Evangelos Makrakis

Dr. Evangelos Makrakis

HYGEIA IVF - EMBRYOGENESIS, Athens, Attikí, Greece
orcid

Research Focus & Metrics

Academic Career Length

23Years (2004-Present)

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

Representative Publications

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1 May 2021 in Maturitas
Verified
Journal Article
Closed access
ILIrene Lambrinoudaki
Irene Lambrinoudaki
SPStavroula A. Paschou
Stavroula A. Paschou
MLMary Ann Lumsden
Mary Ann Lumsden
SFStephanie Faubion
Stephanie Faubion
EMEvangelos Makrakis
Evangelos Makrakis
NPNick Panay
Nick Panay

11 September 2020 in Diagnostics
Verified
Journal Article
Open access
PDF file
Polina GiannelouPolina Giannelou
Polina Giannelou
Mara SimopoulouMara Simopoulou
Mara Simopoulou
Sokratis GrigoriadisSokratis Grigoriadis
Sokratis Grigoriadis
EMEvangelos Makrakis
Evangelos Makrakis
AKAdamantia Kontogeorgi
Adamantia Kontogeorgi
KSKonstantinos Sfakianoudis
Konstantinos Sfakianoudis
Despite recent striking advances in assisted reproductive technology (ART), poor ovarian response (POR) diagnosis and treatment is still considered challenging. Poor responders constitute a heterogeneous cohort with the common denominator of under-responding to controlled ovarian stimulation. Inevitably, respective success rates are significantly compromised. As POR pathophysiology entails the elusive factor of compromised ovarian function, both diagnosis and management fuel an ongoing heated debate depicted in the literature. From the criteria employed for diagnosis to the plethora of strategies and adjuvant therapies proposed, the conundrum of POR still puzzles the practitioner. What is more, novel treatment approaches from stem cell therapy and platelet-rich plasma intra-ovarian infusion to mitochondrial replacement therapy have emerged, albeit not claiming clinical routine status yet. The complex and time sensitive nature of this subgroup of infertile patients indicates the demand for a consensus on a horizontally accepted definition, diagnosis and subsequent effective treating strategy. This critical review analyzes the standing criteria employed in order to diagnose and aptly categorize POR patients, while it proceeds to critically evaluate current and novel strategies regarding their management. Discrepancies in diagnosis and respective implications are discussed, while the existing diversity in management options highlights the need for individualized management.

1 January 2006 in Mediators of Inflammation
Verified
Journal Article
Open access
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NVNicolaos Vitoratos
Nicolaos Vitoratos
EEEmmanuel Economou
Emmanuel Economou
EMEvangelos Makrakis
Evangelos Makrakis
CPConstantinos Panoulis
Constantinos Panoulis
GCGeorge Creatsas
George Creatsas
The purpose of the present study was to examine the profile of selected proinflammatory cytokines in maternal serum of first‐trimester pregnancies complicated by threatened abortion (TACP) and its relevance to obstetric outcome. Serum levels of Th1‐type cytokines interleukin‐1β (IL‐1β), tumor necrosis factor alpha (TNF‐alpha), and Th2‐type cytokine interleukin 6 (IL‐6) were measured, by ELISA, in 22 women with TACP and adverse outcome at admission (group A) and compared with the corresponding levels of 31 gestational age‐matched women with TACP and successful outcome at admission (group B1) and discharge (group B2) and 22 gestational age‐matched women with first‐trimester uncomplicated pregnancy (group C) who served as controls. Mann‐Whitney U or Wilcoxon test was applied as appropriate to compare differences between groups. IL‐1β and TNF‐alpha were detected with significantly higher levels in group A, compared to all other groups. On the contrary, IL‐6 levels were detected with no significant difference among all the other groups studied. It is concluded that in first‐trimester TACP with adverse outcome, a distinct immune response, as reflected by elevated maternal IL‐1β, TNF‐alpha, and unaltered IL‐6 levels, is relevant to a negative obstetric outcome.

1 December 2006 in Fertility and Sterility
Verified
Journal Article
Closed access
EMEvangelos Makrakis
Evangelos Makrakis
IAIrene Angeli
Irene Angeli
KAKristi Agapitou
Kristi Agapitou
KPKonstantinos Pappas
Konstantinos Pappas
ADAlex Dafereras
Alex Dafereras
KPKonstantinos Pantos
Konstantinos Pantos

10 April 2014 in Clinical and Experimental Obstetrics & Gynecology
Verified
Journal Article
Closed access
GPG. Pistofidis
G. Pistofidis
EMEvangelos Makrakis
Evangelos Makrakis
OKO. Koukoura
O. Koukoura
NBN. Bardis
N. Bardis
PBP. Balinakos
P. Balinakos
VAV. Anaf
V. Anaf
Purpose: To analyze laparoscopically treated cases of adenomyosis based on intraoperative and histopathology findings and to correlate different types with patients’ presenting symptoms and characteristics, as well as with the surgical approach. Materials and Methods: Sixtyeight women who underwent laparoscopic treatment of adenomyosis at a referral center for gynecological laparoscopy. Results: Four distinct types of adenomyosis could be identified: diffuse, sclerotic, nodular, and cystic (54.5%, 13%, 28%, and 4.5% of cases, respectively). Menorrhagia as the main presenting symptom was significantly more frequent in patients with the diffuse type (84%) compared to those with sclerotic (44%) and nodular (37%) types (p = 0.025 and p = 0.001, respectively). All cases of cystic and nodular adenomyosis were treated by laparoscopic excision of the lesion. Eighty-nine percent of patients with sclerotic adenomyosis were treated with wide laparoscopic excision of the abnormal tissue. Eighty-one percent of patients with diffuse adenomyosis were treated with laparoscopic hysterectomy. Conclusions: Adenomyosis can be classified in four distinct types with differences in the presenting symptoms, as well as in the ideal surgical approach.

1 May 2004 in Fertility and Sterility
Verified
Journal Article
Closed access
EDEfthimios Deligeoroglou
Efthimios Deligeoroglou
AKAntonios Kontoravdis
Antonios Kontoravdis
EMEvangelos Makrakis
Evangelos Makrakis
PCPanagiotis Christopoulos
Panagiotis Christopoulos
AKApostolos Kountouris
Apostolos Kountouris
GCGeorge Creatsas
George Creatsas