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    Undergraduate and Postgraduate Special Needs Dentistry Curricula for Oral Health Therapists: A Delphi Study
    (Wiley, 2026-04-29) Koh, Dorothy K. L.; Aley, Melanie J.; Leadbeatter, Delyse M.; Sohn, Woosung; Lim, Mathew A. W. T.; Longbottom, Troy; Lansdown, Karen; Rawal, Kadambari; Carrington, Samuel D.; Francis, Jessica; Mandasari, Masita; Cleary, Ceara; Pradhan, Archana
    Aim: To develop a consensus-based curriculum outline for special needs dentistry (SND) tailored to oral health therapists (OHTs),ensuring relevance and applicability across undergraduate and postgraduate education in Australia. Methods: A four-round online modified Delphi study was conducted. The first three rounds involved both Australian and international experts, while the final consensus round was limited to Australian experts. Experts were selected using purposive sampling based on their experience in SND education, clinical practice, or curriculum development. Participants completed semi-structured surveys derived from publicly accessible learning outcomes (LOs) in student handbooks of undergraduate oral health programs and postgraduate SND specialist programs. Additional insights were drawn from the International Association for Disability & Oral Health (iADH) and the Australian Dental Council (ADC) competency guidelines. Across the rounds, experts rated the importance of proposed LOs, identified their appropriate educational level (undergraduate/postgraduate), and provided qualitative feedback. Consensus was defined a priori as ≥ 70% agreement. Modifications were made between rounds based on expert feedback. Results: In Round 1, 24 experts completed, with 66 of 67 LOs reaching consensus. In Round 2, 20 experts assessed 98 LOs(including new and revised items, categorized into undergraduate and postgraduate), with 96 (97.9%) reaching consensus. Round3 involved 16 experts reviewing unresolved and newly added items; two items did not reach consensus. The final round resulted in consensus on all outstanding LOs and confirmed the overall framework’s relevance to the OHT scope and context. Key refinements across rounds included improved clarity in applying Bloom’s Taxonomy, clearer undergraduate/postgraduate differentiation, and increased specificity to SND. The final document, “Undergraduate and Postgraduate Special Needs Dentistry Curricula for Oral Health Therapists” can be downloaded from the Appendices in the Supporting Information.
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    Applying a Health Care Planning Model to Midwifery: Evidence from Germany and New Zealand
    (Oxford University Press, 2025-10-01) Fleming, Tania; Griese, Anne; Leinweber, Julia; Schuessler, Frank
    Background Midwifery workforce planning is essential to ensure equitable access to maternal care but differs widely across countries. Because a dedicated planning tool is lacking, Germany currently does not perform demand-oriented planning for midwifery services. In contrast, New Zealand facilitates planning through centralized data collection and national coordination. This study investigates how planning approaches affect the distribution and accessibility of maternal health care in Germany and New Zealand. Methods Midwifery workforce and population data from Germany and New Zealand were analyzed using a German physician-based demand planning tool adapted for midwifery services. GIS mapping visualized workforce-to-population ratios, spatial accessibility, and socioeconomic disparities in service distribution. Regional care patterns were compared across both systems. Results Application of the adapted physician-based tool in Germany revealed substantial care gaps in rural and peripheral regions, reflecting the absence of a midwifery-specific planning framework. In contrast, assessment in New Zealand showed a more balanced distribution of midwifery services, including remote areas. Centralized workforce monitoring and register-based planning appear to support more equitable access and responsive resource allocation. Conclusions Germany's lack of a dedicated workforce planning system contributes to regional and social inequities in care provision, particularly affecting women with low socioeconomic status. In contrast, New Zealand's structured approach, including centralized monitoring and targeted planning, supports a more balanced distribution across income groups. Adopting such elements may help improve service equity. This study underlines the relevance of tailored planning systems for maternal health and informs policy development. Key messages • Germany’s lack of midwifery planning leads to inequitable access for rural and low-income groups. • New Zealand’s structured system enables more balanced midwifery service provision.
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    Communication Technology Practices Used by Midwives with Pregnant Women/people in Aotearoa New Zealand to Ensure Quality Maternal and Newborn Care
    (Springer Publishing Company, 2024-07-16) Wakelin, Karen J; McAra-Couper, Judith; Fleming, Tania; Erlam, Gwen D.
