Laurel Mimmo
Biographic Data
| ID | 6779312 |
|---|---|
| NAME | Laurel Mimmo |
| GIVEN NAMES | Laurel |
| FAMILY NAME | Mimmo |
| SIGNATURE | MIMMO L |
| AFFILIATIONS | The University of Sydney |
| ORCID | 0000-0001-7738-8275 |
| VERIFIED | Yes |
| TOTAL WORKS | 6 |
| TOTAL CITATIONS | 0 |
| AUTHOR COUNT | 6 |
| EDITOR COUNT | 0 |
| FIRST PUBLICATION YEAR | 2019 |
| LATEST PUBLICATION YEAR | 2026 |
| H-INDEX | 0 |
Procedural Support for Neurodivergent Children During Medical Procedures
Neurodivergent children face unique challenges during medical procedures due to distinct sensory processing patterns and communication difficulties. Evidence-based interventions for procedural pain/distress may inadequately address their specific needs, leading to undertreated distress and negative healthcare experiences. Following Joanna Briggs Institute methodology, we conducted comprehensive searches across six databases on January 10, 2025, f…
Co‐Producing a Patient Reported Experience Measure (PREM) With and for People With Intellectual Disability
BACKGROUND: Patient reported experience measures (PREMs) are widely used as key indicators of value in healthcare towards improved services but are rarely applied among people with intellectual disability. Incorporating the experiences of people with intellectual disability in PREMs data is vital as this group often encounter poor healthcare access and outcomes. This study reports the coproduction of accessible PREMs for people with intellectual …
Co‐Producing Patient‐Reported Experience Measures With People With Intellectual Disability to Improve Healthcare Quality and Outcomes
INTRODUCTION: Intellectual disability, defined by significant limitations in both intellectual functioning and adaptive behaviour with onset during the developmental period, affects an estimated 2% (108 million) of people worldwide. People with intellectual disability experience major health inequity, poor health outcomes and premature deaths, with mortality rates that are 7-12 times higher than the general population. Patient-reported experience…
Epic-CP pilot trial
In children with cerebral palsy (CP), there is evidence that social determinants of health contribute to poorer health outcomes and are barriers to families accessing health services. In the general paediatric population, there is emerging evidence that clinical pathways for the systematised identification and referral of unmet social can support families to address their social needs. The objectives of this Australian pilot are to investigate th…
A qualitative study investigating the experiences of unmet social needs for children with cerebral palsy and their families
There is a social gradient between the unmet needs of an individual with cerebral palsy (CP) and their health and wellbeing outcomes. To date, research has not explored the experience of unmet social needs for children with cerebral palsy and their families and how they may impact their lives. Our study sought to address this knowledge gap through qualitative research methods. Our aim was to understand the experiences of unmet social needs for fa…
Partnerships for safe care
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Partnerships for safe care
Epic-CP pilot trial
In children with cerebral palsy (CP), there is evidence that social determinants of health contribute to poorer health outcomes and are barriers to families accessing health services. In the general paediatric population, there is emerging evidence that clinical pathways for the systematised identification and referral of unmet social can support families to address their social needs. The objectives of this Australian pilot are to investigate th…
A qualitative study investigating the experiences of unmet social needs for children with cerebral palsy and their families
There is a social gradient between the unmet needs of an individual with cerebral palsy (CP) and their health and wellbeing outcomes. To date, research has not explored the experience of unmet social needs for children with cerebral palsy and their families and how they may impact their lives. Our study sought to address this knowledge gap through qualitative research methods. Our aim was to understand the experiences of unmet social needs for fa…
Co‐Producing Patient‐Reported Experience Measures With People With Intellectual Disability to Improve Healthcare Quality and Outcomes
INTRODUCTION: Intellectual disability, defined by significant limitations in both intellectual functioning and adaptive behaviour with onset during the developmental period, affects an estimated 2% (108 million) of people worldwide. People with intellectual disability experience major health inequity, poor health outcomes and premature deaths, with mortality rates that are 7-12 times higher than the general population. Patient-reported experience…
Procedural Support for Neurodivergent Children During Medical Procedures
Neurodivergent children face unique challenges during medical procedures due to distinct sensory processing patterns and communication difficulties. Evidence-based interventions for procedural pain/distress may inadequately address their specific needs, leading to undertreated distress and negative healthcare experiences. Following Joanna Briggs Institute methodology, we conducted comprehensive searches across six databases on January 10, 2025, f…
Co‐Producing a Patient Reported Experience Measure (PREM) With and for People With Intellectual Disability
BACKGROUND: Patient reported experience measures (PREMs) are widely used as key indicators of value in healthcare towards improved services but are rarely applied among people with intellectual disability. Incorporating the experiences of people with intellectual disability in PREMs data is vital as this group often encounter poor healthcare access and outcomes. This study reports the coproduction of accessible PREMs for people with intellectual …
Disability Rights and Representation (3 works) · Family and Disability Support Research (3 works) · Health care (3 works) · Intellectual disability (3 works) · Psychological intervention (3 works) · Cerebral Palsy and Movement Disorders (2 works) · Down syndrome and intellectual disability research (2 works) · Medicine (2 works) · MEDLINE (2 works) · Nursing (2 works)