Is it safe? Talking to teens with HIV/AIDS about death and dying: a 3-month evaluation of Family Centered Advance Care (FACE) planning - anxiety, depression, quality of life

Maureen E Lyon, Patricia A Garvie, Linda Briggs, Jianping He, Robert Malow, Lawrence J D'Angelo, Robert McCarter, Maureen E Lyon, Patricia A Garvie, Linda Briggs, Jianping He, Robert Malow, Lawrence J D'Angelo, Robert McCarter

Abstract

Purpose: To determine the safety of engaging HIV-positive (HIV+) adolescents in a Family Centered Advance Care (FACE) planning intervention.

Patients and methods: We conducted a 2-armed, randomized controlled clinical trial in 2 hospital-based outpatient clinics from 2006-2008 with HIV+ adolescents and their surrogates (n = 76). Three 60-90 minutes sessions were conducted weekly. FACE intervention groups received: Lyon FCACP Survey(©), the Respecting Choices(®) interview, and completion of The Five Wishes(©). The Healthy Living Control (HLC) received: Developmental History, Healthy Tips, Future Planning (vocational, school or vocational rehabilitation). Three-month post-intervention outcomes were: completion of advance directive (Five Wishes(©)); psychological adjustment (Beck Depression, Anxiety Inventories); quality of life (PedsQL(™)); and HIV symptoms (General Health Self-Assessment).

Results: Adolescents had a mean age, 16 years; 40% male; 92% African-American; 68% with perinatally acquired HIV, 29% had AIDS diagnosis. FACE participants completed advance directives more than controls, using time matched comparison (P < 0.001). Neither anxiety, nor depression, increased at clinically or statistically significant levels post-intervention. FACE adolescents maintained quality of life. FACE families perceived their adolescents as worsening in their school (P = 0.018) and emotional (P = 0.029) quality of life at 3 months, compared with controls.

Conclusions: Participating in advance care planning did not unduly distress HIV+ adolescents.

Keywords: HIV/AIDS; adolescents; advance care planning; communication; decision-making; family intervention.

Figures

Figure 1
Figure 1
Transactonal model of coping with stress. Notes: Proximal program mediators are shown in shaded areas. Plans and Actions = statement of treatment preferences and completion of Five Wishes© advance directive. Psychological Adjustment = Symptoms of depressed or anxious mood as measured by the Beck Depression Inventory II or the Beck Anxiety Inventory. Quality of Life = Total, School, Emotion, Physical and Social quality of life as measured by PedsQL™; HIV Specific Symptoms as measured by the General Health Assessment for Children. Abbreviations: A, adolescent; F, family; FACE, Family Centered Advance Care.
Figure 2
Figure 2
Flow of participants through each stage of the trial. Notes: *Kept in analysis, per intent-to-treat design, as if received allocated condition; **n = 1 randomized intervention adolescent became psychotic & ineligible before Session 1; ***n = 1 randomized adolescent control was shot & withdrew from study before Session 1.

