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Patient advocacy

From Wikipedia, the free encyclopedia

Patient advocacy is an area of specialization in health care concerned with advocacy for patients, survivors, and caregivers. The patient advocate may be an individual or an organization, often, though not always, concerned with one specific group of disorders. The terms patient advocate and patient advocacy can refer both to individual advocates providing services that organizations also provide, and to organizations whose functions extend to individual patients. Some patient advocates work for the institutions that are directly responsible for the patient's care.

Typical advocacy activities are the following: patient rights, matters of privacy, confidentiality or informed consent, patient representation, awareness building, support and education of patients, survivors and their carers. Patient advocates give a voice to patients, survivors and their carers on healthcare-related (public) fora, informing the public, the political and regulatory world, health-care providers (hospitals, insurers, pharmaceutical companies etc.), organizations of health-care professionals, the educational world, and the medical and pharmaceutical research communities.


Patient advocacy in the United States emerged in the 1950s in the context of cancer research and treatment.[1] In those early days of cancer treatment, patients and their families raised ethical concerns around the tests, treatment practices, and clinical research being conducted. For instance, they expressed concern to the National Institute of Health (NIH) about the cruelty of the repeated collection of blood samples (for blood marrow examination) and raised questions about whether this was more harmful than beneficial to the patient.[1] Sidney Farber, a Harvard physician and cancer researcher, coined the term "total care", to describe the treatment of children suffering from leukemia.[2] Under total care, a physician "treated the family as a whole, factoring in its psychosocial and economic needs", rather than focusing purely on physical health concerns.[2] Previous researchers had dealt with concerns raised by families, because physicians emphasized patient physical health rather than the inclusion of bedside manners with the families. The practice of practice advocacy emerged to support and represent patients in this medico-legal and ethical discussion.

The 1970s were also an important time in the USA for patient advocacy as the Patient Rights movement grew. As a major advocacy organization during the time, the National Welfare Rights Organization's (NWRO) materials for a patient's bill of rights influenced many additional organizations and writings, including hospital accreditation standards for the Joint Commission in 1970 and the American Hospital Association's Patient Bill of Rights in 1972.[3][4]  The utilisation of advocates by individual patients gained momentum in the early 2000s in the USA, and Australia 10 years later, and the profession is now perceived as a mainstream option to optimise outcomes in both hospital and community based healthcare.


Healthcare Navigation and Support

Examples of patient advocate work include:

  • Educating and walking patients through the management of their disease or chronic illnesses. The social determinants of health can vary significantly from patient to patient. It is the role of the patient advocate to cater to the patient's needs and assist with these factors, such as where to find treatment to manage their illness, assisting with healthcare access due to socioeconomic barriers, or helping find additional health services.[5] Assistance with the management of their illnesses or disease can also include assisting with cooperative purchases of health care materials.
  • Establishing a network of contacts. Examples of contacts patient advocates can assist in connecting patients to include: in the public sector (political and regulatory), in public and private health insurance, in the sector of medical service providers, with medical practitioners, and with pharmaceutical and medical research to provide patients with help in the care and management of their diseases.[6]
  • Providing emotional support in dealing with their health concerns, illnesses, chronic conditions. According to the National Institute of Mental Health, individuals with chronic illnesses are at a higher risk of depression of than patients with other mental health conditions.[7] When managing their illnesses, patients and survivors suffer from the direct effect of the consequences their disease has on their quality of life, and my also go through difficult phases of adaptation of their daily routine and lifestyle to accommodate the disease.[7] Part of the role of patient advocates can include providing emotional support for patients or connecting them to mental health resources.
  • Attending appointments with a patient. Patients can find doctor's appointments intimidating, but also difficult to understand. Issues may stem from differences in language proficiency, educational background, or background in health literacy.[8] A patient advocate's presence can ensure that patient's concerns are highlighted and adequately addressed by physicians. Patient advocates may also be responsible for assisting with scheduling additional appointments as well.
  • Assisting with health insurance and other financial aspects of healthcare. The Institute of Medicine in the United States says fragmentation of the U.S. health care delivery and financing system is a barrier to accessing care.[9] Within the financing system, health insurance plays a significant role. According to a United Health survey, only 9% of Americans surveyed understood health insurance terms, which presents a significant issue for patients, given the importance of health insurance in terms of providing access to healthcare.[10] The patient advocate may help with researching or choosing health insurance plans.

