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The Clinical Guide to Supportive and Palliative Care for HIV/AIDS

The Clinical Guide to Supportive and Palliative Care for HIV/AIDS

The Clinical Guide to Supportive and Palliative Care for HIV/AIDS

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A <strong>Clinical</strong> <strong>Guide</strong> <strong>to</strong> <strong>Supportive</strong> <strong>and</strong> <strong>Palliative</strong> <strong>Care</strong> <strong>for</strong> <strong>HIV</strong>/<strong>AIDS</strong> • Chapter 5: Constitutional Symp<strong>to</strong>msafternoon or evening. <strong>The</strong> dosage can be increased daily as <strong>to</strong>lerated <strong>to</strong> effect or <strong>to</strong> a maximumdaily dose of 60 mg.While generally26 picaswell-<strong>to</strong>lerated, methylphenidate should be used with caution in patients withanxiety, delirium, agitation, or tachyarrhythmias. Any jitteriness, mild anxiety, or hyperactivitythat develop during treatment often can be managed with a dose reduction.Dextroamphetamine has indications <strong>and</strong> properties very similar <strong>to</strong> those of methylphenidate. 43<strong>The</strong> recommended dosage is the same.Pemoline, which is chemically unrelated <strong>to</strong> amphetamine <strong>and</strong> has milder sympathomimeticeffects, also may be effective against fatigue <strong>and</strong> depression in advanced medical illness including<strong>HIV</strong> disease. 45 In the only r<strong>and</strong>omized controlled trial of psychostimulants <strong>for</strong> fatigue in <strong>HIV</strong>positivepeople, methylphenidate (7.5 mg twice daily) <strong>and</strong> pemoline (18.75 mg/day) were significantlybetter than placebo at improving not only fatigue but also depression, psychologicaldistress, <strong>and</strong> overall quality of life. 46 <strong>The</strong> starting dosage of pemoline is 18.75 mg orally at 8 a.m.or twice per day at 8 a.m. <strong>and</strong> noon. <strong>The</strong> dosage can be increased as <strong>to</strong>lerated <strong>to</strong> effect or <strong>to</strong> amaximum daily dose of 112.5 mg. However, due <strong>to</strong> its potential <strong>for</strong> severe hepa<strong>to</strong><strong>to</strong>xicity, pemolineshould be used with caution <strong>and</strong> should not be used in patients with liver disease.VCorticosteroidsCorticosteroids have been shown <strong>to</strong> temporarily improve fatigue in cancer patients. 28 It ispossible that many <strong>HIV</strong>/<strong>AIDS</strong> patients may experience similar benefits in the palliative caresetting. In<strong>for</strong>mation on the use of corticosteroids <strong>for</strong> fatigue <strong>and</strong> other indications in generalpalliative care can be found in this chapter, in the section on <strong>HIV</strong> wasting above.<strong>The</strong>re is direct evidence that corticosteroids improve fatigue in one sub-population of <strong>HIV</strong>/<strong>AIDS</strong>patients: those with disseminated mycobacterium avium complex (MAC) with progressive diseasedespite combination antimycobacterial therapy. Low-dose dexamethasone (4-6 mg/day)led <strong>to</strong> a rapid decrease in fatigue, fever <strong>and</strong> night sweats within one week of initiating treatmentin a series of 12 patients. In similar studies of (low-dose) corticosteroids in small numbers of47, 48patients, weight gain, fever reduction, <strong>and</strong> improved sense of well-being were documented.While r<strong>and</strong>omized controlled trials have not been done, corticosteroids appear <strong>to</strong> be useful inthe palliative care of patients with end-stage <strong>AIDS</strong> <strong>and</strong> MAC refrac<strong>to</strong>ry <strong>to</strong> antimycobacterialtherapy. 49FEVERS AND SWEATS■ Fevers, sweats, or both are frequent causes of suffering <strong>and</strong> poor quality of life in <strong>AIDS</strong> patients.Fever increases metabolic rate, <strong>and</strong> persistent fever is associated with anorexia, weightloss <strong>and</strong> wasting. 6 Etiologies of fever include infections, <strong>HIV</strong>-associated malignancies, side effectsof drugs (e.g., trimethoprim-sulfamethoxazole <strong>and</strong> other sulfa drugs, abacavir <strong>and</strong> otherantiretrovirals, amphotericin B), hormonal dysfunction, <strong>and</strong> au<strong>to</strong>-immune disorders.While any source of fever can cause sweats, sweats without fever may occur in the setting ofsome infections, malignancies, endocrinopathies <strong>and</strong> medications. For example, both opioids<strong>and</strong> withdrawal from opioids may cause sweats in the absence of fever. If possible <strong>and</strong> appropriate,ef<strong>for</strong>ts should be made <strong>to</strong> identify <strong>and</strong> treat the underlying etiology of fevers or sweats.Medications used <strong>to</strong> treat fever <strong>and</strong> sweats of many etiologies include antipyretics, corticosteroids<strong>and</strong> anticholinergics.U.S. Department of Health <strong>and</strong> Human Services • Health Resources <strong>and</strong> Services Administration • <strong>HIV</strong>/<strong>AIDS</strong> Bureau 129

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