References

    1. Justice AC, McGinnis KA, Skanderson M, et al. Towards a combined prognostic index for survival in HIV infection: the role of ‘no-HIV’ biomarkers. HIV Med. 2009;11(2):143–151.
    1. McConnell MS, Byers RH, Frederick T, et al. Trends in antiretroviral therapy use and survival rates for a large cohort of HIV-infected children and adolescents in the United States, 1989–2001. Epidemiology and Social Science. 2005;38(4):488–494.
    1. America’s Children in Brief. Key National Indicators of Well-Being. 2008. Available at: .
    1. Brady MT, Oleske JM, Williams PL, et al. Declines in mortality and changes in causes of death in HIV-1 infected children during the HAART era. J Acquir Immune Defic Syndr. 2010;(5391):86–94.
    1. Hansen L, Archbold PG, Stewart BJ. Role strain and ease in decision-making to withdraw or withhold life support for elderly relatives. J Nurs Scholarsh. 2004;36(3):233–238.
    1. Grady PA. Introduction: Papers from the National Institutes of Health State-of-the-Science Conference on improving end-of-life care. J Palliative Med. 2005;8(Suppl 1):S1–S3.
    1. Bearison D. They Never Want to Tell You. Cambridge, MA: Harvard Univ Press; 1991.
    1. Bluebond-Langner M. Private Worlds of Dying Children. Princeton, NJ: Princeton University Press; 1978.
    1. Hinds PS, Burghen EA, Pritchard M. Conducting end-of-life studies in pediatric oncology. West J Nurs Res. 2007;29:448–465.
    1. Hinds PS, Schum L, Baker JN, Wolfe J. Key factors affecting dying children and their families. J Palliat Med. 2006;8:S70–S78.
    1. Field MJ, Behrman RE, editors. When Children Die: Improving palliative and end-of-life care for children and their families. Washington, DC: Institute of Medicine, National Academy Press; 2002.
    1. Walsh-Kelly CM, Lang KR, Chevako J, et al. Advance directives in a pediatric emergency department. Pediatrics. 1999;103:826–830.
    1. Lyon ME, McCabe MA, Patel K, D’Angelo LJ. What do adolescents want? An exploratory study regarding end-of-life decision-making. J Adolesc Health. 2004;35(6):529 e1–e6.
    1. American Academy of Pediatrics: Committee on Bioethics and Committee on Hospital Care. Palliative care for children. Pediatrics. 2000;106:351–357.
    1. Kane JR. Pediatric palliative care moving forward: Empathy, competence, quality, and the need for systematic change. J Palliat Med. 2006;9:847–849.
    1. Bogart LM, Uyeda K. Community-based participatory research: Partnering with communities for effective and sustainable behavioral health interventions. Health Psychol. 2009;28(4):391–393.
    1. Lyon ME, Garvie PA, Briggs L, He J, D’Angelo L, McCarter R. Development, feasibility and acceptability of the Family-Centered (FACE) Advance Care planning intervention for adolescents with HIV. J Palliat Med. 2009;12(4):363–372.
    1. Lyon ME, Garvie PA, McCarter R, Briggs L, He J, D’Angelo L. Who will speak for me? Improving end-of-life decision-making for adolescents with HIV and their families. Pediatrics. 2009;123(2):e199–e206.
    1. Leventhal HH, Nerenz DR, Steele DJ. Illness representations and coping with health threats. In: Baum A, Taylor SE, Singer JE, editors. Handbook of Psychology and Health, Vol. IV: Social psychological aspects of health. A New Jersey: Laurence Erlbaum Associates, Inc; 1984. pp. 219–252.
    1. Leventhal H, Diefenbach M. The active side of illness cognition. In: Skelton JA, Croyle RT, editors. Mental Representation in Health and Illness. New York, NY: Springer Verlag; 1991. pp. 247–272.
    1. Leventhal H, Benyamini Y, Shafer C. Lay beliefs about health and illness. In: Ayers S, editor. Cambridge Handbook of Psychology, Health and Medicine. Cambridge, MA: Cambridge University Press; 2007. pp. 124–128.
    1. Lazarus RS, Folkman S. Appraisal, and Coping. New York, NY: Springer Publishing Company; 1984.
    1. Power C, Selnes OA, Grim JA, McArthur JC. HIV Dementia Scale: a rapid screening test. J Acquir Immune Defic Syndr Hum Retrovirol. 1995;8:273–278.
    1. Beck AT, Steer RA. Beck Anxiety Inventory Manual. San Antonio, TX: The Psychological Corporation, Harcourt Brace & Company; 1993.
    1. Beck AT, Steer RA, Brown GK. Beck Depression Inventory Manual. 2nd edition. San Antonio, TX: The Psychological Corporation, Harcourt Brace & Company; 1996.