    INTRODUCTION: Communication was identified as a component of high-quality maternity care within an evidence-informed Quality Maternal and Newborn Care framework. Communication technology has been shown to enhance relationships midwives develop with their clients; however, concerns with the safety of the communication have been identified. AIM: This article reports on the contribution that communication technology makes toward quality care when used within a continuity of care relationship between midwives and their pregnant clients. METHODS: This article reports on phase 2A of a multiphase study. Semistructured interviews were conducted with lead maternity carer midwives using the online platform Microsoft Teams. Midwives who had previously undertaken an online survey in phase 1A and had indicated interest in participating in an online interview were emailed an invitation to participate. Fourteen midwives responded to the email invitation. Thematic analysis was used to analyze the interview data. FINDINGS: The findings indicate that communication technology facilitates quality care within a midwifery model of continuity of care. This is achieved in two ways through (a) connectedness and being known and (b) an awareness of challenges which in turn enables midwives to develop strategies for ensuring quality care. DISCUSSION: Communication technology, when used within a continuity of care relationship, facilitates quality care. It does this through enabling a connection continuation of connectedness and knowingness which enables midwives to negotiate safe and appropriate means for contact. It also privileges midwives with knowledge of challenges when using communication technology and enables strategies to be developed.
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    Experiences of Bereaved Māori Whānau in Out‐of‐Hospital Death Where Emergency Ambulance Services Respond
    (Wiley, 2026-04-16) Satchell, Eillish; Moeke‐Maxwell, Tess; Gott, Merryn; Dicker, Bridget; Anderson, Natalie E
    Māori are disproportionately affected by out-of-hospital deaths due to higher rates of cardiac arrest and lower survival outcomes. Ambulance personnel are often the only healthcare professionals present during events, making their role in supporting bereaved whānau (families) critical. However, it remains unclear if current bereavement care meets whānau cultural and spiritual needs. Using kaupapa Māori research principles, this qualitative interview study explores the experiences of bereaved Māori whānau in Aotearoa New Zealand to understand their experiences during an out-of-hospital death when emergency ambulance services respond. Eight interviews with bereaved whānau were completed, with four themes describing how Te Ao Māori (the Māori world) informed whānau needs. Whānau navigated end-of-life collectively, with whānau kotahitanga (family unity) being central to whānau experiences. Tikanga (traditional customs, protocols) during death and dying was important, with such spiritual and cultural needs typically upheld by whānau independently. Whānau presence during the transition between life and death held emotional and cultural significance. Finally, the presence of Māori responders improved whānau experiences. Overall, bereavement care that acknowledges whānau cultural and spiritual needs remains limited during out-of-hospital deaths. Enhancing cultural safety and increasing Māori workforce representation offer key opportunities to strengthen the provision of end-of-life care by emergency ambulance services.
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    Ambulance Personnel’s Experiences With Prehospital Births: A Qualitative Study in Aotearoa New Zealand
    (SAGE Publications, 2025-06-12) Withanarachchie, Vinuli; Todd, Verity; Dicker, Bridget; Maessen, Sarah E
    Births in the prehospital setting are infrequent yet associated with increased odds of maternal and neonatal morbidity and mortality. There is limited understanding of the experiences of emergency medical services staff in handling these potentially high-risk situations. We explored the perspectives of ambulance personnel in Aotearoa New Zealand when responding to out-of-hospital births. Hato Hone St John Ambulance is the largest emergency medical services provider in Aotearoa New Zealand. Between October and November 2023, all Hato Hone St John frontline staff were invited to complete an online survey, including open text questions about their experiences and challenges attending unplanned births. Data was coded and organised into themes using NVivo software and the inductive approach to thematic analysis. One hundred and forty-seven responses were received and included in the survey. Participants encountered a range of challenges in providing intrapartum care in the prehospital setting. Two key themes were identified: (1) navigating complexity and uncertainty in unplanned births, and (2) practical challenges and unsuitable environments; with several subthemes demonstrating that the ambulance personnel responded to obstetric emergencies in diverse circumstances, diligently working to deliver optimal care for both mothers and neonates. This study describes novel challenges faced by ambulance personnel attending unplanned births in Aotearoa New Zealand alongside obstacles previously reported by emergency medical services in other jurisdictions. These findings may be invaluable in guiding further research, curriculum and resource development to better prepare ambulance personnel for the challenging and uncertain situations that characterise prehospital birth events.
