Kathleen J. Ramos
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Kathleen J. Ramos has a total of 159 co-authors. Here are the top co-authors by number of shared publications:
- Christopher Hooper Goss
Division of Pulmonary, Critical Care, and Sleep Medicine, Department of Medicine, University of Washington, Seattle, WA, USA; CF Therapeutics Development Network Coordinating Center, Seattle Children's Research Institute, Seattle, WA, USA; Division of Pulmonary and Sleep Medicine, Department of Pediatrics, University of Washington, Seattle, WA, USA
13 shared publications - Siddhartha G. Kapnadak
Division of Pulmonary, Critical Care, and Sleep Medicine, Department of Medicine, University of Washington, Seattle, WA, USA
12 shared publications Christopher H. Goss
Division of Pulmonary, Critical Care, and Sleep Medicine, Department of Medicine, University of Washington, Seattle WA, United States; Division of Pulmonary and Allergy, Department of Pediatrics, University of Washington, Seattle WA, United States; CFF TDNCC Seattle Children's Research Institute, Seattle, WA, United States
11 shared publications- Albert Faro
Cystic Fibrosis Foundation, Bethesda, MD, USA
5 shared publications - Erika D. Lease
University of Washington
5 shared publications - Joseph M. Pilewski
Division of Pulmonary, Allergy, Critical Care and Sleep Medicine, Department of Medicine, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA
5 shared publications
Latest Publications
- 8 June 2026
- Published by Elsevier in The Journal of Heart and Lung Transplantation
- Vol. 45 (9) , 1470-1473
Approach to prevention and management of chronic lung allograft dysfunction in North American lung transplant centers
- 8 June 2026
- Published by Elsevier in The Journal of Heart and Lung Transplantation
- Vol. 45 (9) , 1470-1473
Approach to prevention and management of chronic lung allograft dysfunction in North American lung transplant centers
- Open Access
- 1 August 2025
- Published by Oxford University Press (OUP) in Annals of the American Thoracic Society
- Vol. 22 (8) , 1132-1133
Lung Donor Utilization Decisions: A Data-Free Zone
- 1 August 2025
- Published by Oxford University Press (OUP) in Annals of the American Thoracic Society
- Vol. 22 (8) , 1132-1133
Open AccessLung Donor Utilization Decisions: A Data-Free Zone
- 2 July 2025
- Published by Elsevier in Journal of Cystic Fibrosis
- Vol. 24 (5) , 929-934
Elexacaftor/tezacaftor/ivacaftor prescription in lung transplant recipients with cystic fibrosis in the US
- 2 July 2025
- Published by Elsevier in Journal of Cystic Fibrosis
- Vol. 24 (5) , 929-934
Elexacaftor/tezacaftor/ivacaftor prescription in lung transplant recipients with cystic fibrosis in the US
- 5 May 2025
- Published by Elsevier in Patient Education and Counseling
- Vol. 137, 108822
Personal narratives to support learning about lung transplant for people with cystic fibrosis
- 5 May 2025
- Published by Elsevier in Patient Education and Counseling
- Vol. 137, 108822
Personal narratives to support learning about lung transplant for people with cystic fibrosis
- 17 October 2024
- Published by Elsevier in The Journal of Heart and Lung Transplantation
- Vol. 44 (2) , 191-192
Lung re-transplantation for recipients with cystic fibrosis: Procedure choice and other considerations
- 17 October 2024
- Published by Elsevier in The Journal of Heart and Lung Transplantation
- Vol. 44 (2) , 191-192
Lung re-transplantation for recipients with cystic fibrosis: Procedure choice and other considerations
- 2 October 2024
- Published by Elsevier in Journal of Cystic Fibrosis
- Vol. 24 (1) , 112-117
Linkage of the CF Foundation Patient Registry with the Scientific Registry of Transplant Recipients database
- 2 October 2024
- Published by Elsevier in Journal of Cystic Fibrosis
- Vol. 24 (1) , 112-117
Linkage of the CF Foundation Patient Registry with the Scientific Registry of Transplant Recipients database
- 18 July 2024
- Published by Wiley in Clinical Transplantation
- Vol. 38 (7) , e15406
