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Journal articles on the topic 'Chronic illness'

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Published: 4 June 2021
Last updated: 11 March 2023

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1

Jonsdottir, Helga. "Chronic illness." Scandinavian Journal of Caring Sciences 15, no. 1 (March 2001): 1–2. http://dx.doi.org/10.1046/j.1471-6712.2001.1510001.x.

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2

Khan, Nadim A., and Constance U. Battle. "Chronic Illness." Topics in Early Childhood Special Education 6, no. 4 (January 1987): 25–32. http://dx.doi.org/10.1177/027112148700600404.

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3

Kunde, Sachin, Mark Riederer, and Kathleen Moltz. "Chronic Illness." Clinical Pediatrics 47, no. 5 (December 5, 2007): 514–16. http://dx.doi.org/10.1177/0009922807311739.

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4

&NA;, &NA;. "CHRONIC ILLNESS." Journal of Developmental & Behavioral Pediatrics 11, no. 1 (February 1990): 41. http://dx.doi.org/10.1097/00004703-199002000-00016.

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5

&NA;. "CHRONIC ILLNESS." Journal of Developmental & Behavioral Pediatrics 13, no. 2 (April 1992): 143. http://dx.doi.org/10.1097/00004703-199204000-00024.

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6

&NA;. "CHRONIC ILLNESS." Journal of Developmental & Behavioral Pediatrics 13, no. 6 (December 1992): 436. http://dx.doi.org/10.1097/00004703-199212000-00019.

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7

SMITH, JEAN C., WILLIAM L. COLEMAN, CATHERINE L. GRUS, and ADRIAN D. SANDLER. "CHRONIC ILLNESS." Journal of Developmental & Behavioral Pediatrics 17, no. 1 (February 1996): 64–65. http://dx.doi.org/10.1097/00004703-199602000-00019.

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8

SK, Campbell, Gardner HG, and V. Ramakrishnan. "CHRONIC ILLNESS." Journal of Developmental & Behavioral Pediatrics 17, no. 4 (August 1996): 284. http://dx.doi.org/10.1097/00004703-199608000-00020.

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9

SMITH, JEAN C., WILLIAM L. COLEMAN, CATHERINE L. GRUS, and ADRIAN D. SANDLER. "CHRONIC ILLNESS." Journal of Developmental & Behavioral Pediatrics 17, no. 6 (December 1996): 436. http://dx.doi.org/10.1097/00004703-199612000-00020.

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10

&NA;, &NA;. "CHRONIC ILLNESS." Journal of Developmental & Behavioral Pediatrics 18, no. 1 (February 1997): 65–66. http://dx.doi.org/10.1097/00004703-199702000-00021.

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11

&NA;, &NA;. "CHRONIC ILLNESS." Journal of Developmental & Behavioral Pediatrics 18, no. 5 (October 1997): 356–57. http://dx.doi.org/10.1097/00004703-199710000-00019.

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12

&NA;, &NA;. "CHRONIC ILLNESS." Journal of Developmental & Behavioral Pediatrics 18, no. 6 (December 1997): 431. http://dx.doi.org/10.1097/00004703-199712000-00018.

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13

MorofLubkin, Ilene. "Chronic Illness." AJN, American Journal of Nursing 87, no. 7 (July 1987): 987–90. http://dx.doi.org/10.1097/00000446-198707000-00043.

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14

Joyce, Robert C. "Chronic Illness." Topics in Geriatric Rehabilitation 7, no. 2 (December 1991): 76. http://dx.doi.org/10.1097/00013614-199112000-00010.

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15

Wolff, Jennifer L. "Chronic Illness." JAMA 295, no. 16 (April 26, 2006): 1947. http://dx.doi.org/10.1001/jama.295.16.1951.

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16

Day, Ally. "Chronic Poetics, Chronic Illness." Journal of Literary & Cultural Disability Studies 11, no. 1 (February 2017): 83–98. http://dx.doi.org/10.3828/jlcds.2017.6.

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17

Abrams, Sarah E. "Chronic Illness: "Chronic" Boredom." Public Health Nursing 20, no. 4 (July 2003): 250–51. http://dx.doi.org/10.1046/j.1525-1446.2003.20401.x.