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    Foetal Movement Information and Maternal Concerns in the Third-Trimester: Findings of an Aotearoa New Zealand National Survey
    (Wiley, 2026-04-03) Bradford, Billie F; Thompson, John MD; McKinlay, Christopher JD; Dukkipati, Likhit S; Cronin, George D; Waller, Nimisha; McAra-Couper, Judith; Cornwall, Tania; McCowan, Lesley ME; Cronin, Robin S
    BACKGROUND: Promoting awareness of foetal movement (FM) is a recognised approach to addressing preventable stillbirth. However, provision of information is inconsistent, and rates of presentation for decreased FM may vary by maternal factors. Information is lacking on maternal views of FM information and knowledge of actions if concerned about FM. AIMS: To describe women's views of FM during late pregnancy in Aotearoa-New Zealand (Aotearoa-New Zealand), including factors that influence maternal actions if concerned. MATERIALS AND METHODS: Online survey of women with singleton third-trimester pregnancies in Aotearoa-New Zealand. Multivariable analysis adjusted for maternal factors. RESULTS: Eligible participants comprised European (1042, 63.5%), Māori (266, 16.2%), Pacific (119, 7.3%), Asian (160, 9.8%) and Other (35, 2.1%). Over half were nulliparous (916, 55.9%) and early third-trimester (median 31, IQR 28-34). Most (1366, 83.3%) had been concerned about FM. Groups that were less likely to seek advice when concerned, included Māori (aOR 0.69, 95% CI 0.51%-0.93%, p = 0.02), Pacific (aOR 0.58, 95% CI 0.38%-0.88%, p = 0.01) and parous (aOR 0.73, 95% CI 0.59%-0.90%, p = 0.003) women. Advice seeking was also less likely with a doctor as the main maternity provider (aOR 0.59, 5% CI 0.39%-0.92%, p = 0.02) compared to a midwife, and those who received fewer than recommended antenatal visits (aOR 0.55, 95% CI 0.34%-0.88%, p = 0.01). CONCLUSIONS: This study identified that FM worries are common in the third-trimester in Aotearoa-New Zealand. Yet, some groups of women were less likely to seek advice when concerned, indicating opportunities to reduce inequity and address barriers to accessing care.
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    Underuse of Bystander Defibrillation on Females During Out-of-Hospital Cardiac Arrest: A Retrospective Observational Study in Aotearoa New Zealand
    (Elsevier BV, 2026-02-03) Todd, Verity; Hutchinson, Heather; Withanarachchie, Vinuli; Swain, Andy; Maessen, Sarah; Brett, Aroha; Dicker, Bridget
    Introduction Early bystander CPR and defibrillation improve cardiac arrest survival. International studies show women receive fewer bystander interventions after out-of-hospital cardiac arrest (OHCA) than men. We investigated associations between sex and bystander interventions in OHCA in Aotearoa New Zealand. Methods Retrospective cohort study of adult OHCA with attempted resuscitation (January 2019–December 2023). Variables included demographics, ethnicity, socioeconomic deprivation, rurality, location type, and witness status. Logistic regression assessed associations between sex and bystander CPR and bystander defibrillation (shock delivered), adjusting for covariates. Results Of 9377 OHCA events, 29.6% occurred in females. Bystander CPR rates were similar between females (75.7%) and males (77.3%) (AOR 1.06, 95% CI: 0.94–1.18, p = 0.36). However, bystander defibrillation occurred in only 1.9% of females versus 5.4% of males. Females had 65% lower odds of receiving bystander defibrillation in unadjusted analysis (UOR 0.35, 95% CI: 0.26–0.47, p ' 0.001) and 39% lower odds after adjustment (AOR 0.61, 95% CI: 0.44–0.84, p = 0.002). Among shockable rhythm cases, sex disparity was not significant (AOR 0.83, 95% CI: 0.59–1.15, p = 0.26). Conclusion Despite equitable bystander CPR rates, females had significantly lower odds of receiving bystander defibrillation. In shockable rhythm cases, the disparity was not significant after adjustment for covariates, suggesting that patient and event characteristics mediate rather than confound this relationship. Findings highlight the need for targeted interventions addressing strategies to improve bystander defibrillation for females in cardiac arrest.
