Allison Tong

Allison Tong's AcademicInfluence.com Rankings

Allison Tong

Biology

#5391

World Rank

#7859

Historical Rank

Biotechnology

#39

World Rank

#40

Historical Rank

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Biology

Allison Tong's Degrees

PhD Biomedical Sciences Stanford University

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Allison Tong's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

Consolidated criteria for reporting qualitative research (COREQ): a 32-item checklist for interviews and focus groups. (2007) (16970)
Enhancing transparency in reporting the synthesis of qualitative research: ENTREQ (2012) (1771)
The views of patients and carers in treatment decision making for chronic kidney disease: systematic review and thematic synthesis of qualitative studies (2010) (449)
Older people's perspectives on participation in physical activity: a systematic review and thematic synthesis of qualitative literature (2015) (422)
Consolidated criteria for reporting qualitative research (COREQ) (2019) (325)
Nomenclature for kidney function and disease: report of a Kidney Disease: Improving Global Outcomes (KDIGO) Consensus Conference. (2020) (309)
Factors that influence the decision to be an organ donor: a systematic review of the qualitative literature. (2012) (212)
Patient and Caregiver Priorities for Outcomes in Hemodialysis: An International Nominal Group Technique Study. (2016) (205)
Patients' experiences and perspectives of living with CKD. (2009) (191)
Experiences of Parents Who Have Children With Chronic Kidney Disease: A Systematic Review of Qualitative Studies (2008) (188)
COREQ (Consolidated Criteria for Reporting Qualitative Studies) (2014) (186)
Developing a Set of Core Outcomes for Trials in Hemodialysis: An International Delphi Survey. (2017) (185)
Catheter-related interventions to prevent peritonitis in peritoneal dialysis: a systematic review of randomized, controlled trials. (2004) (183)
Comparative Survival and Economic Benefits of Deceased Donor Kidney Transplantation and Dialysis in People with Varying Ages and Co-Morbidities (2012) (169)
Calcimimetics for secondary hyperparathyroidism in chronic kidney disease patients. (2014) (151)
Establishing Core Outcome Domains in Hemodialysis: Report of the Standardized Outcomes in Nephrology-Hemodialysis (SONG-HD) Consensus Workshop. (2017) (137)
Parental perspectives on caring for a child with chronic kidney disease: an in-depth interview study. (2010) (136)
The motivations and experiences of living kidney donors: a thematic synthesis. (2012) (136)
Support interventions for caregivers of people with chronic kidney disease: a systematic review. (2008) (136)
Dietary and fluid restrictions in CKD: a thematic synthesis of patient views from qualitative studies. (2015) (126)
Patients' priorities for health research: focus group study of patients with chronic kidney disease. (2008) (125)
Children's experiences of living with juvenile idiopathic arthritis: A thematic synthesis of qualitative studies (2012) (124)
Diagnosis, Monitoring, and Treatment of Systemic Lupus Erythematosus: A Systematic Review of Clinical Practice Guidelines (2015) (122)
Experiences and Perspectives of Adults Living With Systemic Lupus Erythematosus: Thematic Synthesis of Qualitative Studies (2013) (121)
Patient and caregiver perspectives on home hemodialysis: a systematic review. (2015) (120)
Antimicrobial agents to prevent peritonitis in peritoneal dialysis: a systematic review of randomized controlled trials. (2004) (117)
Exercise Training in Solid Organ Transplant Recipients: A Systematic Review and Meta-Analysis (2013) (116)
Motivations, Challenges, and Attitudes to Self-management in Kidney Transplant Recipients: A Systematic Review of Qualitative Studies. (2016) (115)
Clinical Practice Guidelines on Wait-Listing for Kidney Transplantation: Consistent and Equitable? (2012) (114)
Dietary interventions for adults with chronic kidney disease. (2017) (108)
Catheter type, placement and insertion techniques for preventing peritonitis in peritoneal dialysis patients. (2004) (108)
Family Perspectives on Deceased Organ Donation: Thematic Synthesis of Qualitative Studies (2014) (107)
Patient expectations and experiences of remote monitoring for chronic diseases: Systematic review and thematic synthesis of qualitative studies (2019) (106)
Educational Interventions for Patients With CKD: A Systematic Review. (2016) (103)
Adolescent experiences following organ transplantation: a systematic review of qualitative studies. (2009) (103)
Donor Cancer Transmission in Kidney Transplantation: A Systematic Review (2013) (101)
Patients' perspectives on hemodialysis vascular access: a systematic review of qualitative studies. (2014) (101)
The perspectives of adults living with peritoneal dialysis: thematic synthesis of qualitative studies. (2013) (99)
Screening and Follow-Up of Living Kidney Donors: A Systematic Review of Clinical Practice Guidelines (2011) (98)
Important outcomes for kidney transplant recipients: a nominal group and qualitative study. (2012) (98)
Thematic synthesis of qualitative studies on patient and caregiver perspectives on end-of-life care in CKD. (2014) (97)
Implementing core outcomes in kidney disease: report of the Standardized Outcomes in Nephrology (SONG) implementation workshop. (2018) (97)
Challenges in conducting clinical trials in nephrology: conclusions from a Kidney Disease—Improving Global Outcomes (KDIGO) Controversies Conference (2017) (94)
Patient and caregiver values, beliefs and experiences when considering home dialysis as a treatment option: a semi-structured interview study. (2016) (92)
Children’s Experiences of Cystic Fibrosis: A Systematic Review of Qualitative Studies (2014) (90)
Research priority setting in kidney disease: a systematic review. (2015) (85)
Blood pressure and volume management in dialysis: conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference (2020) (84)
Parental perspectives on the financial impact of caring for a child with CKD. (2015) (84)
Children's experiences of dialysis: a systematic review of qualitative studies (2012) (82)
Reporting guideline for priority setting of health research (REPRISE) (2019) (81)
Socio‐economic status and quality of life in children with chronic disease: A systematic review (2016) (78)
Patient and Caregiver Priorities for Outcomes in Peritoneal Dialysis: Multinational Nominal Group Technique Study. (2019) (76)
Aboriginal and Torres Strait Islander people's domains of wellbeing: A comprehensive literature review. (2019) (76)
Perspectives of people with dementia and carers on advance care planning and end-of-life care: A systematic review and thematic synthesis of qualitative studies (2018) (73)
Research Priorities in CKD: Report of a National Workshop Conducted in Australia. (2015) (73)
The perspectives of kidney transplant recipients on medicine taking: a systematic review of qualitative studies. (2011) (72)
Knowledge deficit of patients with stage 1–4 CKD: A focus group study (2014) (72)
Self-management interventions for adults with chronic kidney disease: a scoping review (2018) (71)
Induction and Maintenance Immunosuppression Treatment of Proliferative Lupus Nephritis: A Network Meta-analysis of Randomized Trials. (2017) (70)
Meta-analysis of biochemical and patient-level effects of calcimimetic therapy. (2006) (70)
Standardised outcomes in nephrology – Haemodialysis (SONG-HD): study protocol for establishing a core outcome set in haemodialysis (2015) (69)
Community Preferences for the Allocation of Solid Organs for Transplantation: A Systematic Review (2010) (68)
eHealth interventions for people with chronic kidney disease (2016) (68)
Quality of life of young adults and adolescents with chronic kidney disease. (2013) (68)
Antimicrobial agents for preventing peritonitis in peritoneal dialysis patients. (2004) (68)
Qualitative Research in Organ Transplantation: Recent Contributions to Clinical Care and Policy (2013) (67)
Establishing a Core Outcome Measure for Fatigue in Patients on Hemodialysis: A Standardized Outcomes in Nephrology-Hemodialysis (SONG-HD) Consensus Workshop Report. (2018) (67)
Qualitative research in CKD: an overview of methods and applications. (2014) (67)
Perspectives on pregnancy in women with chronic kidney disease: systematic review of qualitative studies. (2015) (66)
Establishing a Core Outcome Set for Peritoneal Dialysis: Report of the SONG-PD (Standardized Outcomes in Nephrology-Peritoneal Dialysis) Consensus Workshop. (2020) (65)
Patient Perspectives on the Meaning and Impact of Fatigue in Hemodialysis: A Systematic Review and Thematic Analysis of Qualitative Studies. (2019) (65)
Toward Establishing Core Outcome Domains For Trials in Kidney Transplantation: Report of the Standardized Outcomes in Nephrology—Kidney Transplantation Consensus Workshops (2017) (65)
Symptom Clusters in Advanced Cancer Patients: An Empirical Comparison of Statistical Methods and the Impact on Quality of Life. (2016) (65)
Experiences of Latinx Individuals Hospitalized for COVID-19 (2021) (63)
The beliefs and expectations of patients and caregivers about home haemodialysis: an interview study (2013) (61)
Perspectives on Pregnancy in Women With CKD: A Semistructured Interview Study. (2015) (61)
