13 research outputs found
ΠΠΎΡΠ°ΠΆΠ΅Π½ΠΈΠ΅ ΡΠ΅ΡΠ΄ΡΠ° ΠΏΡΠΈ AL-Π°ΠΌΠΈΠ»ΠΎΠΈΠ΄ΠΎΠ·Π΅. Π‘ΠΎΡΡΠΎΡΠ½ΠΈΠ΅ ΠΏΡΠΎΠ±Π»Π΅ΠΌΡ
AL cardiac amyloidosis is a relatively rare disorder that belongs to the group of infiltrative cardiomyopathies. Diagnosis of primary amyloidosis is challenging due to many unspecific symptoms and sings, which often leads to late diagnosis when treatment options are limited. Primary amyloidosis particularly needs to be excluded in patients with heart failure with preserved ejection fraction. Therapy in cardiac amyloidosis has to main vectors: 1) chemotherapy to eliminate amyloidogenic plasmatic cells 2) heart failure treatment. The main challenge for cardiologists is to support hemodynamics until response to chemotherapy occurs. In the article the issue of diagnostics, risk stratification and treatment of primary cardiac amyloidosis is addressed.ΠΠΊΡΡΠ°Π»ΡΠ½ΠΎΡΡΡ. AL-Π°ΠΌΠΈΠ»ΠΎΠΈΠ΄ΠΎΠ· ΡΠ΅ΡΠ΄ΡΠ° ΠΎΡΠ½ΠΎΡΠΈΡΡΡ ΠΊ Π³ΡΡΠΏΠΏΠ΅ ΠΈΠ½ΡΠΈΠ»ΡΡΡΠ°ΡΠΈΠ²Π½ΡΡ
ΠΊΠ°ΡΠ΄ΠΈΠΎΠΌΠΈΠΎΠΏΠ°ΡΠΈΠΉ ΠΈ ΡΠ²Π»ΡΠ΅ΡΡΡ ΠΎΡΠ½ΠΎΡΠΈΡΠ΅Π»ΡΠ½ΠΎ ΡΠ΅Π΄ΠΊΠΈΠΌ Π·Π°Π±ΠΎΠ»Π΅Π²Π°Π½ΠΈΠ΅ΠΌ. ΠΠΈΠ°Π³Π½ΠΎΡΡΠΈΠΊΠ° Π°ΠΌΠΈΠ»ΠΎΠΈΠ΄ΠΎΠ·Π° ΡΠ΅ΡΠ΄ΡΠ° ΠΏΡΠ΅Π΄ΡΡΠ°Π²Π»ΡΠ΅Ρ Π±ΠΎΠ»ΡΡΠΈΠ΅ ΡΡΡΠ΄Π½ΠΎΡΡΠΈ Π²Π²ΠΈΠ΄Ρ ΠΌΠ½ΠΎΠΆΠ΅ΡΡΠ²Π° Π½Π΅ΡΠΏΠ΅ΡΠΈΡΠΈΡΠ½ΡΡ
