Cargando…

A Prospective Randomised Comparative Clinical Trial Study of Luteal Phase Letrozole versus Ganirelix Acetate Administration to Prevent Severity of Early Onset OHSS in ARTs

BACKGROUND: Ovarian hyperstimulation syndrome (OHSS) is the most notable complication in ovulation induction for assisted reproductive techniques (ARTs) like in vitro fertilization (IVF) and intracytoplasmic sperm injection (ICSI). Hence, we decided to evaluate the effect of the aromatase inhibitor,...

Descripción completa

Detalles Bibliográficos
Autores principales: Choudhary, Rana Afzal, Vora, Priyanka H, Darade, Kavita K, Pandey, Seema, Ganla, Kedar N
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royan Institute 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8530210/
https://www.ncbi.nlm.nih.gov/pubmed/34913294
http://dx.doi.org/10.22074/IJFS.2021.139562.1042
_version_ 1784586625922105344
author Choudhary, Rana Afzal
Vora, Priyanka H
Darade, Kavita K
Pandey, Seema
Ganla, Kedar N
author_facet Choudhary, Rana Afzal
Vora, Priyanka H
Darade, Kavita K
Pandey, Seema
Ganla, Kedar N
author_sort Choudhary, Rana Afzal
collection PubMed
description BACKGROUND: Ovarian hyperstimulation syndrome (OHSS) is the most notable complication in ovulation induction for assisted reproductive techniques (ARTs) like in vitro fertilization (IVF) and intracytoplasmic sperm injection (ICSI). Hence, we decided to evaluate the effect of the aromatase inhibitor, letrozole, versus gonadotrophin-releasing hormone (GnRH)-antagonist (ganirelix acetate) on prevention of severity of OHSS and reduction in serum estradiol (E2) levels when administered during the luteal phase after oocyte retrieval in IVF/ICSI cycles. MATERIALS AND METHODS: In this prospective single-centred, randomized, parallel-arm study, 122 patients were rand- omized to receive oral letrozole (n=61, 2.5 mg twice daily) or ganirelix acetate (n=61, 0.25 mg subcutaneously daily) from the day of egg retrieval for the next 7 days. Incidence and severity of early OHSS were the primary endpoints assessed by the signs, symptoms, and laboratory findings of OHSS (e.g., serum E2 levels). The secondary endpoints were patient satisfaction and the additional cost of therapy to prevent the severity of OHSS. RESULTS: Letrozole group had lower incidence of OHSS (13.1%) compared to 19.6% in ganirelix acetate group (P=0.32). Serum E2 levels on post-pick up days 5 and 7 were significantly lower in the letrozole group when com- pared to the ganirelix acetate group (P=0.001). The majority of the patients in both groups had no major complica- tions. No significant difference was found between the study groups with respect to the incidence of OHSS (P=0.33). The additional cost per IVF cycle for prevention of severity of early-onset OHSS in the letrozole group was 5.32 USD compared to 267.26 USD in the ganirelix acetate group, which was almost fifty times costlier. CONCLUSION: Letrozole and ganirelix acetate have the same efficiency for the overall prevention of OHSS, whereas letrozole was more effective in preventing moderate OHSS. Letrozole had better patient satisfaction and is cheaper compared to GnRH antagonists (Registration number: CTRI/2020/10/028674).
format Online
Article
Text
id pubmed-8530210
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Royan Institute
record_format MEDLINE/PubMed
spelling pubmed-85302102021-10-29 A Prospective Randomised Comparative Clinical Trial Study of Luteal Phase Letrozole versus Ganirelix Acetate Administration to Prevent Severity of Early Onset OHSS in ARTs Choudhary, Rana Afzal Vora, Priyanka H Darade, Kavita K Pandey, Seema Ganla, Kedar N Int J Fertil Steril Original Article BACKGROUND: Ovarian hyperstimulation syndrome (OHSS) is the most notable complication in ovulation induction for assisted reproductive techniques (ARTs) like in vitro fertilization (IVF) and intracytoplasmic sperm injection (ICSI). Hence, we decided to evaluate the effect of the aromatase inhibitor, letrozole, versus gonadotrophin-releasing hormone (GnRH)-antagonist (ganirelix acetate) on prevention of severity of OHSS and reduction in serum estradiol (E2) levels when administered during the luteal phase after oocyte retrieval in IVF/ICSI cycles. MATERIALS AND METHODS: In this prospective single-centred, randomized, parallel-arm study, 122 patients were rand- omized to receive oral letrozole (n=61, 2.5 mg twice daily) or ganirelix acetate (n=61, 0.25 mg subcutaneously daily) from the day of egg retrieval for the next 7 days. Incidence and severity of early OHSS were the primary endpoints assessed by the signs, symptoms, and laboratory findings of OHSS (e.g., serum E2 levels). The secondary endpoints were patient satisfaction and the additional cost of therapy to prevent the severity of OHSS. RESULTS: Letrozole group