61 research outputs found
Low fasting glucose is associated with enhanced thrombin generation and unfavorable fibrin clot properties in type 2 diabetic patients with high cardiovascular risk
Objective
To investigate the effect of low blood glucose on thrombin generation and fibrin clot properties in type 2 diabetes (T2DM).
Methods
In 165 patients with T2DM and high cardiovascular risk, we measured ex vivo plasma fibrin clot permeation [Ks], turbidity and efficiency of fibrinolysis including clot lysis time [t50%], together with thrombin generation and platelet activation markers in relation to fasting blood glucose.
Results
As compared to patients in medium (4.5-6.0 mmol/l, nâ=â52) and higher (>6.0 mmol/l, nâ=â75) glucose group, subjects with low glycemia (<4.5 mmol/l, nâ=â38) had lower Ks by 11% (pâ<â0.001) and 8% (pâ=â0.01), respectively, prolonged t50% by 10% (pâ<â0.001) and 7% (pâ=â0.016), respectively, and higher peak thrombin generation by 21% and 16%, respectively (pâ<â0.001 for both). There were no significant differences in Ks and t50% between patients in medium and higher glucose group. In the whole group, a J-shape relationship was observed between glycemia and the following factors: peak thrombin generation, Ks and t50%. Only in patients with HbA1câ<â6.0% (42 mmol/mol) (nâ=â26) fasting glucose positively correlated with Ks (râ=â0.53, Pâ=â0.006) and inversely with t50% (râ=ââ0.46, Pâ=â0.02).
By multiple regression analysis, after adjustment for age, fibrinogen, HbA1c, insulin treatment and T2DM duration, fasting glycemia was the independent predictor of Ks (Fâ=â6.6, dfâ=â2, Pâ=â0.002), t50% (Fâ=â8.0, dfâ=â2, Pâ<â0.001) and peak thrombin generation (Fâ=â13.5, dfâ=â2, Pâ<â0.0001).
Conclusions
In T2DM patients fasting glycemia <4.5 mmol/l is associated with enhanced thrombin formation and formation of denser fibrin clots displaying lower lysability, especially when strict glycemia control was achieved (HbA1c<6.0%)
Knowledge gaps in patients with venous thromboembolism : usefulness of a new questionnaire
The current awareness of venous thromboembolism (VTE) and knowledge of thromboprophylaxis
among patients receiving oral anticoagulation therapy (OAC) are insufficient. We sought to develop and evaluate the usefulness of the Jessa AF Knowledge Questionnaire
(JAKQ), modified for VTE patients. Consecutive patients at least 1 month since the VTE event (n = 273, mean
[SD] age, 51 [17] years; 52.7%, women; 55.9%, unprovoked event) were enrolled to the study. The median percentage of correct responses was 64.2% (interquartile range, 53%-73%; minimum,
12%; maximum, 100%). Younger patients had better knowledge about VTE in general, including a higher
proportion of correct responses to the question about the definition of PE (71.4% vs 57.7%, P = 0.03),
about the possible consequence of DVT, including PE (81.1% vs 62%, P = 0.001) and VTE risk related to
long travels (78.1% vs 59.2%, P = 0.002). There was no difference in overall scoring between patients
taking new oral anticoagulants and those taking vitamin K antagonists (mean [SD], 64.1% [16.3%] vs
63.9% [13.8%], respectively, P = 0.7). Regardless of the type of anticoagulants, 39.3% of patients knew
that VTE is not always symptomatic, 33.6% knew what to do when they missed an OAC dose, and 50%
did not know which painkillers are the safest in combination with anticoagulants. Education applied
in 27 patients resulted in an increase in the median percentage of correct responses from 60% to 80%
(P = 0.0001). Knowledge on VTE and anticoagulation is suboptimal among patients on VKA and NOACs.
Education of VTE patients should be improved especially in older individuals on NOACs
Influence of obstructive sleep apnea on right heart structure and function
Introduction: Obstructive sleep apnea syndrome (OSAS) is a highly prevalent sleep disorder associated with increased cardiovascular morbidity and mortality. This study aimed to investigate heart structure and function and their correlation with the degree of OSAS and sleep indexes in patients diagnosed with OSAS.
