Equity and access
Equity and access to effective cough management in palliative care are influenced by various social, cultural, and economic factors. Aboriginal and Torres Strait Islander peoples often encounter challenges due to geographic isolation and limited availability of culturally safe healthcare services. The integration of traditional healing practices and the involvement of community leaders in care planning are essential to improving access and ensuring effective symptom management for conditions like cough within these communities. [9] Culturally appropriate care models that align with the preferences and needs of these populations can significantly enhance health outcomes and the overall quality of care provided. [9]
For culturally and linguistically diverse (CALD) populations, barriers such as language differences, varying cultural perceptions of illness, and reliance on traditional remedies can delay or complicate the management of cough in palliative care. [9,10] Health literacy remains a critical issue, as patients from CALD backgrounds may not fully understand their conditions or the available treatments, leading to underutilisation of effective therapies such as opioids. [10] Addressing these challenges requires the provision of multilingual resources, the employment of culturally competent healthcare professionals, and the integration of traditional practices into care plans, which can bridge gaps in understanding and ensure that patients receive culturally respectful and effective care. [9,10]
People living in rural and remote settings also face significant barriers to accessing palliative care, including essential services for managing symptoms like cough. Geographic isolation and a shortage of specialised healthcare providers make continuous and comprehensive care challenging. [6] While telemedicine offers a promising solution to bridge these gaps by providing remote consultations, its effectiveness is dependent on reliable internet access and the patient's comfort with digital tools. [6] Similarly, prisoners and people experiencing homelessness often struggle to access consistent palliative care. The prison environment can limit access to specialised care, leading to poor symptom control, while the transient nature of homelessness complicates the delivery of continuous care, resulting in unmanaged symptoms like cough. [11,12] To improve access for these underserved groups, targeted interventions such as mobile health units, dedicated palliative care programs within correctional facilities, and the expansion of telehealth services are crucial. [6,11,12]
Care context
Approaches to the management of cough in palliative care tend to vary across different settings with each setting presenting its own set of challenges and opportunities for symptom control. In hospital settings, the availability of advanced diagnostic tools and multidisciplinary teams can be beneficial for managing acute and severe symptoms, particularly in patients with complex conditions such as lung cancer or interstitial lung disease. [3] However, hospitals may not always provide the most comfortable environment for patients, especially those who are vulnerable to heightened anxiety in clinical settings. Striking a balance between effective symptom management and patient comfort can be challenging in these environments, where the clinical atmosphere might contribute to patient discomfort. [13]
In residential aged care homes, managing cough often requires a more adaptive approach, particularly given the high prevalence of comorbidities among elderly residents. These settings might emphasise non-pharmacological strategies, such as positioning and environmental modifications, to manage cough. [5] The effectiveness of care in these care homes may be enhanced by regular assessments and collaboration with external palliative care teams, which can help ensure that care plans are adjusted as needed to meet the evolving needs of residents. [6] In home-based care, the approach to managing cough is often more personalised, with care plans tailored to the patient's preferences and lifestyle. This setting could be particularly beneficial for patients with chronic conditions, where the familiarity of home might reduce anxiety and improve overall comfort. However, the success of home-based care typically depends on the involvement and capacity of family caregivers, who are often supported by healthcare providers through telemedicine to manage symptoms like cough effectively. [6,13]
Implications for families and carers
The management of cough in palliative care can have various implications for families and carers, who often play a central role in providing day-to-day care and ensuring the patient’s comfort. This role can be physically and emotionally demanding, particularly in home-based care settings, where carers are directly responsible for managing symptoms like persistent cough. The physical demands include continuous monitoring and administering treatments, which may contribute to fatigue and stress, particularly when the cough is severe or disrupts the patient’s overall well-being. [13] Additionally, the emotional burden of witnessing a loved one’s discomfort can lead to feelings of helplessness and anxiety. [6]
Supporting carers in managing these challenges is important. Carers benefit from appropriate education and ongoing support from healthcare providers, including understanding the underlying causes of the cough, administering medications effectively, and using non-pharmacological strategies such as positioning and environmental modifications. Regular communication between carers and healthcare providers, possibly through telemedicine, is important to address emerging concerns and make necessary adjustments to care plans. [13]
The well-being of carers is closely linked to the quality of life of the patient. When carers feel supported and competent in managing symptoms like cough, this can enhance the patient’s comfort and overall well-being. [3] Conversely, insufficient support could lead to carer burnout, potentially affecting the quality of care provided. [6] Recognising and addressing the needs of carers as part of a holistic palliative care approach is important to maintaining both carer well-being and patient care quality. Access to respite care, mental health support, and community resources can help carers manage their responsibilities more effectively and continue to provide compassionate care. [6,13]