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1.
J Thromb Haemost ; 16(3): 474-480, 2018 03.
Article in English | MEDLINE | ID: mdl-29297977

ABSTRACT

Essentials We estimated the cardiovascular risk of patients with idiopathic thrombocytopenic purpura (ITP). The risk of cardiovascular disease was 38% higher in ITP patients compared with controls. Among the ITP patients, splenectomy was associated with higher cardiovascular disease. Clinicians should consider cardiovascular risk when managing ITP patients. SUMMARY: Background Idiopathic thrombocytopenic purpura (ITP) is classically characterized by a transient or persistent decrease of platelet count. Mortality is higher in the ITP population than the general population, with a possible association with increased cardiovascular disease (CVD). Objectives The objective was to assess the strength of the association between ITP and CVD, with a secondary aim to assess the impact of splenectomy on CVD. Methods A population-based retrospective, open cohort study using clinical codes was performed using data from 6591 patients with ITP and 24 275 randomly matched controls (up to 1:4 ratio matched by age, sex, body mass index and smoking status). The main outcome was the risk of CVD, which included ischemic heart disease, stroke, trans-ischemic attack and heart failure. Adjusted incidence rate ratios were calculated using Poisson regression. Results During a median 6-year observation period there was a CVD diagnosis recorded in 392 (5.9%) ITP patients and 1114 (4.5%) control patients. There was an increased risk of developing CVD in the ITP cohort (incidence rate ratio [IRR], 1.38; 95% confidence interval [CI], 1.23-1.55), which remained robust even after a sensitivity analysis only including incident cases of ITP. Findings suggested that patients who had undergone splenectomy were at even further increased risk of developing CVD when compared with the ITP population who had not undergone splenectomy (adjusted IRR, 1.69; 95% CI, 1.22-2.34). Conclusion There is an increased risk of developing CVD in patients with ITP and even further increased risk for those patients with ITP who underwent splenectomy.


Subject(s)
Cardiovascular Diseases/complications , Cardiovascular Diseases/diagnosis , Purpura, Thrombocytopenic, Idiopathic/complications , Purpura, Thrombocytopenic, Idiopathic/diagnosis , Aged , Atherosclerosis/metabolism , Body Mass Index , Female , Follow-Up Studies , Heart Failure , Humans , Incidence , Male , Middle Aged , Myocardial Ischemia , Platelet Count , Poisson Distribution , Prognosis , Regression Analysis , Retrospective Studies , Risk Factors , Smoking , Splenectomy , Treatment Outcome
2.
Br Dent J ; 223(9): 621, 2017 11 10.
Article in English | MEDLINE | ID: mdl-29123274
3.
Br Dent J ; 223(4): 238, 2017 08 25.
Article in English | MEDLINE | ID: mdl-28840872

Subject(s)
Oral Health , Humans
4.
Br Dent J ; 222(7): 497-8, 2017 04 07.
Article in English | MEDLINE | ID: mdl-28387254

Subject(s)
Risk-Taking , Humans
5.
Br Dent J ; 222(7): 549-553, 2017 Apr 07.
Article in English | MEDLINE | ID: mdl-28387295

ABSTRACT

Inflammatory bowel disease (IBD) mainly comprises of two separate inflammatory conditions: Crohn's disease (CD) and ulcerative colitis (UC). The aetiology of these conditions is still being explored with current evidence pointing towards a combination of environmental and genetic components. However, the pathophysiology is understood as a cytokine driven inflammatory response. There is significant association between IBD and dental conditions such as dental caries, other infections and periodontitis. Anti-inflammatory medications such as 5 aminosalicylic acid (5ASA), steroids and biological therapies are the treatment of choice for these chronic conditions, dependent on aetiology. Therefore, this article aims to educate dentists regarding possible implications IBD and its treatment can have for clinical practice and future research.


Subject(s)
Inflammatory Bowel Diseases/complications , Mouth Diseases/etiology , Oral Health , Humans
7.
Br Dent J ; 222(4): 225, 2017 02 24.
Article in English | MEDLINE | ID: mdl-28232673
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