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Fetal and Neonatal Alloimmune ThrombocytopeniaNOFNAITNCT04529382

Neurodevelopmental Outcome After Fetal Neonatal AlloImmune Thrombocytopenia

An observational study of Fetal and Neonatal Alloimmune Thrombocytopenia and Long Term Adverse Effects, run by Leiden University Medical Center at 1 site in Netherlands.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

Fetal and neonatal alloimmune thrombocytopenia (FNAIT) is a disease caused by allo-immunisation during pregnancy. If left untreated, FNAIT can lead to severe fetal intracranial haemorrhage. This complication can be prevented by weekly administration of intravenous immunoglobulin (IVIg) to the mother during pregnancy. Read more about this study

Who is it for?
Ages 18 months to 17 years
What is being tested?
Cognitive testing (Bayley III, WPPSI III and WISC V)
How many people
78 participants
Where
1 siteNetherlands
Study dates
17 Dec 2019to 17 Dec 2021
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 months to 17 years
  • All sexes
  • No healthy volunteers
  • Child

Study population: All children born between 2002 and 2017 and diagnosed with FNAIT are eligible for this study. They will be invited for an assessment at our outpatient clinic. FNAIT cases that were not antenatally treated with IVIg will be eligible for the study (cohort 1), as well as FNAIT cases which were anticipated antenatally by materal IVIg administration (cohort 2).

Who may be able to join

  • Children diagnosed with FNAIT during pregnancy or postnatal, at moment of inclusion 2 to 16 years of age.
  • Children living in the Netherlands.
  • Parents or guardian aged ≥ 18 years old, with parental authority.
  • Written informed consent form both parents with, form being approved by Ethic Committee.

Who cannot join

  • Children born with congenital and/or chromosomal abnormalities.
  • Children that passed away before inclusion.

Trial locations and contacts

1 site in 1 country.

Netherlands1 site
  • Leiden University Medical Center

    Leiden, 2333 ZA

Other trials in Netherlands

About this study

Fetal and neonatal alloimmune thrombocytopenia (FNAIT) is a disease caused by allo-immunisation during pregnancy. If left untreated, FNAIT can lead to severe fetal intracranial haemorrhage. This complication can be prevented by weekly administration of intravenous immunoglobulin (IVIg) to the mother during pregnancy. Knowledge on long-term development of FNAIT survivors with or without IVIg treatment is very limited but an important subject in the counselling of parents of newly diagnosed cases. To evaluate the long-term neurodevelopmental outcome in two groups of children with FNAIT will be asked to participate in our study in an outpatient clinic setting.

Read the detailed description

INTRODUCTION AND RATIONALE Fetal and neonatal alloimmune thrombocytopenia (FNAIT) is the most common cause of thrombocytopenia in otherwise healthy term-born neonates. FNAIT is a rare disease with an incidence estimated around 1 per 1000 live newborns. During pregnancy alloimmunization can occur due to incompatibility of the Human Platelet Antigens (HPA) on the maternal and fetal platelets. Alloimmunization and maternal production of antibodies directed against the HPA-positive fetal platelets, leads to thrombocytopenia and an increased risk of intracranial hemorrhages (ICH) in the fetus. Clinical presentation can vary from skin bleedings to severe ICH leading to lifelong neurologic sequelae or intrauterine death.