ΡΠΈΠΌΠΏΡΠΎΠΌΠΎΠ² ΡΠΈΡΡΠ΅ΠΌΠ½ΠΎΠ³ΠΎ Ρ
Π°ΡΠ°ΠΊΡΠ΅ΡΠ°, ΡΡΠΎ Π·Π°ΡΠ°ΡΡΡΡ ΠΏΡΠΈΠ²ΠΎΠ΄ΠΈΡ ΠΊ ΠΏΠΎΠ·Π΄Π½Π΅ΠΉ ΠΏΠΎΡΡΠ°Π½ΠΎΠ²ΠΊΠ΅ Π΄ΠΈΠ°Π³Π½ΠΎΠ·Π°, ΠΊΠΎΠ³Π΄Π° Π²Π°ΡΠΈΠ°Π½ΡΡ Π»Π΅ΡΠ΅Π½ΠΈΡ Π΄ΠΎΠ²ΠΎΠ»ΡΠ½ΠΎ ΠΎΠ³ΡΠ°Π½ΠΈΡΠ΅Π½Ρ. ΠΠΈΠ°Π³Π½ΠΎΠ· Π°ΠΌΠΈΠ»ΠΎΠΈΠ΄ΠΎΠ·Π° ΠΎΠ±ΡΠ·Π°ΡΠ΅Π»ΡΠ½ΠΎ Π΄ΠΎΠ»ΠΆΠ΅Π½ Π±ΡΡΡ ΠΈΡΠΊΠ»ΡΡΠ΅Π½ Ρ ΠΏΠ°ΡΠΈΠ΅Π½ΡΠΎΠ² Ρ ΡΠ΅ΡΠ΄Π΅ΡΠ½ΠΎΠΉ Π½Π΅Π΄ΠΎΡΡΠ°ΡΠΎΡΠ½ΠΎΡΡΡΡ Ρ ΡΠΎΡ
ΡΠ°Π½Π½ΠΎΠΉ ΡΡΠ°ΠΊΡΠΈΠ΅ΠΉ Π²ΡΠ±ΡΠΎΡΠ°. ΠΠ΅ΡΠ΅Π½ΠΈΠ΅ ΠΏΠ°ΡΠΈΠ΅Π½ΡΠΎΠ² Ρ Π°ΠΌΠΈΠ»ΠΎΠΈΠ΄ΠΎΠ·ΠΎΠΌ ΡΠ΅ΡΠ΄ΡΠ° Π²ΠΊΠ»ΡΡΠ°Π΅Ρ Π΄Π²Π° ΠΎΡΠ½ΠΎΠ²Π½ΡΡ
Π½Π°ΠΏΡΠ°Π²Π»Π΅Π½ΠΈΡ β ΠΏΡΠΎΠ²Π΅Π΄Π΅Π½ΠΈΠ΅ Ρ
ΠΈΠΌΠΈΠΎΡΠ΅ΡΠ°ΠΏΠΈΠΈ Ρ ΡΠ΅Π»ΡΡ ΡΠ½ΠΈΡΡΠΎΠΆΠ΅Π½ΠΈΡ Π°ΠΌΠΈΠ»ΠΎΠΈΠ΄ΠΎΠ³Π΅Π½Π½ΡΡ
ΠΏΠ»Π°Π·ΠΌΠ°ΡΠΈΡΠ΅ΡΠΊΠΈΡ
ΠΊΠ»Π΅ΡΠΎΠΊ ΠΈ Π»Π΅ΡΠ΅Π½ΠΈΠ΅ ΡΠ΅ΡΠ΄Π΅ΡΠ½ΠΎΠΉ Π½Π΅Π΄ΠΎΡΡΠ°ΡΠΎΡΠ½ΠΎΡΡΠΈ. ΠΡΠ½ΠΎΠ²Π½ΠΎΠΉ Π·Π°Π΄Π°ΡΠ΅ΠΉ ΠΊΠ°ΡΠ΄ΠΈΠΎΠ»ΠΎΠ³Π° ΡΠ²Π»ΡΠ΅ΡΡΡ ΠΏΠΎΠ΄Π΄Π΅ΡΠΆΠ°Π½ΠΈΠ΅ Π³Π΅ΠΌΠΎΠ΄ΠΈΠ½Π°ΠΌΠΈΠΊΠΈ Π΄ΠΎ ΠΏΠΎΠ»ΡΡΠ΅Π½ΠΈΡ ΠΎΡΠ²Π΅ΡΠ° Π½Π° Ρ
ΠΈΠΌΠΈΠΎΡΠ΅ΡΠ°ΠΏΠΈΡ. Π ΡΡΠ°ΡΡΠ΅ ΡΠ°ΡΡΠΌΠ°ΡΡΠΈΠ²Π°ΡΡΡΡ Π²ΠΎΠΏΡΠΎΡΡ Π΄ΠΈΠ°Π³Π½ΠΎΡΡΠΈΠΊΠΈ, ΡΡΡΠ°ΡΠΈΡΠΈΠΊΠ°ΡΠΈΠΈ ΡΠΈΡΠΊΠ° ΠΈ Π»Π΅ΡΠ΅Π½ΠΈΡ Π±ΠΎΠ»ΡΠ½ΡΡ
Ρ ΠΏΠ΅ΡΠ²ΠΈΡΠ½ΡΠΌ Π°ΠΌΠΈΠ»ΠΎΠΈΠ΄ΠΎΠ·ΠΎΠΌ ΡΠ΅ΡΠ΄ΡΠ°.
