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1.
Clin Radiol ; 79(2): 107-116, 2024 Feb.
Article in English | MEDLINE | ID: mdl-37968226

ABSTRACT

AIM: To evaluate the impact of recommendations from the 2019 consensus exercise conducted by radiologists and rheumatologists on the use of magnetic resonance imaging (MRI) to investigate axial spondyloarthritis (axSpA) in clinical practice. MATERIALS AND METHODS: A freedom of information (FOI) request was used to assess the use of MRI in the diagnosis of axSpA and radiologists' awareness of the 2019 guidance across all NHS Trusts and Health Boards in the UK, including England, Scotland, Northern Ireland, and Wales. RESULTS: The FOI request was sent to 150 Trusts/Health Boards, and 93 full responses were received. Of the 93 respondents (97%), 90 reported familiarity with the term axSpA and 70/93 (75%) reported familiarity with the 2019 recommendations. Awareness of recommendations regarding specific MRI features supportive of the diagnosis of axSpA was 74/93 (80%) for the sacroiliac joints (SIJs) and 66/93 (71%) for the spine. The median wait for MRI acquisition was 2-3 months. Fifty-two of the 93 (56%) reported at least some outsourcing of axSpA MRI (33%/29% for specialist/non-specialist outsourcing respectively); 32/93 (34%) reported some scans being reported in-house by non-musculoskeletal radiologists. CONCLUSION: There have been several positive developments in the understanding and use of MRI for the diagnosis of axSpA in the UK since the 2017 survey, although substantial scope for further improvement remains. Several new challenges have also emerged, including the increase in waiting times, reliance on outsourcing, and the reporting of MRI by non-musculoskeletal radiologists.


Subject(s)
Axial Spondyloarthritis , Spondylarthritis , Humans , Spondylarthritis/diagnostic imaging , Sacroiliac Joint/diagnostic imaging , Sacroiliac Joint/pathology , Magnetic Resonance Imaging , United Kingdom , Freedom
2.
Semin Arthritis Rheum ; 51(6): 1342-1349, 2021 12.
Article in English | MEDLINE | ID: mdl-34489113

ABSTRACT

BACKGROUND: The current core outcome set for ankylosing spondylitis (AS) has had only minor adaptations since its development 20 years ago. Considering the significant advances in this field during the preceding decades, an update of this core set is necessary. OBJECTIVE: To update the ASAS-OMERACT core outcome set for AS into the ASAS-OMERACT core outcome set for axial spondyloarthritis (axSpA). METHODS: Following OMERACT and COMET guidelines, an international working group representing key stakeholders (patients, rheumatologists, health professionals, pharmaceutical industry and drug regulatory agency representatives) defined the core domain set for axSpA. The development process consisted of: i) Identifying candidate domains using a systematic literature review and qualitative studies; ii) Selection of the most relevant domains for different stakeholders through a 3-round Delphi survey involving axSpA patients and axSpA experts; iii) Consensus and voting by ASAS; iv) Endorsement by OMERACT. Two scenarios are considered based on the type of therapy investigated in the trial: symptom modifying therapies and disease modifying therapies. RESULTS: The updated core outcome set for axSpA includes 7 mandatory domains for all trials (disease activity, pain, morning stiffness, fatigue, physical function, overall functioning and health, and adverse events including death). There are 3 additional domains (extra-musculoskeletal manifestations, peripheral manifestations and structural damage) that are mandatory for disease modifying therapies and important but optional for symptom modifying therapies. Finally, 3 other domains (spinal mobility, sleep, and work and employment) are defined as important but optional domains for all trials. CONCLUSION: The ASAS-OMERACT core domain set for AS has been updated into the ASAS-OMERACT core domain set for axSpA. The next step is the selection of instruments for each domain.