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18

Hash, Joanne, Susan Bodnar-Deren, Elaine Leventhal, and Howard Leventhal. "Chronic Illness with Complexity." OMEGA - Journal of Death and Dying 77, no. 4 (November 22, 2016): 364–85. http://dx.doi.org/10.1177/0030222816675250.

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The present study examines how different chronic illnesses and mental illness comorbidity (chronic illness with complexity [CIC]) associate with components of advance care planning (ACP). We also explore the role self-perceived burden plays in the relationship between illness and ACP. Data were gathered from a cross-sectional survey of 305 elderly participants from the New Jersey End-of-Life study. Participants with diabetes and those with cardiovascular disease (CVD) are less likely, while participants with CIC are more likely, to plan for the end-of-life. Participants with diabetes are less likely to make formal plans, whereas those with CVD are less likely to hold informal discussions. CIC is associated with increased odds of having an advance directive, but no other form of ACP. Self-perceived burden did not appear to be the gateway by which illness groups differentially engaged in ACP. Future research should investigate what aspects of illnesses drive ACP.
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19

O'Neill, Cas, Gerry Silk, Gillian Lowe, Renee Lee, Sultan Cinar, Hong Nguyen, and Binh Ngo. "Chronic Illness and Ethnicity." Australian Journal of Primary Health 6, no. 2 (2000): 94. http://dx.doi.org/10.1071/py00023.

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The expectations which both consumers and service providers bring to health care relationships are based on ethnicity and culture, as well as on individual and family characteristics, education and social circumstances. This article looks at the relationship between ethnicity and prevalence of illness; the interplay between ethnicity and social disadvantage; some cultural meanings attributed to illness; and how meanings may affect treatment. Four accounts are given of how two chronic illnesses - asthma and diabetes - may be viewed within the Timorese, Chinese, Turkish and Vietnamese communities.
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20

Hudson, Joanna L., and Rona Moss-Morris. "Treating Illness Distress in Chronic Illness." European Psychologist 24, no. 1 (January 2019): 26–37. http://dx.doi.org/10.1027/1016-9040/a000352.

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Abstract. Cognitive-behavioral therapy (CBT) is an evidence-based treatment for depression and anxiety recommended for those with and without physical long-term conditions (LTCs). However, the cognitive-behavioral mechanisms targeted in CBT protocols are based on empirical cognitive-behavioral models of depression and anxiety. In these models, emotions are conceptualized as primary mental health disorders rather than a reaction to the challenges of living with a LTC commonly referred to as illness distress. This raises important clinical questions with theoretical implications. These include: Is the experience of illness distress conceptually distinct from primary mental health diagnoses of anxiety and mood disorder? Are there unique cognitive-behavioral mechanisms related to illness self-management, which should be incorporated into CBT for illness distress? How can illness self-management interventions be embedded within existing CBT protocols for depression and anxiety? To address these questions, we distinguish between primary mental health disorders and illness distress conceptually and explore the impact of this on tailored treatment planning and engagement. Second, we review how health psychology theoretical models can help to inform modifications of existing cognitive-behavioral treatments for anxiety and depression to better support the needs of individuals experiencing illness distress. Third, we provide examples of how to embed processes important for illness self-management including, illness cognitions and adherence, alongside existing CBT techniques. The mechanisms and intervention techniques discussed may help to inform the development of integrated CBT treatments for illness distress for future hypothesis testing in comparative effectiveness trials.
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21

Price, Bob. "Illness careers: the chronic illness experience." Journal of Advanced Nursing 24, no. 2 (August 1996): 275–79. http://dx.doi.org/10.1046/j.1365-2648.1996.02047.x.

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22

FOX, JEANNE C. "Chronic Mental Illness." Annual Review of Nursing Research 10, no. 1 (September 1992): 95–112. http://dx.doi.org/10.1891/0739-6686.10.1.95.

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23

Nelson, Judith E., Christopher E. Cox, Aluko A. Hope, and Shannon S. Carson. "Chronic Critical Illness." American Journal of Respiratory and Critical Care Medicine 182, no. 4 (August 15, 2010): 446–54. http://dx.doi.org/10.1164/rccm.201002-0210ci.

