Evidence map›Paper›PMID 34864993›Full record

Trial reportHuman reproduction (Oxford, England)2022

Economic evaluation of endometrial scratching before the second IVF/ICSI treatment: a cost-effectiveness analysis of a randomized controlled trial (SCRaTCH trial).

N E van Hoogenhuijze, R van Eekelen, F Mol, I Schipper, E R Groenewoud, M A F Traas, C A H Janssen, G Teklenburg, J P de Bruin, R H F van Oppenraaij and 27 more

Open access · bronzeAbstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Human reproduction (Oxford, England), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.9field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

12 citing papers in PubMed, 15 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

37 authors at 20 institutions in 1 country.

N E van HoogenhuijzeDepartment of Gynaecology and Reproductive Medicine, University Medical Centre Utrecht, Utrecht University, Utrecht, The Netherlands.ORCID 0000-0001-9057-1306
R van EekelenDutch Consortium for Healthcare Evaluation and Research in Obstetrics and Gynaecology-NVOG Consortium 2.0, Amsterdam, The Netherlands.
F MolAmsterdam UMC, University of Amsterdam, Center for Reproductive Medicine, Reproduction and Development, Amsterdam, The Netherlands.ORCID 0000-0002-6892-5574
I SchipperDivision of Reproductive Endocrinology and Infertility, Department Obstetrics and Gynaecology, Erasmus Medical Centre Rotterdam, Rotterdam, The Netherlands.
E R GroenewoudDepartment of Obstetrics, Gynaecology and Reproductive Medicine, Noordwest Ziekenhuisgroep, Den Helder, The Netherlands.
M A F TraasDepartment of Gynaecology, Gelre Hospital, Apeldoorn, The Netherlands.
C A H JanssenDepartment of Gynaecology, Groene Hart Hospital, Gouda, The Netherlands.
G TeklenburgIsala Fertility Clinic, Isala Hospital, Zwolle, The Netherlands.
J P de BruinDepartment of Gynaecology and Obstetrics, Jeroen Bosch Hospital, Den Bosch, The Netherlands.
R H F van OppenraaijDepartment of Gynaecology, Maasstad Hospital, Rotterdam, The Netherlands.
J W M MaasDepartment of Gynaecology, Maxima Medical Centre, Veldhoven, The Netherlands.
E MollDepartment of Gynaecology, Onze Lieve Vrouwe Gasthuis, Amsterdam, The Netherlands.
K FleischerDepartment of Obstetrics and Gynaecology, Radboud University Medical Centre, Nijmegen, The Netherlands.
M H A van HooffDepartment of Gynaecology, Franciscus Gasthuis en Vlietland, Rotterdam, The Netherlands.
C H de KoningDepartment of Gynaecology, Tergooi Hospital, Hilversum, The Netherlands.
A E P CantineauUniversity of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
C B LambalkDepartment of Reproductive Medicine, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.ORCID 0000-0003-3947-5129
M VerbergFertility Clinic, Fertility Clinic Twente, Hengelo, The Netherlands.
A M van HeusdenFertility Clinic, Medisch Centrum Kinderwens, Leiderdorp, The Netherlands.
A P MangerDepartment of Gynaecology, Diakonessenhuis, Utrecht, The Netherlands.
M M E van RumsteDepartment of Gynaecology, Catharina Hospital, Eindhoven, The Netherlands.
L F van der VoetDepartment of Gynaecology, Deventer Hospital, Deventer, The Netherlands.
Q D PieterseFertility Center, Haga Hospital, The Hague, The Netherlands.
J VisserDepartment of Gynaecology and Obstetrics, Amphia Hospital, Breda, The Netherlands.
E A BrinkhuisDepartment of Gynaecology and Obstetrics, Meander Hospital, Amersfoort, The Netherlands.
J E den HartogDepartment of Obstetrics and Gynaecology, Maastricht UMC+, Maastricht, The Netherlands.
M W GlasFertility Clinic, Wilhelmina Hospital Assen, Assen, The Netherlands.
N F KlijnDepartment of Gynaecology, Leiden University Medical Centre, Leiden, The Netherlands.ORCID 0000-0002-7236-1273
M van der ZandenDepartment of Gynaecology, Haaglanden Medical Centre, The Hague, The Netherlands.
M L BandellDepartment of Gynaecology, Albert Schweitzer Hospital, Sliedrecht, The Netherlands.
J C BoxmeerDepartment of Gynaecology, Reinier de Graaf Gasthuis, Delft, The Netherlands.
J van DisseldorpDepartment of Gynaecology and Obstetrics, St. Antonius Hospital, Nieuwegein, The Netherlands.
J SmeenkDepartment of Reproductive Medicine, Elisabeth-TweeSteden Hospital, Tilburg, The Netherlands.
M van WelyDutch Consortium for Healthcare Evaluation and Research in Obstetrics and Gynaecology-NVOG Consortium 2.0, Amsterdam, The Netherlands.
M J C EijkemansJulius Center for Health Sciences and Primary Care, University Medical Centre Utrecht, Utrecht University, Utrecht, The Netherlands.
H L TorranceDepartment of Gynaecology and Reproductive Medicine, University Medical Centre Utrecht, Utrecht University, Utrecht, The Netherlands.
F J M BroekmansDepartment of Gynaecology and Reproductive Medicine, University Medical Centre Utrecht, Utrecht University, Utrecht, The Netherlands.
Utrecht University · NLRadboud University Nijmegen · NLAmsterdam University Medical Centers · NLNederlandse Vereniging voor Obstetrie en Gynaecologie · NLAlbert Schweitzer Ziekenhuis · NLAmphia Ziekenhuis · NLDe Kinderkliniek · NLDeventer Ziekenhuis · NLDiakonessenhuis hospital · NLElisabeth-TweeSteden Ziekenhuis · NLErasmus University Rotterdam · NLGelre Hospitals · NLGroene Hart Ziekenhuis · NLHaga Hospital · NLIsala · NLJeroen Bosch Ziekenhuis · NLLeiden University · NLMaasstad Ziekenhuis · NLMaastricht University Medical Centre · NLMeander Medisch Centrum · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

