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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 2: Overview of <strong>Clinical</strong> IssuesIn addition, even prior <strong>to</strong> the end of life, providers need <strong>to</strong> develop a keen awareness of theirown feelings regarding patient choices. Providers may actually feel anger at patients over failure<strong>to</strong> adhere <strong>to</strong> antiretroviral therapy or <strong>for</strong> active substance abuse <strong>and</strong> other self-destructivebehaviors. 26 picas Re-examining the goals of care, involving the interdisciplinary team, <strong>and</strong> continuing<strong>to</strong> engage <strong>and</strong> provide follow-up <strong>for</strong> patients—without judging their choices or inability <strong>to</strong> adherewith recommended therapy—will help <strong>to</strong> maintain <strong>and</strong> enhance the clinical relationship.<strong>The</strong> fact that the new generation of <strong>HIV</strong> caregivers has not had the experience of their earliercolleagues—in which there was no avoidance of death <strong>and</strong> no immediate prospect of <strong>for</strong>estallingit with disease-specific therapy—may also be a contributing fac<strong>to</strong>r in the difficulty that providersexperience in addressing end-of-life issues. While we would hope that the experience of theearly years of the <strong>AIDS</strong> epidemic will never have <strong>to</strong> be repeated, we can also hope <strong>to</strong> retain thelessons that it brought regarding the importance of accompanying patients through illness untildeath, of not seeing death as an au<strong>to</strong>matic failure of the clinician, of appreciating the profoundimportance of ‘being there,’ <strong>and</strong> of underst<strong>and</strong>ing the role of the caregiver as ‘caring’ <strong>and</strong> notnecessarily ‘curing.’ 58 As outlined above regarding palliative <strong>and</strong> disease-specific therapy, thestrategy should not be ‘either-or,’ but rather ‘both-<strong>and</strong>,’ <strong>and</strong> providers need <strong>to</strong> be as skilled <strong>and</strong>competent in anticipating <strong>and</strong> addressing the end-of-life issues as they are in interpretingsurrogate marker test results <strong>and</strong> recommending effective combination anti-retroviral treatmentregimens.Another area in which caregivers can have an invaluable impact is in the support <strong>and</strong> educationof families as patients move through the last stages of their illness, especially <strong>for</strong> patients whoremain at home. Ongoing visits by nursing <strong>and</strong> other staff, either at home or in an institutionalsetting, can be extremely helpful in addressing concrete concerns <strong>and</strong> questions about prognosis;the expected changes that occur <strong>to</strong>ward the end of life; <strong>and</strong> some of the physical, emotional, <strong>and</strong>spiritual issues that families can expect. It may be helpful <strong>to</strong> describe these events in terms ofthe estimated prognostic timeframe covering the last months, weeks, <strong>and</strong> days of life, along withthe responses that families may consider <strong>to</strong> help their loved ones through this process. Table 2-6 describes the guidance that the clinician can provide caregivers as the patient moves throughthe last stages of illness. As with other aspects of palliative care, a team approach <strong>and</strong> sustained,consistent interaction over time are key elements in a successful therapeutic relationship.In addition <strong>to</strong> the myriad psychosocial issues outlined above, <strong>and</strong> the more clinical psychiatricissues dealt with in more detail in Chapter 10 (Psychiatric Problems), two other importantpsychosocial themes are (1) multiple loss <strong>and</strong> (2) grief <strong>and</strong> bereavement. While the phenomenonof multiple loss 59 in the <strong>AIDS</strong> epidemic has long been identified <strong>for</strong> patients, providers, <strong>and</strong>communities, this is compounded in the current era because of the long-term relationships thathave been built up over years of patient-provider interaction. Even though the absolute numberof deaths may be declining, the impact of each loss may be as great or greater. This can result ina cumulative burden of grief that can begin <strong>to</strong> have deleterious effects on providers over time. Itis important <strong>to</strong> recognize, anticipate, <strong>and</strong> respond <strong>to</strong> these effects, <strong>and</strong> <strong>to</strong> appreciate that ‘emotionalhealth-maintenance’ <strong>and</strong> self-care are not signs of wasteful self-indulgence but ratherimportant aspects of maintaining our perspective <strong>and</strong> effectiveness as <strong>HIV</strong> care providers.Grief both anticipates the loss <strong>and</strong> follows the loss, with reverberations in<strong>to</strong> the future <strong>for</strong> allthose who have been affected. With the current chronic disease-type trajec<strong>to</strong>ry typical of <strong>HIV</strong>infection (see Figure 2-2), with many exacerbations <strong>and</strong> remissions in the declining stages,28U.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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