Maria Moutafi

Dr. Maria Moutafi

orcid

Research Focus & Metrics

Academic Career Length

5Years (2022-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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28 April 2023 in Polish Heart Journal
Verified
Journal Article
Open access
PDF file
AKAthanasios Kartalis
Athanasios Kartalis
DADimitrios Afendoulis
Dimitrios Afendoulis
MMMaria Moutafi
Maria Moutafi
PVPetros Voutas
Petros Voutas
NPNikolaos Papagiannis
Nikolaos Papagiannis
MDMatthaios Didagelos
Matthaios Didagelos
W w w. j o u r n a l s. v i a m e d i c a. p l / k a r d i o l o g i a _ p o l s k a 400

Verified
Journal Article
Open access
PDF file
AKAthanasios Kartalis
Athanasios Kartalis
DADimitrios Afendoulis
Dimitrios Afendoulis
PVPetros Voutas
Petros Voutas
MMMaria Moutafi
Maria Moutafi
NPNikolaos Papagiannis
Nikolaos Papagiannis
Matthaios DidagelosMatthaios Didagelos
Matthaios Didagelos
Background: Intravenous (IV) flecainide is recommended for the pharmacological cardioversion of recent-onset atrial fibrillation (AF). The aim of this study was to study the efficacy and safety of IV flecainide, co-administered with oral b-blockers, for the cardioversion of paroxysmal AF. Methods: Single-center registry, initiated in the “Skylitseion” General Hospital of Chios in January 2020. The main inclusion criterion was IV flecainide administration plus oral b-blocker for recent-onset AF (≤48 h). The primary outcome was conversion to sinus rhythm at 2 h. Results: A total of 121 (73 males and 48 females, with mean age 61.4 years) consecutive, unselected patients who complied with the study protocol were included. A successful conversion to sinus rhythm at 2 h was achieved in 99 patients (success rate: 81.8%). The median conversion time was 11.7 min (varied from 3 to 23 min). Duration of hospitalization was significantly shorter in patients who were successfully cardioverted with IV flecainide (10.9 vs. 30.7 h, p < 0.001). No serious adverse events were recorded. Conclusion: This is one of the largest registries worldwide, evaluating the effectiveness and safety of IV flecainide co-administered with a b-blocker in the acute management of recent-onset AF. The successful conversion rate at 2 h is very high and quick with no serious adverse events.

1 January 2023 in Korean Circulation Journal
Verified
Journal Article
Open access
PDF file
DADimitrios Afendoulis
Dimitrios Afendoulis
PVPetros Voutas
Petros Voutas
NPNikolaos Papagiannis
Nikolaos Papagiannis
MMMaria Moutafi
Maria Moutafi
PSPanagiotis Sitaras
Panagiotis Sitaras
AKAthanasios Kartalis
Athanasios Kartalis
Korean Circulation Journal 대한심장학회지 순환기 Afendoulis D, et al. Korean Circ J. 2023 Mar;53:e29. https://doi.org/10.4070/kcj.2022.0305

25 August 2023 in Hellenic Journal of Cardiology
Verified
Journal Article
Open access
AKAthanasios Kartalis
Athanasios Kartalis
DADimitrios Afendoulis
Dimitrios Afendoulis
Matthaios DidagelosMatthaios Didagelos
Matthaios Didagelos
MAMichail Ampeliotis
Michail Ampeliotis
MMMaria Moutafi
Maria Moutafi
CVCharalambos Vlachopoulos
Charalambos Vlachopoulos
Chios Mastiha essential oil (CMO) is a natural product extracted from the resin of Mastiha, possessing antioxidant, anti-microbial, anti-ulcer, anti-neoplasmatic and cholesterol lowering capabilities in vitro, and its hypolipidemic effect was confirmed in animal studies. Yet, there are no randomized, placebo-controlled clinical studies in the literature regarding CMO's hypolipidemic effects in humans. A prospective, randomized, placebo-controlled study was designed to study the hypolipidemic effect of CMO capsules on healthy volunteers with elevated cholesterol. 192 healthy volunteers were screened and 160 of them with total cholesterol> 200 mg/dl participated in the study. They were randomized with a 2:1 ratio of receiving CMO capsules (200 mg mastiha-oil/capsule) and placebo for 8 weeks respectively. 113 patients received CMO and 47 were randomized in the control group, and all of them completed the follow-up period. After 8 weeks of CMO administration, total and LDL cholesterol were significantly lower in the CMO compared to the placebo group 215.2±27.5 vs 237.0±27.9 mg/dl (p<0.001) and 135.0±26.1 vs 153.0±23.3 mg/dl (p<0.001) respectively. No gastrointestinal adverse events, liver or renal toxicity were reported. Additionally, in the CMO group total cholesterol was significantly decreased by 20.6 mg/dl (9%) and LDL by 18.1 mg/dl (12%), triglycerides by 21.8 mg/dl (15%) and glucose by 4.6 mg/dl (5%) and HDL was increased by 2.4 mg/dl (5%), compared to their baseline values. MASTIHA-OIL study showed the efficacy and safety of CMO in reduction of Total and LDL-cholesterol after 8 weeks of administration in healthy volunteers with elevated cholesterol levels.

15 October 2022 in Revista Portuguesa de Cardiologia
Verified
Journal Article
Open access
DADimitrios Afendoulis
Dimitrios Afendoulis
Matthaios DidagelosMatthaios Didagelos
Matthaios Didagelos
MMMaria Moutafi
Maria Moutafi
NPNikolaos Papagiannis
Nikolaos Papagiannis
PVPetros Voutas
Petros Voutas
AKAthanasios Kartalis
Athanasios Kartalis

1 January 2023 in Journal of Cardiovascular Imaging
Verified
Journal Article
Open access
PDF file
MMMaria Moutafi
Maria Moutafi
DADimitrios Afendoulis
Dimitrios Afendoulis
NPNikolaos Papagiannis
Nikolaos Papagiannis
AKAthanasios Kartalis
Athanasios Kartalis
NSNikolaos Smyrnioudis
Nikolaos Smyrnioudis
Moutafi M, et al. J Cardiovasc Imaging. 2022 Aug;30:e38. https://doi.org/10.4250/jcvi.2022.0026