In the past, FNAIT was managed with invasive and high-risk interventions including intrauterine platelet transfusion (IUPT). Since the end of the 20th century, invasive intrauterine transfusions (IUT) were replaced by a new, non-invasive therapy: maternal administration of intravenous immunoglobulin (IVIg). This novel therapy resulted in a significant lower risk of intrauterine fetal death and ICH. Intervention with immune modulation in the semi -allogenic environment of the fetus by administration of immunoglobulins (Ig) is successful, especially in preventing ICH. However antenatal treatment with IVIg has been implemented as standard of care without strong methodological follow-up research of children from mothers treated with IVIg. To date, only two follow-up studies have been published in children with anticipated FNAIT cases. The first study of a FNAIT cohort treated with IVIg was done by Ward et al. in 2006. They concluded that development of children treated for FNAIT was better compared to their non-treated siblings. Their conclusions were based on non-validated questionnaires taken by telephone, assessing the behavioral outcome of the children and were limited by a ~40% lost-to-follow-up rate. A second follow-up study including 39 children was published by a research group from our center in 2004. This research stated that the outcome in children with FNAIT and exposed to maternal IVIg treatment was similar to the normal population. However, this study included a heterogenic group of children with different treatment strategies including IUT, hampering definitive conclusions and substantiating the need for more research.

No long-term standardized follow-up studies were performed on FNAIT cases without antenatal treatment and/or ICH. The natural course of the disease and long-term effects of thrombocytopenia on the developing fetus and newborn are unknown. FNAIT is defined as a disease caused by alloantibodies, resulting in thrombocytopenia and a risk of bleeding in the neonate. In the last years, evidence is increasing that the maternal alloantibodies can also bind to the fetal endothelium and may impair angiogenesis in the developing fetuses It is not known at which moment in pregnancy the developing brain is most vulnerable for damage induced by these kind of alloantibodies. The timing in fetal life FNAIT associated ICH ranges from 23 to 42 weeks, but small bleeding may not be diagnosed. It may also be that these type of alloantibodies not lead to ICH but to other type of cerebral damage. These lesions can remain subclinical directly after birth but lead to developmental delay on the long term. This knowledge can be of great interest when counseling parents with a risk of FNAIT or in writing guidelines.

For 3 decades a nationwide screening on FNAIT to detect pregnancies with alloantibodies in time and start treatment to prevent bleedings is being discussed. If alloantibodies lead to cerebral damage on the long term also in patients without large ICH this might have large implications in the debate on the introduction of a national screening programme. Therefore the investigators want to underline that more knowledge about the long-term development of FNAIT survivors is required.

The Leiden University Medical Center (LUMC), a national fetal therapy center in The Netherlands, has a close and long-lasting collaboration with Sanquin. This collaboration offers a unique opportunity to evaluate a large and complete cohort of children with FNAIT. LUMC and Sanquin are both nationwide referral centers for FNAIT and committed to improve timely detection of high-risk cases who need intra-uterine therapy. This research group from the national expertise centers are designated to assess long-term outcome in children with FNAIT and describe the natural history of children affected by FNAIT and the long term effects of a given therapy.

OBJECTIVE The primary objective is to determine the cognitive test score of children diagnosed with FNAIT without and with antenatal treatment.

STUDY DESIGN The investigators will perform an observational cohort study. The long-term neurodevelopmental outcome of children affected by FNAIT will be evaluated. All children born between 2002 and 2017 and diagnosed with FNAIT are eligible for follow-up assessment and will be invited for an assessment at our outpatient clinic. The FNAIT survivors will be collected in two cohorts; cohort 1 will consist of FNAIT survivors without antenatal treatment, cohort 2 will consist of FNAIT survivors that were antenatally anticipated and therefore IVIg treatment to the mother was given.

Enrollment in this study will take place via the LUMC and Stichting Sanquin Bloedvoorziening. The LUMC is national referral center for intrauterine therapy and Sanquin is national reference laboratory to diagnose FNAIT. Retrospectively FNAIT cases will be collected and asked for permission directly or via referring specialist.

After informed consent, child cognitive functioning will be assessed with a formal psychological test of cognitive functioning. According to age, the parents will complete a standardized behavioral and HRQoL questionnaire. Academic performance will be assessed by collecting the most recent CITO test scores from the Dutch Pupil monitoring system developed by the National Institute for Educational Measurement. Assessment of the prevalence of possible late effects of IVIg on the immune system will be assessed by questionnaires about the prevalence of allergies, astma, eczema and course of infections by questionnaires. Parents and children, when 12 years old or older, are asked for consent to request the medical letters from the maternity or neonatology ward to obtain perinatal and neonatal data.