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    Family Experiences of Out-of-Hospital Deaths Where Ambulance Services Respond in Aotearoa New Zealand
    (SAGE Publications, 2025-12-05) Satchell, Eillish; Gott, Merryn; Dicker, Bridget; Moeke-Maxwell, Tess; Anderson, Natalie E
    Background: As ambulance services respond to a growing number of out-of-hospital deaths, supporting bereaved families is increasingly recognised as an important aspect of paramedic care. Actions from ambulance personnel can significantly shape family experiences, underscoring the need for compassionate, evidence-based care in the event of a death. However, currently, little is known about the needs and perspectives of families during these events, particularly from Indigenous and culturally diverse populations. This study explores the experience of Māori and non-Māori families from Aotearoa New Zealand who were present at a death where emergency ambulance services responded. Methods: This qualitative study, underpinned by kaupapa Māori research principles, explored family experiences of emergency ambulance care in the context of a death. Participants were recruited through purposive volunteer sampling, with invitations shared via local and social media. Semi-structured interviews employed a collaborative storytelling approach, where researchers and families co-constructed digital narratives of their experiences. Data were analysed using Braun and Clarke's reflexive thematic analysis. Results: We conducted 21 interviews with 23 bereaved family members. Families described having emotional, cultural and spiritual needs during out-of-hospital deaths. Four themes influenced the experiences of family. Making space for family highlighted the importance of meaningful presence and shared decision-making. Compassionate family care reflected the positive impact of compassionate actions. Communication, which was clear and timely, assisted family understanding. Finally, closure in crisis revealed how follow-up support is needed to help families process and accept death. Conclusion: Care that centres empathy, shared decision making, clear communication and responsiveness to individual family needs can improve the experiences of bereaved families. Greater consideration of family needs during resuscitation and its termination is needed to challenge current care paradigms, which equate family presence with family support. Enhancing cultural and spiritual responsiveness offers an opportunity to provide more holistic and culturally safe bereavement care.
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    Preparing for Death, Dying and Bereavement Care: Student Paramedic Perspectives on a Novel Learning Module
    (Informa UK Limited, 2026-04-07) Anderson, Natalie Elizabeth; Satchell, Eillish; Tseng, Bruce; Shaw, Brayden; McAulay, Mel
    Emergency ambulance personnel are commonly the last health professionals to care for people in the moments before death and the first to provide families with bereavement care, particularly when death is sudden or unexpected. Despite this, paramedic training seldom discusses, simulates or assesses termination of resuscitation, or breaking bad news to family. This paper describes paramedicine students’ experiences of a dedicated learning module designed to prepare them for patient death and caring for bereaved families. A lecture, small-group case studies and actor-led simulations were embedded into paramedic degree students’ final year of study. Students shared their perspectives on learning about death, dying, and bereavement through focus groups or an online survey. Students found talking about death and supporting acute grief unfamiliar and uncomfortable. Eager to provide reassurance in a crisis, many expressed ongoing concerns about saying the wrong thing. Participants wanted greater integration of challenging communication and cultural responsiveness throughout their degree, noting opportunities for learning during clinical placements were precious but limited. Actor-led simulation of patient death and family grief presented an important but unfamiliar divergence from standardized, action-packed resuscitation scenarios. Greater acknowledgement of death, dying and bereavement throughout training could better prepare paramedics for the realities of emergency ambulance work.