Materials and methods: A cohort of 77patients (48 males, aged 58.1 ± 11.0 years, body mass index [BMI] = 32.4 ± 6.2) admitted to the hospital due to suspected OSAS was examined using echocardiography and polysomnography.
Results: Patients with moderate-to-severe OSAS compared to patients without diagnosed OSAS or with mild OSAS had greater right ventricular outflow tract (RVOT) dimensions (32.6 ± 3.6 vs 30.9 ± 2.4 mm; p < 0.05), larger right atrial area (RAA; 21.1 ± 4.8 vs 17.2 ± 3.2 mm; p = 0.002), greater right ventricular mid-cavity diameter (RVD; 35.5 ± 7.0 vs 32.2 ± 4.7 mm; p = 0.02), and diminished tricuspid annular plane systolic excursion (TAPSE, 21.9 ± 4.5 vs 25.8 ± 4.4 mm; p = 0.04), while there were no significant differences in tissue doppler imaging (TDI) parameters (Sâ and Eâ) and in valvular regurgitation gradient for both groups. Moreover, significantly greater RVOT dimensions (31.6 ± 2.6 vs 30.9 ± 3.0 mm, p = 0.04), RVD (39.3 ± 7.0 vs 32.7 ± 5.2 mm, p = 0.003), and RAA (21.4 ± 4.4 vs 18.1 ± 4.2 mm, p = 0.02) as well as reduction in TAPSE (20.9 ± 5.3 vs 25.0 ± 4.3 mm, p = 0.01) were observed in patients having â„ 10 episodes of obstructive apnea (OA) per hour.
Conclusions: In moderate-to-severe OSAS patients, right ventricular (RV) enlargement was observed together with RV dysfunction as measured by TAPSE. Examination using TDI is not superior to standard echocardiography for the detection of heart pathology in OSAS patients. Right heart pathology is present predominantly in patients with obstructive apnea
Obstructive sleep apnea â diagnosis and treatment options
Obturacyjny bezdech senny (OSA) jest schorzeniem polegajÄ
cym na powtarzajÄ
cych siÄ epizodach bezdechĂłw i spĆyceĆ oddechu spowodowanych caĆkowitÄ
bÄ
dĆș czÄĆciowÄ
blokadÄ
przepĆywu powietrza. GĆĂłwnymi objawami OSA sÄ
: nadmierna sennoĆÄ w ciÄ
gu dnia, nagĆe wybudzenia z uczuciem zatrzymania oddechu lub duszenia siÄ, suchoĆÄ w jamie ustnej po przebudzeniu, poranne bĂłle gĆowy, trudnoĆci w koncentracji, potliwoĆÄ nocna i inne. CzÄstoĆÄ wystÄpowania OSA jest wysoka i prawdopodobnie, z powodu zwiÄkszajÄ
cej siÄ czÄstoĆci otyĆoĆci, bÄdzie wiÄksza w przyszĆoĆci. W wielu badaniach wykazano korelacje miÄdzy OSA a innymi schorzeniami, takimi jak: nadciĆnienie tÄtnicze, przewlekĆa niewydolnoĆÄ krÄ
ĆŒenia, choroba niedokrwienna serca, arytmie, udar mĂłzgu. Istnieje rĂłwnieĆŒ wiele publikacji wskazujÄ
cych na korzystny wpĆyw terapii z uĆŒyciem staĆego dodatniego ciĆnienia w drogach oddechowych (CPAP) na schorzenia wspĂłĆistniejÄ
ce. âZĆotym standardemâ w diagnostyce OSA jest tak zwana stacjonarna polisomnografia (PSG), ale urzÄ
dzenia przenoĆne typu 3 (z min. 4 kanaĆami) rĂłwnieĆŒ sÄ
akceptowalne w diagnostyce pacjentĂłw wyjĆciowo obciÄ
ĆŒonych umiarkowanym lub wysokim ryzykiem OSA. DiagnozÄ stawia siÄ na podstawie wynikĂłw PSG i objawĂłw. Na podstawie wyniku PSG moĆŒna podzieliÄ OSA na 3 grupy â Ćagodne, umiarkowane i ciÄĆŒkie. WedĆug aktualnych wytycznych i publikacji CPAP jest leczeniem pierwszego wyboru w umiarkowanej i ciÄĆŒkiej postaci OSA. Strategia lecznicza w przypadku bezdechu Ćagodnego zaleĆŒy od zdrowia pacjenta, schorzeĆ wspĂłĆistniejÄ
cych i indywidualnych decyzji chorego. Innymi opcjami leczenia sÄ
aparaty wewnÄ
trzustne, leczenie pozycyjne i chirurgiczne, ale ĆŒadna z tych metod nie dorĂłwnuje korzyĆciom wynikajÄ