Uncertainty and Communication Preferences Among Patients Undergoing Lung Transplant Evaluation: A Mixed‐Methods Study
Objective: Higher uncertainty is associated with poorer quality of life and may be impacted by clinician communication about the future. We determined how patients undergoing lung transplant evaluation experience uncertainty and communication about the future from clinicians.Methods: We performed a convergent parallel mixed‐methods study using a cross‐sectional survey and semistructured interviews. Patients undergoing lung transplant evaluation at the University of Colorado and the University of Washington answered questions about future communication and completed the Mishel Uncertainty in Illness Scale‐Adult (MUIS‐A; range 33–165, higher scores indicate more uncertainty). Interviews were analyzed using content analysis. Integration of survey and interview results occurred during data interpretation.Results: A total of 101 patients completed the survey (response rate: 47%). Twelve survey participants completed interviews. In the survey, most patients identified changing family roles as important (76%), which was infrequently discussed with clinicians (31%). Most patients (86%) worried about the quality of their life in the future, and 74% said that not knowing what to expect in the future prevented them from making plans. The mean MUIS‐A score was 85.5 (standard deviation 15.3). Interviews revealed three themes: (1) uncertainty of the future distresses participants; (2) participants want practical information from clinicians; and (3) communication preferences vary among participants.Conclusion: Participants experienced distressing uncertainty and wanted information about the future. Communication topics that were important to participants were not always addressed by physicians. Clinicians should address how chronic lung disease and lung transplant can directly impact patients’ lives and support patients to cope with uncertainty.
- 18 July 2024
- Published by Wiley in Clinical Transplantation
- Vol. 38 (7) , e15406
Uncertainty and Communication Preferences Among Patients Undergoing Lung Transplant Evaluation: A Mixed‐Methods Study
Objective: Higher uncertainty is associated with poorer quality of life and may be impacted by clinician communication about the future. We determined how patients undergoing lung transplant evaluation experience uncertainty and communication about the future from clinicians.Methods: We performed a convergent parallel mixed‐methods study using a cross‐sectional survey and semistructured interviews. Patients undergoing lung transplant evaluation at the University of Colorado and the University of Washington answered questions about future communication and completed the Mishel Uncertainty in Illness Scale‐Adult (MUIS‐A; range 33–165, higher scores indicate more uncertainty). Interviews were analyzed using content analysis. Integration of survey and interview results occurred during data interpretation.Results: A total of 101 patients completed the survey (response rate: 47%). Twelve survey participants completed interviews. In the survey, most patients identified changing family roles as important (76%), which was infrequently discussed with clinicians (31%). Most patients (86%) worried about the quality of their life in the future, and 74% said that not knowing what to expect in the future prevented them from making plans. The mean MUIS‐A score was 85.5 (standard deviation 15.3). Interviews revealed three themes: (1) uncertainty of the future distresses participants; (2) participants want practical information from clinicians; and (3) communication preferences vary among participants.Conclusion: Participants experienced distressing uncertainty and wanted information about the future. Communication topics that were important to participants were not always addressed by physicians. Clinicians should address how chronic lung disease and lung transplant can directly impact patients’ lives and support patients to cope with uncertainty.