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    Child Protection in Dental Practice: A Review of Legal and Professional Responsibilities in Aotearoa
    (Tuwhera Open Access, 2026-03-26) Han, Heuiwon
    Social and health inequities persist across Aotearoa New Zealand, disproportionately impacting children and families facing systemic disadvantage. Dental practitioners are uniquely positioned to identify early signs of child abuse and neglect due to their regular interactions with children and their whānau. However, many report uncertainty about their legal and professional obligations when responding to child protection concerns, limiting their ability to provide effective support (Han et al., 2022). This review critically examines the legal statutes and professional standards that inform the role of dental practitioners in child protection (Han et al., 2024). It draws on key legislation, including the Oranga Tamariki Act 1989, and professional standards. A narrative analysis revealed that despite the legal and ethical expectations to report concerns and collaborate with child protection services, current professional guidelines lack the clarity necessary to support confident and timely clinical decision-making. Particularly, requirements to inform the child or their family about information sharing are often inconsistently addressed in organisational documents, creating uncertainty for practitioners and potentially interfering with protective actions. The review emphasises the importance of equity-focused, Te Tiriti-informed guidance to promote culturally responsive practice and enhance capacity to respond to child protection concerns. Key recommendations include providing scaffolded professional education, strengthening interdisciplinary collaboration, and developing practical, accessible protocols for both prevention and early intervention, rather than focusing on detection and reporting. Integrating culturally safe and legally sound child protection practices into oral health care is essential to upholding the rights and wellbeing of tamariki and their whānau. In this presentation, I aim to highlight the critical role of dental practitioners in child protection, explore the legal and ethical frameworks that guide their responsibilities, and propose actionable strategies to strengthen their capacity to respond confidently and culturally safely to concerns of abuse and neglect.  
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    Brushed Aside: A Social Epidemiological Perspective on Asian Children’s Oral Health in Aotearoa New Zealand
    (Te Mātāpuna AUT Library, 2026-03-24) Wang, Ru-Te; Han, Heuiwon; Lee, Bible
    Dental caries remains a prevalent yet largely preventable non-communicable disease. In Aotearoa New Zealand, child caries persists despite publicly funded oral health services. This commentary applies a social epidemiological lens to children’s dental caries, examining how social, political and economic structures shape oral health, and highlighting gaps in evidence for Asian children. The paper draws on New Zealand and international literature on child caries, policy and governance, and equity frameworks, including Te Tiriti o Waitangi and Kaupapa Māori scholarship, with attention to ethnicity data practices and structural racism. National reporting demonstrates persistent inequities for Māori and Pacific children; however, Asian children are often aggregated into an “Other” category, obscuring heterogeneity. Where Asian children are analysed separately, emerging evidence indicates elevated odds of multiple caries at first dental visits and rising hospital admissions for dental treatment under general anaesthesia, challenging “model minority” assumptions. Explanations focused only on language, acculturation or “cultural beliefs” risk reinforcing Eurocentrism when detached from historical and structural determinants. Equity-oriented action requires culturally safe, structurally informed research and policy, including nationally standardised, ethnicity-disaggregated oral health data and prevention and access strategies co-designed with Asian communities.
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    Why Community Water Fluoridation Matters in Clinical Practice: Evidence From the Public Health Association of New Zealand’s New Policy Statement
    (New Zealand Dental Association, 2026-03-27) Han, Heuiwon; Garland, Luke
    Background: Oral health is fundamental to wellbeing in Aotearoa New Zealand, yet dental caries remains a leading cause of childhood hospitalisation and a persistent source of inequity. Community water fluoridation (CWF) is a proven, proportionate, and equitable population measure. This article synthesises the evidence for CWF and translates the Public Health Association of New Zealand’s (PHANZ) 2025 policy position for clinical practice. Methods: A review of national and international evidence on CWF was conducted, incorporating systematic reviews and policy analyses. Policy development drew on engagement with oral health and public health experts and the PHANZ Policy Subcommittee, followed by broader engagement with PHANZ members and final endorsement by the PHANZ Executive Council in June 2025. Findings: CWF can significantly reduce dental caries across the life course, particularly in communities experiencing socioeconomic deprivation. Evidence supports CWF as a safe, cost-effective, and scalable public health measure. The analysis also acknowledges community concerns regarding autonomy and consent, highlighting the importance of community partnership alongside culturally safe implementation of CWF. The PHANZ statement positions CWF as a foundational upstream intervention that should be integrated with broader strategies addressing poverty, access barriers, and wider systemic inequities. Conclusions: Oral health practitioners have a professional and ethical responsibility to advocate for and support CWF through evidence-based communication and culturally safe practice. Implementing and sustaining CWF aligns with clinical ethics and Aotearoa New Zealand’s commitment to equitable oral health outcomes.