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24

Wiencek, Clareen, and Chris Winkelman. "Chronic Critical Illness." AACN Advanced Critical Care 21, no. 1 (January 1, 2010): 44–61. http://dx.doi.org/10.4037/15597768-2010-1008.

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The syndrome of chronic critical illness has well-documented emotional, social, and financial burdens for individuals, caregivers, and the health care system. The purpose of this article is to provide experienced acute and critical care clinicians with essential information about the prevalence and profile of the chronically critically ill patient needed for comprehensive care. In addition, pathophysiology contributing to chronic critical illness is addressed, though the exact mechanism underlying the conversion of acute critical illness to chronic critical illness is unknown. Clinicians can use this information to identify at-risk intensive care unit patients and to institute proactive care to minimize burden and distress experienced by patients and their caregivers.
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25

Plank, Richard E., and Duncan G. Labay. "Chronic Mental Illness." Journal of Nonprofit & Public Sector Marketing 1, no. 2-3 (February 24, 1993): 15–33. http://dx.doi.org/10.1300/j054v01n02_03.

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26

Sjoding, Michael W., and Colin R. Cooke. "Chronic Critical Illness." Critical Care Medicine 43, no. 2 (February 2015): 476–77. http://dx.doi.org/10.1097/ccm.0000000000000780.

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27

SMITH, JEAN C., WILLIAM L. COLEMAN, ADRIAN D. SANDLER, and CATHERINE L. GRUS. "CHRONIC ILLNESS/INJURY." Journal of Developmental & Behavioral Pediatrics 18, no. 2 (April 1997): 133–34. http://dx.doi.org/10.1097/00004703-199704000-00020.

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28

Larsen, Karin E. "Valuing Chronic Illness." Contemporary Psychology: A Journal of Reviews 43, no. 10 (October 1998): 712–13. http://dx.doi.org/10.1037/001821.

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29

Lamas, Daniela. "Chronic Critical Illness." New England Journal of Medicine 370, no. 2 (January 9, 2014): 175–77. http://dx.doi.org/10.1056/nejmms1310675.

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30

Nierman, David M., and Judith E. Nelson. "Chronic critical illness." Critical Care Clinics 18, no. 3 (July 2002): xi—xii. http://dx.doi.org/10.1016/s0749-0704(02)00017-9.

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31

Toles, Mark, Helene Moriarty, Ken Coburn, Sherry Marcantonio, Alexandra Hanlon, Elizabeth Mauer, Paige Fisher, Melissa O’Connor, Connie Ulrich, and Mary D. Naylor. "Managing Chronic Illness." Journal of Applied Gerontology 36, no. 4 (July 9, 2016): 462–79. http://dx.doi.org/10.1177/0733464815602115.

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Models of care coordination can significantly improve health outcomes for older adults with chronic illnesses if they can engage participants. The purpose of this study was to examine the impact of nursing contact on the rate of participants’ voluntary disenrollment from a care coordination program. In this retrospective cohort study using administrative data for 1,524 participants in the Health Quality Partners Medicare Care Coordination Demonstration Program, the rate of voluntary disenrollment was approximately 11%. A lower risk of voluntary disenrollment was associated with a greater proportion of in-person (vs. telephonic) nursing contact (Hazard Ratio [HR] 0.137, confidence interval [CI] [0.050, 0.376]). A higher risk of voluntary disenrollment was associated with lower continuity of nurses who provided care (HR 1.964, CI [1.724, 2.238]). Findings suggest that in-person nursing contact and care continuity may enhance enrollment of chronically ill older adults and, ultimately, the overall health and well-being of this population
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32

Wiencek, Clareen, and Chris Winkelman. "Chronic Critical Illness." AACN Advanced Critical Care 21, no. 1 (January 2010): 44–61. http://dx.doi.org/10.1097/nci.0b013e3181c6a162.

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33

&NA;. "Chronic Critical Illness." AACN Advanced Critical Care 21, no. 1 (January 2010): 62–63. http://dx.doi.org/10.1097/nci.0b013e3181d2b0f2.