No laboratory tests will be performed in this study, however data of the laboratory tests that were performed at timepoint of diagnosing FNAIT will be involved in this study.

After assessment a report will be made from the observations and test results, this report will be sent to the parents.

Being tested
Cognitive testing (Bayley III, WPPSI III and WISC V)
Medical subject headings
Thrombocytopenia, Neonatal Alloimmune, Long Term Adverse Effects

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Cognitive testing (Bayley III, WPPSI III and WISC V)Diagnostic test

    Also called Pediatric Quality of Life Inventory, Child Behavior Checklist, Questionnaire based on 'Richtlijn diagnostiek naar onderliggende aandoeningen bij kinderen met recidiverende luchtweginfecties', Questionnaire composited in collaboration with allergist (Dr. H. de Groot).

    Parents and children will be invited to come for an outpatient clinic visit where cognitive testing and neurologic examination will be performed. In addition to this parents will be asked to fill in questionnaires, provide latest school results and medical files will be requested from treating physicians.

Study groups in NCT04529382
Study groupRoleWhat they receive
Cohort 1: Unanticipated FNAIT casesAll children born between 2002 and 2017 and diagnosed with FNAIT are eligible for this study. Children in cohort 1 will be FNAIT cases that were not antenatally treated with by maternal IVIg administration (or other forms of fetal therapy).
Receives: Diagnostic Test: Cognitive testing (Bayley III, WPPSI III and WISC V)
Cohort 2: Anticipated FNAIT casesAll children born between 2002 and 2017 and diagnosed with FNAIT are eligible for this study. Children in cohort 2 will be FNAIT cases which were anticipated antenatally by maternal IVIg administration according to our local protocol.
Receives: Diagnostic Test: Cognitive testing (Bayley III, WPPSI III and WISC V)

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Cognitive test score

    IQ test score calculated from a standardized cognitive test.

    Measured: From birth until study enrollment. Average age of the participants is expected to be 8 years old.

Secondary outcomes (13)
  1. Neurodevelopmental injury (NDI)

    NDI is a composite outcome of:

    • Cerebral palsy ≥ grade II according to Gross Motor Classification System (GMFCS)
    • Impaired cognitive, language and/or motor development (test scores <70)
    • Bilateral blindness and/or bilateral deafness
    • Bilateral deafness requiring amplification

    Measured: From birth until study enrollment. Average age of the participants is expected to be 8 years old.

  2. Health Related Quality of Life

    Health Related Quality of Life score calculated from the PedsQol questionnaire.

    Measured: From birth until study enrollment. Average age of the participants is expected to be 8 years old.

  3. Cerebral Palsy

    Spastic bilateral, spastic unilateral or mixed Classification by European CP Network

    Measured: From birth until study enrollment. Average age of the participants is expected to be 8 years old.

  4. Bilateral blindness

    Blind or partially sighted.

    Measured: From birth until study enrollment. Average age of the participants is expected to be 8 years old.

  5. Bilateral deafness

    Needing hearing aids.

    Measured: From birth until study enrollment. Average age of the participants is expected to be 8 years old.

  6. Behaviour test score

    Behaviour test score bases on Child Behavior Checklist

    Measured: From birth until study enrollment. Average age of the participants is expected to be 8 years old.

  7. Abnormal course or incidence of infections

    Need to refer to an immunologist or the need to preform diagnostics based on history taking according to the Dutch guidelines.

    Measured: From birth until study enrollment. Average age of the participants is expected to be 8 years old.

  8. Prevalence of eczema

    Number of children that suffer from eczema.

    Measured: From birth until study enrollment. Average age of the participants is expected to be 8 years old.

  9. Prevalence of allergies

    Number of children that suffer from allergies

    Measured: From birth until study enrollment. Average age of the participants is expected to be 8 years old.

