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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 3: Assessment of Physical Symp<strong>to</strong>ms• Studies of caregivers have found that caregivers are commonly inaccuratewhen reporting on subjective aspects of the patient experience. 21,2226 picasThis includes, <strong>for</strong> example, symp<strong>to</strong>ms such as pain <strong>and</strong> depression.A tendency has been demonstrated <strong>for</strong> caregivers <strong>to</strong> be more accuratewhen reporting on objective measures, such as the patient’s ability <strong>to</strong>dress independently. Of note, this is not <strong>to</strong> imply that caregiver reportsshould be neglected as they can provide vital insights in<strong>to</strong> the patientexperience, especially over time.• Objective signs can be usefully moni<strong>to</strong>red <strong>to</strong> complement subjective data, butthis in<strong>for</strong>mation cannot substitute <strong>for</strong> self-report.For example, nausea assessment should involve a subjective rating by thepatient <strong>and</strong> may be supplemented by assessment of the frequency of emesis.• In some groups of patients, such as cognitively impaired adults or preverbalchildren, it may be impossible <strong>to</strong> obtain or interpret patient self-reports.<strong>The</strong>se populations need special care <strong>and</strong> attention. When such patients areencountered, reports from family members <strong>and</strong> staff may be the only usefulproxies <strong>and</strong> the in<strong>for</strong>mation obtained from these sources should be combinedwith a physical assessment of the patient so that the clinician can fully assessthe situation. Although proxy data should be interpreted with caution, theobservations of a caregiver who knows the patient well or is a highly skillednurse should certainly be considered as important insights in<strong>to</strong>, or indica<strong>to</strong>rsof, patient distress.Symp<strong>to</strong>ms Are Multidimensional ExperiencesSymp<strong>to</strong>ms are multidimensional experiences that may be evaluated in terms of their specificcharacteristics <strong>and</strong> impact. 6, 25-28 Symp<strong>to</strong>m multidimensionality is portrayed in Table 3-3. 16, 17 It isnot uncommon <strong>for</strong> researchers or clinicians <strong>to</strong> describe a symp<strong>to</strong>m simply by stating that it ispresent. Although prevalence data alone may be useful in<strong>for</strong>mation, a more detailed assessmen<strong>to</strong>f the characteristics of specific symp<strong>to</strong>ms is usually more helpful, especially in the clinicalsetting.Significant variability has been demonstrated in relation <strong>to</strong> symp<strong>to</strong>m characteristics. 6, 25-28 Threecrucial variable dimensions are frequency, severity <strong>and</strong> distress. Although symp<strong>to</strong>m characteristicsare often variable, the proportion of patients who describe a symp<strong>to</strong>m as relatively intenseor frequent usually exceeds the proportion describing it as highly distressing. 28, 29 <strong>The</strong> frequencydimension does not apply <strong>to</strong> some symp<strong>to</strong>ms, <strong>for</strong> example, constipation.44U.S. Department of Health <strong>and</strong> Human Services • Health Resources <strong>and</strong> Services Administration • <strong>HIV</strong>/<strong>AIDS</strong> Bureau

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