Subject(s)
Axial Spondyloarthritis , Spondylarthritis , Spondylitis, Ankylosing , Consensus , Humans , Outcome Assessment, Health Care , Rheumatologists , Spondylarthritis/diagnosis , Spondylarthritis/drug therapy , Spondylitis, Ankylosing/drug therapy
4.
Ann Rheum Dis ; 76(5): 862-868, 2017 May.
Article in English | MEDLINE | ID: mdl-28122761

ABSTRACT

OBJECTIVES: Autoantibodies directed against cytosolic 5'-nucleotidase 1A have been identified in many patients with inclusion body myositis. This retrospective study investigated the association between anticytosolic 5'-nucleotidase 1A antibody status and clinical, serological and histopathological features to explore the utility of this antibody to identify inclusion body myositis subgroups and to predict prognosis. MATERIALS AND METHODS: Data from various European inclusion body myositis registries were pooled. Anticytosolic 5'-nucleotidase 1A status was determined by an established ELISA technique. Cases were stratified according to antibody status and comparisons made. Survival and mobility aid requirement analyses were performed using Kaplan-Meier curves and Cox proportional hazards regression. RESULTS: Data from 311 patients were available for analysis; 102 (33%) had anticytosolic 5'-nucleotidase 1A antibodies. Antibody-positive patients had a higher adjusted mortality risk (HR 1.89, 95% CI 1.11 to 3.21, p=0.019), lower frequency of proximal upper limb weakness at disease onset (8% vs 23%, adjusted OR 0.29, 95% CI 0.12 to 0.68, p=0.005) and an increased prevalence of excess of cytochrome oxidase deficient fibres on muscle biopsy analysis (87% vs 72%, adjusted OR 2.80, 95% CI 1.17 to 6.66, p=0.020), compared with antibody-negative patients. INTERPRETATION: Differences were observed in clinical and histopathological features between anticytosolic 5'-nucleotidase 1A antibody positive and negative patients with inclusion body myositis, and antibody-positive patients had a higher adjusted mortality risk. Stratification of inclusion body myositis by anticytosolic 5'-nucleotidase 1A antibody status may be useful, potentially highlighting a distinct inclusion body myositis subtype with a more severe phenotype.


Subject(s)
5'-Nucleotidase/immunology , Autoantibodies/blood , Muscle Fibers, Skeletal/pathology , Myositis, Inclusion Body/blood , Myositis, Inclusion Body/diagnosis , Age of Onset , Aged , Aged, 80 and over , Biomarkers/blood , Cytosol , Electron Transport Complex IV/analysis , Female , Humans , Kaplan-Meier Estimate , Male , Middle Aged , Muscle Fibers, Skeletal/chemistry , Muscle Weakness/etiology , Myositis, Inclusion Body/pathology , Prognosis , Proportional Hazards Models , Retrospective Studies , Self-Help Devices/statistics & numerical data , Survival Rate , Time Factors
5.
Clin Exp Rheumatol ; 33(6): 910-6, 2015.
Article in English | MEDLINE | ID: mdl-25797345

ABSTRACT

OBJECTIVES: Patient reported outcomes (PROs) are relevant in rheumatology. Variable accessibility and validity of commonly used PROs are obstacles to homogeneity in evidence synthesis. The objective of this project was to provide a comprehensive library of "validated PROs". METHODS: A launch meeting with rheumatologists, PROs methodological experts, and patients, was held to define the library's aims and scope, and basic requirements. To feed the library we performed systematic reviews on selected diseases and domains. Relevant information on PROs was collected using standardised data collection forms based on the COSMIN checklist. RESULTS: The EULAR Outcomes Measures Library (OML), whose aims are to provide and to advise on PROs on a user-friendly manner albeit based on scientific grounds, has been launched and made accessible to all. PROs currently included cover any domain and, are generic or specifically target to the following diseases: rheumatoid arthritis, osteoarthritis, spondyloarthritis, low back pain, systemic lupus erythematosus, gout, osteoporosis, juvenile idiopathic arthritis, and fibromyalgia. Up to 236 instruments (106 generic and 130 specific) have been identified, evaluated, and included. The systematic review for SLE, which yielded 10 specific instruments, is presented here as an example. The OML website includes, for each PRO, information on the construct being measured and the extent of validation, recommendations for use, and available versions; it also contains a glossary on common validation terms. CONCLUSIONS: The OML is an in progress library led by rheumatologists, related professionals and patients, that will help to better understand and apply PROs in rheumatic and musculoskeletal diseases.


