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Highly active antiretroviral therapy (HAART) has transformed infection with the human immunodeficiency virus (HIV) from a terminal illness to a chronic, treatable condition.
Psychiatric and substance use disorders are frequent concomitants of HIV infection and complicate its diagnosis and treatment.
Evaluation of affective, behavioral, and cognitive symptoms must be broad and include primary psychiatric disorders and secondary conditions related to HIV infection, opportunistic infections, and neoplasms.
Because both psychotropic and antiretroviral agents are metabolized by the cytochrome P-450 enzyme system, pharmacokinetic interactions between these two classes of medication must be considered when treating psychiatric disorders in HIV-infected patients.
Successful psychiatric treatment can be lifesaving if poor adherence to HAART is due to untreated psychiatric illness.
Once a dread illness that portended certain death after years—or even just months—of inexorable decline, infection with HIV has become a chronic, treatable illness. The advent of HAART in 1995 marked a critical turning point in the pandemic. Various combinations of potent medications, each targeting a different step in the virus's hijacking of its human host, reduced the incidence of the acquired immunodeficiency syndrome (AIDS) and improved life expectancy for many patients with HIV infection. Well into the fourth decade of the epidemic, now nearly 30 medications in five classes are available, at least in developed nations and increasingly in developing areas.
The successes of the past 30 years notwithstanding, diagnosis with HIV infection still foreshadows an arduous course of frequent examinations, serial monitoring of cell count and viral load, and difficult treatments with potentially disabling and disfiguring adverse effects (e.g., neuropathy, lipodystrophy). Effective treatment is not obtainable in all parts of the world, and, even in countries where medications are available, not all patients have access to them. At each step of what has been termed the HIV care cascade , significant attrition curtails the number of patients who receive the evaluation and care required to achieve the most critical outcome—full viral suppression. For example, in the US in 2009, 81.9% of HIV-infected people knew their status, 65.8% received care, 36.7% stayed in treatment, 32.7% received HAART, and only 25.3% achieved viral suppression. Blacks and Hispanics/Latinos were significantly less likely to be aware of their HIV status; young people were significantly more adversely affected at each level of the cascade. Closing these gaps in care will require overcoming several barriers, including health beliefs, mental illness, and stigma around HIV, sexual orientation, and substance use.
For the reasons listed in Box 57-1 , the general psychiatrist—regardless of venue and type of practice—will be called on to evaluate and to treat a fair share of patients with HIV infection. This chapter reviews the epidemiology, basic biology, classification, and diagnosis of HIV infection; a general approach to psychiatric care of HIV-infected patients; psychiatric and neurological disorders common in this population and their treatments; and special clinical problems encountered in HIV psychiatry.
Many patients with HIV infection have psychiatric problems, both antecedent and consequent to contracting the virus.
Many patients with psychiatric problems have HIV infection, in part related to poor judgment.
Patients with HIV infection develop medical problems that can manifest as psychiatric illness.
Patients with HIV infection take medications with affective, behavioral, and cognitive effects and that interact with psychotropic agents.
HIV, Human immunodeficiency virus.
At the end of 2011, 34 million people were living with HIV infection worldwide. Sub-Saharan Africa remains the epicenter of the pandemic, followed by the Caribbean. In the US, at the end of 2011, 1.3 million people were living with HIV infection. Since 2001, approximately 50,000 new infections have occurred yearly. Of these, the largest proportion continue to occur in men who have sex with men (MSM).
The HIV ( Figure 57-1 ) is a retrovirus—a virus containing ribonucleic acid and the enzyme reverse transcriptase for replication—that affects the immune system and the central nervous system (CNS), gaining entry to cells (e.g., Tlymphocytes, monocytes, macrophages) that express the CD4 receptor on their membranes. The life cycle of the virus once inside an infected cell is depicted in Figure 57-2 . All of the currently available antiretroviral medications target one of five key steps and enzymes in this process: fusion of the virus with the host cell membrane; entry into the cell; reverse transcriptase; integrase; and protease.
