Pruritus in Palliative Care: A Narrative Review of Essential Oil-Based Strategies to Alleviate Cutaneous Discomfort
Abstract
1. Introduction
2. Literature Search
3. Pathophysiology of Pruritus in Palliative Care
3.1. Mechanisms Involved in Pruritus
3.1.1. Neuropathic Pruritus
3.1.2. Inflammatory Pruritus
3.1.3. Cholestatic Pruritus
3.1.4. Uremic Pruritus
3.1.5. Other Contributing Factors
3.2. Common Underlying Conditions in Palliative Care
- Cancer: Hematologic malignancies such as Hodgkin’s lymphoma are particularly associated with severe, unexplained pruritus. Solid tumors may also contribute indirectly via paraneoplastic syndromes, metastasis to the skin, or cholestasis from hepatic involvement [2].
- Liver Disease: Patients with primary biliary cholangitis, metastatic liver disease, or obstructive cholangiopathies frequently report intractable itch, often preceding other symptoms of hepatic dysfunction [26].
- Kidney Disease: In chronic kidney disease, particularly ESRD, pruritus can become a debilitating symptom that affects up to 40–50% of patients on dialysis [27].
- Neurological Disorders: Conditions such as multiple sclerosis, post-stroke syndromes, or spinal cord compression due to metastatic cancer can provoke neuropathic pruritus [28].
- HIV/AIDS: Immune dysregulation, opportunistic infections, and medication side effects contribute to a high prevalence of pruritus in terminal-stage HIV patients [29].
3.3. Impact on Quality of Life and Psychological Well-Being
3.4. Diagnostic Considerations in Pruritus Assessment
4. Essential Oil-Based Care in Palliative Care: Mechanisms, Applications, and Clinical Integration
4.1. Introduction to Aromatherapy and Essential Oils
4.2. Proposed Mechanisms of Action for Antipruritic Effects
- Anti-inflammatory Effects: Many EOs, including lavender (Lavandula angustifolia), chamomile (Matricaria recutita), and tea tree (Melaleuca alternifolia), have demonstrated anti-inflammatory activity. These actions are mediated through the inhibition of pro-inflammatory cytokines (e.g., IL-1β and TNF-α), reduction in oxidative stress, and suppression of cyclooxygenase pathways, which may reduce skin irritation and inflammation-driven itch [47,48,49].
- Neuromodulatory Effects: Certain EOs interact with neurotransmitter systems. For example, lavender has demonstrated affinity for GABA-A receptors, producing anxiolytic and sedative effects that may indirectly reduce itch perception. Menthol-containing EOs such as peppermint (Mentha piperita) can also modulate TRPM8 ion channels, providing a cooling sensation that may counteract the itch–scratch cycle [53,54].
4.3. Review of the Evidence
4.4. Safety Considerations and Routes of Application
4.4.1. Topical Application
4.4.2. Inhalation
4.4.3. Oral Ingestion
4.4.4. Precautions
- Always consider allergies, sensitivities, and potential interactions with existing medications.
- Avoid known dermal irritants (e.g., cinnamon, clove, and oregano) on broken or sensitive skin.
- EOs should not be used on mucosal areas or open wounds unless under specialist guidance.
4.5. Clinical and Ethical Considerations for Use of Essential Oils in Pruritus Management
4.5.1. Patient Preferences and Values
4.5.2. Safety and Contraindications
- Skin integrity: Avoid use on broken, fragile, or highly inflamed skin.
- Sensitivities and allergies: Patch testing may be advisable before topical application.
- Organ function: Patients with hepatic or renal impairment may have altered metabolism or excretion of oil constituents.
- Potential drug interactions: Though rare, interactions with sedatives, anticoagulants, or hormone-sensitive conditions may occur with some oils (e.g., fennel and clary sage).
- Mode of application: Topical use should involve proper dilution (typically 0.5–2% in a carrier oil), while inhalation should be conducted in a well-ventilated environment to avoid overwhelming fragrance [72].
4.5.3. Ethical and Cultural Sensitivity
4.6. Role of Multidisciplinary Teams
4.7. Practical Guidelines and Protocols
- Assessment and documentation of pruritus characteristics, severity (e.g., using a Visual Analog Scale or 5-D Itch Scale), triggers, and patient history [37]. The 5-D Itch Scale is a validated tool designed to assess five dimensions of pruritus: Duration (frequency of itching episodes), Degree (severity), Direction (change over time), Disability (impact on daily activities such as sleep, leisure, housework, and work/school), and Distribution (affected body areas). It provides a more comprehensive evaluation compared to unidimensional scales, such as the NRS or VAS, offering valuable insights into both symptom severity and functional impact [37]. The scale is particularly useful in chronic and complex cases of pruritus, allowing clinicians to monitor therapeutic responses over time.
