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506  n  TERMINAL ILLNESS



           applications  involving  human  touch  have   cure. Furthermore, unlike hospice or end-of-
           occurred using robotic technology (DeKastle,   life care, palliative medicine is recognized as
   T       2009; Eckberg, 1998; peck, 1992). The ability   a medical specialty. As such, the likelihood
           to touch patients, change dressings, perform   that  this  service  will  be  incorporated  into
           wound care, or hug an elderly patient remain   treatment is enhanced.
           a distant possibility.                       Research in the area of terminal illness
              Telepresence  is  a  new  and  challenging   has focused on the individual (patient needs,
           aspect being added to the nursing practice.   symptom  management,  and  holistic  care),
           Nurses  are  expected  to  take  an  active  role,   family  needs  (meaning-making,  empower-
           embrace this technology, and work to max-  ment, anticipatory grief, managing time, and
           imize its potential for patient care.    the impact of terminal illness on the family),
                                                    and system issues (adequacy of care, ethical
                                      Josette Jones  issues, impact of ethnicity on care, terminally
                                                    ill patients and research, transfer to hospice
                                                    and  palliative  are,  and  incarcerated  termi-
                                                    nally ill patients).
                   Terminal illness                     A  continuing  question  in  the  care  of
                                                    those  with  a  terminal  illness  is  the  role  of
                                                    food and hydration. For relatives and signif-
           What is a terminal illness? The term gener-  icant others, food has a symbolic value, con-
           ally is applied to a person with a degenerative   noting nurturing and life and the hope that
           process  rather  than  an  episode  engendered   death will be forestalled. “What if my loved
           by trauma sustained as a result of some exter-  one stops eating/Will my loved one starve”
           nal force. “A person may be regarded as hav-  was one of a number of questions that fam-
           ing a terminal illness when broad agreement   ily caregivers wanted to discuss with health
           has been reached among health professionals   care professionals in a study of 33 current and
           that there is no longer the possibility of cure   bereaved health caregivers (Herbert, Schulz,
           and that life-expectancy is limited” (Hughes   Copeland, & Arnold, 2008). Nurses in Taiwan
           & Neal, 2000, p. 4).                     also were influenced by the cultural maxim
              “When  is  an  illness  terminal?”  is  still   of “food comes first for people” and thus con-
           a question that both providers and patients   sidered artificial nutrition and hydration as
           may  be  reluctant  to  discuss.  The  emphasis   basic care for terminally ill persons (Ke, Chui,
           on curative treatment, no matter the dimin-  Lo, & Hu, 2008). plonk and Arnold (2005) dis-
           ishing chances for prolonged life, abets the   aggregate  nutrition  and  hydration,  noting
           reluctance  to  label  a  condition  as  terminal.   that the consensus is that the former is not
           Failure to do so, however, may result in dying   beneficial to dying persons whereas the lat-
           persons not having the time to attend to the   ter is controversial. Also controversial is the
           tasks  they  would  wish  to,  were  the  reality   use of palliative sedation when other means
           of their condition openly shared (gawande,   of pain relief are ineffective to relieve intrac-
           2010). Interestingly, nurses were more likely to   table  suffering  (De  graeff  &  Dean,  2007).
           be willing to disclose “bad” news to patients   Although the previous studies focus on the
           than were physicians (Ben Natan, Shahar, &   needs of the dying person, the needs of the
           garfunkel, 2009). At the same time, with the   families of those who are terminally ill also
           new emphasis on palliative care at the diag-  have been of concern to health care practitio-
           nosis of a life-threatening illness, the poten-  ners and of interest to researchers.
           tial  for  such  discussions  may  be  enhanced.   The quality of life of the informal care-
           And unlike hospice care, there is no require-  giver  is  predicted  by  their  physical  health
           ment to forego aggressive treatment aimed at   and  spirituality (Tang,  2009).  Consequently,
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