Background: Rheumatoid
arthritis (RA) is an autoimmune disease
characterized by chronic systemic inflammation, leading to joint deformities
and functional loss. RA progression is accompanied by abnormalities
in the coagulation–fibrinolysis system, clinically manifested
as a hypercoagulable state. However, there are currently no bibliometrics
or visualization analysis in this field. Objective: The present study
aims to reveal the knowledge structure, research status, and research
trends related to hypercoagulability in RA through bibliometric analysis
and to evaluate the utility of inflammatory and coagulation markers
in RA disease activity through retrospective data mining. Methods:
English articles and reviews on RA hypercoagulability published from
2010 to 2023 were extracted from the Web of Science Core Collection
(WoSCC) database on March 1, 2023. VOSviewer and CiteSpace software
were used for knowledge mapping analysis of the included papers in
terms of countries/regions, institutions, journals, authors, keywords,
research hotspots, and frontiers. A retrospective analysis was conducted
on the general information on RA patients. The demographic and clinical
indicators of all participants were collected to determine the correlation
of inflammatory and coagulation markers with the Chinese patient-reported
activity index for rheumatoid arthritis (CPRI-RA). Results: A total
of 957 papers were retrieved. The United States was the most productive
country in this field and had the highest h-index, and the most prolific
institution was the Karolinska Institute. The Annals of the Rheumatic
Diseases was the journal with the most publications, and KLARESKOG
L. was the most productive author. From keyword analysis, it could
be seen that “inflammation”, “activation”,
“disease-activity”, and “risk” had long
been the focuses of RA hypercoagulability research. “Criteria”,
“validation”, “coagulation”, “target”,
and “anemia” were the latest popular keywords in the
past 5 years. Retrospective data mining revealed that the levels of
inflammation (RF, ESR, and CRP) and coagulation (PLT and DD) were
significantly increased in RA patients. FBG, CRP, and ESR were significantly
correlated with CPRI-RA. Additionally, ESR, CRP, and FBG were identified
as independent risk factors for CPRI-RA. Conclusion: The mechanism
and application of hypercoagulability in RA have been research hotspots
in recent years. Inflammation and coagulation markers are independent
risk factors for CPRI-RA.