Browsing by Author "Mueller, Isabelle"
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- Some of the metrics are blocked by yourconsent settingsAcute Maternal Stress Disrupts Infant Regulation of the Autonomic Nervous System and Behavior: A CASP Study(Frontiers Media S.A., 2021)
;Mueller, Isabelle ;Snidman, Nancy ;DiCorcia, Jennifer A.Tronick, EdExposure to maternal stress is assumed to influence infant health and development across the lifespan. The autonomic nervous system (ANS) is especially sensitive to the effects of the early caregiving environment and linked to predictors of later mental health. Understanding how exposure to maternal stress adversely affects the developing ANS could inform prevention. However, there is no agreed upon definition of maternal stress making its study difficult. Here we use the Caretaker Acute Stress Paradigm (CASP) to study the effects of maternal stress in an experimentally controlled laboratory setting. The CASP has 5 episodes, a natural play, followed by a caretaker stressor (or control) condition, another play, a classic still face episode, followed by another play. A total of 104 4-months-old infants and their mothers were randomly assigned to either the caretaker-stress or caretaker-control condition. Changes in behavior, heart rate (HR), and respiratory sinus arrhythmia (RSA) before and after the introduction of the stressor (or control condition) were recorded and compared. Infants in the maternal stress condition showed significantly more behavioral distress [ X 2 = (1, N = 104) = 4.662, p = 0.031]. Moreover, infants whose mothers were in the stress condition showed an significant increase in heart rate after the caretaker condition [ F (1, 102) = 9.81, p = 0.002]. Finally we observed a trend to faster RSA recovery in infants of the control condition [ F (1, 75) = 3.539, p = 0.064]. Results indicate that exposure to acute maternal stress affects infant regulation of the autonomic nervous system and behavior. - Some of the metrics are blocked by yourconsent settingsFactorial validity and comparability of the six translations of the Rivermead Post-Concussion Symptoms Questionnaire translations: results from the CENTER-TBI study(2023-09-08)
;Zeldovich, Marina ;Bockhop, Fabian; ;Mueller, Isabelle ;Polinder, Suzanne ;Mikolic, Ana ;van der Vlegel, MarjoleinBackground: Comparison of patient-reported outcomes in multilingual studies requires evidence of the equivalence of translated versions of the questionnaires. The present study examines the factorial validity and comparability of six language versions of the Rivermead Post-Concussion Symptoms Questionnaire (RPQ) administered to individuals following traumatic brain injury (TBI) in the Collaborative European NeuroTrauma Effectiveness Research (CENTER-TBI) study. Methods: Six competing RPQ models were estimated using data from Dutch (n = 597), English (n = 223), Finnish (n = 213), Italian (n = 268), Norwegian (n = 263), and Spanish (n = 254) language samples recruited six months after injury. To determine whether the same latent construct was measured by the best-fitting model across languages and TBI severity groups (mild/moderate vs. severe), measurement invariance (MI) was tested using a confirmatory factor analysis framework. Results: The results did not indicate a violation of the MI assumption. The six RPQ translations were largely comparable across languages and were able to capture the same construct across TBI severity groups. The three-factor solution comprising emotional, cognitive, and somatic factors provided the best fit with the following indices for the total sample: χ2 (101) = 647.04, ${\chi }^{2}/df$ χ2/ df= 6.41, p < 0.001, CFI = 0.995, TLI = 0.994, RMSEA = 0.055, CI90%[0.051, 0.059], SRMR = 0.051. Conclusion: The RPQ can be used in international research and clinical settings, allowing direct comparisons of scores across languages analyzed within the full spectrum of TBI severity. To strengthen the aggregated applicability across languages, further analyses of the utility of the response scale and comparisons between different translations of the RPQ at the item level are recommended. - Some of the metrics are blocked by yourconsent settingsLongitudinal Internal Validity of the Quality of Life after Brain Injury: Response Shift and Responsiveness(2023-04-29)
