Literature DB >> 36186160

Families following pediatric traumatic medical events: identifying psychosocial risk profiles using latent profile analysis.

Yaara Sadeh1,2,3, Rachel Dekel1, Amichai Brezner2, Jana Landa2,4, Tamar Silberg2,5.   

Abstract

Background: Post-traumatic stress symptoms (PTSS) are often experienced by children and family members after pediatric traumatic medical events (PTMEs). Assessing families' psychosocial risk factors is a crucial part of trauma-informed practice as it helps identify risk for PTSS in the aftermath of PTME.
Objectives: Using the Psychosocial Assessment Tool 2.0 (PAT2.0), this study describes the psychosocial risk of families following PTMEs in two ways: 1. Describing the psychosocial risk defined by the PAT2.0 based on three-tiered risk levels; 2. Using latent profile analysis (LPA); identifying psychosocial risk profiles and examining how child- and injury-related factors can affect profile membership.
Methods: Caregivers of 374 children following PTMEs admitted to a pediatric rehabilitation department in Israel completed the PAT2.0. Total PAT2.0 score and the seven PAT2.0 subscales (family structure/resources, social support, child problems, sibling problems, family problems, caregiver stress reactions, and family beliefs) were included in the first analysis. Mean PAT2.0 scores of three risk categories (universal, targeted, clinical) were calculated; LPA, which allows for cross-sectional latent variable mixture models to identify heterogeneity within a population, and multinomial logistic regressions using six out of the seven PAT2.0 subscales, were used to determine distinct profile differences and predictors of profile membership.
Results: The three-tiered risk levels revealed were relatively high, as compared to levels in families of children with other clinical diagnoses. LPA yielded a three-profile solution: low family risk (63.53%); high caregiver stress, above-average levels of family risk (22.5%); and sibling problems, above-average levels of family risk (13.94%). Ethnicity and type of injury predicted group membership.
Conclusion: Families of children following PTMEs are at increased psychosocial risk. A clinically useful approach to identifying and preventing PTSS may be to evaluate specific domain patterns rather than just the total PAT2.0 risk level alone, based on the PAT2.0 subscales.
© 2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.

Entities:  

Keywords:  PAT; Psychosocial; child illness; child injury; family; posttraumatic stress

Mesh:

Year:  2022        PMID: 36186160      PMCID: PMC9518403          DOI: 10.1080/20008066.2022.2116825

Source DB:  PubMed          Journal:  Eur J Psychotraumatol        ISSN: 2000-8066


Introduction

Pediatric injuries and illnesses have a significant impact on children, adolescents, and families worldwide (Kullgren & Carter, 2020). In Israel, approximately 200,000 children visit emergency rooms annually (Nir et al., 2017), with 20,600 children hospitalised as a consequence of unintentional injury. These injuries/illnesses are often associated with prolonged hospitalisation, impaired physical functioning, and significant psychosocial distress for both child and family (McCarthy, Hearps, et al., 2016). In some cases, children and youth following pediatric traumatic medical events (PTMEs) are admitted to a pediatric rehabilitation centre to further assist recovery (Jones et al., 2018). Given the high levels of emotional distress, providers and families in pediatric healthcare settings can benefit from trauma-informed care which may help prevent or reduce the risk of further traumatic responses (Marsac et al., 2016). Pediatric care has increasingly promoted in recent years family-centred approaches that highlight the importance of the family for the child’s health and well-being by routinely assessing the family and providing family-level support so that all members are met in terms of their needs (Christofferson et al., 2020). Studies conducted among various pediatric populations have identified a variety of negative effects experienced by families and children following PTMEs (Price et al., 2015). Such effects include increased financial burden on the family, lack of social support, parents’ mental-health problems, reduced family relationship quality, and reduced sibling well-being (Kazak, Schneider, et al., 2015). Furthermore, these effects may increase the risk of pediatric medical traumatic stress (PMTS). Symptoms of PMTS include hyperarousal, avoidance, and re-experiencing events that occurred as a result of a serious disease or medical intervention that threatened the child's health and entailed intrusive, painful, and frightening medical care for the child (National Child Traumatic Stress Network, 2020). Previous studies conducted in pediatric rehabilitation settings have indicated that approximately 20% of mothers report significant emotional distress (Silberg et al., 2016). Additionally, 21% of mothers and 27% of children following PTMEs have self-reported significant levels of PMTS (Sadeh et al., 2020), interacting with other psychosocial risk factors, which may in turn increase child's risk of developing PTSS (Sadeh et al., 2020).

