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Efficacy and safety of perioperative use of epinephrine for laparoscopic myomectomy in infertile women with symptomatic solitary intramural uterine fibroids A randomized clinical trial

Identifikátory výsledku

  • Kód výsledku v IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F65269705%3A_____%2F16%3A00065721" target="_blank" >RIV/65269705:_____/16:00065721 - isvavai.cz</a>

  • Nalezeny alternativní kódy

    RIV/00216224:14110/16:00091846

  • Výsledek na webu

  • DOI - Digital Object Identifier

Alternativní jazyky

  • Jazyk výsledku

    angličtina

  • Název v původním jazyce

    Efficacy and safety of perioperative use of epinephrine for laparoscopic myomectomy in infertile women with symptomatic solitary intramural uterine fibroids A randomized clinical trial

  • Popis výsledku v původním jazyce

    OBJECTIVE: To determine the efficacy and safety of intramyometrial application of epinephrine during a laparoscopic myomectomy in women of reproductive age desiring pregnancy and with clinically symptomatic uterine fibroids, in comparison with a placebo-based patient control group. STUDY DESIGN: The study group (n=96, 53.3%) underwent an application of 12 mu g epinephrine hydrochloride diluted in 20 mL of NaCl solution, while the control group (n=84, 46.7%) received 20 mL of NaCl only. Perioperative blood loss, duration of surgery, length of hospital stay, and incidence of perioperative and postoperative complications were evaluated. RESULTS: A significantly lower blood loss (mean +/- SD: 57 +/- 23 mL) was observed in the group with local application of epinephrine as compared to the control group (143 +/- 106 mL) (p<0.001), along with a significantly shortened duration of surgery (53 +/- 16 min) vs. control group (72 +/- 26 min) (p=0.006), and a significantly shortened hospital stay (3.0 +/- 1.2 days) vs. the control group (4.3 +/- 1.4 days) (p= 0.003). No serious perioperative complications were observed in either group, and no statistically significant difference in the incidence of postoperative complications was recorded with our study group when compared to the control group (2.1% vs. 7.1%) (p=0.143). CONCLUSION: Epinephrine use during a laparoscopic myomectomy is both effective and safe.

  • Název v anglickém jazyce

    Efficacy and safety of perioperative use of epinephrine for laparoscopic myomectomy in infertile women with symptomatic solitary intramural uterine fibroids A randomized clinical trial

  • Popis výsledku anglicky

    OBJECTIVE: To determine the efficacy and safety of intramyometrial application of epinephrine during a laparoscopic myomectomy in women of reproductive age desiring pregnancy and with clinically symptomatic uterine fibroids, in comparison with a placebo-based patient control group. STUDY DESIGN: The study group (n=96, 53.3%) underwent an application of 12 mu g epinephrine hydrochloride diluted in 20 mL of NaCl solution, while the control group (n=84, 46.7%) received 20 mL of NaCl only. Perioperative blood loss, duration of surgery, length of hospital stay, and incidence of perioperative and postoperative complications were evaluated. RESULTS: A significantly lower blood loss (mean +/- SD: 57 +/- 23 mL) was observed in the group with local application of epinephrine as compared to the control group (143 +/- 106 mL) (p<0.001), along with a significantly shortened duration of surgery (53 +/- 16 min) vs. control group (72 +/- 26 min) (p=0.006), and a significantly shortened hospital stay (3.0 +/- 1.2 days) vs. the control group (4.3 +/- 1.4 days) (p= 0.003). No serious perioperative complications were observed in either group, and no statistically significant difference in the incidence of postoperative complications was recorded with our study group when compared to the control group (2.1% vs. 7.1%) (p=0.143). CONCLUSION: Epinephrine use during a laparoscopic myomectomy is both effective and safe.

Klasifikace

  • Druh

    J<sub>x</sub> - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)

  • CEP obor

    FK - Gynekologie a porodnictví

  • OECD FORD obor

Návaznosti výsledku

  • Projekt

  • Návaznosti

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Ostatní

  • Rok uplatnění

    2016

  • Kód důvěrnosti údajů

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Údaje specifické pro druh výsledku

  • Název periodika

    Journal of reproductive medicine

  • ISSN

    0024-7758

  • e-ISSN

  • Svazek periodika

    61

  • Číslo periodika v rámci svazku

    7-8

  • Stát vydavatele periodika

    US - Spojené státy americké

  • Počet stran výsledku

    5

  • Strana od-do

    380-384

  • Kód UT WoS článku

    000380580600013

  • EID výsledku v databázi Scopus