;Zeldovich, Marina ;Hahm, Stefanie ;Mueller, Isabelle ;Krenz, Ugne ;Bockhop, Fabian; ;Zeldovich, Marina; 1Institute of Medical Psychology and Medical Sociology, University Medical Center Göttingen, Waldweg 37A, 37073 Göttingen, Germany; marina.zeldovich@med.uni-goettingen.de (M.Z.); im2622@cumc.columbia.edu (I.M.); ugne.krenz@med.uni-goettingen.de (U.K.); fabian.bockhop@med.uni-goettingen.de (F.B.) ;Hahm, Stefanie; 2Department Health & Prevention, Institute of Psychology, University of Greifswald, Robert-Blum-Str. 13, 17489 Greifswald, Germany; stefanie.hahm@uni-greifswald.de ;Mueller, Isabelle; 1Institute of Medical Psychology and Medical Sociology, University Medical Center Göttingen, Waldweg 37A, 37073 Göttingen, Germany; marina.zeldovich@med.uni-goettingen.de (M.Z.); im2622@cumc.columbia.edu (I.M.); ugne.krenz@med.uni-goettingen.de (U.K.); fabian.bockhop@med.uni-goettingen.de (F.B.) ;Krenz, Ugne; 1Institute of Medical Psychology and Medical Sociology, University Medical Center Göttingen, Waldweg 37A, 37073 Göttingen, Germany; marina.zeldovich@med.uni-goettingen.de (M.Z.); im2622@cumc.columbia.edu (I.M.); ugne.krenz@med.uni-goettingen.de (U.K.); fabian.bockhop@med.uni-goettingen.de (F.B.) ;Bockhop, Fabian; 1Institute of Medical Psychology and Medical Sociology, University Medical Center Göttingen, Waldweg 37A, 37073 Göttingen, Germany; marina.zeldovich@med.uni-goettingen.de (M.Z.); im2622@cumc.columbia.edu (I.M.); ugne.krenz@med.uni-goettingen.de (U.K.); fabian.bockhop@med.uni-goettingen.de (F.B.)von Steinbuechel, Nicole; 1Institute of Medical Psychology and Medical Sociology, University Medical Center Göttingen, Waldweg 37A, 37073 Göttingen, Germany; marina.zeldovich@med.uni-goettingen.de (M.Z.); im2622@cumc.columbia.edu (I.M.); ugne.krenz@med.uni-goettingen.de (U.K.); fabian.bockhop@med.uni-goettingen.de (F.B.)The Quality of Life after Brain Injury (QoLIBRI) questionnaire was developed and validated to assess disease-specific health-related quality of life (HRQoL) in individuals after TBI. The present study aims to determine its longitudinal validity by assessing its responsiveness and response shift from 3 to 6 months post-injury. Analyses were based on data from the European longitudinal observational cohort Collaborative European NeuroTrauma Effectiveness Research in Traumatic Brain Injury study. A total of 1659 individuals recovering from TBI were included in the analyses. Response shift was assessed using longitudinal measurement invariance testing within the confirmatory factor analyses framework. Responsiveness was analyzed using linear regression models that compared changes in functional recovery as measured by the Glasgow Outcome Scale–Extended (GOSE) with changes in the QoLIBRI scales from 3 to 6 months post-injury. Longitudinal tests of measurement invariance and analyses of discrepancies in practical significance indicated the absence of response shift. Changes in functional recovery status from three to six months were significantly associated with the responsiveness of the QoLIBRI scales over the same time period. The QoLIBRI can be used in longitudinal studies and is responsive to changes in an individual’s functional recovery during the first 6 months after TBI. - Some of the metrics are blocked by yourconsent settingsSensitivity of outcome instruments in a priori selected patient groups after traumatic brain injury: Results from the CENTER-TBI study(2023)
;von Steinbuechel, Nicole ;Rauen, Katrin ;Covic, Amra ;Krenz, Ugne ;Bockhop, Fabian ;Mueller, Isabelle ;Cunitz, Katrin ;Polinder, Suzanne ;Steyerberg, Ewout W. ;Vester, Johannes ;the CENTER-TBI participants investigatorsAi, JingluTraumatic brain injury (TBI) can negatively impact patients’ lives on many dimensions. Multiple instruments are available for evaluating TBI outcomes, but it is still unclear which instruments are the most sensitive for that purpose. This study examines the sensitivity of nine outcome instruments in terms of their ability to discriminate within and between specific patient groups, selected a priori as identified from the literature, at three different time points within a year after TBI (i.e., 3, 6, and 12 months post injury). The sensitivity of the instruments to sociodemographic (sex, age, education), premorbid (psychological health status), and injury-related (clinical care pathways, TBI and extracranial injury severity) factors was assessed by means of cross-sectional multivariate Wei-Lachin analyses. The Glasgow Outcome Scale Extended (GOSE)–the standard in the field of TBI for measuring functional recovery–demonstrated the highest sensitivity in most group comparisons. However, as single functional scale, it may not be able to reflect the multidimensional nature of the outcome. Therefore, the GOSE was used as a reference for further sensitivity analyses on more specific outcome scales, addressing further potential deficits following TBI. The physical component summary score (PCS) of the generic health-related quality of life (HRQOL) instruments (SF-36v2/-12v2) and the TBI-specific HRQOL instruments (QOLIBRI/-OS) were most sensitive in