During the first weeks after infection, the population of CD4+ Tlymphocytes (i.e., the CD4 count) decreases as the amount of virus in the blood (i.e., the viral load) increases ( Figure 57-3 ). Following a weak and short-lived rebound, the CD4 count steadily declines. At the same time, the viral load oscillates around a “set-point” until ultimately viral replication intensifies and peripheral viremia surges. Administration of HAART, when effective, halts this process. Opportunistic infections (OIs), neoplasms, and neuropsychiatric conditions occur with increasing frequency as the immune deficiency worsens; prophylaxis for certain OIs (e.g., Pneumocystis jirovecii [formerly Pneumocystis carinii ] pneumonia and toxoplasmosis) is instituted during the course of infection according to the CD4 count.
According to the Centers for Disease Control and Prevention (CDC), AIDS is defined by a CD4 count below 200 cells/µl (or less than 14% of total lymphocytes) or the presence of an AIDS-defining condition ( Box 57-2 ).
Candidiasis
Cervical cancer, invasive
Coccidioidomycosis
Cryptococcosis
Cryptosporidiosis
Cytomegalovirus disease or retinitis
Herpes simplex virus infection
Histoplasmosis
HIV-related encephalopathy
HIV-related wasting syndrome
Isosporiasis
Kaposi's sarcoma
Lymphoma (Burkitt's, immunoblastic, or primary CNS)
Mycobacterial infection ( M. avium complex, M. kansasii, M. tuberculosis, or other species)
Pneumocystis jirovecii pneumonia
Pneumonia, recurrent
Progressive multifocal leukoencephalopathy
Salmonella septicemia, recurrent
Toxoplasmosis, cerebral
AIDS, Acquired immunodeficiency syndrome; CNS, central nervous system; HIV, human immunodeficiency virus.
Infection with HIV is usually diagnosed in two steps. The initial test is an enzyme-linked immunosorbent assay (ELISA). A positive result on this test is then confirmed by a Western blot test. Because one-fifth of HIV-infected people in the US are unaware of their serostatus, the CDC and the United States Preventive Services Task Force (USPSTF) recommend that HIV testing be done as part of routine clinical care for all patients, regardless of risk factors.
The approach to the psychiatric care of the patient with HIV infection focuses on accurate diagnosis; an appreciation of the differences in response to, and tolerability of, psychotropic medications; and the prognostic importance of optimal adherence to effective antiretroviral treatment, which psychiatric illness often compromises.
Psychiatric symptoms in a patient with HIV infection may be primary or secondary ( Box 57-3 ); the CD4 count provides useful initial guidance in making this differential diagnosis. A CD4 count greater than 500 cells/µl suggests a primary psychiatric cause, whereas a CD4 count less than 200 cells/µl, and a fortiori less than 50 cells/µl, suggests the psychiatric problem is secondary to the effects of immune compromise. For example, a patient who has just been told that he is HIV-positive but whose CD4 count is still normal and whose viral load is low may become depressed as part of an adjustment disorder (a primary psychiatric problem). However, 10 years later, when he again has depressed mood and his CD4 count is 100 cells/µl, he may very likely have an OI or a neoplasm affecting his CNS and causing depression (a secondary psychiatric problem).
Delirium
Substance intoxication or withdrawal
Primary HIV syndromes
Seroconversion illness
Acute HIV meningoencephalitis
HIV-associated neurocognitive disorder
Opportunistic infections
Fungi
Aspergillus fumigatus
Candida albicans
Coccidioides immitis
Cryptococcus neoformans
Histoplasma capsulatum
Mucormycosis
Protozoa/parasites
Amebas
Toxoplasma gondii
Viruses
Adenovirus type 2
Cytomegalovirus (CMV)
Herpes simplex virus
JC virus
Varicella-zoster virus
Bacteria
Gram-negative organisms
Listeria monocytogenes
Mycobacterium avium-intracellulare
Mycobacterium tuberculosis
Nocardia asteroides
Treponema pallidum
Neoplasms
Primary CNS lymphoma
Non-Hodgkin's lymphoma
Metastatic Kaposi's sarcoma (rare)
Medication side effects
Endocrinopathies and nutrient deficiencies
Addison's disease (CMV, Cryptococcus, HIV, ketoconazole)
Hypothyroidism
Hypogonadism
Vitamins A, B 6 , B 12 , and E deficiencies
Non–HIV-related conditions
HIV, Human immunodeficiency virus.