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    The Roles and Purposes of Caring Touch in Health Professional Practice: A Discourse Analysis
    (Wiley, 2026-03-23) Power, Nicola; Fadyl, Joanna; Walters, Simon; Payne, Deborah
    Research literature concludes that caring touch contributes to physical and psychological wellness. However, in health practice, touch is constructed as acceptable in some situations and not in others. Utilising interviews with nurses and other health professionals, the aim of this study was to explore the discourses shaping the role and purpose of caring touch in health practice. Poststructural methodology, drawn from the work of Michele Foucault, was employed to make visible what discourses of caring touch were legitimised or marginalised in a health setting. At times, caring touch was constructed as an expression of humanness, whilst at others it was expressly part of a professional practice. Findings showed that discourses shaping choices to engage in acts of caring touch with patients were linked to the social construction of the relationship between the patient and the professional. Whilst some practitioners talked about integrating caring touch into practice with little difficulty, for others, caring touch was constructed as an ‘extra’. Discourses that shaped professional subjectivities were key to those differences. Findings from this paper build on existing understandings of caring touch in literature by highlighting the unique interplay of discourses in practice.
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    Applying a Health Care Planning Model to Midwifery: Evidence from Germany and New Zealand
    (Oxford University Press (OUP), 2025-10-27) Griese, A; Schüssler, F; Fleming, T; Leinweber, J
    Background Midwifery workforce planning is essential to ensure equitable access to maternal care but differs widely across countries. Because a dedicated planning tool is lacking, Germany currently does not perform demand-oriented planning for midwifery services. In contrast, New Zealand facilitates planning through centralized data collection and national coordination. This study investigates how planning approaches affect the distribution and accessibility of maternal health care in Germany and New Zealand. Methods Midwifery workforce and population data from Germany and New Zealand were analyzed using a German physician-based demand planning tool adapted for midwifery services. GIS mapping visualized workforce-to-population ratios, spatial accessibility, and socioeconomic disparities in service distribution. Regional care patterns were compared across both systems. Results Application of the adapted physician-based tool in Germany revealed substantial care gaps in rural and peripheral regions, reflecting the absence of a midwifery-specific planning framework. In contrast, assessment in New Zealand showed a more balanced distribution of midwifery services, including remote areas. Centralized workforce monitoring and register-based planning appear to support more equitable access and responsive resource allocation. Conclusions Germany's lack of a dedicated workforce planning system contributes to regional and social inequities in care provision, particularly affecting women with low socioeconomic status. In contrast, New Zealand's structured approach, including centralized monitoring and targeted planning, supports a more balanced distribution across income groups. Adopting such elements may help improve service equity. This study underlines the relevance of tailored planning systems for maternal health and informs policy development. Key messages • Germany’s lack of midwifery planning leads to inequitable access for rural and low-income groups. • New Zealand’s structured system enables more balanced midwifery service provision.
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    Simulation of Phased Alerting of Community First Responders for Cardiac Arrest
    (Public Library of Science (PLoS), 2026-03-03) van den Berg, Pieter L; Henderson, Shane G; Li, Hemeng; Dicker, Bridget; Jagtenberg, Caroline J
    BACKGROUND: Community First Responders (CFRs) are commonly used for out-of-hospital cardiac arrests, and advanced systems send so-called phased alerts: notifications with built-in time delays. The policy that defines these delays affects both response times and volunteer fatigue. METHODS: We compare alert policies by Monte Carlo Simulation, estimating patient survival, coverage, number of alerts and redundant CFR arrivals. In the simulation, acceptance probabilities and response delays are bootstrapped from 29,307 rows of historical data covering all GoodSAM alerts in New Zealand between 1-12-2017 and 30-11-2020. We simulate distances between the patient and CFRs by assuming that CFRs are located uniformly at random in a 1-km circle around the patient, for different CFR densities. Our simulated CFRs travel with a distance-dependent speed that was estimated by linear regression on observed speeds among those responders in the above-mentioned data set that eventually reached the patient. RESULTS: The alerting policy has a large impact on the four metrics above, and the best choice depends on volunteer density. For each volunteer density, we are able to identify a policy that improves GoodSAM New Zealand's current policy on all four metrics. For example, when there are 30 volunteers within 1 km from the patient, sending out alerts to 7 volunteers and replacing each volunteer that rejects by a new one, is expected to save 10 additional lives per year compared to the current policy, without increasing volunteer fatigue. Our results also shed light on polices that would improve one metric while worsening another, for example, when there are 10 volunteers within 1 km from the patient, dispatching them all immediately increases our survival estimate by 11% compared to the current policy, with the downside of also increasing the redundant arrivals by 137%. CONCLUSIONS: Monte Carlo simulation can help CFR system managers identify a good policy before implementing it in practice. We recommend balancing survival and volunteer fatigue, aiming to ultimately further improve a CFR system's effectiveness.