Developing Consensus-Based Priority Outcome Domains for Trials in Kidney Transplantation: A Multinational Delphi Survey With Patients, Caregivers, and Health Professionals (2017) (60)
Neurocognitive and Educational Outcomes in Children and Adolescents with CKD: A Systematic Review and Meta-Analysis. (2018) (60)
Lupus Means Sacrifices: Perspectives of Adolescents and Young Adults With Systemic Lupus Erythematosus (2016) (58)
Immunosuppressive treatment for proliferative lupus nephritis. (2018) (56)
Patient-Reported Outcome Measures for Fatigue in Patients on Hemodialysis: A Systematic Review. (2017) (56)
Experiences and perspectives of adolescents and young adults with advanced CKD. (2013) (55)
An international Delphi survey helped develop consensus-based core outcome domains for trials in peritoneal dialysis. (2019) (52)
Consumer involvement in topic and outcome selection in the development of clinical practice guidelines (2012) (52)
The Expectations and Attitudes of Patients With Chronic Kidney Disease Toward Living Kidney Donor Transplantation: A Thematic Synthesis of Qualitative Studies (2015) (51)
What factors influence people's decisions to register for organ donation? The results of a nominal group study (2014) (51)
Parental perspectives on evaluation and management of fever in young infants: an interview study (2014) (51)
Screening and prevention for latent tuberculosis in immunosuppressed patients at risk for tuberculosis: a systematic review of clinical practice guidelines (2018) (51)
‘Suspended in a paradox’—patient attitudes to wait‐listing for kidney transplantation: systematic review and thematic synthesis of qualitative studies (2015) (51)
Membranous nephropathy (2020) (50)
Men’s perspectives of prostate cancer screening: A systematic review of qualitative studies (2017) (49)
Research priorities in health communication and participation: international survey of consumers and other stakeholders (2018) (48)
Identifying Outcomes Important to Patients with Glomerular Disease and Their Caregivers. (2020) (48)
Children’s Experiences of Epilepsy: A Systematic Review of Qualitative Studies (2016) (48)
Patients’ Perspectives and Experiences Living with Systemic Sclerosis: A Systematic Review and Thematic Synthesis of Qualitative Studies (2016) (47)
Clinicians' Perspectives on Providing Emergency-Only Hemodialysis to Undocumented Immigrants (2018) (46)
A painful inheritance-patient perspectives on living with polycystic kidney disease: thematic synthesis of qualitative research. (2015) (46)
Motivations, experiences, and perspectives of bone marrow and peripheral blood stem cell donors: thematic synthesis of qualitative studies. (2013) (46)
Incidence and Outcomes of COVID-19 in People With CKD: A Systematic Review and Meta-analysis (2021) (46)
Perspectives of Older Kidney Transplant Recipients on Kidney Transplantation. (2017) (46)
Patient satisfaction with in-centre haemodialysis care: an international survey (2014) (45)
Public Awareness and Attitudes to Living Organ Donation: Systematic Review and Integrative Synthesis (2013) (45)
Patient beliefs and attitudes to taking statins: systematic review of qualitative studies. (2018) (44)
A guide to reading and using systematic reviews of qualitative research. (2016) (44)
Patient and Caregiver Priorities for Outcomes in CKD: A Multinational Nominal Group Technique Study. (2020) (43)
Composing a new song for trials: the Standardized Outcomes in Nephrology (SONG) initiative. (2017) (43)
“When I had my transplant, I became normal.” Adolescent perspectives on life after kidney transplantation (2010) (42)
The experiences of commercial kidney donors: thematic synthesis of qualitative research (2012) (42)
Standardized Outcomes in Nephrology—Peritoneal Dialysis (SONG-PD): Study Protocol for Establishing a Core Outcome Set in PD (2017) (42)
Studying the post-COVID-19 condition: research challenges, strategies, and importance of Core Outcome Set development (2022) (41)
Community Attitudes to Deceased Organ Donation: A Focus Group Study (2012) (41)
Establishing core outcome domains in pediatric kidney disease: report of the Standardized Outcomes in Nephrology - Children and Adolescents (SONG-KIDS) consensus workshops. (2020) (41)
Report of the Standardized Outcomes in Nephrology-Hemodialysis (SONG-HD) Consensus Workshop on Establishing a Core Outcome Measure for Hemodialysis Vascular Access. (2018) (41)
Assessment of kidney function in type 2 diabetes (2010) (40)
Patient and Caregiver Perspectives on Terms Used to Describe Kidney Health. (2020) (40)
Living Kidney Donor Assessment: Challenges, Uncertainties and Controversies Among Transplant Nephrologists and Surgeons (2013) (40)
A Discrete Choice Study of Patient Preferences for Dialysis Modalities. (2018) (39)
Standardised Outcomes in Nephrology—Children and Adolescents (SONG-Kids): a protocol for establishing a core outcome set for children with chronic kidney disease (2016) (39)
The Preferences and Perspectives of Nephrologists on Patients’ Access to Kidney Transplantation: A Systematic Review (2014) (39)
Patients’ experiences and perspectives of multiple concurrent symptoms in advanced cancer: a semi-structured interview study (2016) (39)
An Interview Study of Patient and Caregiver Perspectives on Advance Care Planning in ESRD. (2017) (39)
“It was just an unconditional gift.” Self reflections of non‐directed living kidney donors (2012) (38)
Adolescent views on transition in diabetes and nephrology (2013) (38)
Quality of life of children and adolescents with chronic kidney disease: a cross-sectional study (2018) (38)
Patients’ Attitudes and Experiences of Disease‐Modifying Antirheumatic Drugs in Rheumatoid Arthritis and Spondyloarthritis: A Qualitative Synthesis (2018) (37)
Child and Parental Perspectives on Communication and Decision Making in Pediatric CKD: A Focus Group Study. (2018) (37)
Core Outcomes Set for Trials in People With Coronavirus Disease 2019 (2020) (37)
Knowledge, beliefs and attitudes of kidney transplant recipients regarding their risk of cancer (2012) (37)
“You know your own fistula, it becomes a part of you”—Patient perspectives on vascular access: A semistructured interview study (2016) (37)
Children’s experiences of congenital heart disease: a systematic review of qualitative studies (2018) (37)
Prevention, detection and management of early chronic kidney disease: A systematic review of clinical practice guidelines (2013) (36)
Vascular Access Outcomes Reported in Maintenance Hemodialysis Trials: A Systematic Review. (2017) (36)
Meaning of empowerment in peritoneal dialysis: focus groups with patients and caregivers. (2020) (36)
Lifestyle behaviour change for preventing the progression of chronic kidney disease: a systematic review (2019) (36)
Māori patients' experiences and perspectives of chronic kidney disease: a New Zealand qualitative interview study (2017) (33)
Range and Heterogeneity of Outcomes in Randomized Trials of Pediatric Chronic Kidney Disease (2017) (33)
Qualitative Research in Transplantation: Ensuring Relevance and Rigor (2016) (33)
Identifying and integrating consumer perspectives in clinical practice guidelines on autosomal‐dominant polycystic kidney disease (2016) (33)
Nephrologists' Perspectives on Defining and Applying Patient-Centered Outcomes in Hemodialysis. (2017) (32)
An analysis of media coverage on the prevention and early detection of CKD in Australia. (2008) (32)
The perspectives of Aboriginal patients and their health care providers on improving the quality of hemodialysis services: A qualitative study (2014) (32)
Experiences and Perspectives of Dietary Management Among Patients on Hemodialysis: An Interview Study. (2018) (32)
‘Beats the alternative but it messes up your life’: Aboriginal people's experience of haemodialysis in rural Australia (2014) (32)
Service providers’ perspectives, attitudes and beliefs on health services delivery for Aboriginal people receiving haemodialysis in rural Australia: a qualitative study (2013) (31)
Scope and Consistency of Outcomes Reported in Randomized Trials Conducted in Adults Receiving Hemodialysis: A Systematic Review. (2018) (31)
Consensus Methods: Nominal Group Technique (2019) (31)
Identifying Needs for Self-management Interventions for Adults With CKD and Their Caregivers: A Qualitative Study. (2019) (31)
Communication during childhood cancer: Systematic review of patient perspectives (2019) (31)
Standardized Outcomes in Nephrology-Transplantation: A Global Initiative to Develop a Core Outcome Set for Trials in Kidney Transplantation (2016) (30)
Research priority setting in childhood chronic disease: a systematic review (2018) (30)
Identifying Outcomes that Are Important to Living Kidney Donors: A Nominal Group Technique Study. (2018) (30)
Nephrologists' perspectives on waitlisting and allocation of deceased donor kidneys for transplant. (2011) (30)
Quality of life of adolescent kidney transplant recipients. (2011) (30)
Eliciting patient preferences, priorities and trade-offs for outcomes following kidney transplantation: a pilot best–worst scaling survey (2016) (30)
KHA‐CARI guideline recommendations for the diagnosis and management of autosomal dominant polycystic kidney disease (2016) (29)
Patient preferences for the allocation of deceased donor kidneys for transplantation: a mixed methods study (2012) (29)