The pediatric psychosocial preventative health model (PPPHM)

Screening families for psychosocial risk and stress symptoms is considered a necessary factor for the development of early and effective prevention programmes (Kazak, Abrams, et al., 2015). The Pediatric Psychosocial Preventative Health Model (PPPHM) outlines three dimensions meant to distinguish between degrees of risk for maladaptation associated with pediatric medical conditions (Kazak, Schneider, et al., 2015). This model suggests that screening should involve all families entering the pediatric healthcare system, not just those thought to be at elevated risk. Based on the PPPHM, the Psychosocial Assessment Tool 2.0 (PAT2.0) was developed (Pai et al., 2008). The PAT2.0 is a family-centred screening tool used to measure psychosocial risk in pediatric settings; has been widely used in the US (Kazak et al., 2019), Australia (McCarthy, Hearps, et al., 2016), Canada (Barrera et al., 2014), and the Netherlands (Sint Nicolaas et al., 2016); and is suitable for families from different races, ethnicities, and socioeconomic status (SES) (Kazak et al., 2018). It assesses seven dimensions affecting a family’s functioning and health, such as problems among multiple family members or difficulties in social domains (Pai et al., 2008), as well as a total psychosocial risk score. The total score is a sum of the subscales, with three tiers of risk – universal, targeted, and clinical. Universal risk forms the bottom tier and represents the largest group of families (50–60%); this group has the lowest psychosocial risk and most favourable outcome and ability to adjust to the child’s health condition. Targeted risk forms the middle tier and represents approximately 25–33% of families; this group has identifiable challenges and psychosocial risks. At the top of the pyramid are families at clinical risk; this group comprises the smallest group (≤ 15%), has more serious or chronic psychosocial challenges, and consists of families with increased risk for severe or escalating difficulties. To the best of our knowledge, a systematic screening for psychosocial risk in families in Israel and more specifically in families whose child has been admitted to pediatric rehabilitation following PTMEs has not been conducted. Thus, the first aim of the current study was to describe levels of psychosocial risk among families of children following PTMEs admitted to pediatric rehabilitation, according to the PAT2.0 three-tiered model of risk (i.e. universal, targeted, clinical). Studies have found that PAT2.0 screening increases the amount of care provided and that such care is in line with the PPPHM tiers both in the US (Kazak et al., 2011) and the Netherlands (Schepers et al., 2017). However, McCarthy, Wakefield, et al. (2016) found that PAT2.0 screening does not necessarily lead to services that match families’ needs, and other recent studies have indicated that categorisation into three risk groups may not accurately demonstrate the full extent of heterogeneity of within-group problems experienced in particular domains (e.g. child or siblings problems, financial burden, emotional distress) (Muscara et al., 2017; Sharkey et al., 2020). Thus, although the PAT2.0 is a multi-dimensional screener with the potential of providing more information about various domains of psychosocial risk, existing studies examining psychosocial risk in pediatric populations have predominantly used a cumulative frequency score (i.e. summing the subscale scores to create a total PAT2.0 score with the three-tiered model of risk) (Kazak et al., 2018) potentially limiting the multidimensional, qualitative-based conceptualisation of family psychosocial risk (Spurk et al., 2020). Thus, it is often not clear what drives overall risk; diverse symptomatic manifestation may not be captured; and substantial information may be lost (Kotov et al., 2017). Using an approach that allows the study of relationships among individual difficulties and family factors, and illustrates the dynamic nature of the interaction between components, can be useful for improving our understanding of the characteristics of the problems and the domains central to the development of psychosocial difficulties (Colliva et al., 2020). For example, according to a recent study, epilepsy and asthma both have the same overall PAT score, but different domains have different interrelationships with each other that influence the risk for other domains (Colliva et al., 2020). Our second aim was to identify latent patterns of psychosocial risk experienced by families of children in pediatric rehabilitation following PTMEs, by examining associations across the different PAT2.0 sub-domains. An increasingly accepted method for studying complex multidimensional phenomena, such as family psychosocial risk, is latent profile analysis (LPA). LPA is a cross-sectional latent variable mixture modelling approach which aims to find heterogeneity within a given population (Petersen et al., 2019). The LPA approach uses multiple aspects of individual/family functioning that can be studied holistically by finding common types, called profiles (Petersen et al., 2019). Each individual/family is probabilistically assigned to a specific profile, according to both level of similarity to other members in the profile and level of dissimilarity from those in other profiles. Therefore, to better understand the psychosocial context surrounding children, we conceptualised psychosocial risk as a set of interdependent domains and explored the hypothesis that different profiles of needs and risks are associated with different demographic and illness factors. Examining the factors that may be universally related to adjustment outcomes and those that may be culture- or diagnosis-dependent could enhance our understanding of specific risk and protective factors following PTMEs (Sharkey et al., 2020). Studies have indicated that due to social structures that drive oppression and racism, ethnic minorities such as the Israeli-Arab population, may have an increased risk of developing PTSS following PTMEs (Hussien et al., 2021; Randall, 1996). These may be related to disparities in access to economic and social resources, perceptions of discrimination, or due to culturally-specific attitudes and beliefs that mediate coping with a traumatic event (Wolmer et al., 2014). Furthermore, due to the relatively wide range of medical conditions and etiologies among children admitted to pediatric rehabilitation, recovery pathways also differ widely (Kullgren & Carter, 2020). Child’s gender and age at time of PTME may also contribute to family’s psychosocial risk (Price et al., 2015). Research shows that parents of female-gender and younger-aged children are more likely to be at risk for parental PTSS following various types of trauma (Cox et al., 2008) and following accidental trauma specifically (Trickey et al., 2012). Thus, examining specific profile predictors, such as ethnicity, etiology, illness/injury phase, age, and gender as predictors of profile membership could be particularly important for the development of person- and family-centred interventions.