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34

Walker, Christine. "Recognising the changing boundaries of illness in defining terms of chronic illness." Australian Health Review 24, no. 2 (2001): 207. http://dx.doi.org/10.1071/ah010207.

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Definitions of chronic illness do not reflect the changing nature of chronic illnesses. When definitions in the literature,which guide and inform thinking in a field, remain static they are in danger of creating stereotypes. This can havean adverse influence on the care of people with chronic illness. Debates over the use of terms associated with chronicillness will lead to a better understanding of the place of chronic illness in the world of health and illness andultimately lead to services that better meet the needs of consumers.
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35

BRUNK, DOUG. "Chronic Pain Deemed a Chronic Illness." Caring for the Ages 11, no. 2 (February 2010): 11. http://dx.doi.org/10.1016/s1526-4114(10)60039-x.

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36

Robinson, Carole A. "Families Living Well With Chronic Illness." Qualitative Health Research 27, no. 4 (October 25, 2016): 447–61. http://dx.doi.org/10.1177/1049732316675590.

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Chronic illness is a global issue of escalating importance. While prevention, control, and management of chronic disease are imperative, it is also critical to shift our focus away from illness and toward living. In particular, attention needs to focus on living well despite illness. This article reports a grounded theory study with 43 members from 17 families who perceived they were managing well with serious chronic illnesses. The theory that captures the circular, iterative healing process of moving on is comprised of five phases: the fight, accepting, living with the chronic illness, sharing the experience, and reconstructing life. Families moved on through the process and moved on over time toward healing where they lived well alongside chronic illness. Family issues associated with each phase are identified as well as implications for health care providers. The theory provides a way of conceptualizing wellness in illness that supports patient- and family-centered care.
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37

Lindsay, Sally. "Prioritizing Illness: Lessons in Self-Managing Multiple Chronic Diseases." Canadian Journal of Sociology 34, no. 4 (May 29, 2009): 983–1002. http://dx.doi.org/10.29173/cjs1776.

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Chronic disease management strategies are largely based on single disease models, yet patients often need to manage multiple conditions. This study uses the concepts of ‘chronic illness trajectory’ and ‘biographical disruption’ to examine how patients self-manage multiple chronic conditions and especially how they prioritize which condition(s) will receive the greatest attention. Fifty-three people with multiple chronic illnesses participated in one of 6 focus groups. The results suggest that people who were disrupted tended to be younger than 60, lived on their own, cared for other family members, or other barriers. Many participants anticipated subsequent illnesses given their age and prior experience with illness. In order to cope with their multiple illnesses most felt it was necessary to prioritize their ‘main’ illness. Their reasons for prioritizing a particular illness included: (1) the unpredictable nature of the disease; (2) the condition could not be controlled by tablets; and (3) the condition tended to set off the rest of their health problems. Social context played a key role in shaping patients’ biography and chronic illness trajectory.
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38

Shute, Rosalyn H. "Childhood Chronic Illness and the School." Journal of Psychologists and Counsellors in Schools 9, S1 (August 1999): 109–22. http://dx.doi.org/10.1017/s1037291100003034.

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This paper introduces to school personnel some important issues with regard to chronic illness in children and adolescents. Current approaches to understanding the adaptation of young people to chronic illness are introduced, and the present state of knowledge about its psychosocial impact is outlined. Specific effects on education are then discussed, followed by a consideration of the role of school personnel, particularly guidance officers and school counsellors, in ensuring that the needs of students with chronic illnesses are appropriately met.
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39

Koenig, Harold G. "Depression in Chronic Illness." Journal of Christian Nursing 31, no. 1 (January 2014): 40–46. http://dx.doi.org/10.1097/cnj.0000000000000016.

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40

Gore, Susan L., Gary L. Albrecht, and Judith A. Levy. "Life with Chronic Illness." Contemporary Sociology 22, no. 5 (September 1993): 747. http://dx.doi.org/10.2307/2074672.

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41

MISHEL, MERLE H. "Uncertainty in Chronic Illness." Annual Review of Nursing Research 17, no. 1 (January 1999): 269–94. http://dx.doi.org/10.1891/0739-6686.17.1.269.

