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1. Identifying Existing Guidelines, Frameworks, Checklists, and Recommendations for Implementing Patient-Reported Outcome Measures: Protocol for a Scoping Review

2. Patient-Reported Outcome Measures in High-Risk Medical Device Registries: A Scoping Review

3. Informing a national rare disease registry strategy in Australia: a mixed methods study

4. Current state of rare disease registries and databases in Australia: a scoping review

5. Response rates in clinical quality registries and databases that collect patient reported outcome measures: a scoping review

6. Evaluation and acceptability of patient-reported outcome measures in women following pelvic organ prolapse procedures

7. Bayesian Spatio-Temporal Multilevel Modelling of Patient-Reported Quality of Life following Prostate Cancer Surgery

8. History of the Australian Breast Device Registry

9. Bayesian spatio-temporal modelling of child anemia in Ethiopia using conditional autoregressive model

10. Survival of people with cystic fibrosis in Australia

11. Evaluations of statistical methods for outlier detection when benchmarking in clinical registries: a systematic review

12. Registry randomised trials: a methodological perspective

13. Preliminary development of recommendations for the inclusion of patient-reported outcome measures in clinical quality registries

14. Academic health science centre models across the developing countries and lessons for implementation in Indonesia: a scoping review

15. Measurement properties of the 12-item Short Form Health Survey version 2 in Australians with lung cancer: a Rasch analysis

16. Using data linkage for national surveillance of clinical quality indicators for dementia care among Australian aged care users

17. The protocol of a clinical quality registry for dementia and mild cognitive impairment (MCI): the Australian dementia network (ADNeT) Registry

18. Development of a percutaneous coronary intervention patient level composite measure for a clinical quality registry

19. Acceptability of patient reported outcome measures (PROMs) in a cystic fibrosis data registry

20. What matters most to patients following percutaneous coronary interventions? A new patient-reported outcome measure developed using Rasch analysis.

21. Enhancing Value and Uptake for Whole-Population Cohorts of Children and Parents: Methods to Integrate Registries into the Generation Victoria Cohort

22. Comorbidity data collection across different spine registries: an evidence map

24. Forecasting of overall and aggressive prostate cancer incident counts at the small area level

25. Comparing patient-reported outcome measures for pain in women with pelvic floor disorders pre- and post-surgical management: A systematic review protocol

26. The role of Australian clinical quality registries in pregnancy care: A scoping review

28. Patient-reported outcome measures for pain in women with pelvic floor disorders: a systematic review

29. Clinical quality registries: urgent reform is required to enable best practice and best care

30. Establishment and initial implementation of the Australasian Pelvic Floor Procedure Registry

31. Hereditary Endocrine Tumor Registries

32. Development of a conceptual framework for a new patient-reported outcome measure for pain in women following mesh surgery for pelvic floor disorders: a qualitative study

33. Evaluation and acceptability of patient-reported outcome measures in women following pelvic organ prolapse procedures

34. Clinical outcomes of adults and children with cystic fibrosis during the COVID-19 pandemic

35. Identification of Predictive Factors for Patient-Reported Outcomes in the Prospective Australian Breast Device Registry

36. Outcomes collected in female pelvic floor surgical procedure registries and databases: a scoping review

37. Redesign of the Australian Cystic Fibrosis Data Registry: A multidisciplinary collaboration

38. The Australian Early Psychosis Collaborative Consortium (AEPCC): Improving Clinical Care in Early Psychosis

39. Registry randomised trials: a methodological perspective

40. Geospatial and temporal variation of prostate cancer incidence

41. Influence of timeliness and receipt of first treatment on geographic variation in non‐small cell lung cancer mortality

42. Leadership during the COVID-19 pandemic: building and sustaining trust in times of uncertainty

43. Primary and secondary care related quality indicators for dementia care among australian aged care users: national trends, risk factors, and variation

44. Developing a Preliminary Conceptual Framework for Guidelines on Inclusion of Patient Reported-Outcome Measures (PROMs) in Clinical Quality Registries

45. Health-related quality of life following percutaneous coronary intervention during the COVID-19 pandemic

46. Academic health science centre models across the developing countries and lessons for implementation in Indonesia: a scoping review

47. The Australasian Pelvic Floor Procedure Registry: Not before time

48. Measurement properties of the 12-item Short Form Health Survey version 2 in Australians with lung cancer: a Rasch analysis

49. Hereditary Endocrine Tumors and Associated Syndromes: A Narrative Review for Endocrinologists and Endocrine Surgeons

50. Forecasting of Lung Cancer Incident Cases at the Small-Area Level in Victoria, Australia

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