Distinguishing between primary and secondary causes has therapeutic implications because results of standard psychiatric treatment for secondary problems may be inferior to those achieved if the problem were primary. As in a patient with traumatic brain injury, stroke, dementia, or advanced age, the brain of a patient with HIV infection can be considered to be more sensitive to psychotropics and to have less reserve capacity. Thus a standard dose of a psychotropic medication may have a more (or less) profound effect in an HIV-infected patient or may cause adverse effects that usually occur only at higher dosages.
Optimum treatment of HIV infection and related conditions is essential for effective psychiatric care. Close collaboration between the psychiatrist and the physician providing the HIV care (usually a specialist in infectious diseases) is crucial.
Substance use disorders are well represented among HIV-infected patients. The 12-month prevalence of drug dependence in the HIV Cost and Services Utilization Study (HCSUS)—a study of a nationally representative sample of nearly 3,000 HIV-infected adults in the US—was 12.5%. Substance use disorders affect the transmission, course, and treatment of HIV infection in numerous ways ( Box 57-4 ).
Impaired judgment
Disinhibition
Risky sexual practices
Viral transmission
Interactions with psychotropic medications
Poor adherence to antiretroviral therapy
Possible immune suppression
HIV, Human immunodeficiency virus.
So-called “club drugs”—methylenedioxymethamphetamine (MDMA, “ecstasy”), gamma-hydroxybutyrate (GHB, “liquid ecstasy”), and ketamine (“special K”)—and other related compounds (e.g., methamphetamine [speed, crystal meth]) have become increasingly popular drugs of abuse, in part because of their effects on social disinhibition and sexual enhancement. As a result, they can pave the way to HIV transmission. By virtue of pharmacokinetic interactions with the cytochrome P-450 system, the co-administration of “club drugs” with antiretroviral medications can have harmful consequences. Adverse effects of MDMA and GHB, thought to be due to interactions with protease inhibitors, have been reported. Protease inhibitors, especially ritonavir, may inhibit the metabolism of amphetamines and ketamine.
Many stressors during the course of HIV infection threaten both the establishment and the maintenance of sobriety in patients with substance use disorders ( Box 57-5 ).
Diagnosis and Treatment
Testing seropositive
Serial determinations of CD4 count and viral load
Initiation of highly active antiretroviral therapy
Initiation of prophylaxis for opportunistic infections
First hospitalization
Transfer to hospice care
Experience of Symptoms
Wasting
Diarrheal illness
Treatment-resistant pain and insomnia
Vision-impairing disease (e.g., cytomegalovirus retinitis)
Cognitive and motor dysfunction
Side effects of medications (e.g., fat redistribution syndrome)
Psychosocial Consequences
Disclosure of HIV serostatus
Disclosure of sexual orientation (e.g., leading to loss of family support)
Loss of employment and health insurance
Application for welfare and disability insurance
Financial and social impoverishment (e.g., loss of friends to AIDS)
AIDS, Acquired immunodeficiency syndrome; HIV, human immunodeficiency virus.
Interactions between methadone and various antiretroviral agents are presented in Box 57-6 . While these interactions may produce measurable changes in methadone plasma levels, such alterations do not consistently result in clinical manifestations. Withdrawal phenomena have been observed with efavirenz, nevirapine, and nelfinavir.
Antiretrovirals that decrease methadone concentrations
Amprenavir
Efavirenz
Fosamprenavir
Lopinavir/ritonavir
Nelfinavir
Nevirapine
Ritonavir
Methadone decreases the concentration of:
Didanosine
Stavudine
Methadone increases the concentration of:
Zidovudine
Less is known about buprenorphine, which, like methadone, is metabolized by cytochrome P-450 3A4. The co-administration of buprenorphine/naloxone and efavirenz to 10 volunteers did not precipitate opioid withdrawal, despite decreased buprenorphine exposure; efavirenz plasma levels remained therapeutic. The combination of ritonavir and atazanavir caused symptoms consistent with opioid excess when given to three patients also taking buprenorphine; pharmacokinetic measures of buprenorphine and the two protease inhibitors were not reported. Buprenorphine's partial agonism at opioid receptors limits its utility in patients who require narcotic analgesics, as many HIV-infected patients do.