The current study

Our first aim was to categorise psychosocial risk based on the classification of the overall PAT2.0 total risk score into the previously established three levels of risk (i.e. universal, targeted, clinical). We hypothesised that due to the unique circumstances (prolonged rehabilitation, possible chronicity of the child’s healthcare needs, and long-term implications for child and family) of families and children admitted to pediatric rehabilitation following PTMEs, the distribution of PAT2.0 scores would lean toward the increased risk categories (i.e. targeted and clinical) as compared to those reported in the literature (Kazak et al., 2018). Our second aim was to identify latent profiles of psychosocial risk using LPA, based on the six sub-domains measured by the PAT2.0. The literature suggests that various factors may be associated with PTSS risk (Marsac et al., 2014); however to the best of our knowledge, only one study employed latent analysis using PAT2.0 subscales (Sharkey et al., 2020). Thus, the current study used exploratory analysis to reveal specific psychosocial risk profiles associated with PTSS risk, above the PAT2.0 general risk categories. We expected to observe several distinct latent risk profiles, with related elevations in different domains. Lastly, as LPA has the potential to develop and expand theoretical thinking regarding the existence of different configurations of profiles in variables relevant to health and children, including their predictors (Spurk et al., 2020), our third aim was to examine, in an exploratory fashion, whether the following – ethnicity, type of etiology, illness/injury phase, child's age, gender – were sensitive predictors of risk profiles.

Methods

Participants

We used a cross-sectional retrospective design extracted from the medical records of 374 children (221 males), 0–18 years of age (M = 9.11, SD = 5.42), who were admitted to a pediatric rehabilitation department between 2011 and 2019 (see Table 1 for a detailed description of the demographic and injury/illness characteristics of study participants).
Table 1.

Demographics and injury/illness characteristics.

VariableN = 374 (SD/%)
Child age in years M (SD), range9.11 (5.42), 0.3–18
Child gender, male n (%)221 (59.1)
Child ethnicity n (%) 
Jews324 (86.6)
Arabs48 (12.8)
Highest Parental Education n (%) 
Less than Highschool Education41 (10.9)
Highschool Education131(35.4)
Some college/vocational school or higher200 (53.7)
Relationship Status n (%) 
Single10 (2.4)
Married/Partnered318 (85.1)
Separated/Divorced45 (12.2)
Widow1 (0.3)
Injury/illness characteristics 
Injury/illness phase, n (%) 
Up to one month after Injury/illness153 (40.9)
Up to two months after Injury/illness91(24.3)
Up to one year after Injury/illness79 (21.1)
More than one year after Injury/illness51 (13.6)
Child injury/illness type n (%) 
ABI*212 (56.7)
Spinal Cord30 (8.0)
Orthopedic61 (16.3)
Others71 (18.9)
Length of hospitalisation in days100 (83.5)
Accident-related admissions100 (27%)
Illness-related admissions274 (73%)

*ABI: acquired brain injury; includes tumours, viral infections, stroke, and traumatic head injury.

Demographics and injury/illness characteristics. *ABI: acquired brain injury; includes tumours, viral infections, stroke, and traumatic head injury. Inclusion criteria were: (1) child hospitalised in the pediatric rehabilitation department between 2011 and 2019, (2) parents’ agreement to complete the department’s screening procedure, and (3) sufficient mastery of the native language to complete the questionnaires. Potential participants were excluded if their injuries were due to family violence or suspected child abuse. Among the 537 children who were eligible to be included in the analyses, N = 120 families declined to participate, and N = 43 families could not complete the questionnaires due to lack of sufficient proficiency in their native language. Between those who provided data to be included in the analyses, M(374) = 9.11, SD = 5.42, and those who did not provide such data, M(163) = 9.02 SD = 11.11, there were no significant differences in child’s age, t(496) = 1.535, p = .25, gender, χ2(1) = 2.689, p = .12, or etiology type χ2(42) = 49.47, p = .20.