Attitudes and beliefs about deceased organ donation in the Arabic-speaking community in Australia: a focus group study (2016) (29)
“It's Not Me, It's Not Really Me.” Insights From Patients on Living With Systemic Sclerosis: An Interview Study (2017) (28)
Antimicrobial agents for preventing peritonitis in peritoneal dialysis patients. (2017) (28)
Perspectives on childhood resilience among the Aboriginal community: an interview study (2017) (28)
Clinician beliefs and attitudes about home haemodialysis: a multinational interview study (2012) (28)
Perspectives of transplant physicians and surgeons on reimbursement, compensation, and incentives for living kidney donors. (2014) (28)
Recent advances in autosomal‐dominant polycystic kidney disease (2016) (28)
Catheter type, placement and insertion techniques for preventing catheter-related infections in chronic peritoneal dialysis patients. (2019) (28)
Patient Preferences for Outcomes After Kidney Transplantation: A Best-Worst Scaling Survey (2017) (28)
Donor and Recipient Views on Their Relationship in Living Kidney Donation: Thematic Synthesis of Qualitative Studies. (2017) (26)
Research priority setting in organ transplantation: a systematic review (2017) (26)
Building trust and sharing power for co-creation in Aboriginal health research: a stakeholder interview study (2019) (26)
Stakeholder Views of Clinical Trials in Low- and Middle-Income Countries: A Systematic Review (2016) (26)
Patients' Perspectives on the Prevention and Treatment of Peritonitis in Peritoneal Dialysis: A Semi-Structured Interview Study (2016) (26)
The Consistency and Reporting of Quality-of-Life Outcomes in Trials of Immunosuppressive Agents in Kidney Transplantation: A Systematic Review and Meta-analysis. (2016) (26)
Patient experiences of training and transition to home haemodialysis: A mixed‐methods study (2017) (26)
Patient and caregiver preferences for home dialysis—the home first study: a protocol for qualitative interviews and discrete choice experiments (2015) (26)
Healthcare and Research Priorities of Adolescents and Young Adults with Systemic Lupus Erythematosus: A Mixed-methods Study (2017) (25)
Identifying Important Outcomes for Young People With CKD and Their Caregivers: A Nominal Group Technique Study. (2019) (25)
Patient-centred approaches for the management of unpleasant symptoms in kidney disease (2022) (25)
Identifying critically important vascular access outcomes for trials in haemodialysis: an international survey with patients, caregivers and health professionals. (2019) (24)
Health and wealth in children and adolescents with chronic kidney disease (K-CAD study) (2014) (24)
Range and Consistency of Outcomes Reported in Randomized Trials Conducted in Kidney Transplant Recipients: A Systematic Review (2018) (24)
Experiences and Perspectives of Transgender Youths in Accessing Health Care: A Systematic Review. (2021) (24)
Advance care planning in chronic kidney disease: A survey of current practice in Australia (2017) (23)
Preferences for engagement in health technology assessment decision-making: a nominal group technique with members of the public (2016) (23)
Preferences for Policy Options for Deceased Organ Donation for Transplantation: A Discrete Choice Experiment (2015) (23)
Core Outcome Measures for Trials in People With Coronavirus Disease 2019: Respiratory Failure, Multiorgan Failure, Shortness of Breath, and Recovery (2021) (23)
Selecting, refining and identifying priority Cochrane Reviews in health communication and participation in partnership with consumers and other stakeholders (2019) (23)
'I feel stronger and younger all the time'-perspectives of elderly kidney transplant recipients: thematic synthesis of qualitative research. (2016) (22)
Researchers’, Regulators’, and Sponsors’ Views on Pediatric Clinical Trials: A Multinational Study (2016) (22)
Validation of a Core Patient-Reported Outcome Measure for Fatigue in Patients Receiving Hemodialysis: The SONG-HD Fatigue Instrument. (2020) (22)
Parental views on otitis media: systematic review of qualitative studies (2016) (22)
Clinicians' Perspectives on Advance Care Planning for Patients With CKD in Australia: An Interview Study. (2017) (22)
Rationing scarce organs for transplantation: healthcare provider perspectives on wait‐listing and organ allocation (2013) (21)
Community Preferences for the Allocation of Donor Organs for Transplantation: A Discrete Choice Study (2013) (21)
General practitioners’ perspectives on the prevention of cardiovascular disease: systematic review and thematic synthesis of qualitative studies (2018) (21)
How do people with chronic kidney disease value cancer‐related quality of life? (2012) (21)
Perspectives of healthcare providers on the nutritional management of patients on haemodialysis in Australia: an interview study (2018) (21)
The patient experience of kidney disease and pregnancy. (2019) (21)
Considerations and Challenges in Selecting Patient-Reported Outcome Measures for Clinical Trials in Nephrology. (2017) (20)
Nephrologists' Perspectives on Recipient Eligibility and Access to Living Kidney Donor Transplantation (2016) (20)
A Coaching Program to Improve Dietary Intake of Patients with CKD: ENTICE-CKD. (2020) (20)
The CARI guidelines. Prevention and management of chronic kidney disease in type 2 diabetes. (2010) (20)
Research priorities for COVID-19 sensor technology (2021) (20)
Transition Between Different Renal Replacement Modalities: Gaps in Knowledge and Care—The Integrated Research Initiative (2019) (20)
Living well with kidney disease by patient and care-partner empowerment: kidney health for everyone everywhere. (2021) (20)
Community views and perspectives on public engagement in health technology assessment decision making. (2017) (20)
Use of patient‐reported outcome measures and patient‐reported experience measures in renal units in Australia and New Zealand: A cross‐sectional survey study (2019) (20)
Research priorities for COVID-19 sensor technology (2021) (20)
In their own words: the value of qualitative research to improve the care of children with chronic kidney disease (2017) (20)
Health coaching and pedometers to enhance physical activity and prevent falls in community-dwelling people aged 60 years and over: study protocol for the Coaching for Healthy AGEing (CHAnGE) cluster randomised controlled trial (2016) (19)
Frontline interdisciplinary clinician perspectives on caring for patients with COVID-19: a qualitative study (2021) (19)
Unexpected donor‐derived infectious transmissions by kidney transplantation: A systematic review (2018) (19)
Health benefits and costs of screening for colorectal cancer in people on dialysis or who have received a kidney transplant. (2013) (19)
Patient awareness and beliefs about the risk factors and comorbidities associated with chronic kidney disease : A mixed‐methods study (2017) (19)
Patient‐reported outcome measures for life participation in kidney transplantation: A systematic review (2019) (19)
Suspension and resumption of kidney transplant programmes during the COVID‐19 pandemic: perspectives from patients, caregivers and potential living donors – a qualitative study (2020) (19)
Consumer Perspectives on Pediatric Rheumatology Care and Service Delivery: A Qualitative Study (2013) (19)
Peritoneal dialysis-associated peritonitis outcomes reported in trials and observational studies: A systematic review (2020) (19)
Patient and Caregiver Priorities for Medication Adherence in Gout, Osteoporosis, and Rheumatoid Arthritis: Nominal Group Technique (2020) (18)
Outcome Measures in Rheumatology - Interventions for medication Adherence (OMERACT-Adherence) Core Domain Set for Trials of Interventions for Medication Adherence in Rheumatology: 5 Phase Study Protocol (2018) (18)
Autosomal Dominant Polycystic Kidney Disease: A Path Forward. (2015) (18)
Patients’ Perspectives and Experience of Psoriasis and Psoriatic Arthritis: A Systematic Review and Thematic Synthesis of Qualitative Studies (2020) (18)
Preferences for a self-management e-health tool for patients with chronic kidney disease: results of a patient-oriented consensus workshop. (2019) (18)
Indigenous Australian women's experiences of participation in cervical screening (2020) (18)
KHA-CARI Autosomal Dominant Polycystic Kidney Disease Guideline: Diet and Lifestyle Management. (2015) (17)
How Qualitative Research Informs Clinical and Policy Decision Making in Transplantation: A Review (2016) (17)
Identifying patient‐important outcomes in polycystic kidney disease: An international nominal group technique study (2019) (17)
The Lived Experience of "Being Evaluated" for Organ Donation: Focus Groups with Living Kidney Donors. (2017) (17)
Clinicians’ experiences with remote patient monitoring in peritoneal dialysis: A semi-structured interview study (2020) (17)
Cardiovascular Outcomes Reported in Hemodialysis Trials. (2018) (17)
The Fabric of Aboriginal and Torres Strait Islander Wellbeing: A Conceptual Model (2021) (17)
Health-Related Quality of Life in People Across the Spectrum of CKD (2020) (17)
Beliefs and Attitudes to Bowel Cancer Screening in Patients with CKD: A Semistructured Interview Study. (2017) (17)
Identifying and integrating patient and caregiver perspectives for clinical practice guidelines on the screening and management of infectious microorganisms in hemodialysis units (2017) (17)