  10. Patient reported anaphylaxis

    Serious allergic reaction, requiring urgent medical treatment with epinephrine.

    Measured: From birth until study enrollment. Average age of the participants is expected to be 8 years old.

  11. Poor control of allergic rhinitis

    CARAT score of upper airways < 8

    Measured: From birth until study enrollment. Average age of the participants is expected to be 8 years old.

  12. Poor control of asthma

    CARAT score of lower airways < 16.

    Measured: From birth until study enrollment. Average age of the participants is expected to be 8 years old.

  13. Academic performance

    The latest test scores from primary school will be requested. Three academic domains will be assessed; arithmetic and spelling performance and measurements on reading comprehension.

    Measured: From birth until study enrollment. Average age of the participants is expected to be 8 years old.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted27 Aug 2020
  2. Study start17 Dec 2019
  3. Primary completion17 Dec 2020 (estimated)
  4. Study completion17 Dec 2021 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Retrospective
Enrolment
78 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04529382
Sponsor's protocol ID
P19.069
Acronym
NOFNAIT
Status last verified
Aug 2020
First submitted
15 Jul 2020
Last updated
27 Aug 2020
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: In principle we do not share individual participant data with other researchers. If there is a request on sharing data this request is first submitted to the project leader (J.M.M. van Klink) or the principal investigators (E. Lopriore or M. de Haas). If they agree upon sharing data this request will be sent to the scientific committee of the Department of Pediatrics. If the project leader or scientific committees give permission for access to the data, the request is sent to a the METC of the LUMC. The METC will evaluate whether the purpose of reuse is in line with the informed consent.

Publications

  • Dreyfus M, Kaplan C, Verdy E, Schlegel N, Durand-Zaleski I, Tchernia G. Frequency of immune thrombocytopenia in newborns: a prospective study. Immune Thrombocytopenia Working Group. Blood. 1997 Jun 15;89(12):4402-6.

    PubMed 9192764
  • Williamson LM, Hackett G, Rennie J, Palmer CR, Maciver C, Hadfield R, Hughes D, Jobson S, Ouwehand WH. The natural history of fetomaternal alloimmunization to the platelet-specific antigen HPA-1a (PlA1, Zwa) as determined by antenatal screening. Blood. 1998 Oct 1;92(7):2280-7.

    PubMed 9746765
  • Winkelhorst D, Kamphuis MM, Steggerda SJ, Rijken M, Oepkes D, Lopriore E, van Klink JMM. Perinatal Outcome and Long-Term Neurodevelopment after Intracranial Haemorrhage due to Fetal and Neonatal Alloimmune Thrombocytopenia. Fetal Diagn Ther. 2019;45(3):184-191. doi: 10.1159/000488280. Epub 2018 May 4.

    PubMed 29730660
  • Bussel JB, Berkowitz RL, Lynch L, Lesser ML, Paidas MJ, Huang CL, McFarland JG. Antenatal management of alloimmune thrombocytopenia with intravenous gamma-globulin: a randomized trial of the addition of low-dose steroid to intravenous gamma-globulin. Am J Obstet Gynecol. 1996 May;174(5):1414-23. doi: 10.1016/s0002-9378(96)70582-3.

    PubMed 9065105
  • Winkelhorst D, Murphy MF, Greinacher A, Shehata N, Bakchoul T, Massey E, Baker J, Lieberman L, Tanael S, Hume H, Arnold DM, Baidya S, Bertrand G, Bussel J, Kjaer M, Kaplan C, Kjeldsen-Kragh J, Oepkes D, Ryan G. Antenatal management in fetal and neonatal alloimmune thrombocytopenia: a systematic review. Blood. 2017 Mar 16;129(11):1538-1547. doi: 10.1182/blood-2016-10-739656. Epub 2017 Jan 27.

