Bipolar Disorder, Major Depressive Disorder
Conditions
Keywords
lithium, pharmacokinetics, renal, kidney
Brief summary
Lithium is a mainstay in the treatment of bipolar disorder, and a frequently used adjunctive therapy for major depressive disorder. It is accepted practice to monitor lithium serum levels to monitor for efficacy and toxicity. However, studies on the difference in lithium levels between once and twice daily dosing, which also assess the impact of kidney function are scarce. The aim of this study is to quantify this pharmacokinetic difference, identify the impact of kidney function, in the context of estimating effects to inform feasibility and sample size needed for a larger well-powered study.
Detailed description
Bipolar disorder is a chronic and recurring condition which causes functional impairment and increases lifetime suicide risk. Major depressive disorder likewise confers a high burden of illness on the affected population, and treatment is complicated by the fact 50-70% of patients treated with an initial agent do not achieve full remission of symptoms. There are numerous clinical practice guidelines which support the use of lithium as a first-line agent for bipolar disorder, and as an adjunctive therapy for major depressive disorder. Therapeutic ranges for lithium were established in the 1970s using multiple daily dose regimens, and therefore should not be directly applied to patients taking lithium once daily. The current standard of practice is to measure levels 12 hours post dose irrespective of once or twice daily administration. There is some evidence that lithium levels drawn 12 hours post dose are 10 - 26% higher when dosing lithium once daily compared to twice daily, however, the impact of kidney function on this difference has not been studied, and this difference in 12h post levels has not been confirmed via prospective data. Guidance on therapeutic drug monitoring (TDM) is vague with respect to interpretation of specific lithium blood levels for once daily dosing. Physicians may reduce a patient's dose based on a lithium level that is seemingly higher that target, even if the patient is clinically stable, putting the patient at risk for re-emergence of symptoms. Though it is known that lithium is excreted by the kidney, the impact of kidney function on the difference in lithium levels when dosed once daily compared to twice daily is not well understood. The results of this pilot study will help identify the impact of kidney function on lithium therapeutic drug monitoring in current practice, and potentially lead to a larger multi-center study.
Interventions
DIAGNOSTIC_TESTLithium level
The level of lithium in the serum
DIAGNOSTIC_TESTSerum Creatinine
The level of creatinine (as an indicator of kidney function, to approximate GFR) in the serum
Sponsors
Mount Sinai Hospital, Canada
Study design
Allocation
NON_RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Adult patients admitted to the inpatient psychiatry unit at Mount Sinai Hospital treated with lithium therapy (i.e. taking lithium before admission, or initiated on lithium therapy during hospitalization)
Exclusion criteria
* any patients who are currently pregnant * patients taking lithium three times daily * patients taking lithium with a specific dosing frequency for a documented clinical reason.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Difference in lithium levels between once and twice daily dosing | once 2 steady state levels have been taken (4-12 days of intervention) | The average of the difference in 12 hour post-dose serum level between the two dosing regimens (once daily and twice daily dosing) |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Correlation between renal function and difference in lithium level | once 2 steady state levels have been taken (4-12 days of intervention) and average creatinine clearance has been calculated | Calculated correlation coefficient (r) for renal function (as estimated by calculation of creatinine clearance via Cockroft Gault) and mean percent change in serum lithium concentration when transitioning between once and twice daily dosing |
| Frequency of selected concurrent medication use | recorded upon enrollment, and every 4-6 days until study completion, up to 12 months | Frequency of thiazide diuretic, loop diuretic, NSAID, and ACE inhibitor/ARB use |
Countries
Canada
Contacts
Primary ContactVirginia Fernandes, PharmD
Backup ContactDario A Moscoso, PharmD
Outcome results
None listed