distinguishing recovery after TBI across all time points and patient groups, followed by the RPQ assessing post-concussion symptoms and the PHQ-9 measuring depression. The SF-36v2/-12v2 mental component summary score and the GAD-7 measuring anxiety were less sensitive in several group comparisons. The assessment of the functional recovery status combined with generic HRQOL (the PCS of the SF-12v2), disease-specific HRQOL (QOLIBRI-OS), and post-concussion symptoms (RPQ) can provide a sensitive, comprehensive, yet time-efficient evaluation of the health status of individuals after TBI in different patient groups. - Some of the metrics are blocked by yourconsent settingsThe Association of Post-Concussion and Post-Traumatic Stress Disorder Symptoms with Health-Related Quality of Life, Health Care Use and Return-to-Work after Mild Traumatic Brain Injury(MDPI, 2021)
;van der Vlegel, Marjolein ;Polinder, Suzanne ;Mikolic, Ana ;Kaplan, Rana; ; ;Zeldovich, Marina ;van Praag, Dominique ;Bockhop, Fabian ;Haagsma, Juanita ;Cunitz, Katrin ;Mueller, IsabelleThe CENTER-TBI Participants and InvestigatorsPatients with mild traumatic brain injury (mTBI) are at risk for post-concussion (PC) symptoms and post-traumatic stress disorder (PTSD). The co-occurrence of PC and PTSD symptoms after mTBI in relation to health-related quality of life (HRQoL), health care utilization, and return to work has not yet been investigated. PC and PTSD symptoms were measured six months post-TBI by respectively the Rivermead Post-Concussion Symptoms Questionnaire (RPQ) and the Post-Traumatic Stress Disorder Checklist for DSM-5 (PCL-5). Of the 1566 individuals after mTBI who met the inclusion criteria, 26.1% experienced PC symptoms (RPQ ≥16). Additionally, 9.8% experienced PTSD symptoms (PCL-5 ≥ 33), of which the vast majority (81%) also reported experiencing PC symptoms. Differences between patients with no/mild symptoms, with only PC, only PTSD, and both PC and PTSD symptoms in HRQoL, return to work, and rehabilitation were analyzed using logistic and linear regression analyses. Patients with PC and/or PTSD symptoms reported lower HRQoL, higher rates of rehabilitation, and lower return to work rates compared to patients with no/mild symptoms. Patients with both PC and PTSD symptoms reported significantly lower HRQoL (B = −2.73, CI = −4.65; −0.83, p < 0.001) compared to those with only PC symptoms, while there were no significant differences in their ongoing rehabilitation care (OR = 1.39, CI = 0.77–2.49, p = 0.272) and return to work rates (OR = 0.49, CI = 0.15–1.63, p = 0.246) at six months. These results underline the importance of the diagnosis and appropriate treatment of patients with mTBI, experiencing PC and/or PTSD symptoms. - Some of the metrics are blocked by yourconsent settingsTranslation and Linguistic Validation of Outcome Instruments for Traumatic Brain Injury Research and Clinical Practice: A Step-by-Step Approach within the Observational CENTER-TBI Study(MDPI, 2021)
; ;Rauen, Katrin ;Krenz, Ugne ;Wu, Yi-Jhen; ; ;Cunitz, Katrin ;Mueller, Isabelle ;Bockhop, Fabian ;Zeldovich, Marina ;Polinder, Suzanne ;Wilson, Lindsay ;Steyerberg, Ewout ;Maas, Andrew ;Menon, DavidThe Linguistic Validation Group of CENTER-TBIAssessing outcomes in multinational studies on traumatic brain injury (TBI) poses major challenges and requires relevant instruments in languages other than English. Of the 19 outcome instruments selected for use in the observational Collaborative European NeuroTrauma Effectiveness Research in TBI (CENTER-TBI) study, 17 measures lacked translations in at least one target language. To fill this gap, we aimed to develop well-translated linguistically and psychometrically validated instruments. We performed translations and linguistic validations of patient-reported measures (PROMs), clinician-reported (ClinRO), and performance-based (PerfO) outcome instruments, using forward and backward translations, reconciliations, cognitive debriefings with up to 10 participants, iterative revisions, and international harmonization with input from over 150 international collaborators. In total, 237 translations and 211 linguistic validations were carried out in up to 20 languages. Translations were evaluated at the linguistic and cultural level by coding changes when the original versions are compared with subsequent translation steps, using the output of cognitive debriefings, and using comprehension rates. The average comprehension rate per instrument varied from 88% to 98%, indicating a good quality of the translations. These outcome instruments provide a solid basis for future TBI research and clinical practice and allow the aggregation and analysis of data across different countries and languages.