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Dive into the research topics where Kirsten R. Heineman is active.

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Featured researches published by Kirsten R. Heineman.


Journal of Developmental and Behavioral Pediatrics | 2008

Evaluation of neuromotor function in infancy - A systematic review of available methods

Kirsten R. Heineman; Mijna Hadders-Algra

Objective: Neuromotor function in infancy can be evaluated in various ways. Assessment instruments are used for early detection of children with a high risk for developmental disorders. Early detection enables clinicians to provide intervention at a young age when plasticity of the nervous system is high. The assessments may also be used to monitor intervention. The present article will review the psychometric properties of methods to assess neuromotor function in infancy. Method: A literature search was performed in PubMed, Medline, and PsycINFO (1966–2007) on instruments to assess neuromotor functioning of infants. Results: Fifteen instruments were included and classified into 4 groups: (1) Comprehensive neurological examinations (n = 4). These techniques are widely used, though little is known about their reliability. Their validity in predicting major developmental disorders such as cerebral palsy is good; their predictive validity for minor motor disorders is moderate at best. (2) Procedures with standardized scoring (n = 7). These have good reliability, but only moderate predictive validity for major developmental disorders. No data available for prediction of minor developmental disorders. (3) Observation of milestones (n = 2). Its predictive validity for major developmental disorders is only moderate, whereas reliability is good. (4) Assessment of quality of motor behavior or motor patterns (n = 2). These instruments have the best predictive validity for major and minor developmental motor disorders, but current methods are only useful under the age of 4 months. Conclusion: Prediction of developmental outcome at an early age is difficult. In medical evaluations of high-risk infants, the best predictions are achieved through a combination of multiple, complementary tools, that is, achieved milestones, neurological examination and assessment of the quality of motor behavior.


Developmental Medicine & Child Neurology | 2008

The Infant Motor Profile: A Standardized and Qualitative Method to Assess Motor Behaviour in Infancy.

Kirsten R. Heineman; Arend F. Bos; Mijna Hadders-Algra

A reliable and valid instrument to assess neuromotor condition in infancy is a prerequisite for early detection of developmental motor disorders. We developed a video‐based assessment of motor behaviour, the Infant Motor Profile (IMP), to evaluate motor abilities, movement variability, ability to select motor strategies, movement symmetry, and fluency. The IMP consists of 80 items and is applicable in children from 3 to 18 months. The present study aimed to test intra‐ and interobserver reliability and concurrent validity of the IMP with the Alberta Infant Motor Scale (AIMS) and Touwen neurological examination. The study group consisted of 40 low‐risk term (median gestational age [GA] 40wks, range 38‐42wks) and 40 high‐risk preterm infants (median GA 29.6wks, range 26‐33wks) with corrected ages 4 to 18 months (31 females, 49 males). Intra‐ and interobserver agreement of the IMP were satisfactory (Spearmans rho=0.9). Concurrent validity of IMP and AIMS was good (Spearmans rho=0.8, p<0.005). The IMP was able to differentiate between infants with normal neurological condition, simple minor neurological dysfunction (MND), complex MND, and abnormal neurological condition (p<0.005). This means that the IMP may be a promising tool to evaluate neurological integrity during infancy, a suggestion that needs confirmation by means of assessment of larger groups of infants with heterogeneous neurological conditions.


Developmental Medicine & Child Neurology | 2010

The assessment of minor neurological dysfunction in infancy using the Touwen Infant Neurological Examination: strengths and limitations.

Mijna Hadders-Algra; Kirsten R. Heineman; Arend F. Bos; Karin J. Middelburg

Aim  Little is known of minor neurological dysfunction (MND) in infancy. This study aimed to evaluate the inter‐assessor reliability of the assessment of MND with the Touwen Infant Neurological Examination (TINE) and the construct and predictive validity of MND in infancy.


Developmental Medicine & Child Neurology | 2010

Construct validity of the Infant Motor Profile: relation with prenatal, perinatal, and neonatal risk factors.

Kirsten R. Heineman; Sacha la Bastide-van Gemert; Vaclav Fidler; Karin J. Middelburg; Arend F. Bos; Mijna Hadders-Algra

Aim  The Infant Motor Profile (IMP) is a qualitative assessment of motor behaviour of infants aged 3 to 18 months. The aim of this study was to investigate construct validity of the IMP through the relation of IMP scores with prenatal, perinatal, and neonatal variables, including the presence of brain pathology indicated by neonatal ultrasound imaging of the brain.


Acta Paediatrica | 2010

Development of adaptive motor behaviour in typically developing infants

Kirsten R. Heineman; Karin J. Middelburg; Mijna Hadders-Algra

Aim:  During motor development, infants learn to select adaptive motor strategies out of their motor repertoire. The aim of this study is twofold: first, to investigate whether the presence of adaptive motor behaviour can be observed reliably, and second, to explore the ages at which clinically observable transition to adaptive motility emerges for four specific motor functions: abdominal progression, sitting motility, reaching and grasping.


Developmental Medicine & Child Neurology | 2013

Reliability and concurrent validity of the Infant Motor Profile

Kirsten R. Heineman; Karin J. Middelburg; Arend F. Bos; Lieke Eidhof; Sacha la Bastide-van Gemert; Edwin R. van den Heuvel; Mijna Hadders-Algra

The Infant Motor Profile (IMP) is a qualitative assessment of motor behaviour in infancy. It consists of five domains: movement variation, variability, fluency, symmetry, and performance. The aim of this study was to assess interobserver reliability and concurrent validity of the IMP with the Alberta Infant Motor Scale (AIMS) and an age‐specific neurological examination.