Clinicians' Perspectives on Managing Symptom Clusters in Advanced Cancer: A Semistructured Interview Study. (2016) (16)
Establishing a Core Outcome Measure for Graft Health: A Standardized Outcomes in Nephrology-Kidney Transplantation (SONG-Tx) Consensus Workshop Report (2018) (16)
Establishing a Core Outcome Set for Autosomal Dominant Polycystic Kidney Disease: Report of the Standardized Outcomes in Nephrology-Polycystic Kidney Disease (SONG-PKD) Consensus Workshop. (2020) (16)
Public Attitudes and Beliefs About Living Kidney Donation: Focus Group Study (2014) (16)
Research priorities for childhood chronic conditions: a workshop report (2018) (16)
Cancer Screening in People Who Have Chronic Disease: The Example of Kidney Disease (2011) (16)
Standardised Outcomes in Nephrology—Polycystic Kidney Disease (SONG-PKD): study protocol for establishing a core outcome set in polycystic kidney disease (2017) (16)
Recruitment and retention in clinical trials in chronic kidney disease: report from national workshops with patients, caregivers and health professionals. (2020) (16)
Targeted, structured text messaging to improve dietary and lifestyle behaviours for people on maintenance haemodialysis (KIDNEYTEXT): study protocol for a randomised controlled trial (2019) (16)
Living well with kidney disease by patient and care partner empowerment: kidney health for everyone everywhere (2020) (15)
Psychosocial care of living kidney donors (2010) (15)
Establishing a Core Outcome Measure for Life Participation: a Standardized Outcomes in Nephrology - Kidney Transplantation (SONG-Tx) Consensus Workshop Report. (2019) (15)
A Web-Based Self-Management Support Prototype for Adults With Chronic Kidney Disease (My Kidneys My Health): Co-Design and Usability Testing (2021) (15)
Community-Based Interventions and Individuals' Willingness to be a Deceased Organ Donor: Systematic Review and Meta-Analysis (2015) (15)
Core Outcome Domains for Trials in Autosomal Dominant Polycystic Kidney Disease: An International Delphi Survey. (2020) (15)
One-Time Fecal Immunochemical Screening for Advanced Colorectal Neoplasia in Patients with CKD (DETECT Study). (2019) (15)
Tuning into Qualitative Research-A Channel for the Patient Voice. (2016) (15)
A case study of enhanced clinical care enabled by Aboriginal health research: the Hearing, EAr health and Language Services (HEALS) project (2016) (15)
Transparency, trust and minimizing burden to increase recruitment and recruitment in trials: a systematic review. (2021) (14)
Community preferences for the allocation of deceased donor organs for transplantation: a focus group study. (2013) (14)
Patient perspectives of a young adult renal clinic: A mixed‐methods evaluation (2015) (14)
The association between socioeconomic disadvantage and parent-rated health in children and adolescents with chronic kidney disease—the Kids with CKD (KCAD) study (2019) (14)
eHealth Interventions for Solid Organ Transplant Recipients: A Systematic Review and Meta-analysis of Randomized Controlled Trials. (2020) (14)
Standardized Outcomes in Nephrology-Glomerular Disease (SONG-GD): establishing a core outcome set for trials in patients with glomerular disease. (2019) (13)
Health professional and community perspectives on reducing barriers to accessing specialist health care in metropolitan Aboriginal communities: A semi‐structured interview study (2017) (13)
Patients’ and caregivers’ expectations and experiences of remote monitoring for peritoneal dialysis: A qualitative interview study (2020) (13)
Nephrologists’ Perspectives on Gender Disparities in CKD and Dialysis (2021) (13)
NAV-KIDS2 trial: protocol for a multi-centre, staggered randomised controlled trial of a patient navigator intervention in children with chronic kidney disease (2019) (13)
Community Preferences for the Allocation &Donation of Organs - The PAraDOx Study (2011) (13)
What Matters 2 Adults: a study protocol to develop a new preference-based wellbeing measure with Aboriginal and Torres Strait Islander adults (WM2Adults) (2020) (13)
Promoting deceased organ and tissue donation registration in family physician waiting rooms (RegisterNow-1 trial): study protocol for a pragmatic, stepped-wedge, cluster randomized controlled registry (2017) (13)
Patients’ and caregivers’ perspectives on access to kidney replacement therapy in rural communities: systematic review of qualitative studies (2020) (12)
Case‐control study of end‐of‐life treatment preferences and costs following advance care planning for adults with end‐stage kidney disease (2019) (12)
Patients' Experiences and Perspectives of Telehealth Coaching with a Dietitian to Improve Diet Quality in Chronic Kidney Disease: A Qualitative Interview Study. (2019) (12)
Content and Quality of Websites for Patients With Chronic Kidney Disease: An Environmental Scan (2019) (12)
Feasibility and acceptability of telehealth coaching to promote healthy eating in chronic kidney disease: a mixed-methods process evaluation (2019) (12)
Nephrologists' perspectives on the effect of guidelines on clinical practice: a semistructured interview study. (2010) (12)
Principles and strategies for involving patients in research in chronic kidney disease: report from national workshops. (2020) (11)
Radiologists’ perspectives about evidence-based medicine and their clinical practice: a semistructured interview study (2014) (11)
Making Decisions About Long-Term Institutional Care Placement Among People With Dementia and Their Caregivers: Systematic Review of Qualitative Studies. (2020) (11)
Expectations and Experiences of Follow-up and Self-Care After Living Kidney Donation: A Focus Group Study (2017) (11)
Public preferences for engagement in Health Technology Assessment decision-making: protocol of a mixed methods study (2015) (11)
Perspectives on mental health among patients receiving dialysis. (2020) (10)
Patient- and parent proxy-reported outcome measures for life participation in children with chronic kidney disease: a systematic review. (2020) (10)
Perspectives on life participation by young adults with chronic kidney disease: an interview study (2020) (10)
Patients' perspectives of pain in dialysis: systematic review and thematic synthesis of qualitative studies. (2020) (10)
International perspectives on Patient Involvement in Clinical Trials in Nephrology. (2020) (10)
The CARI guidelines. Cost-effectiveness and socioeconomic implications of prevention and management of chronic kidney disease in type 2 diabetes. (2010) (10)
Patient-reported outcomes and experiences in the transition of undocumented patients from emergency to scheduled hemodialysis. (2020) (10)
Range and Variability of Outcomes Reported in Randomized Trials Conducted in Patients With Polycystic Kidney Disease: A Systematic Review. (2020) (10)
Clinicians’ and researchers’ perspectives on establishing and implementing core outcomes in haemodialysis: semistructured interview study (2018) (10)
Establishing a Core Outcome Measure for Life Participation: A Standardized Outcomes in Nephrology – Kidney Transplantation (SONG-Tx) Consensus Workshop Report. (2018) (10)
The experiences and impact of being deemed ineligible for living kidney donation: Semi‐structured interview study (2020) (9)
Children and adolescents’ experiences of primary lymphoedema: semistructured interview study (2018) (9)
Developing Consensus-Based Outcome Domains for Trials in Children and Adolescents With CKD: An International Delphi Survey. (2020) (9)
Identifying and integrating patient and caregiver perspectives in clinical practice guidelines for percutaneous renal biopsy (2019) (9)
Focus group study of public opinion about paying living kidney donors in Australia. (2015) (9)
Living kidney donor and recipient perspectives on their relationship: longitudinal semi-structured interviews (2019) (9)
Top 10 research priorities for people living with pulmonary fibrosis, their caregivers, healthcare professionals and researchers (2020) (9)
Costs and outcomes of advance care planning and end-of-life care for older adults with end-stage kidney disease: A person-centred decision analysis (2019) (8)
International Survey to Establish Prioritized Outcomes for Trials in People With Coronavirus Disease 2019 (2020) (8)
Feasibility and acceptability of e-PROMs data capture and feedback among patients receiving haemodialysis in the Symptom monitoring WIth Feedback Trial (SWIFT) pilot: protocol for a qualitative study in Australia (2020) (8)
Standardised Outcomes in Nephrology – Chronic Kidney Disease (SONG-CKD): a protocol for establishing a core outcome set for adults with chronic kidney disease who do not require kidney replacement therapy (2021) (8)
Living well with kidney disease by patient and care-partner empowerment: Kidney health for everyone everywhere. (2021) (8)
KHA-CARI Autosomal Dominant Polycystic Kidney Disease Guideline: Genetic Testing for Diagnosis. (2015) (8)
Building better research partnerships by understanding how Aboriginal health communities perceive and use data: a semistructured interview study (2016) (8)
"Someone's Got My Back": Older People's Experience of the Coaching for Healthy Ageing Program for Promoting Physical Activity and Preventing Falls. (2020) (7)
The Lived Experience of ‘Being Evaluated’ for Organ Donation: Focus Groups with Living Kidney Donors (2017) (7)
