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2. Capturing the young child's reports of cancer treatment tolerability: Does our practice reflect an assumption that they cannot report?. Issue 1 (17th October 2022)

3. Concept‐elicitation phase for the development of the pediatric patient‐reported outcome version of the Common Terminology Criteria for Adverse Events. Issue 1 (30th September 2015)

4. Eliciting the child's voice in adverse event reporting in oncology trials: Cognitive interview findings from the Pediatric Patient‐Reported Outcomes version of the Common Terminology Criteria for Adverse Events initiative. Issue 3 (21st September 2016)

5. Expanding construct validity of established and new PROMIS Pediatric measures for children and adolescents receiving cancer treatment. Issue 4 (6th January 2020)

6. Lack of Concordance in Symptomatic Adverse Event Reporting by Children, Clinicians, and Caregivers: Implications for Cancer Clinical Trials. Issue 15 (20th May 2022)

7. Longitudinal use of patient reported outcomes in pediatric leukemia and lymphoma reveals clinically relevant symptomatic adverse events. Issue 12 (24th September 2022)

8. Mapping child and adolescent self‐reported symptom data to clinician‐reported adverse event grading to improve pediatric oncology care and research. Issue 1 (25th September 2019)

9. Patients' Experiences With Staphylococcus aureus and Gram-Negative Bacterial Bloodstream Infections: Results From Cognitive Interviews to Inform Assessment of Health-Related Quality of Life. (8th December 2021)

10. Patients, caregivers, and clinicians differ in performance status ratings: Implications for pediatric cancer clinical trials. Issue 19 (1st July 2021)