    1. King CA, Katz SH, Ghaziuddin N, Brand E, Hill E, McGovern L. Diagnosis and assessment of depression and suicidality using the NIMH Diagnostic Interview Scale for Children-DISC-2.3-National Institute of Mental Health. J Abnormal Child Psych. 1997;25(3):173–181.
    1. Barkley RA. Attention-Deficit Hyperactivity Disorder: A clinical workbook. New York, NY: The Guilford Press; 1993.
    1. American Academy of Pediatrics. Bright Futures. 2005. [Accessed January 10, 2010]. Available from: .
    1. Wolf-Branigin M, Schuyler V, White P. Improving quality of life and career attitudes of youth with disabilities: Experiences from the Adolescent Employment Readiness Center. Res Soc Work Prac. 2007;17:324–334.
    1. Wiener L, Ballard E, Brennan T, Battles H, Martinez P, Pao M. How I wish to be remembered: the use of an advance care planning document in adolescent and young adult populations. J Palliat Med. 2008;11:1309–1313.
    1. Hammes BJ, Briggs L. Includes Statement of Treatment Preferences. La Crosse, WI: Gundersen Lutheran Medical Foundation; 2000. Respecting choices: advance care planning facilitator manual.
    1. Watcher RM, Lo B. Advance directives for patients with Human Immunodeficiency Virus infection. Crit Care Clin. 1993;9:125–135.
    1. Varni JW, Seid M, Rode CA. The PEDSQL: measurement model for the pediatric quality of life inventory. Med Care. 1999;37:126–139.
    1. Varni JW, Seid M, Kurtin PS. PedsQL 4.0: reliability and validity of the Pediatric Quality of Life Inventory version 4.0 generic core scales in healthy and patient populations. Med Care. 2001;39:800–812.
    1. Varni JW, Burwinkle TM, Seid M, Skarr D. The PedsQLTM 4.0 as a pediatric population health measure: Feasibility, reliability, and validity. Ambul Pediatr. 2003;3:329–341.
    1. Gortmaker SL, Lenderking WR, Clark C, et al. Development and Use of a Pediatric Quality of Life Questionnaire in AIDS Clinical Trials: Reliability and Validity of the General Health Assessment for Children. In: Drotar D, editor. Measuring Health-Related Quality of Life in Children and Adolescents: Implications for Research and Practice. Mahway, NJ: Lawrence Erlbaum Associates; 1998. pp. 219–235.
    1. Centers for Disease Control and Prevention. 1993 revised classification system for HIV infection and expanded surveillance case definition for AIDS among adolescents and adults. MMWR: Recomm Rep. 1992;41:1–17.
    1. Morrison RS, Zayas LH, Mulvihill M, Baskin SA, Meier DE. Barriers to completion of health care proxies: An examination of ethnic differences. Arch Intern Med. 1998;158:2493–2497.
    1. Blackhall LJ, Frank G, Murphy ST, Michel V, Palmer JM, Azen SP. Ethnicity and attitudes towards life sustaining technology. Soc Sci Med. 1999;48:1779–1789.
    1. Kiely DK, Mitchell SL, Marlow A, Murphy KM, Morris JN. Racial and state differences in the designation of advance directives in nursing home residents. J Am Geriatr Soc. 2001;49:1346–1352.
    1. Degenholtz HB, Arnold RA, Meisel A, Lave JR. Persistence of racial disparities in advance care plan documents among nursing home residents. J Am Geriatr Soc. 2002;50:378–381.
    1. Degenholtz HB, Thomas SB, Miller MJ. Race and the intensive care unit: Disparities in preferences for end-of-life care. Crit Care Med. 2003;31(5 Suppl):S373–S378.
    1. Smith DB. Health Care Divided: Race and Healing a Nation. Ann Arbor, MI: The University of Michigan Press; 2002. pp. 24–27.
    1. Phillips RS, Hamel MB, Teno JM, et al. Patient race and decisions to withhold or withdraw life-sustaining treatments for seriously ill hospitalized adults. SUPPORT Investigators. Study to Understand Prognoses and Preferences for Outcomes and Risks of Treatment. Am J Med. 2000;108:14–19.
    1. Krakauer EL, Crenner C, Fox K. Barriers to optimum end-of-life care for minority patients. J AM Geriatr Soc. 2002;50(1):182–190.
    1. Crawley LM. Racial, cultural and ethnic factors influencing end-of-life care. J Palliative Med. 2005;8:S58–S69.
    1. Lyon ME, Williams PL, Woods ER, et al. Do not resuscitate orders and/or hospice care, psychological health and quality of life among children/adolescents with AIDS. J Palliative Med. 2008;11:459–469.
    1. Washington R. Press Release: Study by former DC Commissioner of mental health finds hospice care benefits black families. Montgomery Hospice. Jun 24, 2004. [Accessed January 10, 2010]. Available from: . [June 24, 2004]