The oral solution (but not the capsules) of amprenavir contains propylene glycol, which is metabolized by aldehyde dehydrogenase. Disulfiram inhibits this enzyme and can thus lead to propylene glycol toxicity; therefore, the combination of disulfiram and amprenavir oral solution is contraindicated.
Mood and anxiety disorders are two of the most frequent major psychiatric concomitants of HIV infection. In the HCSUS, 36% screened positive for major depression, 26.5% for dysthymia, 15.8% for generalized anxiety disorder, and 10.5% for panic attack. While individual studies have failed to document a greater risk for depressive disorders in HIV-positive patients compared to HIV-negative controls, a meta-analysis found the frequency of major depressive disorder to be nearly twice as high in the HIV-positive group. This finding may suggest that the various consequences of HIV infection (e.g., effects of the virus within the CNS, immune dysfunction, and systemic viral burden) exert a depressogenic effect.
The differential diagnosis of depression and anxiety is broad ( Box 57-7 ). The patient's complaint of “depression” or “anxiety” should be taken solely as a description of his subjective feeling state rather than as a proclamation of his diagnosis. The patient may simply have a depressed mood or feel anxious, isolated from other symptoms and signs of psychiatric illness. Such a state, for example, would not be unusual in a patient who was recently told that he is HIV-positive or in a patient who is starting an antiretroviral regimen. Dysphoria or apprehension in this situation may be more consistent with grief over loss of health. Moreover, because of their drug use or sexual orientation, many HIV patients have friends who also are HIV-positive. When these friends die of the disease, bereavement can overwhelm the surviving members of their social circles. Many patients, particularly women, will have experienced psychological trauma due to childhood abuse and partner violence and may have post-traumatic stress disorder, which can be easily missed without specific inquiry.
Normal depressed or anxious mood
Grief
Primary depressive disorder (first or recurrent episode)
Primary anxiety disorder
HIV-associated neurocognitive disorder
Hypoactive delirium
Secondary causes (see Box 57-3 )
HIV, Human immunodeficiency virus.
At later stages of illness, OIs and neoplasms affecting the CNS, other complications of advanced disease, cognitive disorders, and adverse effects of HAART can cause secondary depressive disorders. Delirium and HIV-associated neurocognitive disorder (HAND), including HIV-associated dementia (HAD), are characterized by apathy and psychomotor slowing that can easily be mistaken for a depressive disorder.
Treatment of depression and anxiety includes the usual modalities: psychopharmacology, psychotherapy, and electroconvulsive therapy (ECT).
Choice of psychotropic medication is not usually limited by the presence of HIV infection per se . However, owing to the sensitivity of the brain in HIV-infected patients, especially at later stages, initiation of treatment with half the usual starting dose and titration at half the usual speed is recommended; most patients will ultimately tolerate (and need) standard doses. Tricyclic antidepressants (TCAs) may have an advantage in this regard because their serum levels can be measured to gauge any pharmacokinetic effects of interactions between them and HAART. If apathy or psychomotor slowing is prominent—due to depression, dementia, or both (or in unclear cases)—psychostimulants, bupropion, or desipramine can be particularly effective. Bupropion is metabolized by cytochrome P-450 isoform 2B6, which is inhibited by ritonavir, nelfinavir, and efavirenz and induced by nevirapine. The triazolobenzodiazepines—alprazolam, midazolam, and triazolam—are metabolized by cytochrome P-450 3A4, an isoform inhibited by protease inhibitors (PIs), which can thus enhance the effects of these anxiolytics. Use of those benzodiazepines in patients on HAART is relatively contraindicated; other benzodiazepines should be considered.
ECT can be lifesaving when a more rapid response is required and when catatonia is present.
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