Evidence map›Paper›PMID 37369184›Full record

ArticleGynecologic and obstetric investigation2023

Dosing Characteristics of Recombinant Human Luteinizing Hormone or Human Menopausal Gonadotrophin-Derived LH Activity in Patients Undergoing Ovarian Stimulation: A German Fertility Database Study.

Valerie Strezsak, Arthur Allignol, Klaus Bühler, Robert Fischer, Julie Hubbard, Salvatore Longobardi, Monica Lispi, Joan Schertz, Patrice Verpillat

Open access · hybridAbstract read
In one paragraph

Article in Gynecologic and obstetric investigation, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

9 authors at 4 institutions in 2 countries.

Valerie StrezsakGlobal Clinical Development, Research and Development, EMD Serono Research and Development Institute, Inc., an affiliate of Merck KGaA, Billerica, Massachusetts, USA.
Arthur AllignolGlobal Epidemiology, Research and Development, Merck Healthcare KGaA, Darmstadt, Germany.
Klaus BühlerDepartment of Gynaecology and Reproductive Medicine, University Hospital Jena, Friedrich-Schiller-University Jena, Jena, Germany.
Robert FischerFertility Centre Hamburg, Hamburg, Germany.
Julie HubbardGlobal Clinical Development, Research and Development, EMD Serono Research & Development Institute, Inc., an affiliate of Merck KGaA, Billerica, Massachusetts, USA.
Salvatore LongobardiGlobal Clinical Development, Research and Development, Merck Healthcare KGaA, Darmstadt, Germany.
Monica LispiGlobal Medical Affairs Fertility, Research and Development, Merck Healthcare KGaA, Darmstadt, Germany.
Joan SchertzGlobal Clinical Development, Research and Development, EMD Serono Research & Development Institute, Inc., an affiliate of Merck KGaA, Billerica, Massachusetts, USA.
Patrice VerpillatGlobal Epidemiology, Research and Development, Merck Healthcare KGaA, Darmstadt, Germany.
Merck (Germany) · DEMerck Serono (Italy) · ITJena University Hospital · DEUniversity of Modena and Reggio Emilia · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesThe aim of the study was to evaluate dosing of recombinant human luteinizing hormone (r-hLH) or human menopausal gonadotrophin (hMG)-derived medications with LH activity in ovarian stimulation (OS) cycles for in vitro fertilization (IVF)/intracytoplasmic sperm injection (ICSI).

designA non-interventional study was performed to analyse data from the German RecDate database (January 2007-December 2011). PARTICIPANTS/MATERIALS, SETTING,

methodsStarting/total r-hLH/hMG dose, OS duration/cycle number, r-hLH/hMG initiation day (first day of administration), and population/cycle characteristics were assessed in women (≥18 years) undergoing OS for IVF/ICSI using r-hLH or hMG-derived medications (excluding corifollitropin alfa, clomiphene citrate, letrozole, mini/micro-dose human chorionic gonadotrophin, and urofollitropin alone). Data were summarized descriptively.

results67,858 identified cycles utilized medications containing r-hLH (10,749), hMG (56,432), or both (677). Mean (standard deviation) OS duration with r-hLH and hMG was 10.1 (4.43) and 9.8 (6.16) days, respectively. Median (25th-75th percentile) r-hLH starting dose (75.0 [75.0-150.0] IU) was consistent across patients regardless of age, infertility diagnosis, or gonadotrophin-releasing hormone (GnRH) protocol. Median (25th-75th percentile) hMG-derived LH activity starting dose was 225.0 (150.0-300.0) IU, regardless of GnRH protocol, but was lower in women aged <35 years and those with ovulation disorders/polycystic ovary syndrome. Median (25th-75th percentile) total dose for r-hLH (750.0 [337.5-1,125.0] IU) and hMG-derived LH activity (1,575.0 [750.0-2,625.0] IU) varied according to patients' age, infertility diagnosis, cycle number, and r-hLH/hMG initiation day. GnRH antagonist use resulted in a numerically higher median total hMG-derived LH activity dose than GnRH agonist use. LIMITATIONS: The data used in this study were taken from electronic medical records relating to a specific timeframe (2007-2011) and therefore may not accurately reflect current clinical practice; however, it is likely that the differences between the two compounds would be maintained. Additionally, secondary data sources may suffer from uniformity and quality issues.

conclusionsThe standard of care for OS cycles is described with respect to IVF/ICSI treatment including an LH component in Germany during the specified timeframe.

Indexed as

InfertilitySemenFemaleFertilityFertilization in VitroGonadotropin-Releasing HormoneHumansLuteinizing HormoneMaleMenopauseMenotropinsOvulation InductionGonadotropin-Releasing HormoneLuteinizing HormoneMenotropinsHuman menopausal gonadotrophinLuteinizing hormoneOvarian stimulationReal-world dataRecombinant human luteinizing hormone

Identifiers

PMID37369184
PMCPMC10614274
OpenAlexW4382344288

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.