To study PsO patients in the outpatient dermatology clinic in order to 1) to compare the sensitivity and specificity of the easy to use questionnaire: the Psoriasis Epidemiology Screening Tool (PEST) and ultrasonography in identifying PsO patients…
ID
Source
Brief title
Condition
- Autoimmune disorders
- Epidermal and dermal conditions
Synonym
Research involving
Sponsors and support
Intervention
Outcome measures
Primary outcome
The sensitivity and specificity of the PEST-questionnaire and ultrasonography
in identifying PsO patients having PsA according to a rheumatologist and meet
the CASPAR-criteria.
Secondary outcome
Quality of life and physical functioning after 1 year after screening
Background summary
Psoriasis (PsO) is a chronic skin disorder with a prevalence of approximately
2-3% in the Western population. Between 6 and 42% of patients with psoriasis
will develop psoriatic arthritis (PsA), a chronic inflammatory rheumatic
disorder. Increasing evidence suggests that diagnosing PsA early and
subsequently providing early treatment, improves patients* outcomes
substantially. Since in the majority of cases the symptoms of the skin precede
the musculoskeletal symptoms, an opportunity for screening arises at outpatient
dermatology clinics. However, it is difficult for physicians treating patients
with psoriasis, e.g. dermatologists, to discriminate musculoskeletal symptoms
caused by PsA from other causes of musculoskeletal symptoms. A standardised
screening (zorgpad) at the dermatology outpatient clinic could enhance the
early identification of PsO patients having PsA. An easy to use questionnaire
and ultrasonography, could be valuable tools for such a standardised screening.
Study objective
To study PsO patients in the outpatient dermatology clinic in order to 1) to
compare the sensitivity and specificity of the easy to use questionnaire: the
Psoriasis Epidemiology Screening Tool (PEST) and ultrasonography in identifying
PsO patients having PsA 2) to evaluate the value of screening with the PEST and
with ultrasonography for relevant patient health outcomes
Study design
Prospective observational cohort study with a nested case-control study
Study burden and risks
In total, all PsO patients will be scheduled for one initial study visit and
for an additional study visit if they have positive PEST score (meaning risk
for PsA) in the follow-up. Visits as well as the collection of data will be as
much as possible integrated with regular patient care. The additional
measurements are questionnaires, ultrasound of entheses and painful joints, and
additional blood samples (±80 mL). All patients will be discussed with a
rheumatologist and the patients having PsA at baseline will be referred to the
rheumatologist for further treatment. A large benefit for the participating PsO
patient is the possible earlier identification of PsA with subsequent earlier
treatment.
Maasstadweg 21
Rotterdam 3079 DZ
NL
Maasstadweg 21
Rotterdam 3079 DZ
NL
Listed location countries
Age
Inclusion criteria
* Patients that are diagnosed with psoriasis by their dermatologist
* be able to read/write the Dutch language
* provide a written informed consent
* age > 18 years
Exclusion criteria
- Patients who already have the diagnosis of PsA according to a rheumatologist
- Patients using conventional disease-modifying antirheumatic drugs (DMARDs) or biological DMARDs such as TNF-, IL-17A or IL-23 inhibitors.
* Patients using cyclosporin or tacrolimus.
* Patients using systemic corticosteroids.
Design
Recruitment
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
Register | ID |
---|---|
CCMO | NL64545.101.18 |