    1. Allison S, Wolters PL, Brouwers P. Youth with HIV/AIDS: Neurobehavioral consequences. In: Paul RH, Sachtor NC, Valcour V, Tashima KT, editors. HIV and the Brain. Totowa, NJ: Current Clinical Neurology, Humana Press; 2009. pp. 187–211.
    1. Lyon ME, McCarter R, D’Angelo L. Detecting HIV associated neurocognitive disorders in adolescents: what is the best screening tool? J Adolesc Health. 2009;44(2):133–135.
    1. Wood SM, Shah SS, Steenhoff AP, Rutstein RM. The impact of AIDS diagnoses on long-term neurocognitive and psychiatric outcomes of surviving adolescents with perinatally acquired HIV. AIDS. 2009;23(14):1859–1865.
    1. Lautrette A, Darmon M, Megarbane B, et al. A communication strategy and brochure for relatives of dying patients in the ICU. N Engl J Med. 2007;356(5):469–478.
    1. Lilly CM, DeMeo DL, Sonna LA, et al. An intensive communication intervention for the critically ill. Am J Med. 2000;109(6):469–475.
    1. Lilly CM, Sonna LA, Haley KJ, Massaro AF. Intensive communication: four-year follow-up from a clinical practice study. Crit Care Med. 2003;31(5):S394–S399.
    1. Romer AL, Hammes BJ. Comunication, trust, and making choices: advance care planning four years on. J Palliat Med. 2004;7:35–40.
    1. Tulsky JA. Beyond advance directives: importance of communication skills at the end of life. JAMA. 2005;294(3):395–365.
    1. Tulsky JA. Interventions to enhance communication among patients, providers, and families. J Palliat Med. 2005;8:S95–S102.
    1. AARP. AARP North Carolina End of Life Care Survey: African American Members. Report prepared by Rachelle Cummins, MA. 2003. [Accessed on January 10, 2010]. Available from:
    1. Haas JS, Weissman JS, Cleary PD, et al. Discussion of preferences for life-sustaining care by persons with AIDS. Arch Intern Med. 1993;153:1241–1248.
    1. Emanuel EJ, Fairclough DL, Emanuel L. Attitudes and desires related to euthanasia and physician-assisted suicide among terminally ill patients and their caregivers. JAMA. 2000;284:2460–2468.
    1. Thompson BL, Lawson D, Croughan-Minihane M, Cooke M. Do patients’ ethnic and social factors influence the use of do-not-resuscitate orders? Ethn Dis. 1999;9:132–139.
    1. Baker JN, Rai S, Lui W, et al. Race does not influence Do-Not-Resuscitate Status or the number or timing of End-of-Life discussions at a pediatric oncology referral center. J Palliat Med. 2009;12(1):71–76.
    1. Bakitas M, Lyons KD, Hegel MT, et al. Effects of a palliative care intervention on clinical outcomes in patients with advanced cancer: the Project ENABLE II randomized controlled trial. JAMA. 2009;302:746–749.
    1. Davies B, Reimer JC, Brown P, Martens N. Challenges of conducting research in palliative care. Omega (Westport) 1995;31:263–273.
    1. Hudson P, Aranda S, McMurray N. Randomized controlled trials in palliative care: overcoming the obstacles. Int J Palliat Nurs. 2001;7:427–434.
    1. McMillan SC, Weitzner MA. Methodologic issues in collecting data from debilitated patients with cancer near the end of life. Oncol Nurs Forum. 2003;30:123–126.
    1. Kirchhoff KT, Kehl KA. Recruiting participants in end-of-life research. Am J Hosp Palliat Care. 2008;24:515–521.
    1. Ingram BL, Flannery D, Elkavich A, Rotheram-Borus MJ. Common processes in evidence-based adolescent HIV prevention. Aids Behav. 2008;12:374–383.
    1. Malow RM, Kershaw T, Sipsma H, Rosenberg R, Devieux JG. HIV preventive interventions for adolescents: A look back and ahead. Curr HIV/AIDS Rep. 2007;4:173–180.
    1. Tevendale HD, Lightfoot M. Programs that work: Prevention for positives. In: Lyon ME, D’Angelo LJ, editors. Teenagers HIV and AIDS: Insights from youths living with the virus. Westport, CT: Praeger Publishers; 2006. pp. 105–126.
    1. Lyon ME, Woodward K. Nonstigmatizing ways to engage HIV-positive African-American teens in mental health and supportive services: A commentary. J Natl Med Assoc. 2003;95:196–200.
    1. US Department of Health and Human Services. Call To Action: Eliminating racial and ethnic disparities in health. Washington, DC: Grantmakers in Health; 1998.
    1. Dickens DS. Building competence in pediatric end-of-life care. J Palliative Med. 2009;12(7):617–622.

Source: PubMed

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