Patient and caregiver perspectives on burnout in peritoneal dialysis (2020) (7)
Qualitative Research in CKD: How to Appraise and Interpret the Evidence. (2021) (7)
Perspectives of solid organ transplant recipients on medicine‐taking: Systematic review of qualitative studies (2021) (7)
Informative for Decision Making? The Spectrum and Consistency of Outcomes After Living Kidney Donation Reported in Trials and Observational Studies (2019) (7)
Kidney transplant recipient perspectives on telehealth during the COVID‐19 pandemic (2021) (7)
What Matters 2 Adults (WM2Adults): Understanding the Foundations of Aboriginal and Torres Strait Islander Wellbeing (2021) (7)
Horses for courses: promoting transparent reporting of qualitative research in AJKD. (2014) (7)
Patients' attitudes and experiences of transition from paediatric to adult healthcare in rheumatology: a qualitative systematic review. (2020) (7)
Anti‐infective (antiseptics and antibiotics) agents for preventing peritonitis in peritoneal dialysis patients (2003) (7)
Establishing Core Cardiovascular Outcome Measures for Trials in Hemodialysis: Report of an International Consensus Workshop. (2020) (7)
Completeness of reporting of adverse events in trials of maintenance immunosuppression in kidney transplantation: a systematic review (2017) (7)
Scope and Consistency of Outcomes Reported in Trials of Patients With Systemic Sclerosis (2020) (6)
Parents' and carers' views on factors contributing to the health and wellbeing of urban Aboriginal children. (2020) (6)
Test performance of faecal occult blood testing for the detection of bowel cancer in people with chronic kidney disease (DETECT) protocol (2011) (6)
Disparities in end-stage kidney disease care for children: a global survey. (2020) (6)
Health care provider perspectives on cervical screening for Aboriginal and Torres Strait Islander women: a qualitative study (2021) (6)
Interventions for fatigue in people with chronic kidney disease requiring dialysis (2018) (6)
STANDARDISED OUTCOMES IN NEPHROLOGY-HAEMODIALYSIS (SONG-HD): USING THE DELPHI METHOD TO GAIN CONSENSUS ON CORE OUTCOMES FOR HAEMODIALYSIS TRIALS. (2015) (6)
Patient experiences of sleep in dialysis: systematic review of qualitative studies. (2021) (6)
Qualitative research methods and its application in nephrology (2021) (6)
Identifying critically important cardiovascular outcomes for trials in hemodialysis: an international survey with patients, caregivers and health professionals. (2020) (6)
Patient needs and priorities for patient navigator programmes in chronic kidney disease: a workshop report (2020) (6)
A Mixed Method Investigation to Determine Priorities for Improving Information, Interaction, and Individualization of Care Among Individuals on In-center Hemodialysis: The Triple I Study (2020) (6)
Patient and caregiver perspectives on sleep in dialysis (2020) (6)
Patient-reported outcome measures for life participation in peritoneal dialysis: a systematic review. (2020) (6)
The measurement properties of tests and tools used in cystic fibrosis studies: a systematic review (2021) (6)
Qualitative Research in Rheumatology: An Overview of Methods and Contributions to Practice and Policy (2020) (5)
Patient, Caregiver, and Provider Perspectives on Challenges and Solutions to Individualization of Care in Hemodialysis: A Qualitative Study (2020) (5)
Perspectives of Transplant Professionals on the Values, Ethics, and Challenges of Living Kidney Donor Evaluation in Asia (2015) (5)
A working partnership: A review of shared decision‐making in nephrology (2021) (5)
Clinicians’ attitudes and approaches to evaluating the potential living kidney donor‐recipient relationship: An interview study (2019) (5)
NAV-KIDS 2 trial : protocol for a multi-centre , staggered randomised controlled trial of a patient navigator intervention in children with chronic kidney disease (2019) (5)
Perspectives of Medical Specialists From Different Disciplines on the Management of Systemic Lupus Erythematosus: An Interview Study (2018) (5)
Perspectives on ability to work from patients’ receiving dialysis and caregivers: analysis of data from the global SONG initiative (2021) (5)
The Power of the Patient Voice: Conducting and Using Qualitative Research to Improve Care and Outcomes in Peritoneal Dialysis (2018) (5)
Patient and parent perspectives on transition from paediatric to adult healthcare in rheumatic diseases: an interview study (2021) (5)
A Systematic Review of Scope and Consistency of Outcome Measures for Physical Fitness in Chronic Kidney Disease Trials (2021) (5)
Identifying dimensions of fatigue in haemodialysis important to patients, caregivers and health professionals: An international survey (2020) (5)
Scope of Outcomes in Trials and Observational Studies of Interventions Targeting Medication Adherence in Rheumatic Conditions: A Systematic Review (2019) (5)
A Text Messaging Intervention for Dietary Behaviors for People Receiving Maintenance Hemodialysis: A Feasibility Study of KIDNEYTEXT. (2021) (5)
Factors Associated With Advanced Colorectal Neoplasia in Patients With CKD. (2021) (5)
‘Knowledge is power’: A framework for partnering with consumers in developing and delivering a scientific meeting in nephrology (2020) (5)
Management of Anemia in Nondialysis Chronic Kidney Disease: Current Recommendations, Real-World Practice, and Patient Perspectives. (2020) (5)
Patient-led identification and prioritization of exercise interventions for fatigue on dialysis: a workshop report (2020) (5)
“A good death but there was all this tension around”- perspectives of residential managers on the experience of delivering end of life care for people living with dementia (2021) (4)
KHA-CARI Autosomal Dominant Polycystic Kidney Disease Guideline: Genetics and Genetic Counseling. (2015) (4)
Aboriginal and Torres Strait Islander women's views of cervical screening by self‐collection: a qualitative study (2022) (4)
Behavioural and pharmaceutical interventions for the prevention of skin cancers in solid organ transplant recipients: a systematic review of randomised controlled trials (2020) (4)
“Can I go to Glasgow?” Learnings from patient involvement at the 17th Congress of the International Society for Peritoneal Dialysis (ISPD) (2020) (4)
Clinicians’ perspectives of shared care of psoriatic arthritis and psoriasis between rheumatology and dermatology: an interview study (2020) (4)
Living Well With Kidney Disease by Patient and Carepartner Empowerment: Kidney Health for Everyone Everywhere. (2021) (4)
Perspectives on blood pressure by patients on haemo‐ and peritoneal dialysis (2020) (4)
Living well with kidney disease by patient and care-partner empowerment: Kidney health for everyone everywhere. (2021) (4)
‘A sword of Damocles’: patient and caregiver beliefs, attitudes and perspectives on presymptomatic testing for autosomal dominant polycystic kidney disease: a focus group study (2020) (4)
World Kidney Day 2021: Living Well With Kidney Disease by Patient and Care Partner Empowerment-Kidney Health for Everyone Everywhere. (2021) (4)
Patient-reported outcome measures for pain in autosomal dominant polycystic kidney disease: A systematic review (2021) (4)
Sex Differences in Kidney Transplantation: Austria and the United States, 1978–2018 (2022) (4)
Targeted Education ApproaCH to improve Peritoneal Dialysis Outcomes (TEACH-PD): A feasibility study (2020) (4)
Hypoxia-inducible factor stabilisers for the anaemia of chronic kidney disease. (2020) (4)
PATIENTS' EXPERIENCES AND PERSPECTIVES OF LIVING WITH CHRONIC KIDNEY DISEASE (2009) (4)
Outcome measures for technique survival reported in peritoneal dialysis: A systematic review (2021) (4)
Patients' Perspectives on Shared Decision‐Making About Medications in Psoriatic Arthritis: An Interview Study (2021) (3)
DIALYSIS VASCULAR ACCESS (2014) (3)
Influenza vaccination uptake and factors influencing vaccination decision among patients with chronic kidney or liver disease (2021) (3)
Dietary patterns for adults with chronic kidney disease (2015) (3)
Cost-effectiveness of a mobile phone text messaging program (KIDNEYTEXT) targeting dietary behaviours in people receiving haemodialysis. (2021) (3)
Patient-centred clinical trial design (2022) (3)
Large-scale, mixed-methods, knowledge exchange to establish core outcomes - the SONG approach. (2020) (3)
D-mannose for preventing and treating urinary tract infections. (2020) (3)
Country-specific sex disparities in living kidney donation (2021) (3)
Patient and Caregiver Experiences and Attitudes about Their Involvement in Research in Chronic Kidney Disease (2022) (3)
Study protocol: Yarning about HPV Vaccination: a qualitative study of factors influencing HPV vaccination among Aboriginal and Torres Strait Islander adolescents in Australia (2021) (3)
KHA-CARI Autosomal Dominant Polycystic Kidney Disease Guideline: Psychosocial Care. (2015) (3)
Patients' experiences and perspectives of a mobile phone text messaging intervention to improve dietary behaviours in haemodialysis. (2021) (3)
eHealth interventions for people with chronic kidney disease. (2019) (3)
Establishing a core outcome measure for life participation in patients receiving peritoneal dialysis: A Standardised Outcomes in Nephrology–Peritoneal Dialysis consensus workshop report (2022) (3)
