A Journey to Hospice: Reflecting on One Patient’s Barriers to Service

2021 ◽  
Vol 17 (4) ◽  
pp. 246-249
Author(s):  
Kimberly E. Giamportone
Keyword(s):  
2014 ◽  
Vol 23 (1) ◽  
pp. 42-54 ◽  
Author(s):  
Tanya Rose Curtis

As the field of telepractice grows, perceived barriers to service delivery must be anticipated and addressed in order to provide appropriate service delivery to individuals who will benefit from this model. When applying telepractice to the field of AAC, additional barriers are encountered when clients with complex communication needs are unable to speak, often present with severe quadriplegia and are unable to position themselves or access the computer independently, and/or may have cognitive impairments and limited computer experience. Some access methods, such as eye gaze, can also present technological challenges in the telepractice environment. These barriers can be overcome, and telepractice is not only practical and effective, but often a preferred means of service delivery for persons with complex communication needs.


2015 ◽  
Author(s):  
Jeffry L. Moe ◽  
Narketta M. Sparkman
Keyword(s):  

2019 ◽  
pp. 1-18 ◽  
Author(s):  
Hannah Jelley ◽  
Liselot Kerpershoek ◽  
Frans Verhey ◽  
Claire Wolfs ◽  
Marjolein de Vugt ◽  
...  

AbstractTimely access to care services is crucial to support people with dementia and their family carers to live well. Carers of people with dementia (N = 390), recruited from eight countries, completed semi-structured interviews about their experiences of either accessing or not using formal care services over a 12-month period in the Access to Timely Formal Care (Actifcare) study. Participant responses were summarised using content analysis, categorised into clusters and frequencies were calculated. Less than half of the participants (42.3%) reported service use. Of those using services, 72.8 per cent reported timely access and of those not using services 67.2 per cent were satisfied with this situation. However, substantial minorities either reported access at the wrong time (27.2%), or feeling dissatisfied or mixed feelings about not accessing services (32.8%). Reasons for not using services included use not necessary yet, the carer provided support or refusal. Reasons given for using services included changes in the condition of the person with dementia, the service's ability to meet individual needs, not coping or the opportunity to access services arose. Facilitators and barriers to service use included whether participants experienced supportive professionals, the speed of the process, whether the general practitioner was helpful, participant's own proactive attitude and the quality of information received. To achieve timely support, simplified pathways to use of formal care services are needed.


Author(s):  
Carmen Ortiz Hendricks

Latinos are a heterogeneous and highly complex population that presents the profession with one of the greatest challenges in understanding diversity and what constitutes culturally and linguistically competent social work interventions. At this point in history, Latinos are the fastest growing racial and ethnic group in the United States. This has given rise to strong anti‐immigration sentiment, English only legislation, and increased discrimination and racism, which Latino newcomers must contend with upon arrival in the United States. Social workers need to work to reduce both external and internal institutional barriers to service delivery for Latinos while responding effectively to their interpersonal and familial needs.


2000 ◽  
Vol 23 (4) ◽  
pp. 134 ◽  
Author(s):  
Jane Lloyd ◽  
Gawaine Powell Davies ◽  
Mark Harris

The aim of the study reported here was to evaluate current initiatives in GP-hospital integration and highlight areaswhere further research, development and evaluation are required. Seven pre-existing GP-hospital programs wereselected and given supplementary funding to allow for more effective evaluation. These local evaluations were thenincorporated into a national program on GP-hospital collaboration.We found that the seven projects made substantial progress towards their goals, and in the process highlighted importantaspects of successful collaboration. The collective evaluation of DHIP identified expected benefits of collaboration forpatients (improved access to services, reduced anxiety, and fewer post discharge complications), for GPs (increasedinvolvement in acute care and in hospital decision making), and for service organisations (stronger workingrelationships, increased capacity, and greater efficiency). Barriers to service integration were also identified, includingthe different cultures of Divisions and hospitals, their lack of internal coherence and the Commonwealth-state divide.The evaluation showed that much has been achieved in building the relationships and the capacity needed for GP-hospitalcollaboration, and that effective models exist. The current challenge is to extend successful models acrosshealth areas and make effective collaboration part of the normal system of care. Substantial progress towardsintegrated care relies on a shift from a focus on systems within general practice or hospital environments to a patientcentred approach. This will require general practice, hospitals, community services and consumer organisations toform long term partnerships and move beyond their currently disjointed view of acute and community care. Thedevelopment of practical indicators for integrated care will support the process and facilitate shared learning acrossCommonwealth and state divides.


1998 ◽  
Vol 13 (3) ◽  
pp. 191-200 ◽  
Author(s):  
Leyland Pitt ◽  
Pierre Berthon ◽  
Nikala Lane

While the external measurement of service quality, and even the measurement of the expectations and perceptions of internal customers, is well established in the services literature, less attention has been given to the assessment of the ‘gaps’ which cause the customer discrepancy. This paper describes a study which ascertained internal gaps (‘1 through 4') in a large information systems department within a major consulting and accounting firm.


Author(s):  
Alida J. van der Ham ◽  
Laura S. Shields ◽  
Roddy van der Horst ◽  
Jacqueline E. W. Broerse ◽  
Maurits W. van Tulder

1994 ◽  
Vol 25 (1) ◽  
pp. 36-42 ◽  
Author(s):  
Lee Ann Watson-Armstrong ◽  
Barbara O'Rourke ◽  
John Schatzlein

While persons with disabilities face an increased risk of sexual abuse (Sobsey & Varnhagen, 1991), awareness of the severity of the problem is still lacking among most health care professionals, including rehabilitation practitioners. The purpose of this paper is to increase awareness of the issues evolving around sexual abuse and persons with disabilities by addressing the following; the prevalence of sexual abuse, including case examples; the increased vulnerability of persons with disabilities; sexual abuse reporting; barriers to service or sexual abuse treatment; and social and cultural issues. Recommendations for addressing sexual abuse issues within the counseling relationship are provided, as are resources for additional information concerning sexual abuse among persons with disabilities.


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