Public policy

Private advocacy

As global healthcare systems started to become more complex, and as the role of the cost of care continues to place more of a burden on patients, a new profession of private professional advocacy began to take root in the mid-2000s. At that time, two organizations were founded to support the work of these new private practitioners, professional patient advocates.[citation needed] The National Association of Healthcare Advocacy Consultants was started to provide broad support for advocacy.[11] The Alliance of Professional Health Advocates was started to support the business of being a private advocate.[12]

Proponents of private advocacy, such as Australian advocate Dorothy Kamaker, have noted that the patient advocates employed by healthcare facilities have an inherent conflict-of-interest in situations where the needs of an individual patient are at odds with the business interests of an advocate's employer. Kamaker argues that hiring a private advocate eliminates this conflict because the private advocate “…has only one master and very clear priorities.”[13]


Patient opinion leaders, also sometimes called patient advocates, are individuals who are well versed in a disease, either as patients themselves or as caretakers, and share their knowledge on the particular disease with others. Such POLs can have an influence on health care providers and may help persuade them to use evidence-based therapies or medications in the management of other patients. Identifying such people and persuading them is one goal of market access groups at pharmaceutical and medical device companies.[14]


Professional groups

Alliance of Professional Health Advocates
The Alliance of Professional Health Advocates (APHA) is an international membership organization for private, professional patient advocates, and those who are exploring the possibility of becoming private advocates. It provides business support such as legal, insurance and marketing. It also offers a public directory of member advocates called AdvoConnection.[12] Following the 2011 death of Ken Schueler — a charter member of the APHA, described as "the Father of Private Patient Advocacy" — the organization established the H. Kenneth Schueler Patient Advocacy Compass Award. The award recognizes excellence in private practice including the use of best practices, community outreach, support of the profession and professional ethics.[15]
Dialysis Patient Citizens
Dialysis Patient Citizens is a patient-led, non-profit organization dedicated to improving dialysis citizens’ quality of life by advocating for favorable public policy. One of DPC’s goals is to provide dialysis patients with the education, access and confidence to be their own advocates. Through their grassroots advocacy campaigns, Patient Ambassador program; Washington, DC patient fly-ins; conference calls and briefings, DPC works to train effective advocates for dialysis-related issues.[16] Membership is free.[17]
National Association of Healthcare Advocacy Consultants
National Association of Healthcare Advocacy Consultants (NAHAC) is a nonprofit organization located in Berkeley, California. Joanna Smith founded NAHAC on July 15, 2009 as a broad-based, grassroots organization for health care and patient advocacy. To that end, it is a multi-stakeholder organization, with membership open to the general public.[11]
National Patient Advocate Foundation
The National Patient Advocate Foundation is a non-profit organization in the United States dedicated to "...improving access to, and reimbursement for, high-quality healthcare through regulatory and legislative reform at the state and federal levels."[18] The National Patient Advocate Foundation was founded simultaneously with the non-profit Patient Advocate Foundation, "...which provides professional case management services to Americans with chronic, life-threatening and debilitating illnesses."[19]
Patient Advocates Australia
Patient Advocates Australia, founded by Dorothy Kamaker, is a support option for consumers of aged, health and disability care in Australia. For the elderly, an emerging need has arisen for patient advocacy in residential aged facilities. The Aged Care Royal Commission Report published in 2021 has made recommendations regarding a need for vigilant advocacy for residents of nursing homes to protect them against rampant abuse and neglect with one submission calling for the routine provision of independent patient advocates ( For the disabled, funding for support to overcome healthcare barriers is available through the NDIS ( The Australian Patient’s Association says “More and more, patients are realizing they can improve their medical outcomes..” and recommends the use of (independent) patient advocates (

Center for Patient Partnerships

Founded in 2000,[20] the interprofessional Center for Patient Partnerships (CPP) at University of Wisconsin–Madison offers a health advocacy certificate with a focus on either patient advocacy or system-level health policy advocacy.[21] The book chapter "Educating for Health Advocacy in Settings of Higher Education" describes CPP's pedagogy and curriculum.[22]

Government agencies

United States

In the United States, state governmental units have established ombudsmen to investigate and respond to patient complaints and to provide other consumer services.

