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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 4: Pain• Predominantly Sensory Neuropathy (PSN) of <strong>AIDS</strong><strong>The</strong> most frequently encountered neuropathy is a symmetrical predominantly sensory painful peripheralneuropathy.26 picasThis is typically a late manifestation, occurring most often in patients with an<strong>AIDS</strong>-defining illness. 30 <strong>The</strong> prevalence of this neuropathy in hospice populations ranges from 19%17, 31, 32<strong>to</strong> 26%.<strong>The</strong> predominant symp<strong>to</strong>m in about 60% of patients is pain in the soles of the feet. Paraesthesia isfrequent <strong>and</strong> usually involves the dorsum of the feet <strong>and</strong> soles. Most patients have signs of peripheralneuropathy (most commonly, absent or reduced ankle jerks <strong>and</strong> elevated thresholds <strong>to</strong> pain <strong>and</strong>30, 33,vibration sense); <strong>and</strong>, while the signs progress, the symp<strong>to</strong>ms often remain confined <strong>to</strong> the feet.34Although the patients’ complaints are predominantly sensory, electrophysiological studies demonstrateboth sensory <strong>and</strong> mo<strong>to</strong>r involvement.IV• Immune-mediated NeuropathiesAcute Guillain-Barré syndrome has been described in association with seroconversion (group-Iinfection) but may occur at any time. Both acute <strong>and</strong> chronic inflamma<strong>to</strong>ry demyelinatingpolyneuropathies are predominantly mo<strong>to</strong>r-related, <strong>and</strong> sensory abnormalities are rare. 35Mononeuritis multiplex presents with sensory or mo<strong>to</strong>r deficits in the distribution of multiple spinal,cranial or peripheral nerves <strong>and</strong> may progress in<strong>to</strong> a chronic inflamma<strong>to</strong>ry demyelinating35, 36polyneuropathy.• Infectious NeuropathiesPolyradiculopathies (associated with CMV infection) often present with radicular pain <strong>and</strong> followa distinct course. 37 <strong>The</strong> onset is usually subacute <strong>and</strong> the deficit initially confined <strong>to</strong> sacral <strong>and</strong>lumbar nerve roots. Both sensory <strong>and</strong> mo<strong>to</strong>r functions are involved, <strong>and</strong> there is usually early involvemen<strong>to</strong>f sphincters. Progression is relentless. 35Harrison <strong>and</strong> colleagues identified three variables related <strong>to</strong> herpes zoster pain: extent of lesionhealing; extension of lesion crusting; <strong>and</strong> the number of new vesicles. 38 According <strong>to</strong> their study, thesignificance of baseline pain due <strong>to</strong> herpes zoster was a predic<strong>to</strong>r of return <strong>to</strong> daily life functioning.Furthermore, the significance of pain at presentation <strong>and</strong> at one month was a significant predic<strong>to</strong>rof chronic pain. 38• Toxic/nutritional NeuropathiesToxic <strong>and</strong> nutritional neuropathies in patients with <strong>HIV</strong> disease have been reported with the following:29, 33• Alcohol• Vitamin deficiencies (B 6 , B 12 )• Antiretroviral drugs: ddI (didanosine), ddC (zalcitabine), d4T (stavudine)• Anti-virals: foscarnet• PCP prophylaxis: dapsone• Anti-bacterial drugs: metronidazole• Anti-mycobacterial drugs: INH, rifampin, ethionamide• Anti-neoplastics: vincristine, vinblastineU.S. Department of Health <strong>and</strong> Human Services • Health Resources <strong>and</strong> Services Administration • <strong>HIV</strong>/<strong>AIDS</strong> Bureau 93

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