Nephrologists' perspectives on cancer screening in patients with chronic kidney disease: An interview study (2019) (3)
Development of an international Delphi survey to establish core outcome domains for trials in adults with glomerular disease. (2021) (3)
Appraisal of Qualitative Studies (2019) (3)
Evaluation of the Cochrane Consumers and Communication Group’s systematic review priority-setting project (2020) (3)
New approaches to trials in glomerulonephritis. (2017) (3)
SUN-073 DEVELOPING CONSENSUS-BASED OUTCOME DOMAINS FOR TRIALS IN PERITONEAL DIALYSIS: AN INTERNATIONAL DELPHI SURVEY (2019) (3)
Patient, Caregiver, and Provider Perspectives on Improving Information Delivery in Hemodialysis: A Qualitative Study (2021) (3)
Living well with kidney disease by patient and care-partner empowerment: Kidney health for everyone everywhere. (2021) (3)
Patient and Caregiver Priorities for Outcomes in Peritoneal Dialysis (2018) (3)
Addressing Challenges in Developing a Core Domain Set in Adherence Interventions in Rheumatology: A Report from the OMERACT-Adherence Group (2019) (3)
Trajectories of quality of life in chronic kidney disease: a novel perspective of disease progression. (2021) (2)
M (cid:1) aori patients ’ experiences and perspectives of chronic kidney disease: a New Zealand qualitative interview study (2017) (2)
Patients’ Perspectives on Access to Dialysis and Kidney Transplantation in Rural Communities in Australia (2021) (2)
Systematic Review of Qualitative Studies Experiences of Parents Who Have Children With Chronic Kidney Disease: A (2013) (2)
#PatientsIncluded: Patient involvement in nephrology conferences (2020) (2)
A Core Outcome Set for Trials in Glomerular Disease (2021) (2)
Patient and Clinician Perspectives on the use of Remote Patient Monitoring in Peritoneal Dialysis (2022) (2)
Scope and heterogeneity of outcomes reported in randomized trials in patients receiving peritoneal dialysis (2020) (2)
RANGE AND CONSISTENCY OF INFECTION OUTCOMES REPORTED IN TRIALS CONDUCTED IN KIDNEY TRANSPLANT RECIPIENTS: A SYSTEMATIC REVIEW (2021) (2)
Living well with kidney disease by patient and care-partner empowerment: kidney health for everyone everywhere (2021) (2)
Living Well with Kidney Disease by Patient and Care-Partner Empowerment: Kidney Health for Everyone Everywhere (2021) (2)
A Focus Group Study of Self-Management in Patients With Glomerular Disease (2021) (2)
Living Well with Kidney Disease by Patient and Care-Partner Empowerment: Kidney Health for Everyone Everywhere (2021) (2)
Living Well With Kidney Disease by Patient and Care Partner Empowerment: Kidney Health for Everyone Everywhere. (2021) (2)
A Web-Based Self-Management Support Prototype for Adults With Chronic Kidney Disease (My Kidneys My Health): Co-Design and Usability Testing (Preprint) (2020) (2)
Quality of Life Outcomes Reported in Randomised Controlled Trials of Immunosuppressive Drug Regimens in Kidney Transplantation: A Systematic Review: 971 (2012) (2)
MAKING DECISIONS ABOUT LONG-TERM INSTITUTIONAL CARE PLACEMENT AMONG PEOPLE WITH DEMENTIA AND THEIR CAREGIVERS: SYSTEMATIC REVIEW OF QUALITATIVE STUDIES (2019) (2)
Nephrologistsʼ Preferences and Perspectives On Patientsʼ Access to Kidney Transplantation: A Systematic Review.: Abstract# B834 (2014) (2)
A practical guide to interpreting and applying systematic reviews of qualitative studies in rheumatology (2020) (2)
Core outcome measures for trials in people with COVID-19: respiratory failure, multiorgan failure, shortness of breath and recovery (2020) (2)
Establishing a core outcome measure for pain in patients with autosomal dominant polycystic kidney disease: a consensus workshop report (2021) (2)
Chronic disease prevention programs offered by Aboriginal Community Controlled Health Services in New South Wales, Australia (2021) (2)
Marketing systems for smallholders: a comparison of assembly markets in areas of production with farmer marketing at Mbare Musika in Harare (1997) (2)
Albaramki J, Hodson EM, Craig JC, Webster AC .Parenteral versus oral iron therapy for adults and children with chronic kidney disease. Cochrane Database of Systematic Reviews of Systematic (2013) (2)
Living Well with Kidney Disease by Patient and Care-Partner Empowerment: Kidney Health for Everyone Everywhere (2021) (2)
Preferences for Biologic Treatment in Patients With Psoriatic Arthritis: A Discrete Choice Experiment (2021) (2)
CLINICIAN BELIEFS AND ATTITUDES ABOUT HOME HAEMODIALYSIS: QUALITATIVE INTERVIEW STUDY (2012) (2)
Fecal Immunochemical Screening for Advanced Colorectal Neoplasia in Patients with CKD: Accurate or Not? Reply (2019) (2)
Using self-determination theory to understand and improve recruitment for the Coaching for Healthy Ageing (CHAnGE) trial (2021) (2)
Qualitative Research in Nephrology: An Introduction to Methods and Critical Appraisal. (2021) (2)
Patient and caregiver perspectives on blood pressure in children with chronic kidney disease. (2021) (2)
eHealth Interventions for Solid Organ Transplant Recipients: A Systematic Review and Meta-analysis of Randomized Controlled Trials. (2020) (1)
“WHEN I HAD MY TRANSPLANT, I BECAME NORMAL.” ADOLESCENT EXPERIENCES AND PERSPECTIVES ON LIFE AFTER KIDNEY TRANSPLANTATION: 175 (2010) (1)
Older People's Perspectives on Participation in Exercise: A Systematic Review and Thematic Synthasis of Qualitative Literature (2013) (1)
Authors' Reply. (2019) (1)
Young Kidney Professionals' Perspectives and Attitudes about Consuming Scientific Information: A Focus Group Study. (2018) (1)
Scope and consistency of outcomes reported in randomised trials of haemodialysis (2015) (1)
Promoting deceased organ and tissue donation registration in family physician waiting rooms (RegisterNow-1): a pragmatic stepped-wedge, cluster randomized controlled registry trial (2022) (1)
Identifying important outcomes for young people with chronic kidney disease and their caregivers: a nominal group technique study (2019) (1)
Discrete choice experiments to elicit patient preferences for decision-making in transplantation. (2020) (1)
Patient preferences for cancer screening in chronic kidney disease: a best-worst scaling survey. (2021) (1)
FRI0655 Title: the consistency of outcomes reported in trials of systemic sclerosis. improving over time? (2018) (1)
Equity in national policies for Australians with kidney disease (2021) (1)
Living well with kidney disease by patient and care‐partner empowerment: Kidney health for everyone everywhere (2021) (1)
Outcomes of Interest to Living Kidney Donors (2019) (1)
P-52 Delivering advance care planning in chronic kidney disease (CKD): The perspectives of healthcare providers (2015) (1)
Correction to: The association between socioeconomic disadvantage and parent-rated health in children and adolescents with chronic kidney disease—the Kids with CKD (KCAD) study (2022) (1)
Perspectives of patients, family members, health professionals and the public on the impact of COVID-19 on mental health (2022) (1)
SUN-244 RANGE AND VARIABILITY OF OUTCOMES REPORTED IN RANDOMIZED TRIALS CONDUCTED IN POLYCYSTIC KIDNEY DISEASE: A SYSTEMATIC REVIEW (2019) (1)
Perspectives of Clinicians on Shared Decision Making in Pediatric CKD: A Qualitative Study. (2022) (1)
Experiences and challenges faced by patients with COVID-19 who were hospitalised and participated in a randomised controlled trial: a qualitative study (2022) (1)
Patient and caregiver perspectives on telehealth in kidney transplantation (2020) (1)
Reply to “Review of Living Kidney Donor Guidelines is Out of Date Before Publication” (2012) (1)
Epidemiology and outcome research in CKD 5D (2012) (1)
Planning implementation and scale-up of physical activity interventions for people with walking difficulties: study protocol for the process evaluation of the ComeBACK trial (2022) (1)
The evaluation of individualised telehealth intensive coaching to promote healthy eating and lifestyle in chronic kidney disease (ENTICE-CKD): A pilot randomised controlled trial (2018) (1)
CKD GENERAL AND CLINICAL EPIDEMIOLOGY 2 (2014) (1)
Indigenous peoples' perspectives of living with chronic kidney disease: systematic review of qualitative studies. (2022) (1)
Living well with kidney disease by patient and care-partner empowerment: kidney health for everyone everywhere (2021) (1)
Patient Preferences for the Allocation of Deceased Donor Kidneys for Transplantation: A Mixed Methods Study: 946 (2012) (1)
Correction to: Living Well with Kidney Disease by patient and care-partner empowerment: Kidney Health for Everyone Everywhere (2021) (1)
Patientsʼ Attitudes Towards Living Kidney Donation: Systematic Review and Thematic Synthesis of Qualitative Research.: Abstract# B832 (2014) (1)
Living Well With Kidney Disease by Patient and Care-Partner Empowerment: Kidney Health for Everyone Everywhere. (2021) (1)
Living well with kidney disease by patient and care-partner empowerment: Kidney health for everyone everywhere. (2021) (1)
Murradambirra Dhangaang (make food secure): Aboriginal community and stakeholder perspectives on food insecurity in urban and regional Australia (2021) (1)
Establishing a Core Outcome Measure for Peritoneal Dialysis-related Peritonitis: A Standardized Outcomes in Nephrology—Peritoneal Dialysis Consensus Workshop Report (2022) (1)
Living Well With Kidney Disease by Patient and Care-Partner Empowerment: Kidney Health for Everyone Everywhere (2021) (1)