New York
In New York, the Office of Patient Advocacy within the New York State Office of Alcoholism and Substance Abuse Services (OASAS) is responsible for protecting the rights of patients in OASAS-certified programs. The office answers questions from patients and their families; provides guidance for health care professionals on topics related to patient rights, state regulations, and treatment standards, and intervenes to resolve problems that cannot be handled within treatment programs themselves.[23]
In California, the Office of the Patient Advocate (OPA), an independent state office established in July 2000 in conjunction with the Department of Managed Health Care, is responsible for the creation and distribution of educational materials for consumers, public outreach, evaluation and ranking of health care service plans, collaboration with patient assistance programs, and policy development for government health regulation.[citation needed]

Such state government offices may also be responsible for intervening in disputes within the legal and insurance systems and in disciplinary actions against health care professionals. Some hospitals, health insurance companies, and other health care organizations also employ people specifically to assume the role of patient advocate. Within hospitals, the person may have the title of Ombudsman or Patient Representative.[citation needed]

Nursing and advocacy

The American Nurses Association (ANA) includes advocacy in its definition of nursing:

Nursing is the protection, promotion, and optimization of health and abilities, prevention of illness and injury, facilitation of healing, alleviation of suffering through the diagnosis and treatment of human response, and advocacy in the care of individuals, families, groups, communities, and populations.[24][25][26]

Advocacy in nursing finds its theoretical basis in nursing ethics. For instance, the ANA's Code of Ethics for Nurses includes language relating to patient advocacy:[27]

  1. The nurse's primary commitment is to the patient, whether an individual, family, group, or community.
  2. The nurse promotes, advocates for, and strives to protect the health, safety, and rights of the patient.

Relationship to pharmaceutical industry

Some patient advocacy groups receive donations from pharmaceutical companies. In 2015, 14 companies donated $116 million to patient advocacy groups. A database identifying more than 1,200 patient groups showed that six pharmaceutical companies contributed $1 million or more in 2015 to individual groups representing patients who use their drugs, and 594 groups in the database received donations from pharmaceutical companies. Fifteen patient groups relied on pharmaceutical companies for at least 20 percent of their revenue in the same year, and some received more than half of their revenue from pharmaceutical companies. Recipients of donations from pharmaceutical companies include the American Diabetes Association, Susan G. Komen, and the Caring Ambassadors Program.[28]