- Open Access
- 22 June 2024
- Published by Elsevier in CHEST Pulmonary
- Vol. 2 (4)
A Dramatic Decline in Lung Transplantation for Cystic Fibrosis in the United States
- 22 June 2024
- Published by Elsevier in CHEST Pulmonary
- Vol. 2 (4)
Open AccessA Dramatic Decline in Lung Transplantation for Cystic Fibrosis in the United States
- 1 February 2024
- Published by Oxford University Press (OUP) in Annals of the American Thoracic Society
- Vol. 21 (2) , 271-278
Lung Allocation Score Exceptions in Persons with Cystic Fibrosis Undergoing Lung Transplant
Rationale: Lung transplantation can extend the lives of individuals with advanced cystic fibrosis (CF). Until March 2023, the Lung Allocation Score (LAS) was used in the United States to determine transplant priority. Certain clinical events or attributes (“risk events”) that are not included in the LAS (e.g., massive hemoptysis) are relatively common and prognostically important in CF and may prompt an exception request to increase priority for donor lungs. The new Lung Composite Allocation Score (CAS) also allows for exceptions based on the same principles. Objectives: To evaluate the frequency of LAS exceptions in persons with CF (PwCFs) listed for lung transplantation and assess whether LAS exceptions are associated with improved waitlist outcomes for PwCFs compared with similarly “at-risk” individuals without LAS exceptions. Methods: A merged dataset combining data from the CF Foundation Patient Registry and the Organ Procurement and Transplantation Network (2005–2019) was used to identify PwCFs listed for lung transplantation. We compared waitlist outcomes between PwCFs with a LAS exception versus those without an exception despite having a risk event. Risk events were defined as an episode of massive hemoptysis, pneumothorax, at least three moderate/severe pulmonary exacerbations, and/or a decrease in forced expiratory volume in 1 second by ⩾30% predicted (absolute) in the prior 12 months. Analyses were performed using competing risk regression with time to transplantation as the primary outcome and death without a transplant as a competing risk. Results: Of 3,538 listings from 3,309 candidates, 2% of listings (n = 81) had at least one exception. Candidates with an exception and those with a risk event but no exception received lung transplants more slowly than people without an exception or risk event (subdistribution hazard ratio [95% confidence interval]: LAS exception cohort, 0.66 [0.52–0.85]; risk event cohort without exceptions, 0.79 [0.72–0.86]). There was no difference between those with LAS exceptions and those at risk without LAS exceptions: subdistribution hazard ratio, 0.84 (0.66–1.08). Conclusions: LAS exceptions are rare in PwCFs listed for lung transplantation. LAS exceptions resulted in a similar time to transplantation for PwCFs compared with similarly at-risk individuals. As we enter the CAS era, these LAS-based results are pertinent to improve risk stratification among PwCFs being considered for lung transplantation.
- 1 February 2024
- Published by Oxford University Press (OUP) in Annals of the American Thoracic Society
- Vol. 21 (2) , 271-278
Lung Allocation Score Exceptions in Persons with Cystic Fibrosis Undergoing Lung Transplant
Rationale: Lung transplantation can extend the lives of individuals with advanced cystic fibrosis (CF). Until March 2023, the Lung Allocation Score (LAS) was used in the United States to determine transplant priority. Certain clinical events or attributes (“risk events”) that are not included in the LAS (e.g., massive hemoptysis) are relatively common and prognostically important in CF and may prompt an exception request to increase priority for donor lungs. The new Lung Composite Allocation Score (CAS) also allows for exceptions based on the same principles. Objectives: To evaluate the frequency of LAS exceptions in persons with CF (PwCFs) listed for lung transplantation and assess whether LAS exceptions are associated with improved waitlist outcomes for PwCFs compared with similarly “at-risk” individuals without LAS exceptions. Methods: A merged dataset combining data from the CF Foundation Patient Registry and the Organ Procurement and Transplantation Network (2005–2019) was used to identify PwCFs listed for lung transplantation. We compared waitlist outcomes between PwCFs with a LAS exception versus those without an exception despite having a risk event. Risk events were defined as an episode of massive hemoptysis, pneumothorax, at least three moderate/severe pulmonary exacerbations, and/or a decrease in forced expiratory volume in 1 second by ⩾30% predicted (absolute) in the prior 12 months. Analyses were performed using competing risk regression with time to transplantation as the primary outcome and death without a transplant as a competing risk. Results: Of 3,538 listings from 3,309 candidates, 2% of listings (n = 81) had at least one exception. Candidates with an exception and those with a risk event but no exception received lung transplants more slowly than people without an exception or risk event (subdistribution hazard ratio [95% confidence interval]: LAS exception cohort, 0.66 [0.52–0.85]; risk event cohort without exceptions, 0.79 [0.72–0.86]). There was no difference between those with LAS exceptions and those at risk without LAS exceptions: subdistribution hazard ratio, 0.84 (0.66–1.08). Conclusions: LAS exceptions are rare in PwCFs listed for lung transplantation. LAS exceptions resulted in a similar time to transplantation for PwCFs compared with similarly at-risk individuals. As we enter the CAS era, these LAS-based results are pertinent to improve risk stratification among PwCFs being considered for lung transplantation.