28 research outputs found
Histological, Morphometrical, and Enzyme Histochemical Studies on Varicocele Orchiopathy
Uterus Transplantation as a Therapy Method in Mayer-Rokitansky-Kuster-Hauser Syndrome
The Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome is the most common
cause of uterine aplasia (underdevelopment or absence) at a frequency
estimated to be worldwide of 1/4500 births of new-born female infants.
This is a literature review aiming to determine the sufficiency of the
uterine transplantation (UTx) method as a therapeutic protocol for the
MRKH syndrome.
Online searches were carried out in PubMed, Embase, CINAHL and Google
scholar databases, during January and February 2019. The search included
a combination of the various terms (see key words) as well as a
combination of these terms in Greek and English so as to identify and
display articles that would be as close as possible to the subject of
research.
The online search yielded 95 articles. Eighty-five of these were
considered as eligible and possible sources from the title and abstract
presented but later were excluded, whereas 10 of them were selected to
be included in the literature review. The literature review results
showed that two therapeutic methods that are now successfully applied
are the Vecchietti method and the Davydov method, which is the latest
and less invasive technique but with equally if not improved immediate
results. However, this treatment is not adequate to satisfy or provide a
solution for the reproduction requirements of this patient group. The
UTx proved sufficient.
Although uterus transplant could be considered the ideal solution for
the management of infertility and the satisfaction of the reproductive
and sexual needs of women with MRKH syndrome, since the first successful
pregnancy after uterine transplantation is a reality in the recent
years, it is early days to be considered as a safe mode of management
Layperson's Esthetic Preference to the Presence or Absence of the Interdental Papillae in the Low Smile Line: A Web‐based Study
Rehabilitation Challenge in Patient With High Smile Line: Case Report and Review of Surgical Protocols
Pain and discomfort following immediate and delayed loading by overdentures in the single mandibular implant study (SMIS)
Survival and Complications of Single Dental Implants in the Edentulous Mandible Following Immediate or Delayed Loading: A Randomized Controlled Clinical Trial
It was the aim of this 24-mo randomized controlled clinical trial to investigate whether the survival of a single median implant placed in the edentulous mandible to retain a complete denture is not compromised by immediate loading. Secondary outcomes were differences in prosthetic complications between the loading principles. Each of the 158 patients who received an implant was randomly assigned to the immediate loading group (n = 81) or the delayed loading group (n = 77). Recall visits were performed 1 mo after implant placement (for only the delayed loading group) and 1, 4, 12, and 24 mo after implant loading. Nine implants failed in the immediate loading group, all within the first 3 mo of implant loading, and 1 implant failed in the delayed loading group prior to loading. Noninferiority of implant survival of the immediate loading group, as compared with the delayed loading group, could not be shown (P = 0.81). Consistent with this result, a secondary analysis with Fisher exact test revealed that the observed difference in implant survival between the treatment groups was indeed statistically significant (P = 0.019). The most frequent prosthetic complications and maintenance interventions in the mandible were retention adjustments, denture fractures, pressure sores, and matrix exchanges. There was only 1 statistically significant difference between the groups regarding the parameter “fracture of the denture base in the ball attachment area” (P = 0.007). The results indicate that immediate loading of a single implant in the edentulous mandible reveals inferior survival than that of delayed loading and therefore should be considered only in exceptional cases (German Clinical Trials Register: DRKS00003730)