European Journal of Paediatric Neurology | 2015

Myoclonus in childhood-onset neurogenetic disorders: The importance of early identification and treatment

Martje E. van Egmond; Jan Willem Elting; Anouk Kuiper; Rodi Zutt; Kirsten R. Heineman; Oebele F. Brouwer; Deborah A. Sival; M.A.A.P. Willemsen; Marina A. J. Tijssen; Tom J. de Koning

BACKGROUND In clinical practice, myoclonus in childhood-onset neurogenetic disorders frequently remains unrecognized, because it is often overshadowed by other neurological features. Since treatment can lead to significant functional improvement, accurate phenotyping is essential. To demonstrate the importance of early identification and treatment, we report on four patients with various childhood-onset neurogenetic disorders suffering from myoclonus. METHODS We evaluated four patients with established childhood-onset neurogenetic disorders and involuntary jerky movements, who visited our young-onset movement disorder outpatient clinic. RESULTS We present the clinical data of four patients (aged 8-21 years) with childhood-onset neurogenetic disorders, including ataxia-telangiectasia, Coffin-Lowry syndrome and epileptic encephalopathy due to SCN1A mutations. All four suffered from jerky movements that hampered normal daily activities and that had gone unrecognized for several years. The presence of multifocal myoclonus was confirmed by polymyography. In all patients, treatment resulted in marked improvement of both myoclonus and overall functioning. CONCLUSION These cases highlight the relevance of actively searching for myoclonus in childhood-onset neurogenetic disorders, even when a molecular diagnosis has already been established. To further improve the awareness and recognition of myoclonus in children, we provide a list of childhood-onset neurogenetic disorders with myoclonus as important associated feature.


Developmental Medicine & Child Neurology | 2011

Infant Motor Profile and cerebral palsy : promising associations

Kirsten R. Heineman; Arend F. Bos; Mijna Hadders-Algra

Aim  The Infant Motor Profile (IMP) is a novel qualitative assessment of motor behaviour in infancy. The aim of this study was to determine whether IMP scores throughout infancy differ between children with and without cerebral palsy (CP) at 18 months. Furthermore, we evaluated the predictive ability of IMP scores throughout infancy for CP.


Early Human Development | 2013

Movement variation in infants born following IVF/ICSI with and without ovarian hyperstimulation

Pamela Schendelaar; Kirsten R. Heineman; Maas Jan Heineman; M. Jongbloed-Pereboom; Sacha la Bastide-van Gemert; Karin J. Middelburg; Edwin R. van den Heuvel; Mijna Hadders-Algra

BACKGROUND The effect of in vitro fertilisation (IVF) on neurodevelopment is not fully understood. Probably, IVF does not affect traditional measures of neurodevelopment in infancy. Recently, an instrument, the Infant Motor Profile (IMP), was developed that evaluates the quality of motor behaviour. It includes the evaluation of movement variation (i.e. movement repertoire size), a parameter reflecting the integrity of cortical connectivity. AIM To evaluate the effect of ovarian hyperstimulation and the in vitro procedure on movement variation during infancy. STUDY DESIGN Prospective cohort study. SUBJECTS Singletons born following IVF or intracytoplasmic sperm injection (ICSI) with conventional controlled ovarian hyperstimulation (COH-IVF/ICSI, n=68), in a modified natural cycle (MNC-IVF/ICSI, n=57) and natural conception born to subfertile couples (Sub-NC, n=90). OUTCOME MEASURES Children were assessed with the IMP at 4, 10 and 18 months, resulting in a total IMP score and five domain scores: variation, variability, symmetry, fluency and performance. Primary outcome was the domain score variation. RESULTS A significant effect of study group was observed for the variation score up until 18 months of age (p=0.039). COH-IVF/ICSI children had a significantly lower mean variation score than MNC-IVF/ICSI children (mean difference [95% confidence interval] -1.010 [-1.766; -0.254]). Mean variation scores of COH-IVF/ICSI and Sub-NC children were similar; the same held true for the comparison between MNC-IVF/ICSI and Sub-NC. Total IMP scores and other domain scores of the three groups were similar. CONCLUSION The present study did not demonstrate a clear effect of ovarian hyperstimulation and the in vitro procedure on movement variation throughout infancy.


Developmental Medicine & Child Neurology | 2018

Motor development in infancy is related to cognitive function at 4 years of age

Kirsten R. Heineman; Pamela Schendelaar; Edwin R. van den Heuvel; Mijna Hadders-Algra

Evidence is accumulating that motor and cognitive development are interrelated. This study investigates associations between motor development in infancy and cognitive function at 4 years of age.

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Mijna Hadders-Algra

University Medical Center Groningen

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Karin J. Middelburg

University Medical Center Groningen

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Arend F. Bos

University Medical Center Groningen

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Pamela Schendelaar

University Medical Center Groningen

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Sacha la Bastide-van Gemert

University Medical Center Groningen

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Edwin R. van den Heuvel

Eindhoven University of Technology

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Vaclav Fidler

University Medical Center Groningen

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la Sacha Bastide-van Gemert

University Medical Center Groningen

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