ReviewCNS drugs2026
Sublingual Administration for Pain Control: Pharmacology, Clinical Applications and Future Directions.
Review in CNS drugs, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
10 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Sublingual (SL) drug delivery represents an important alternative route of analgesic administration, particularly in settings where rapid pain control is desired or oral and parenteral routes are limited. By enabling direct absorption through the oral mucosa, SL administration partially bypasses first-pass hepatic metabolism, potentially improving bioavailability and accelerating the onset of action for select medications. Historically, SL analgesia has been most closely associated with opioid formulations such as fentanyl, buprenorphine, and sufentanil. SL fentanyl has demonstrated efficacy in breakthrough cancer pain among opioid-tolerant patients because of its rapid absorption and potent analgesic properties, whereas buprenorphine remains widely utilized for chronic pain and opioid use disorder owing to its partial µ-opioid receptor agonism and ceiling effect on respiratory depression. More recently, SL sufentanil has gained interest for the supervised management of acute pain in perioperative and emergency settings. Beyond opioids, expanding interest in SL therapeutics has included ketamine, cannabinoids, α2-adrenergic agonists, and investigational nonsteroidal anti-inflammatory drug (NSAID) formulations. Ketamine has shown potential utility in neuropathic and refractory pain syndromes, while cannabinoids are being explored for chronic, inflammatory, neuropathic, and cancer-related pain. Clonidine and dexmedetomidine may also serve as opioid-sparing adjuncts in selected settings. This review summarizes currently available and emerging SL analgesics, emphasizing pharmacologic mechanisms, pharmacokinetics, clinical applications, safety considerations, and therapeutic limitations. Although SL delivery offers advantages, such as noninvasive administration and rapid systemic exposure, limitations including variable bioavailability, formulation challenges, adverse effects, and limited comparative clinical evidence continue to restrict broader adoption.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.