cym z terapii CPAP.Obstructive sleep apnea (OSA) is a disease characterized by recurrent episodes of apneas and hypopneas, caused by total or partial airway obstruction. Main symptoms of OSA are: excessive daytime sleepiness, snoring, waking up suddenly feeling like gasping or choking, dry mouth or sore throat after waking up, morning headaches, trouble concentrating, night sweats and others. Prevalence of OSA is high and probably â due to increasing prevalence of obesity â will be higher in the future. Many studies show correlation between OSA and other diseases such as hypertension, chronic heart failure, coronary artery disease, arrhythmias and stroke. There are also many publications showing positive impact of CPAP treatment on managing comorbidities. Gold standard in diagnosis of OSA is in-laboratory polysomnography (PSG), although type 3 portable monitors (with at least 4 channels) are also acceptable to diagnose patients with pre- -test moderate to high risk of OSA. Diagnosis is made based on PSG results and symptoms. Based on PSG results, we can divide OSA into 3 groups: mild, moderate and severe. Based on current guidelines and publications, continuous positive airway pressure (CPAP) is a first choice treatment in moderate and severe OSA. Treatment strategies in mild OSA depend on patient health, comorbidities and individual patient decisions. Other treatment options are oral appliances, positional treatment and surgery but none of them equals CPAPâs benefits
Polish regional differences in patient knowledge on atrial fibrillation and its management as well as in patterns of oral anticoagulant prescription
Background: The Jessa Atrial Fibrillation Knowledge Questionnaire (JAKQ) was successfully used to assess knowledge gaps in patients with atrial fibrillation (AF).
Aims: To evaluate the regional differences among Polish patients in their awareness of AF diagnosis and oral anticoagulation use.
Methods: A total of 1583 patients with AF at a median (IQR) age of 72 (66â79) years completed the JAKQ in 3 cardiology centers (center I, KrakĂłw; center II, ToruĆ; center III, Kielce) from January 2017 to June 2018. The final analysis included 1525 patients, 32.9% were on vitamin K antagonists (VKAs) and 67.1% on non-VKA oral anticoagulants (NOACs), that is, rivaroxaban and dabigatran (28.9% each), and apixaban (9.3%).
Results: The mean (SD) score on the JAKQ was 55.5% (18.4%) with better results among patients on VKAs compared with NOACs (58% [18.3%] vs 54.3% [18.4%]; P = 0.0002) with time from AF diagnosis more than 12 months (57.4% [17.5%] vs 50% [19.9%]; P < 0.0001). There was a significant difference in the knowledge scores between the 3 centers (I, 59.5%; II, 48.5%; III, 54.3%; P < 0.0001). In all centers the number of correct answers correlated inversely with patientâs age (r = â0.20; P < 0.0001). NOACs were more frequently used in center III. The percentage of correct responses was lower in patients on reduced NOAC doses (35.4% of patients on NOACs), compared with the full-dose NOAC groups in center I (56.9% vs 62.5%; P = 0.012) and II (48.1% vs 56.2%; P = 0.003).
Conclusions: Patients from a high-volume academic center showed better knowledge than their peers from district hospitals. There are large regional differences in prescription patterns of oral anticoagulants, including the preferred NOAC
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