ΠΠ°ΠΊΠ»ΡΡΠ΅Π½ΠΈΠ΅. ΠΡΠΏΠΎΠ»ΡΠ·ΠΎΠ²Π°Π½ΠΈΠ΅ ΡΠΎΠ²ΡΠ΅ΠΌΠ΅Π½Π½ΠΎΠΉ Ρ
ΠΈΠΌΠΈΠΎΡΠ΅ΡΠ°ΠΏΠΈΠΈ Π΄Π΅ΠΌΠΎΠ½ΡΡΡΠΈΡΡΠ΅Ρ Π·Π½Π°ΡΠΈΡΠ΅Π»ΡΠ½ΠΎΠ΅ ΡΠ»ΡΡΡΠ΅Π½ΠΈΠ΅ Π²ΡΠΆΠΈΠ²Π°Π΅ΠΌΠΎΡΡΠΈ
Review of novel clinical recommendations on diagnosis and treatment of atrial fibrillation (2016) of the European society of cardiology developed in collaboration with the European association for cardio-thoracic surgery
[No abstract available
Review of novel clinical recommendations on diagnosis and treatment of atrial fibrillation (2016) of the European society of cardiology developed in collaboration with the European association for cardio-thoracic surgery
[No abstract available
THE EFFECT OF SYSTEMICALLY-ADMINISTERED RENOKINASE ON VOLUMETRIC CORONARY VENOUS FLOW-RATE IN PATIENTS WITH ACUTE MYOCARDIAL-INFARCTION
THE EFFECT OF SYSTEMICALLY-ADMINISTERED RENOKINASE ON VOLUMETRIC CORONARY VENOUS FLOW-RATE IN PATIENTS WITH ACUTE MYOCARDIAL-INFARCTION
Prevalence of Advanced Chronic Kidney Disease in Patients with Nonvalvular Atrial Fibrillation Hospitalized in Cardiology Departments
Objective To estimate the prevalence of chronic kidney disease (CKD) 3b-5 stages and the newly diagnosed sustained reduction in glomerular filtration rate (GFR) <30 ml/min/1.73 m2 in patients with atrial fibrillation (AF) in real clinical practice, as well as the features of their anticoagulant therapy. Materials and Methods Retrospectively, data of all discharge epicrisis from cardiological departments of five Moscow hospitals from June 1, 2016 to May 31, 2017 were analyzed. Patients over 18 years old with AF were enrolled. At the next stage, patients with CKD 3 b-5 st and newly diagnosed sustained reduction in GFR <30 ml/min/1.73 m2 (at least 2 measurements during hospitalization) were selected. Results Data of 9725 patients were analyzed, AF was diagnosed in 2983 (31 %) cases, of which a decreased GFR <45 ml/min/1.73 m2 was detected in 27 % (n = 794) cases. Among them, 349 (44 %) were diagnosed with CKD 3b st, 123 (15 %) with CKD 4 st, 44 (6 %) with CKD 5 st, 278 (35 %) had a newly diagnosed sustained reduction in GFR. In 63 % of patients with AF and GFR <45 ml/min/1.73 m2, anemia was diagnosed, 39 % of them had moderate and severe one. 711 (89 %) patients were prescribed anticoagulants, 53 % were assigned direct oral anticoagulants (DOACs). Patients with CKD 3 b st. more often rivaroxaban 15 mg (29 %) was prescribed, with CKD 4 and CKD 5-warfarin (48 % and 25 %, respectively), in patients with newly diagnosed sustained reduction in GFR <30 ml/min/1.73 m2- A pixaban 10 mg/day (16.2 %). Conclusion A quarter of patients with AF revealed a decreased GFR <45 ml/min/1.73 m2, half of them were recommended DOACs. 42 % of patients with GFR <30 ml/min/1.72 m2 were prescribed DOACs, 27 %-warfarin. Patients with CKD 5 st DOACs were not assigned; in half of cases, none of the anticoagulants was recommended. Most often, the dose of the prescribed anticoagulant was not counted according to GFR in patients with newly diagnosed sustained reduction in GFR <30 ml/min/1.73 m2. Β© 2020 Rockefeller University Press. All rights reserved
Safety performance of rivaroxaban versus warfarin in patients with atrial fibrillation and advanced chro-nic kidney disease
Aim To evaluate safety of using rivaroxaban in patients with stage 4 chronic kidney disease (CKD) or transient, stable decline of glomerular filtration rate (GFR) to 15-29βmlβ/minβ/β1.73βm2 in the presence of atrial fibrillation (AF).Material and methods This multicenter prospective, randomized study included patients admitted to cardiology departments from 2017 through 2019. Of 10β224 admitted patients 109 (3β%) patients with AF and stage 4 CKD or a stable decline of GFR to 15-29βmlβ/minβ/β1.73βm2 were randomized at 2:1 ratio to the rivaroxaban 15βmgβ/day (n=73) treatment group or to the warfarin treatment group (n=36). The primary endpoint was development of BARC and ISTH major, minor, and clinically relevant minor bleeding. Mean follow-up duration was 18 months.Results Patients receiving warfarin had a significantly higher incidence of BARC (n=26 (72.2β%) vs. n=31 (42.4β%), Ρ<0.01) and ISTH (n=22 (61.1β%) vs. n=27 (36.9β%), p<0.01) minor bleeding and all ISTH clinically relevant (minor clinically relevant and major bleedings) n=10 (27.7β%) vs. n=8 (10.9β%), Ρ=0.03]. The number of repeated hospitalizations was 65 (43% of patients) in the rivaroxaban treatment group and 27 (48% of patients) in the warfarin treatment group (Ρ=0.57), including 24 (36.9β%) and 11 (40.7β%) emergency admissions in the rivaroxaban and warfarin treatment groups, respectively (Ρ=0.96). Significant improvement of changes in creatinine clearance and GFR (by CKD-EPI and Cockroft-Gault) was observed in the rivaroxaban treatment group.Conclusion The study provided evidence for a more beneficial safety profile of rivaroxaban compared to warfarin in patients with AF and advanced CKD