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    Mental Health Related Callouts to the Ambulance Service in Aotearoa New Zealand: A Descriptive Analysis
    (Pasifika Medical Association Group, 2026-02-27) Harding, Gabrielle; Fortune, Sarah; Ramalho,, Rodrigo; Swain, Andrew; Brett, Aroha; Dicker, Bridget
    Aims: This study aimed to determine the association between demographic and clinical characteristics of mental health–related callouts to the ambulance services in Aotearoa New Zealand, focussing on differences among Māori, Pacific peoples and non-Māori non-Pacific peoples (NMNPP). Methods: A retrospective cross-sectional study analysed routinely collected data from electronic patient report forms between 1 July 2022 and 30 June 2023. Mental health–related callouts were identified using clinician-coded impressions from the Aotearoa New Zealand Paramedic Care Collection. Results: Of 26,847 callouts, a higher proportion involved individuals under the age of 24 among Māori (31.9%) and Pacific people (29.3%) compared to NMNPP (19.1%) (p<0.001). Callout proportion was higher in the most deprived areas, particularly among Māori (47.7%) and Pacific peoples (49.9%) versus NMNPP (24.5%) (p<0.001). Of total individual callouts, 15.8% presented more than once, with a higher proportion among Māori. Conclusions: This study demonstrates an association between ethnicity, deprivation and mental health–related ambulance callouts, with Māori and Pacific populations in deprived areas experiencing proportionately higher callouts. Findings highlight the need for culturally responsive interventions and equitable access to care. Ambulance data can inform policy and monitor mental health trends.
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    'Flipping the Chair': A Satellite Model for Dental Education in Rural and Remote Communities in Aotearoa New Zealand.
    (Wiley, 2025-12-28) Lansdown, Karen; Han, Heuiwon; Fernandez, Daniel; Cleland, Tanya; Martin, Melody; Hamer, Helen Paris; Khareedi, Rohini
    AIM: This article introduces an innovative educational model, 'flipping the chair,' a dynamic approach to delivering rural and remote education. Drawing on 4 years of satellite teaching experiences at Auckland University of Technology (AUT), we share key insights and lessons learnt to inform future initiatives in other university and educational settings. CONTEXT: Delivering comprehensive oral health education to rural and remote communities can be a complex challenge due to geographic isolation, limited resources, and workforce shortages. To address these inequities, a strategic partnership was formed in 2022 with Health New Zealand-Te Whatu Ora in Northland. This collaborative initiative prioritises the recruitment of Māori (Indigenous population of Aotearoa New Zealand) students who may experience significant barriers to accessing higher education in urban regions, with the benefit of academic study in familiar surroundings. APPROACH: Our satellite model of dental education was introduced in 2022 with an initial cohort of six first-year students, five students in 2023, nine in 2024, and five in 2025. Across all years, 56% of students identified as Māori. The first graduating cohort of five students completed the programme in 2024. This article discusses how AUT developed and implemented dental education within rural and remote communities. CONCLUSION: By adapting and 'flipping' the traditional university model, we have developed a sustainable approach to rural and remote dental education with promising educational outcomes.
