confidentiality:
Only the PI will see the patient's identified information before deidentifying it. To ensure
patient privacy, the informed consent discussion will happen in the patient's private room
Risks:
Melatonin has been proven to safe in every patient population by multiple studies. A
consensus statement by the World Sleep Foundation in 2000 confirms that there have been no
significant side-effects in healthy adults. Specifically, the use of melatonin in seizure
disorders is controversial, with some data showing detriment and some showing benefit. For
this reason, patients with a seizure disorder have been excluded from the study. The
investigators will be using USP (United States Pharmacopeia)- certified melatonin as well.
USP is a non-profit organization that regulates over-the-counter (OTC) supplements in the US.
Its seal verifies that the manufacturer adheres to good manufacturing practices.
The attending physician on the case can choose to withdraw the patient from the study at any
time if they feel that participation is adversely affecting the patient.
Compensation:
There will be no compensation provided for participation in this study.
Benefits:
Considering the multiple studies that have suggested safety and efficacy, critically ill
patients stand to benefit from a lack of delirium and possibly shorter hospital stays. This
would benefit Parkview Medical Center as well.
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