Establishing a Core Outcome Measure for Peritoneal Dialysis-related Peritonitis: A Standardized Outcomes in Nephrology—Peritoneal Dialysis Consensus Workshop Report (2022) (1)
O-93 Current practice and barriers to advance care planning in the australian and New Zealand nephrology setting: A national survey (2015) (1)
Stakeholder perspectives on the implementation and impact of Indigenous health interventions: A systematic review of qualitative studies (2021) (1)
The CKD bowel health study: understanding the bowel health and gastrointestinal symptom management in patients with chronic kidney disease: a mixed-methods observational longitudinal study (protocol) (2021) (1)
Living Well With Kidney Disease by Patient and Care-Partner Empowerment: Kidney Health for Everyone Everywhere (2021) (1)
Exercise Training in Solid Organ Transplant Recipients - A Systematic Review: 991 (2012) (1)
Longitudinal assessment of the health-related quality of life of children and adolescents with chronic kidney disease. (2022) (1)
Living well with kidney disease by patient and care-partner empowerment: Kidney health for everyone everywhere. (2021) (1)
Clinicians’ perspectives on equity of access to dialysis and kidney transplantation for rural people in Australia: a semistructured interview study (2022) (1)
Prize Orals (2017) (1)
Vascular access outcomes reported in randomised trials conducted in patients requiring haemodialysis: a systematic review (2017) (1)
Transplant Professionals’ Attitudes and Approaches to the Living Kidney Donor-Recipient Relationship: Interview study (2017) (1)
Horticultural marketing in Zimbabwe: experiences from the Mutoko-Uzumba smallholder farmer project. (1990) (1)
The cost and role of transport in smallholder horticultural production: experiences from the Mashonaland East fruit and vegetable project (1997) (1)
Synbiotics, prebiotics and probiotics for solid organ transplant recipients. (2021) (1)
A viewpoint describing the American Society of Transplantation rationale to conduct a comprehensive patient survey assessing unmet immunosuppressive therapy needs (2022) (1)
Clinicians’ Attitudes and Perspectives on Ante-Mortem Interventions in Deceased Organ Donation: An International Interview Study (2018) (1)
Establishing a Core Outcome Measure for Graft Health: A Sandardized Outcomes in Nephrology – Kidney Transplantation (song-tx) Consensus Workshop Report (2018) (1)
FP657STAKEHOLDER PRIORITIES FOR CARDIOVASCULAR OUTCOMES IN HEMODIALYSIS TRIALS: AN INTERNATIONAL SURVEY (2018) (1)
An eHealth self-management intervention for adults with chronic kidney disease, My Kidneys My Health: a mixed-methods study (2022) (1)
Novel treatments and trials in COVID-19 (2021) (0)
Sex and gender as predictors for allograft and patient-relevant outcomes after kidney transplantation (2022) (0)
Cognitive and academic outcomes in children with chronic kidney disease (2022) (0)
SUN-019 IDENTIFYING OUTCOMES IMPORTANT TO PATIENTS WITH GLOMERULONEPHRITIS AND THEIR CAREGIVERS: A MULTINATIONAL NOMINAL GROUP STUDY (2019) (0)
Public Attitudes and Beliefs About Living Kidney Donation: Focus Group Study.: Abstract# B839 (2014) (0)
CARI Autosomal Dominant Polycystic Kidney Disease Guideline : Genetics and Genetic Counseling (2015) (0)
Study protocol for Vascular Access outcome measure for function: a vaLidation study In hemoDialysis (VALID) (2022) (0)
Everyoneʼs Got Their Own Threshold. Nephrologistsʼ Perspectives On Patient Eligibility and Access to Living Donor Kidney Transplantation.: Abstract# B836 (2014) (0)
AB 1237 PATIENTS ’ PERSPECTIVES AND EXPERIENCE OF PSORIASIS AND PSORIATIC ARTHRITIS : A SYSTEMATIC REVIEW AND THEMATIC SYNTHESIS OF QUALITATIVE STUDIES (2019) (0)
Perspectives of a proposed patient navigator programme for people with chronic kidney disease in rural communities: Report from national workshops (2022) (0)
OP-IJEJ210168_6 225..226 ++ (2021) (0)
“A Good Death But There Was All This Tension Around” - Perspectives of Residential Managers on the Experiences and Challenges of Delivering end of Life Care for People Living with Dementia. (2020) (0)
What Outcomes Matter Most for Kidney Transplant Recipients? Results of a Mixed Methods Study: 970 (2012) (0)
Child and caregiver perspectives on access to psychosocial and educational support in pediatric chronic kidney disease: a focus group study (2022) (0)
Perspectives of Kidney Transplant Recipients on eHealth: Semistructured Interviews (2022) (0)
254 Induction and maintenance treatment of proliferative lupus nephritis: an updated cochrane review (2017) (0)
Coaching for Healthy Ageing: Recruiting and Older Population (2016) (0)
Improving renal services for Aboriginal people with end-stage kidney disease in rural NSW (2013) (0)
Identifying principles and strategies for involving patients and caregivers in research in chronic kidney disease: A report of three workshops (2018) (0)
Protocol for establishing a core outcome set for evaluation in studies of pulmonary exacerbations in people with cystic fibrosis (2022) (0)
Let's Talk About Sex…and Chronic Kidney Disease. (2023) (0)
Baseline characteristics of participants in the NAVKIDS2 trial: a patient navigator program in children with chronic kidney disease (2022) (0)
AB1360 Range and consistency of outcome measures reported in randomised trials in dermatomyositis: a systematic review (2018) (0)
FP784CHILD AND PARENTAL VIEWS ON COMMUNICATION AND DECISION-MAKING IN PEDIATRIC CHRONIC KIDNEY DISEASE (2018) (0)
Living Well With Kidney Disease by Patient and Care Partner Empowerment: Kidney Health for Everyone Everywhere (2021) (0)
Research priorities in chronic kidney disease: a priority setting partnership (2014) (0)
Towards consumer-centred health care and health research in nephrology: understanding patient and family caregiver experiences and perspectives in chronic kidney disease (2008) (0)
[Living well with kidney disease by patient and care-partner empowerment: kidney health for everyone everywhere]. (2021) (0)
THE PERSPECTIVES OF KIDNEY AND KIDNEY-PANCREAS TRANSPLANT RECIPIENTS ON CANCER RISK, PREVENTION AND SCREENING BEHAVIOURS: A QUALITATIVE STUDY.: 698 (2010) (0)
SAT-233 BEHAVIOR CHANGE TECHNIQUES IN LIFESTYLE INTERVENTIONS FOR PREVENTING THE PROGRESSION OF CHRONIC KIDNEY DISEASE: A SYSTEMATIC REVIEW (2019) (0)
MP822DEVELOPING CONSENSUS BASED PRIORITY OUTCOME DOMAINS FOR TRIALS IN KIDNEY TRANSPLANTATION: A MULTINATIONAL DELPHI SURVEY WITH PATIENTS, CAREGIVERS AND HEALTH PROFESSIONALS (2017) (0)
Australian Workshops on Patients’ Perspectives on Hemodialysis and Incremental Start (2022) (0)
MO048DEVELOPING CORE VASCULAR ACCESS OUTCOMES FOR TRIALS IN HAEMODIALYSIS: AN INTERNATIONAL MULTISTAKEHOLDER SURVEY (2017) (0)
Announcement (1976) (0)
Title: Decision Making around Living and Deceased Donor Kidney Transplantation: a Qualitative Study Exploring the Importance of Expected Relationship Changes (0)
Researchers’ perspectives on methodological challenges and outcomes selection in interventional studies targeting medication adherence in rheumatic diseases: an OMERACT-adherence study (2021) (0)
Establishment of a Young Adult Renal Clinic and Effects On Qualitative and Quantitative Assessments of Quality of Life (QOL): A Longitudinal Study.: Abstract# D2727 (2014) (0)
The perspectives of healthcare providers on the nutritional management of patients on haemodialysis: An interview study (2017) (0)
Exercise Training and Dietary Program in Kidney Transplant Recipients: 1432 (2012) (0)
ELICITING PRIORITIES FOR RESEARCH FROM PATIENTS WITH CHRONIC KIDNEY DISEASE (2007) (0)
SAT-238 IDENTIFYING IMPORTANT OUTCOMES FOR YOUNG PEOPLE WITH CHRONIC KIDNEY DISEASE AND THEIR CAREGIVERS: FOCUS GROUPS WITH NOMINAL GROUP TECHNIQUE (2019) (0)
Insights From Transplant Professionals on the Use of Social Media: Implications and Responsibilities (2022) (0)
Patient Preferences and Priorities for Outcomes Following Kidney Transplantation.: Abstract# D2716 (2014) (0)
Opinions of Transplant Nephrologists and Surgeons On Reimbursement, Compensation and Incentives for Living Kidney Donors.: Abstract# B828 (2014) (0)
Eliciting the Priorities of Patients, Caregivers and Health Professionals for Important Outcomes in Nephrology Using International Best-Worst Scaling Surveys (2017) (0)
Feasibility and acceptability of telehealth coaching to promote healthy eating in chronic kidney disease (2019) (0)
Patient and parent proxy-reported outcome measures for life participation in children with CKD (2020) (0)
SAT-236 IDENTIFYING AND INTEGRATING PATIENT AND CAREGIVER PERSPECTIVES IN CLINICAL PRACTICE GUIDELINES FOR PERCUTANEOUS RENAL BIOPSY (2019) (0)
NAVKIDS2 trial: a multi-centre, waitlisted randomised controlled trial of a patient navigator intervention in children with chronic kidney disease — statistical analysis plan and update to the protocol (2022) (0)
Living Well with Kidney Disease by Patient and Care-Partner Empowerment: Kidney Health for Everyone Everywhere (2021) (0)
They put funerals and family in front of their dialysis?: a qualitative study of service provider's perspectives on service delivery for Aboriginal people receiving haemodialysis in rural NSW (2014) (0)
Desperation, Despair, and Debasement: Thematic Synthesis of Qualitative Research on the Experiences of Commercial Kidney Donors: 942 (2012) (0)