study questionIs a single endometrial scratch prior to the second fresh IVF/ICSI treatment cost-effective compared to no scratch, when evaluated over a 12-month follow-up period? SUMMARY ANSWER: The incremental cost-effectiveness ratio (ICER) for an endometrial scratch was €6524 per additional live birth, but due to uncertainty regarding the increase in live birth rate this has to be interpreted with caution. WHAT IS KNOWN ALREADY: Endometrial scratching is thought to improve the chances of success in couples with previously failed embryo implantation in IVF/ICSI treatment. It has been widely implemented in daily practice, despite the lack of conclusive evidence of its effectiveness and without investigating whether scratching allows for a cost-effective method to reduce the number of IVF/ICSI cycles needed to achieve a live birth. STUDY DESIGN, SIZE, DURATION: This economic evaluation is based on a multicentre randomized controlled trial carried out in the Netherlands (SCRaTCH trial) that compared a single scratch prior to the second IVF/ICSI treatment with no scratch in couples with a failed full first IVF/ICSI cycle. Follow-up was 12 months after randomization.Economic evaluation was performed from a healthcare and societal perspective by taking both direct medical costs and lost productivity costs into account. It was performed for the primary outcome of biochemical pregnancy leading to live birth after 12 months of follow-up as well as the secondary outcome of live birth after the second fresh IVF/ICSI treatment (i.e. the first after randomization). To allow for worldwide interpretation of the data, cost level scenario analysis and sensitivity analysis was performed. PARTICIPANTS/MATERIALS, SETTING,

methodsFrom January 2016 until July 2018, 933 women with a failed first IVF/ICSI cycle were included in the trial. Data on treatment and pregnancy were recorded up until 12 months after randomization, and the resulting live birth outcomes (even if after 12 months) were also recorded.Total costs were calculated for the second fresh IVF/ICSI treatment and for the full 12 month period for each participant. We included costs of all treatments, medication, complications and lost productivity costs. Cost-effectiveness analysis was carried out by calculating ICERs for scratch compared to control. Bootstrap resampling was used to estimate the uncertainty around cost and effect differences and ICERs. In the sensitivity and scenario analyses, various unit costs for a single scratch were introduced, amongst them, unit costs as they apply for the United Kingdom (UK). MAIN RESULTS AND THE ROLE OF CHANCE: More live births occurred in the scratch group, but this also came with increased costs over a 12-month period. The estimated chance of a live birth after 12 months of follow-up was 44.1% in the scratch group compared to 39.3% in the control group (risk difference 4.8%, 95% CI -1.6% to +11.2%). The mean costs were on average €283 (95% CI: -€299 to €810) higher in the scratch group so that the point average ICER was €5846 per additional live birth. The ICER estimate was surrounded with a high level of uncertainty, as indicated by the fact that the cost-effectiveness acceptability curve (CEAC) showed that there is an 80% chance that endometrial scratching is cost-effective if society is willing to pay ∼€17 500 for each additional live birth. LIMITATIONS, REASONS FOR CAUTION: There was a high uncertainty surrounding the effects, mainly in the clinical effect, i.e. the difference in the chance of live birth, which meant that a single straightforward conclusion could not be ascertained as for now. WIDER IMPLICATIONS OF THE

findingsThis is the first formal cost-effectiveness analysis of endometrial scratching in women undergoing IVF/ICSI treatment. The results presented in this manuscript cannot provide a clear-cut expenditure for one additional birth, but they do allow for estimating costs per additional live birth in different scenarios once the clinical effectiveness of scratching is known. As the SCRaTCH trial was the only trial with a follow-up of 12 months, it allows for the most complete estimation of costs to date. STUDY FUNDING/COMPETING INTEREST(S): This study was funded by ZonMW, the Dutch organization for funding healthcare research. A.E.P.C., F.J.M.B., E.R.G. and C.B. L. reported having received fees or grants during, but outside of, this trial. TRIAL REGISTRATION NUMBER: Netherlands Trial Register (NL5193/NTR 5342).

Indexed as

Fertilization in VitroSperm Injections, IntracytoplasmicBirth RateCost-Benefit AnalysisFemaleHumansLive BirthMalePregnancyPregnancy RateARTcost-effectivenesseconomic analysisendometrial injuryendometrial scratchICSIIVFlive birth

Identifiers

PMID34864993
PMCPMC8804332
OpenAlexW4200116517

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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.