Undifferentiated connective tissue disease: state of the art on clinical practice guidelines

Author:

Antunes Margarida,Scirè Carlo AlbertoORCID,Talarico Rosaria,Alexander TobiasORCID,Avcin Tadej,Belocchi Chiara,Doria Andrea,Franceschini Franco,Galetti Ilaria,Govoni Marcello,Hachulla Eric,Launay David,Lepri Gemma,Macieira Carla,Matucci-Cerinic Marco,Montecucco Carlo Maurizio,Moraes-Fontes Maria FranciscaORCID,Mouthon Luc,Paolino Sabrina,Ramoni Veronique,Tani Chiara,Tas Sander W,Tincani Angela,Van Vollenhoven Ronald,Zen Margherita,Fonseca Joao,Bombardieri Stefano,Fonseca João Eurico,Schneider Matthias,Smith Vanessa,Cutolo Maurizio,Mosca Marta,Beretta LorenzoORCID

Abstract

The term ‘undifferentiated connective tissue disease’ (UCTD) is generally used to describe clinical entities characterised by clinical and serological manifestations of systemic autoimmune diseases but not fulfilling the criteria for defined connective tissue diseases (CTDs). In this narrative review, we summarise the results of a systematic literature research, which was performed as part of the ERN ReCONNET project, aimed at evaluating existing clinical practice guidelines (CPGs) or recommendations.No specific CPG on UCTD were found, potential areas of intervention are absence of a consensus definition of UCTD, need for specific monitoring and therapeutic protocols, stratification of UCTD based on the risk of developing a defined CTD and preventive measure for the future development of a more severe condition.Patients feel uncertainty regarding the name of the disease and feel the need of a better education and understanding of these conditions and its possible changes over time.

Funder

European Union’s Health Programme

Publisher

BMJ

Subject

Immunology,Immunology and Allergy,Rheumatology

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