    PubMed 28130210
  • Ward MJ, Pauliny J, Lipper EG, Bussel JB. Long-term effects of fetal and neonatal alloimmune thrombocytopenia and its antenatal treatment on the medical and developmental outcomes of affected children. Am J Perinatol. 2006 Nov;23(8):487-92. doi: 10.1055/s-2006-954958. Epub 2006 Nov 8.

    PubMed 17094038
  • Radder CM, de Haan MJ, Brand A, Stoelhorst GM, Veen S, Kanhai HH. Follow up of children after antenatal treatment for alloimmune thrombocytopenia. Early Hum Dev. 2004 Oct;80(1):65-76. doi: 10.1016/j.earlhumdev.2004.05.007.

    PubMed 15363839
  • Yougbare I, Lang S, Yang H, Chen P, Zhao X, Tai WS, Zdravic D, Vadasz B, Li C, Piran S, Marshall A, Zhu G, Tiller H, Killie MK, Boyd S, Leong-Poi H, Wen XY, Skogen B, Adamson SL, Freedman J, Ni H. Maternal anti-platelet beta3 integrins impair angiogenesis and cause intracranial hemorrhage. J Clin Invest. 2015 Apr;125(4):1545-56. doi: 10.1172/JCI77820. Epub 2015 Mar 16.

    PubMed 25774504
  • van Gils JM, Stutterheim J, van Duijn TJ, Zwaginga JJ, Porcelijn L, de Haas M, Hordijk PL. HPA-1a alloantibodies reduce endothelial cell spreading and monolayer integrity. Mol Immunol. 2009 Jan;46(3):406-15. doi: 10.1016/j.molimm.2008.10.015. Epub 2008 Nov 26.

    PubMed 19038456
  • Tiller H, Kamphuis MM, Flodmark O, Papadogiannakis N, David AL, Sainio S, Koskinen S, Javela K, Wikman AT, Kekomaki R, Kanhai HH, Oepkes D, Husebekk A, Westgren M. Fetal intracranial haemorrhages caused by fetal and neonatal alloimmune thrombocytopenia: an observational cohort study of 43 cases from an international multicentre registry. BMJ Open. 2013 Mar 22;3(3):e002490. doi: 10.1136/bmjopen-2012-002490.

    PubMed 23524102
  • Janssen J, V.N., Engelen R, et al., Wetenschappelijke verantwoording van de toetsen LOVS rekenen-wiskunde voor groep 3 tot en met 8. [Scientific justification of the mathematics test for grade 1 until grade 6]. 2010, Cito: Arnhem.

  • Mols A, K.F., Wetenschappelijke verantwoording van de toetsen Spelling nietwerkwoorden voor groep 7 en 8. [Scientific justification of the spelling test for grade 5 and 6]. . 2010, Cito: Arnhem.

  • Weekers A, G.I., Kleintjes F, et al., Wetenschappelijke verantwoording papieren toetsen Begrijpend lezen voor groep 7 en 8. [Scientific justification of the reading comprehension test for grade 5 and 6]. 2011, Cito: Arnhem.

  • Gilijns P, V.L., Het CITO leerlingvolgsysteem: Met het oog op de praktijk [The CITO pupil monitoring system: focus on practice]. Pedagogische Studiën 1992. 86:291-6.

  • Touwen BC, Hempel MS, Westra LC. The development of crawling between 18 months and four years. Dev Med Child Neurol. 1992 May;34(5):410-6. doi: 10.1111/j.1469-8749.1992.tb11453.x.

    PubMed 1592193

Questions about this trial

What is this clinical trial studying?

An observational study of Fetal and Neonatal Alloimmune Thrombocytopenia and Long Term Adverse Effects, run by Leiden University Medical Center at 1 site in Netherlands.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 27 Aug 2020. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Netherlands. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Cognitive test score (time frame: From birth until study enrollment. Average age of the participants is expected to be 8 years old.). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT04529382, which also lists 29 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 27 Aug 2020.

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