Funded by the WITH Foundation
Jennifer McLaren, MD
- Communicating with Patients with IDD and Their Family Members
- Considerations for Waiting Rooms
- Sensory Considerations for Medical Providers
- Cultural Competency and Prescribing
- Abilities Based on Level of IDD
- Developmental considerations that impact psychiatric assessment
Best Practices in MH Diagnosis and Treatment
- Trauma and Stressor Related Disorders
- Anxiety Disorders
- Obsessive Compulsive and Related Disorders
- Depressive Disorders
- Bipolar Disorders
- Grief and Loss
- Schizophrenia and Other Psychotic Disorders
This section provides a brief overview of Depressive Disorders in individuals with Intellectual and Developmental Disabilities (IDD) and Autism Spectrum Disorders (ASD). Depressive Disorders are common among individuals with IDD, with lifetime prevalence rates of 37%.1 Common antecedents for depression in individuals with IDD include personal loss (e.g., caregiver, friend, staff), isolation, marginalization, meaninglessness, lack of autonomy, trauma, bullying, victimization, or other adverse experiences. It is important to ask about these losses as it should impact the therapeutic intervention chosen.
The core features of Depressive Disorders are a depressed and/or irritable mood with a marked change from an individual’s baseline and impairment in functioning. The severity of an individual’s ID impacts the presentation of depression. Individuals with mild to moderate ID may report feeling sad or depressed, making depression easier to recognize. Individuals with a more significant intellectual impairment may not be able to verbalize their internal feelings, making a depression diagnosis more nuanced. For all individuals, observation of presentation and collateral information are key.
The diagnosis of Depressive Disorders requires meeting current diagnostic criteria for one of the following: Disruptive Mood Dysregulation Disorder, Major Depressive Disorder, Persistent Depressive Disorder, Pre-menstrual Dysphoric Disorder, Other Specified and Unspecified Depressive Disorders, and Depressive Disorder Due to Another Medical Condition. These disorders are frequently comorbid with anxiety disorders. Consider utilizing a standardized rating scale when assessing and treating depression such as the PHQ-9. Adaptations to the PHQ-92 have been made for individuals with IDD.
For moderate to severe depression consider a combination of therapy plus antidepressants. There is a lack of research on psychopharmacologic treatments for individuals with depression and IDD. The psychotropic medications used to treat depression in typically developing individuals are utilized for individuals with IDD. It is important to start antidepressants at a low dose and slowly titrate and consider comorbid medical issues and drug-to-drug interactions. Consider utilizing a SSRI as the initial pharmacologic treatment based on their efficacy and tolerability (Figure 1). If an SSRI is not appropriate, then consider serotonin-norepinephrine reuptake inhibitors, atypical antidepressants, and serotonin modulators (Figure 1). Studies show the efficacy of the various antidepressants as comparable across and within the different classes for both acute and maintenance treatment. The selection of an antidepressant is based on the following: symptoms, comorbid diagnosis, safety, side effect profile, drug-to-drug interaction, patient preference, cost, first-degree relative with a history of a positive response to an antidepressant, and patient’s previous response to medications.
Some side effects to consider when selecting an antidepressant include the following:
- Citalopram: increase in irritability for individuals with ASD; QT prolongation
- Sertraline: higher rates of diarrhea
- Venlafaxine: more nausea and vomiting
- Bupropion: less sexual dysfunction; contraindicated in eating disorders
- Mirtazapine: greater weight gain
Tricyclic antidepressants and monoamine oxidase inhibitors are typically not utilized as initial treatment for depression given their more serious side effect profile and elevated risk with overdose.
After initiation of an antidepressant, improvement can be seen in 2-4 weeks. If the individual is not improving and tolerating the antidepressant, then titrate the antidepressant in stepwise increments as tolerated up to lowest effective dose.
1 American Psychiatric Association. Practice Guidelines for the Treatment of Patients with Major Depressive Disorder. Washington DC: American Psychiatric Association, 2010.
2 Breen J. Adapting the GAD-7 and PHQ-9 Clinical Measures for People with Learning Disabilities [PhD thesis]. Royal Holloway, University of London; 2017.
Table 1. Key Components in Assessing Depression in Individuals with ID and ASD
|Comprehensive history with collateral information, including behavioral observations from caregivers, residential staff, day staff, etc.|
Physical examination: Assess for illnesses can be associated with depression (e.g., Hypothyroidism, Epilepsy, Stroke, Anemia).
Review individual’s medication list. Assess if medications are causing/contributing to depression.
Mental Status Examination: Assess suicidality and homicidality, psychotic symptoms, catatonic symptoms, and future orientation.
Labs to consider: Thyroid stimulating hormone (TSH), complete blood count (CBC), vitamin D level, liver function tests (LFTs), renal function tests
For individuals not showing improvement with antidepressant treatment, consider re-evaluating their diagnosis and compliance with treatment. Switching antidepressants should be considered if symptoms fail to improve after a 6 to 12-week medication trial at a therapeutic dose (See Figure 1). If the individual shows a partial response to treatment, consider augmenting the initial antidepressant with second-generation antipsychotics (aripiprazole, quetiapine, and risperidone), lithium, or other antidepressants. Risks and harms of adding additional medications must be carefully considered. After three adequate trials of antidepressants, if the individual continues to have significant symptoms of depression, consider neurostimulation such as repetitive transcranial magnetic stimulation (rTMS) and then electroconvulsive therapy (ECT). ECT should only be utilized when symptoms are severe, refractory to medication treatment, or when medication options run out.
Figure 1. Consensus treatment psychotropic algorithm – Depressive Disorders
* Combination Medication Treatment with medications that complement each other such as Buproprion plus SSRI, TCA plus SSRI
- For individuals with severe suicidality or malnutrition secondary to depression and food refusal: consider electroconvulsive therapy
- For individuals with psychotic symptoms: add an antipsychotic to antidepressant treatment
- For individuals with catatonic features due to depression: add a benzodiazepine to antidepressant treatment
American Psychiatric Association. Diagnostic and Statistical Manual of Mental Disorders (5th ed.). Washington, DC: American Psychiatric Association, 2013.
American Psychiatric Association. Practice Guideline for the Treatment of Patients with Major Depressive Disorder. Washington DC: American Psychiatric Association, 2010.
Breen J. Adapting the GAD-7 and PHQ-9 Clinical Measures for People with Learning Disabilities [PhD Thesis]. Royal Holloway, University of London; 2017.
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