Range and consistency of outcome measures reported in randomised trials in dermatomyositis: a systematic review (2022) (0)
MO027EVALUATING THE FEASIBILITY AND IMPACT OF A MOBILE PHONE TEXT MESSAGING INTERVENTION ON ADHERENCE TO DIETARY RECOMMENDATIONS IN PATIENTS ON HAEMODIALYSIS (KIDNEYTEXT) (2020) (0)
Reporting of Qualitative Health Research (2018) (0)
Improving Clinical Care for Children With CKD: A Report From a National Kidney Foundation Scientific Workshop. (2022) (0)
SP583VASCULAR ACCESS OUTCOMES REPORTED IN RANDOMISED TRIALS CONDUCTED IN PATIENTS REQUIRING HAEMODIALYSIS: A SYSTEMATIC REVIEW (2017) (0)
Under-screened Aboriginal and Torres Strait Islander women’s perspectives on cervical screening (2022) (0)
SO046SCOPE AND CONSISTENCY OF OUTCOMES REPORTED IN RANDOMISED TRIALS CONDUCTED IN ADULTS ON HAEMODIALYSIS (2017) (0)
SUN-124 RANGE AND CONSISTENCY OF CARDIOVASCULAR OUTCOMES REPORTED IN CONTEMPORARY RANDOMISED TRIALS IN KIDNEY TRANSPLANT PATIENTS: A SYSTEMATIC REVIEW (2019) (0)
Range and consistency of gastrointestinal outcomes reported in peritoneal dialysis trials: A systematic review. (2022) (0)
Association between socioeconomic status and academic performance in children and adolescents with chronic kidney disease (2022) (0)
THU0565 RESEARCHERS’ PERSPECTIVES ON ADHERENCE INTERVENTION RESEARCH AND OUTCOMES IN RHEUMATOLOGY: AN INTERNATIONAL QUALITATIVE STUDY (2020) (0)
Effectiveness of Behavioral Interventions for Promoting Sun-Protection and Preventing Skin Cancer in Solid Organ Transplant Recipients: A Systematic Review.: Abstract# A538 (2014) (0)
S70– Consumer involvement in guideline development (2010) (0)
Living well with kidney disease by patient and care-partner empowerment: kidney health for everyone everywhere (2021) (0)
Scope and Consistency of Cancer Outcomes Reported in Randomized Trials in Kidney Transplant Recipients (2022) (0)
One-Time Faecal Immunochemical Screening for Advanced Colorectal Neoplasia in Patients with Chronic Kidney Disease (Detect Study) (2018) (0)
Identifying a core vascular access outcome for all trials in haemodialysis: an international survey with patients and health professionals (2017) (0)
Living well with kidney disease by patient and care partner empowerment: kidney health for everyone everywhere. (2021) (0)
Outcome Measures for Life Participation in Patients with Kidney Transplantation (2018) (0)
Range and Consistency of Cardiovascular Outcomes Reported by Clinical Trials in Kidney Transplant Recipients: A Systematic Review (2022) (0)
Gut microbial biomarkers for predicting adverse outcomes in people with chronic kidney disease (2022) (0)
Delivering health programs for Aboriginal and Torres Strait Islander children: Carer and staff views on what's important (2022) (0)
SP597DEVELOPING A CORE OUTCOME MEASURE FOR VASCULAR ACCESS FOR TRIALS IN HAEMODIALYSIS: AN INTERNATIONAL MULTISTAKEHOLDER CONSENSUS WORKSHOP (2017) (0)
Living well with kidney disease by patient and care partner empowerment: kidney health for everyone everywhere (2021) (0)
Reprint of: Living well with kidney disease by patient and care-partner empowerment: kidney health for everyone everywhere (2021) (0)
Living Well with Kidney Disease by patient and care-partner empowerment: Kidney Health for Everyone Everywhere (2021) (0)
MO034DIETARY PATTERNS FOR PEOPLE WITH CHRONIC KIDNEY DISEASE: META-ANALYSIS OF RANDOMIZED CLINICAL TRIALS (2017) (0)
Synbiotics, prebiotics and probiotics for people with chronic kidney disease (2020) (0)
SAT-235 PRINCIPLES AND STRATEGIES FOR INVOLVING PATIENTS IN RESEARCH IN CHRONIC KIDNEY DISEASE: REPORT FROM NATIONAL WORKSHOPS (2019) (0)
SUN-066 PATIENT AND CAREGIVER PERSPECTIVES, BELIEFS, AND EXPERIENCES OF EMPOWERMENT IN PERITONEAL DIALYSIS (2019) (0)
The Spectrum of Patient and Caregiver Experiences (2021) (0)
AB1237 Patients’ perspectives and experience of psoriasis and psoriatic arthritis: a systematic review and thematic synthesis of qualitative studies (2018) (0)
Clinical Practice Guidelines on Waitlisting for Kidney Transplantation: A Systematic Review: 1247 (2012) (0)
Full Review New approaches to trials in glomerulonephritis (2016) (0)
SUN-097 PATIENTS' LIVED EXPERIENCE OF FATIGUE IN HEMODIALYSIS: SYSTEMATIC REVIEW AND THEMATIC ANALYSIS OF QUALITATIVE STUDIES (2019) (0)
Perspectives and experiences of self-monitoring of blood pressure among patients with hypertension: a systematic review of qualitative studies. (2023) (0)
Staff perspectives on end-of-life care for people living with dementia in residential aged care homes: qualitative study (2023) (0)
Improving renal services for Aboriginal people in rural NSW: avoiding the 'costly' crisis (2014) (0)
Australian Rural Caregivers' Experiences in Supporting Patients With Kidney Failure to Access Dialysis and Kidney Transplantation: A Qualitative Study. (2022) (0)
HEALS (Hearing EAr health Language and Speech services) project (2016) (0)
International Guidelines for Diabetes, Heart Disease, and Kidney Disease (2011) (0)
Prize Orals (2020) (0)
WCN23-0574 THE ELLEN MEDICAL DEVICES AFFORDABLE POINT-OF-CARE PERITONEAL DIALYSIS SYSTEM - A PILOT STUDY (2023) (0)
Award Orals (2022) (0)
Incremental versus standard dialysis for people with kidney failure (2023) (0)
Qualitative analysis of stakeholder perspectives on engaging Latinx patients in kidney-related research (2023) (0)
Broadening the diversity of consumers engaged in guidelines: a scoping review (2022) (0)
P0275SCOPE AND CONSISTENCY OF OUTCOME MEASURES FOR PHYSICAL FITNESS IN TRIALS IN PATIENTS WITH CHRONIC KIDNEY DISEASE: A SYSTEMATIC REVIEW (2020) (0)
Patient Perspectives on Outcome Domains of Medication Adherence Trials in Inflammatory Arthritis: An International OMERACT Focus Group Study (2021) (0)
SUN-096 STANDARDIZED OUTCOMES IN NEPHROLOGY-HEMODIALYSIS (SONG-HD): DEVELOPING A CORE OUTCOME MEASURE FOR FATIGUE IN HEMODIALYSIS (2019) (0)
Living well with kidney disease by patient and care-partner empowerment: kidney health for everyone everywhere (2021) (0)
SP734THE BREADTH AND CONSISTENCY OF OUTCOMES REPORTED IN RANDOMISED TRIALS CONDUCTED IN ADULT KIDNEY TRANSPLANT RECIPIENTS (2017) (0)
Sources of Clinician Burnout in Providing Care for Underserved Patients in a Safety-Net Healthcare System (2022) (0)
Disparities in decision-making practices for dialysis modality in advanced chronic kidney disease: closing the gap across Europe. (2021) (0)
Living well with kidney disease by patient and care partner empowerment: kidney health for everyone everywhere. (2021) (0)
384 Multi-specialists’ perspectives on clinical decision making in systemic lupus erythematosus: an interview study (2017) (0)
Defining Myocardial Infarction in trials of people receiving hemodialysis: consensus report from the SONG-HD MI Expert Working group. (2023) (0)
Parental Perspectives On the Financial Impact of Caring for a Child With Chronic Kidney Disease.: Abstract# B1218 (2014) (0)
Living well with kidney disease by patient and care-partner empowerment: Kidney health for everyone everywhere (2021) (0)
OP56 The cost-effectiveness of advance care planning for older adults with end-stage kidney disease (2019) (0)
For peer review only "Service providers' perspectives, attitudes and beliefs on health services delivery for Aboriginal people receiving haemodialysis in rural Australia" (2013) (0)
Epidemiology and CKD - 1 (2009) (0)
1454Renal disease in Aboriginal children and young adults (ARDAC): evolution to a data linkage study (2021) (0)
Title : Identifying and integrating consumer perspectives in clinical practice guidelines on autosomal dominant polycystic kidney disease 1 Running title : Consumer involvement in ADPKD guidelines (0)
FP783 GLOMERULONEPHRITIS WITH CRESCENTS IN CHILDREN (2018) (0)
SuO008STANDARDISED OUTCOMES IN NEPHROLOGY (SONG): ESTABLISHING A CORE VASCULAR ACCESS OUTCOME MEASURE FOR TRIALS IN HAEMODIALYSIS (2018) (0)
Child and parental perspectives on communication and decision-making in pediatric chronic kidney disease: a focus group study (2018) (0)
Engagement and fidelity of a cardiovascular disease prevention-focused digital health intervention in cardiology outpatient waiting rooms: a mixed-methods study (2022) (0)
FP628A CORE OUTCOME SET FOR TRIALS IN HAEMODIALYSIS ESTABLISHED BY THE STANDARDISED OUTCOMES IN NEPHROLOGY - HAEMODIALYSIS INITIATIVE (2018) (0)
Critically important outcomes for infection in trials in kidney transplantation: An international survey of patients, caregivers, and health professionals (2022) (0)
SPECTRUM AND CONSISTENCY OF CANCER OUTCOMES IN RANDOMIZED TRIALS IN KIDNEY TRANSPLANT RECIPIENTS: A SYSTEMATIC REVIEW (2020) (0)
Living well with kidney disease by patient and care-partner empowerment: Kidney health for everyone everywhere (2021) (0)
Living well with kidney disease by patient and care‐partner empowerment: kidney health for everyone everywhere (2021) (0)
PATIENT AND CAREGIVER BELIEFS, ATTITUDES AND PERSPECTIVES ON GENETIC SCREENING AND TESTING FOR AUTOSOMAL POLYCYSTIC KIDNEY DISEASE (2018) (0)
Novel Endpoints in Solid Organ Transplantation: Targeting Patient-reported Outcome Measures. (2023) (0)

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What Schools Are Affiliated With Allison Tong?

Allison Tong is affiliated with the following schools:

Medical University of Vienna
University of Sydney
Stanford University