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    "The whole thing is just really difficult": Experiences of Dental Services for Children and Adults With Cerebral Palsy in Australia - A Qualitative Study
    (Informa UK Limited, 2025-11-29) Lansdown, Karen; Smithers-Sheedy, Hayley; Bulkeley, Kim; Zagreanu, Claudia; Irving, Michelle; McGrath, Margaret
    PURPOSE: People with cerebral palsy (CP) often experience significant barriers to accessing dental care, yet this area remains under researched in Australia. This study explored how people with CP and their caregivers experience dental services in Australia. METHODS: Semi structured interviews were conducted with a total of (n = 13) participants, including caregivers of children with CP (n = 4), adults with CP (n = 5) and caregivers of adults with CP (n = 4). RESULTS: Reflexive thematic analysis revealed three key themes: (1) "The whole thing is just really difficult-Difficulties in identifying and accessing dental services for people with CP," (2) When care stops at the chair-Ableism in oral health care and (3) Person-centred care-How the dental profession can be more welcoming to people with CP. Two of these themes included sub-themes. People with CP experience complex and often overlooked challenges in accessing dental services, influenced by clinical and structural barriers, as well as by systemic failures and the quality of interaction with dental practitioners. When dental care is positive, it is underpinned by trust, effective communication, respect, and genuine partnership. CONCLUSION: People with CP and their caregivers in this study identified structural and interpersonal barriers to dental service access, while also suggesting practical, inclusive, and coordinated solutions to improve access to dental care.
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    Provider Perspectives on Heart Healthcare Inequities Among Māori and Pacific Peoples in Aotearoa New Zealand: A Qualitative Study
    (Elsevier BV, 2025-12-18) Taueetia-Su'a, T; Brewer, KM; Ameratunga, S; Hanchard, S; Selak, V; Dicker, B; Rahiri, JL; Grey, C; Harwood, M
    Objective: We explored service providers’ views on evidence–practice gaps and inequities in heart health care for Māori and Pacific peoples, alongside solutions to address these issues. Methods: Employing Kaupapa Māori and Pacific research methodologies, we recruited Māori, Pacific, and non-Māori/Pacific providers, purposively sampled from a range of disciplines. Semi-structured interviews were conducted individually and in focus groups. Differences in perspectives offered by Māori and Pacific providers are compared to those of non-Māori/Pacific providers. Results: Twenty-three providers, identifying as Māori (6), Pacific (5), or non-Māori/Pacific (12), shared their views of the healthcare system, experiences of providing care, and observations of Māori and Pacific patient and whānau experiences. Results were grouped into three themes: Tikanga Māori and Fa'a Pasifika versus non-Māori/Pacific ways; gaps in the health system for Māori and Pacific patients; and solutions. Māori and Pacific providers emphasised structural determinants, systemic failures and workforce inadequacies underlying inequities. Conclusions: There is a critical need for equity-focused, holistic and relational models of heart health care that are co-designed with Māori and Pacific patients and whānau, and delivered by a culturally safe workforce. Implications for Public Health: Adequately resourced services, designed by and for Māori and Pacific peoples, have the potential to achieve equitable heart health care outcomes.
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    Emergency Ambulance Care of Families During Death, Dying, and Bereavement: A Document Analysis of Australian and Aotearoa New Zealand Clinical Practice Guidelines
    (Elsevier, 2025-06-26) Satchell, Eillish; Gott, Merryn; Juhrmann, Madeleine; Dicker, Bridget; Anderson, Natalie Elizabeth
    BACKGROUND: Ambulance personnel play an important role in supporting families during death, dying, and bereavement. Evidence-based clinical practice guidelines are crucial for ensuring high-quality ambulance care. However, it is unknown what guidance currently informs care of bereaved families. This document analysis examines ambulance guidelines pertaining to family care in out-of-hospital death in Australia and Aotearoa New Zealand. METHODS: Clinical practice guidelines were sourced from all Australian and Aotearoa New Zealand ambulance services. Using qualitative document analysis, guidance addressing family care during death, dying, and bereavement was examined. Analysis was conducted using a customised coding framework informed by the Australian National Consensus Statement: Essential Elements for safe and high-quality end-of-life care. RESULTS: While most guidelines included essential elements of end-of-life care, there was significant heterogeneity in the scope, detail and nature of guidance. Care instructions varied between services, populations and clinical scenarios. Guidance pertaining to culturally safe care was limited. CONCLUSIONS: Ambulance clinical guidance remains focused on technical skills during resuscitation, death, and dying. More guidance is needed to inform important elements of family care such as communication, family partnership, and cultural safety. Incorporating evidenced-based principles of end-of-life care presents an opportunity to improve ambulance support for bereaved families.
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