Study register · detail
Harm
GRADE
Very low
9 citations
Samplen = 1 Pat.
Duration5 years of nabilone treatment…
EndpointCannabinoid hyperemesis…
Blindingn.a.
DesignFallserie
Cannabinoidthc
Max. dose2.0 mg
Routeoral
Key finding
Nabilone led to worsening of nausea and vomiting (cannabinoid hyperemesis syndrome) instead of the expected relief; after discontinuation no return of symptoms.
Summary
Single case report (n=1): 70-year-old patient with small cell lung carcinoma in palliative care; nabilone (incrementally increased from 0.5 to 2 mg over 5 years) led to refractory vomiting (cannabinoid hyperemesis syndrome suspected). After discontinuation of nabilone complete remission of nausea/emesis, pain control successful with opioids.
P
Population70-year-old woman with small cell lung carcinoma in palliative care, n=1
I
InterventionNabilone (synthetic cannabinoid), dose escalation from 0,5 to 2 mg over 5 years, most recently discontinued after 7 weeks of increased dose
O
OutcomeAfter discontinuation of nabilone complete cessation of refractory nausea and vomiting; pain management successful with opioids and adjuvants
Confidence in the evidence
Very low
The lowest GRADE level, the effect estimate remains uncertain.
Downgraded for
Imprecision
Quality profile
Sample size
★★★★★
Blinding
—
Effect size
Harm
Citations / year
★★★★★
Authors
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Abstract
Introduction: Synthetic cannabinoids are commonly used to manage pain, nausea, and vomiting in oncology and palliative care. Despite the current acceptance of cannabinoids as a treatment option for nausea and vomiting, there is a lack of data regarding the side effects of its prolonged use leading to possible toxicity due to accumulation, and as a result, exacerbation of nausea and vomiting rather than alleviation. Case Report Presentation: The patient, a 70-year-old female, was residing in the palliative care unit with the diagnosis of small-cell lung cancer. She underwent a course of chemotherapy consisting of paclitaxel, docetaxel, and cisplatin. She presented with hair loss, sore mouth, a loss of appetite, diarrhea, neuralgia, nausea, and vomiting which developed approximately 5 h after chemotherapy. Nabilone was used for the last 5 years to manage the patient's neuralgia. As her cancer progressed, a dosage of nabilone was incrementally increased from 0.5 to 2 mg to control her pain; however, it exacerbated refractory nausea and vomiting. Nabilone was discontinued 7 weeks after administration due to suspicion of cannabinoid hyperemesis syndrome. Hot baths were attempted with temporary relief. Her pain became well controlled with opioids and adjuvants and there has been no recurrence of nausea and vomiting since the cessation of nabilone.
Discussion/Conclusion: Successful recognition and management of cannabinoid hyperemesis syndrome is especially important in individuals with comorbid disorders in order to avoid cannabis toxicity.
The impediment to action advances action.