Subject(s)
Lupus Erythematosus, Systemic , Outcome and Process Assessment, Health Care/standards , Patient Care Management , Evidence-Based Practice , Humans , Library Collection Development , Lupus Erythematosus, Systemic/diagnosis , Lupus Erythematosus, Systemic/therapy , Patient Care Management/methods , Patient Care Management/standards , Reproducibility of Results
6.
Parasitol Res ; 97(6): 436-44, 2005 Dec.
Article in English | MEDLINE | ID: mdl-16151731

ABSTRACT

Diplostomum (Austrodiplostomum) compactum (Lutz, 1928) metacercariae (Platyhelminthes, Digenea) were found in six fish species, belonging to two orders (Characiformes and Perciformes) and three families (Erythrinidae, Sciaenidae and Cichlidae). A total of 477 individuals were collected, from August 1999 to May 2001, in the upper Paraná River floodplain, Brazil. The metacercariae were infecting the eyes of six host species and the brain of five of them. Plagioscion squamosissimus, Satanoperca pappaterra and Cichla monoculus presented the highest values of prevalence, mean intensity and mean abundance. Diplostomum (A.) compactum was over-dispersed in the population of Hoplias aff. malabaricus, S. pappaterra, P. squamosissimus, Crenicichla britskii and C. monoculus. No significant difference was observed in the metacercariae distribution in the right and left eyes. The abundance of D. (A.) compactum metacercariae was positively correlated with the host's relative condition factor in H. aff. malabaricus and S. pappaterra. No significant difference of the abundance of parasitism between the sex of the hosts was evidenced. In relation to the prevalence, significant difference was observed only in C. britskii. Positive correlations were verified between the prevalence of infection and the standard length of the specimens in C. britskii and the intensity of infection and the standard length of the hosts in P. squamosissimus and C. monoculus. In relation to parasite abundance and the standard length class of the host, significant differences were observed in P. squamosissimus, C. britskii and C. monoculus.


Subject(s)
Brain Diseases/veterinary , Eye Infections, Parasitic/veterinary , Fishes/parasitology , Fresh Water/parasitology , Helminthiasis, Animal/parasitology , Platyhelminths/isolation & purification , Animals , Body Size , Brain/parasitology , Brain Diseases/parasitology , Brazil , Eye/parasitology , Eye Infections, Parasitic/parasitology , Female , Fishes/anatomy & histology , Male , Perciformes/anatomy & histology , Perciformes/parasitology , Species Specificity
7.
Arq. bras. med. vet. zootec ; 57(3): 295-299, jun. 2005. tab
Article in Portuguese | LILACS | ID: lil-415144

ABSTRACT

Estudaram-se os efeitos anestésicos e cardiorrespiratórios produzidos pela infusão contínua de propofol em gatos pré-medicados com a associação cetamina-midazolam. Catorze gatos adultos foram igualmente distribuídos em dois grupos (TX1 e TX3) aos quais administraram-se, pela via intramuscular, cetamina (3,0mg/kg) e midazolam (0,3mg/kg). Decorridos cinco minutos procedeu-se a indução anestésica pela administração intravenosa de propofol (5,0mg/kg), imediatamente seguida pela infusão contínua do agente hipnótico nas doses de 0,1 ou 0,3mg/kg/min, aos animais de TX1 e TX3, respectivamente. Foram mensuradas as freqüências cardíaca e respiratória, temperatura retal, saturação de oxihemoglobina, concentração exalada de dióxido de carbono e pressão arterial. Em TX3 observou-se manutenção de adequado plano anestésico, enquanto que os animais do TX1 apresentaram-se sedados. Houve decréscimo acentuado da freqüência cardíaca, pressão arterial e elevação da concentração de dióxido de carbono exalado no TX3. Conclui-se que o emprego de propofol na dose de infusão de 0,3mg/kg/min em gatos pré-medicados com cetamina-midazolam produz anestesia satisfatória, bradicardia, depressão da função respiratória e pressão arterial.


Subject(s)
Animals , Male , Female , Anesthetics/administration & dosage , Cats , Propofol/administration & dosage
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