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In this chapter, the research on uncertainty in chronic illness is reviewed and critiqued. Two theoretical perspectives of uncertainty that can be applied across the range of chronic illness are presented. Research on the causes and consequences of uncertainty in chronic illness are considered and critiqued. The review addresses research on adults and on parents of chronically ill children. Conclusions include the areas requiring further investigation.
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42

Sawyer, Michael G., Jennifer J. Couper, A. James Martin, and J. Declan Kennedy. "Chronic illness in adolescents." Medical Journal of Australia 179, no. 5 (September 2003): 237. http://dx.doi.org/10.5694/j.1326-5377.2003.tb05525.x.

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43

McInnes, Rosemary A. "Chronic illness and sexuality." Medical Journal of Australia 179, no. 5 (September 2003): 263–66. http://dx.doi.org/10.5694/j.1326-5377.2003.tb05535.x.

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44

Sánchez Herrera, Beatriz, Lucy Barrera Ortiz, and Gloria Mabel Carrillo Gonzàlez. "Incontinence and Chronic Illness." Aquichan 13, no. 3 (December 1, 2013): 421–32. http://dx.doi.org/10.5294/aqui.2013.13.3.9.

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Objetivo: explorar la producción y contenido de la información disponible a nivel mundial sobre el abordaje de la incontinencia urinaria (IU) e incontinencia fecal (IF) y su relación con la enfermedad crónica (EC). Materiales y métodos: a partir de una revisión de literatura en las bases de datos Cinahl, Ovid, Scielo, Medline y Psychoinfo, entre los años 2009 y 2012, bajo los descriptores de incontinencia urinaria e incontinencia fecal, en combinación con enfermedad crónica, con su traducción al inglés, se identificaron, analizaron y clasificaron los planteamientos sobre el tema de la incontinencia según relevancia para la comprensión de la misma en la situación de EC. Resultados: se presentan los estudios encontrados clasificados en cinco grandes grupos sobre IU e IF que incluyen los que ilustran la magnitud del problema por su frecuencia y tipología, los que establecen relación directa entre la incontinencia y la EC, los que describen otros factores asociados con la incontinencia y con la EC, los que abordan la forma de valorar la incontinencia y los que dan aportes respecto al manejo de la IU o IF en la EC. Conclusiones: la literatura tiene abundante producción científica en sus dos últimos años y a nivel mundial sobre la IU pero no en igual proporción sobre la IF. Existen modelos para la valoración, medición y comprensión del fenómeno así como para la intervención y atención puntual sobre la misma. No se reportan abordajes integrales al problema de la IU e IF en personas con EC.
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45

Pollock, Susan E. "Adaptation to Chronic Illness." Nursing Clinics of North America 22, no. 3 (September 1987): 631–44. http://dx.doi.org/10.1016/s0029-6465(22)01314-7.

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46

Katzin, Louise. "Chronic Illness and Sexuality." American Journal of Nursing 90, no. 1 (January 1990): 54. http://dx.doi.org/10.2307/3426228.

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47

Schaefer, Karen Moore. "Breastfeeding in Chronic Illness." MCN, The American Journal of Maternal/Child Nursing 29, no. 4 (2004): 248–53. http://dx.doi.org/10.1097/00005721-200407000-00010.

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48

Shortell, Stephen M., Robin Gillies, Juned Siddique, Lawrence P. Casalino, Diane Rittenhouse, James C. Robinson, and Rodney K. McCurdy. "Improving Chronic Illness Care." Medical Care 47, no. 9 (September 2009): 932–39. http://dx.doi.org/10.1097/mlr.0b013e31819a621a.

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49

Koenig, Harold G. "Depression in Chronic Illness." Journal of Christian Nursing 31, no. 1 (2014): 40–46. http://dx.doi.org/10.1097/cnj.0b013e3182893752.

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50

Madrigal, Vanessa N., and Jennifer K. Walter. "Pediatric Chronic Critical Illness." Pediatric Critical Care Medicine 20, no. 12 (December 2019): 1206–7. http://dx.doi.org/10.1097/pcc.0000000000002154.

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