See also


  1. ^ a b "National Cancer Institute (NCI)". National Institutes of Health (NIH). 2015-07-07. Retrieved 2021-04-26.
  2. ^ a b Keating, Peter; Cambrosio, Alberto (2011). Cancer on Trial. University of Chicago Press. doi:10.7208/chicago/9780226428932.001.0001. ISBN 978-0-226-14304-0.
  3. ^ "A Journey Through the History of the Joint Commission". Retrieved 2021-04-25.
  4. ^ Rothman, David (1997). Beginnings Count. Oxford University Press. p. 23.
  5. ^ Lara, Alice Ann; Salberg, Lisa (2009). "Patient Advocacy: What Is Its Role?". Pacing and Clinical Electrophysiology. 32 (s2): S83–S85. doi:10.1111/j.1540-8159.2009.02392.x. ISSN 1540-8159. PMID 19602171. S2CID 38477053.
  6. ^ National Research Council; Woolf, S. H.; Aron, L. (2013-03-12). U.S. Health in International Perspective. 4. doi:10.17226/13497. ISBN 978-0-309-26414-3. PMID 24006554.
  7. ^ a b "Chronic Illness and Mental Health: Recognizing and Treating Depression" (PDF). National Institute of Mental Health. 2021. Retrieved 6 May 2021.
  8. ^ Aelbrecht, Karolien; Hanssens, Lise; Detollenaere, Jens; Willems, Sara; Deveugele, Myriam; Pype, Peter (2019-04-01). "Determinants of physician–patient communication: The role of language, education and ethnicity". Patient Education and Counseling. 102 (4): 776–781. doi:10.1016/j.pec.2018.11.006. ISSN 0738-3991. PMID 30527850.
  9. ^ Bruhn, John G. (2014), Understanding Health Disparities, SpringerBriefs in Public Health, Cham: Springer International Publishing, pp. 35–51, doi:10.1007/978-3-319-06462-8_2, ISBN 978-3-319-06461-1, retrieved 2021-05-15
  10. ^ "UnitedHealth survey: Most Americans don't understand basic health plan terms". Healthcare Dive. Retrieved 2021-04-24.
  11. ^ a b Smith, Joanna. "History of NAHAC". National Association of Healthcare Advocacy Consultants. Retrieved 10 October 2017.
  12. ^ a b "About APHA". The Alliance of Professional Health Advocates. Retrieved 6 July 2016.
  13. ^ Kamaker, Dorothy (26 September 2015). "Patient advocacy services ensure optimum health outcomes". Business. Sydney Morning Herald. Fairfax Media.
  14. ^ Flodgren, Gerd; O'Brien, Mary Ann; Parmelli, Elena; Grimshaw, Jeremy M. (24 June 2019). "Local opinion leaders: effects on professional practice and healthcare outcomes". The Cochrane Database of Systematic Reviews. 6: CD000125. doi:10.1002/14651858.CD000125.pub5. ISSN 1469-493X. PMC 6589938. PMID 31232458.
  15. ^ "The H. Kenneth Schueler Patient Advocacy Compass Award". The Alliance of Professional Health Advocates. Retrieved 19 February 2015.
  16. ^ "About Dialysis Patient Citizens". Dialysis Patient Citizens. Retrieved 9 December 2020.
  17. ^ "Join DPC". Dialysis Patient Citizens. Retrieved 9 December 2020.
  18. ^ "Mission Statement". National Patient Advocate Foundation. Archived from the original on 16 February 2015. Retrieved 16 February 2015.
  19. ^ "Our History & Mission". Patient Advocate Foundation. Retrieved 16 February 2015.
  20. ^ "Our History". Center for Patient Partnerships. Retrieved 10 October 2017.
  21. ^ "Adult and Returning Students: Health Advocacy Certificate Program". Center for Patient Partnerships. Retrieved 10 October 2017.
  22. ^ Hurst, Marsha; Gaines, Martha E.; Grob, Rachel N.; Weil, Laura; Davis, Sarah (2008). "Educating for Health Advocacy in Settings of Higher Learning". In Earp, Jo Anne L.; French, Elizabeth A.; Gilkey, Melissa B. (eds.). Patient Advocacy for Health Care Quality: Strategies for Achieving Patient-Centered Care. Jones and Bartlett. pp. 481–506. ISBN 978-0-7637-4961-3. OCLC 79256746.
  23. ^ "Patient Advocacy Services". Office of Alcoholism and Substance Abuse Services. New York State.
  24. ^ "What is Nursing?". American Nurses Association. Retrieved 10 October 2017.
  25. ^ American Nurses Association (2003). Nursing's Social Policy Statement (2nd ed.). Washington, DC: American Nurses Association. p. 6. ISBN 978-1-55810-214-9. OCLC 300247546.
  26. ^ American Nurses Association (2004). Nursing: Scope and Standards of Practice (1st ed.). Washington, DC: American Nurses Association. p. 7. ISBN 978-1-55810-215-6. OCLC 300966858.
  27. ^ "2001 Approved Provisions". NursingWorld. American Nurses Association, Inc. Archived from the original on 15 June 2010. Retrieved 2010-06-08.
  28. ^ "Patient Advocacy Groups Take in Millions from Drugmakers. Is There a Payback?". 6 April 2018.
This page was last edited on 29 June 2021, at 21:55
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