had lower incidence of OHSS (13.1%) compared to 19.6% in ganirelix acetate group (P=0.32). Serum E2 levels on post-pick up days 5 and 7 were significantly lower in the letrozole group when com- pared to the ganirelix acetate group (P=0.001). The majority of the patients in both groups had no major complica- tions. No significant difference was found between the study groups with respect to the incidence of OHSS (P=0.33). The additional cost per IVF cycle for prevention of severity of early-onset OHSS in the letrozole group was 5.32 USD compared to 267.26 USD in the ganirelix acetate group, which was almost fifty times costlier. CONCLUSION: Letrozole and ganirelix acetate have the same efficiency for the overall prevention of OHSS, whereas letrozole was more effective in preventing moderate OHSS. Letrozole had better patient satisfaction and is cheaper compared to GnRH antagonists (Registration number: CTRI/2020/10/028674). Royan Institute 2021 2021-10-16 /pmc/articles/PMC8530210/ /pubmed/34913294 http://dx.doi.org/10.22074/IJFS.2021.139562.1042 Text en The Cell Journal (Yakhteh) is an open access journal which means the articles are freely available online for any individual author to download and use the providing address. The journal is licensed under a Creative Commons Attribution-Non Commercial 3.0 Unported License which allows the author(s) to hold the copyright without restrictions that is permitting unrestricted use, distribution, and reproduction in any medium provided the original work is properly cited. https://creativecommons.org/licenses/by/3.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Choudhary, Rana Afzal
Vora, Priyanka H
Darade, Kavita K
Pandey, Seema
Ganla, Kedar N
A Prospective Randomised Comparative Clinical Trial Study of Luteal Phase Letrozole versus Ganirelix Acetate Administration to Prevent Severity of Early Onset OHSS in ARTs
title A Prospective Randomised Comparative Clinical Trial Study of Luteal Phase Letrozole versus Ganirelix Acetate Administration to Prevent Severity of Early Onset OHSS in ARTs
title_full A Prospective Randomised Comparative Clinical Trial Study of Luteal Phase Letrozole versus Ganirelix Acetate Administration to Prevent Severity of Early Onset OHSS in ARTs
title_fullStr A Prospective Randomised Comparative Clinical Trial Study of Luteal Phase Letrozole versus Ganirelix Acetate Administration to Prevent Severity of Early Onset OHSS in ARTs
title_full_unstemmed A Prospective Randomised Comparative Clinical Trial Study of Luteal Phase Letrozole versus Ganirelix Acetate Administration to Prevent Severity of Early Onset OHSS in ARTs
title_short A Prospective Randomised Comparative Clinical Trial Study of Luteal Phase Letrozole versus Ganirelix Acetate Administration to Prevent Severity of Early Onset OHSS in ARTs
title_sort prospective randomised comparative clinical trial study of luteal phase letrozole versus ganirelix acetate administration to prevent severity of early onset ohss in arts
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8530210/
https://www.ncbi.nlm.nih.gov/pubmed/34913294
http://dx.doi.org/10.22074/IJFS.2021.139562.1042
work_keys_str_mv AT choudharyranaafzal aprospectiverandomisedcomparativeclinicaltrialstudyoflutealphaseletrozoleversusganirelixacetateadministrationtopreventseverityofearlyonsetohssinarts
AT vorapriyankah aprospectiverandomisedcomparativeclinicaltrialstudyoflutealphaseletrozoleversusganirelixacetateadministrationtopreventseverityofearlyonsetohssinarts
AT daradekavitak aprospectiverandomisedcomparativeclinicaltrialstudyoflutealphaseletrozoleversusganirelixacetateadministrationtopreventseverityofearlyonsetohssinarts
AT pandeyseema aprospectiverandomisedcomparativeclinicaltrialstudyoflutealphaseletrozoleversusganirelixacetateadministrationtopreventseverityofearlyonsetohssinarts
AT ganlakedarn aprospectiverandomisedcomparativeclinicaltrialstudyoflutealphaseletrozoleversusganirelixacetateadministrationtopreventseverityofearlyonsetohssinarts
AT choudharyranaafzal prospectiverandomisedcomparativeclinicaltrialstudyoflutealphaseletrozoleversusganirelixacetateadministrationtopreventseverityofearlyonsetohssinarts
AT vorapriyankah prospectiverandomisedcomparativeclinicaltrialstudyoflutealphaseletrozoleversusganirelixacetateadministrationtopreventseverityofearlyonsetohssinarts
AT daradekavitak prospectiverandomisedcomparativeclinicaltrialstudyoflutealphaseletrozoleversusganirelixacetateadministrationtopreventseverityofearlyonsetohssinarts
AT pandeyseema prospectiverandomisedcomparativeclinicaltrialstudyoflutealphaseletrozoleversusganirelixacetateadministrationtopreventseverityofearlyonsetohssinarts
AT ganlakedarn prospectiverandomisedcomparativeclinicaltrialstudyoflutealphaseletrozoleversusganirelixacetateadministrationtopreventseverityofearlyonsetohssinarts