- Trial interventions starting with a patch test and observation of response to a low-dose topical or inhaled preparation [75].
- Standardized dilution protocols, typically:
- ○
- 0.5–1% for frail, elderly, or terminally ill patients.
- ○
- 1–2% for more robust individuals with intact skin [65].
- Choice of carrier oils such as jojoba, sweet almond, or fractionated coconut oil, depending on skin condition and allergies.
- Clear documentation of EOs used, dose, route of application, frequency, and patient feedback.
5. Discussion
5.1. Clinical Implications
5.2. Limitations
5.3. Future Research
6. Conclusions
Funding
Conflicts of Interest
References
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Essential Oil | Key Active Compounds | Mechanisms of Action | Target Pathways/Effects | Indications in Pruritus | Efficacy Evidence |
---|---|---|---|---|---|
Lavender (Lavandula angustifolia) | Linalool, linalyl acetate | Neuromodulation via GABA-A receptor modulation; anti-inflammatory; anxiolytic | CNS calming, decreased itch perception, reduced inflammation | Neuropathic itch, anxiety-related itch, generalized pruritus | Aromatherapy massage ↓ pruritus and improved sleep in cancer patients [57] |
Chamomile (Matricaria recutita/Chamaemelum nobile) | α-bisabolol, chamazulene | Inhibition of pro-inflammatory cytokines (IL-1β, TNF-α); antioxidant; skin barrier repair | Anti-inflammatory, barrier support | Inflammatory dermatoses, dry-skin-related itch, atopic-prone skin | Bath therapy ↓ skin irritation in pediatric eczema [58] |
Peppermint (Mentha piperita) | Menthol, menthone | TRPM8 ion channel activation (cooling sensation); local analgesic effect | Sensory nerve modulation, anti-itch signaling | Uremic pruritus, cholestatic pruritus, thermal/irritant pruritus | RCT in CKD patients: ↓ itch intensity with 1.5% solution vs. placebo [59] |
Tea Tree (Melaleuca alternifolia) | Terpinen-4-ol, α-terpineol | Antimicrobial; inhibits prostaglandins and histamine release | Skin infection control, inflammation reduction | Secondary infection from scratching, contact dermatitis | Preclinical studies show ↓ histamine-induced itching [56] |
Sandalwood (Santalum album) | Santalol | Soothing, emollient, and anti-inflammatory activity | Skin hydration, TNF-α modulation | Xerotic pruritus, chronic inflammatory pruritus | Preclinical and dermatological use shows anti-inflammatory and skin-soothing effects in xerosis [50] |
Geranium (Pelargonium graveolens) | Citronellol, geraniol | Antioxidant and mild anti-inflammatory properties | Oxidative stress reduction, peripheral sensory modulation | Stress-related or multifactorial pruritus | No direct RCT; antioxidant and sensory-modulating properties suggest potential benefit in stress-related pruritus |
Bergamot (Citrus bergamia) † | Limonene, linalool, bergapten (furocoumarin) † | Anxiolytic via serotonergic pathways; potential phototoxicity | Mood enhancement, CNS neuromodulation | Psychological pruritus, anxiety-exacerbated itch | In combination with lavender, showed reduced pruritus and improved mood in elderly/palliative care patients [60] |
Aspect | Details |
---|---|
Recommended EOs | Lavender (Lavandula angustifolia), Roman chamomile (Chamaemelum nobile), Peppermint (Mentha × piperita), Frankincense (Boswellia carterii), Tea tree (Melaleuca alternifolia) |
Dilution Ratios |
|
Routes of Administration |
|
Carrier Oils | Jojoba, Sweet almond, Fractionated coconut oil |
Contraindications |
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Diogo Gonçalves, S. Pruritus in Palliative Care: A Narrative Review of Essential Oil-Based Strategies to Alleviate Cutaneous Discomfort. Diseases 2025, 13, 232. https://doi.org/10.3390/diseases13080232
Diogo Gonçalves S. Pruritus in Palliative Care: A Narrative Review of Essential Oil-Based Strategies to Alleviate Cutaneous Discomfort. Diseases. 2025; 13(8):232. https://doi.org/10.3390/diseases13080232
Chicago/Turabian StyleDiogo Gonçalves, Sara. 2025. "Pruritus in Palliative Care: A Narrative Review of Essential Oil-Based Strategies to Alleviate Cutaneous Discomfort" Diseases 13, no. 8: 232. https://doi.org/10.3390/diseases13080232
APA StyleDiogo Gonçalves, S. (2025). Pruritus in Palliative Care: A Narrative Review of Essential Oil-Based Strategies to Alleviate Cutaneous Discomfort. Diseases, 13(8), 232. https://doi.org/10.3390/diseases13080232