Facial Pain
Conditions
Brief summary
The purpose of this study is to describe midfacial segment pain phenotype, burden and comorbidities in a multicentre and multidisciplinary setting. The ultimate goal is a comprehensive description of this type of pain allowing for its implementation in future classifications. This cross-sectional study is designed to describe midfacial segment pain in a clinical setting. Patients from rhinologic, headache and facial pain or oral medicine/dentistry secondary care centres will be recruited during a one year period. Individuals with other facial pain according to current classification such as sinonasal disorders, neoplasms, local infections, history of significant trauma associated with pain onset will be excluded. Data will be collected through a structured questionnaire covering pain characteristics, coexisting diagnoses, pain-related burden and consequences, physical examination and paranasal sinuses imaging.
Detailed description
https://journals.sagepub.com/doi/10.1177/25158163241235642
Interventions
None listed
Sponsors
Swiat Zdrowia
Study design
Observational model
CASE_ONLY
Time perspective
CROSS_SECTIONAL
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
The study will include patients consulting rhinologic, oral medicine/dentistry, headache or pain specialists because of facial pain with the following features: * located at least partially within an area innervated by the second or third division of the trigeminal nerve (both bilateral and unilateral) * duration of attacks of \> 5 minutes and \< 1 month * attacks recur for \> 1 month * at least one pain-free day per month (this pain-free day must be unrelated to the use of abortive or prophylactic treatment modalities).
Exclusion criteria
1. Facial pain can be attributed to other ICOP-1 diagnosis, apart from tension-type orofacial pain. This means that investigators should exclude especially: * facial migraine by ensuring that facial pain is not accompanied by either migraine aura AND/OR nausea/vomiting AND/OR photo- and phonophobia * persistent idiopathic facial pain by ensuring that the patient experienced a pain-free day or days in the last month (this day or days must be unrelated to use of abortive or prophylactic treatment modalities). * stomatognathic disorders incl. myofascial orofacial pain (chapter 1-3 of ICOP-1) by ensuring that pain is neither unrelated to jaw motion, function or parafunction nor that signs of temporomandibular disorders are present on physical examination. 2. Facial pain with clear rhinogenic cause, such as acute and chronic rhinosinusitis fulfilling both clinical and endoscopic/imaging diagnostic criteria according to the European Position Paper on Rhinosinusitis and Nasal Polyps (EPOS 2020). 3. Facial pain that can be attributed to neoplasms. 4. Facial pain that can be attributed to local infection including post-herpetic neuralgia. 5. History of significant trauma associated with pain onset (pain developed within 7 days from trauma). Patients who additionally and independently suffer from primary headaches whose mid-facial pain cannot be explained as orofacial headaches are explicitly not excluded. In other words, patients with migraine are not excluded, as long as their facial pain has no typical migraine features (i.e. nausea/vomiting, photo- AND phonophobia or aura) and facial pain attacks occur independently of headache episodes. Also, patients showing signs of mucosal contact points or deviated nasal septum will be included, but the presence of these conditions should be noted in the patients' history. Moreover, patients with Lund-Mackay score of 4 or less can be included in the study, unless any singular sinus can be scored with 2 points.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Pain characteristics | 1 month prior to study visit. | Following pain features will be assessed with structured questionnaire: location, frequency, duration, quality, intensity, accompanying symptoms, provoking/relieving factors. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Coexisting diagnoses | 1 month prior to study visit. | Other headache/pain-related disorders (assessed with structured questionnaire). |
| Pain-related burden and consequences | 1 month prior to study visit. | Medications used and their efficacy, consultations in the past, surgical procedures in the past, cost of treatment (assessed with structured questionnaire). |
Countries
Malta, Poland, United Kingdom
Outcome results
None listed