Procedure

As part of the pediatric rehabilitation department’s admissions process, each family was asked by their psychologist/social worker to complete the questionnaires regarding their current situation in order to screen for the family’s psychosocial factors. All study procedures were approved by the Institutional Review Board at The Sheba Medical Center.

Measures

Child- and injury-related factors were abstracted from electronic health records, including ethnicity categories, type of etiology, illness/injury phase, age, and gender.

Psychosocial assessment tool 2.0

The PAT2.0 (Pai et al., 2008) comprises seven subscales including family structure and resources (8 items; e.g. financial difficulties); social support (4 items; e.g. provision of emotional/financial support); child problems (16 items; e.g. being distracted); sibling problems (16 items; e.g. school or learning difficulties); family problems (15 items; e.g. marital difficulties, separation); parent stress reactions (3 items; e.g. arousal and avoidance); and family beliefs (10 items; e.g. the ability to make good treatment decisions). The seven subscales are calculated by dividing the number of item responses indicative of risk by the total number of items in the respective domain, yielding a subscale score ranging from 0.0–1.0, with higher scores indicating higher psychosocial risk, for each subscale. Total score is a sum of 7 subscales (each subscale is a sum of endorsed risk items on that subscale) from 0 to 7, mapping onto the three tiers of the PPPHM (Kazak, 2006). In a study by Kazak et al. (2018) the PAT2.0 subscales showed good internal consistency using the Kuder–Richardson 20 coefficient (child problems were KR20 > 0.80, and family structure/resources, social support, and family problems were adequate, ranging from 0.59 to 0.64). The PAT2.0 has shown excellent convergent validity in a range of pediatric conditions (Guerra-Peña & Steinley, 2016; McCarthy, Hearps, et al., 2016; Sint Nicolaas et al., 2016). In this study, internal reliability was good for the PAT2.0 total score (α = 0.703). The PAT2.0 questionnaire has been translated into 13 languages, including Hebrew: the version that was used in this study.

Statistical analysis

An initial descriptive analysis was conducted, and mean scores for those who provided data were compared with those who did not (using Pearson correlations and chi-square). According to our first goal, we calculated the prevalence of psychosocial risk for every PAT2.0 risk category (universal, targeted, clinical) as a percentage of all participating families (Table 2). A one-sample t-test was conducted to compare our mean level with those of other samples that also measured psychosocial risk among caregivers of specific pediatric populations using the total PAT2.0 score. Furthermore, descriptive analyses identified unacceptable skewness due to floor effect (3.56; >2) in the social support domain across the entire sample, resulting in the removal of the social support domain from our second analysis. LPA studies have shown that a great challenge is identifying the true or meaningful profiles rather than the ‘spurious’ profiles (Spurk et al., 2020). One of the reasons for detecting spurious profiles in LPA can be caused by non-normally distributed data (skewed data) (Spurk et al., 2020) related to a floor/ceiling effect. When data is non-normally distributed, fit indices tend to favour models with more latent profiles than those used to simulate them, potentially creating spurious profiles in LPA (Guerra-Peña & Steinley, 2016). As a solution to this problem, formulating a preliminary test that takes account of higher-order moments (e.g. skewness and krtosis) of the observed data is recommended (Muthén, 2003), as was done in this study.
Table 2.

Descriptive statistics of the PAT2.0.

PAT2.0 scaleN (%)Scale rangeMSDRange
PAT2.0 total3740.00–3.991.18.771.00–3.82
Universal174 (46.5)0.00–1.00.535.278.00–0.98
Targeted146 (39.0)1.01–2.001.42.2781.01–2.00
Clinical54 (14.4)2.01–3.992.568.4762.01–3.82
1. Family structure/resources374.00–1.00.155.165.00–.75
2. Social support374.00–1.00.056.16.00–1.00
3. Child problems374.00–1.00.283.228.00–.93
4. Sibling problems374.00–1.00.100.172.00–.73
5. Family problems374.00–1.00.149.18.00–1.00
6. Stress reactions374.00–1.00.295.353.00–1.00
7. Family beliefs374.00–1.00.57.127.00–1.00

PAT2.0 – Psychosocial Assessment Tool 2.0.

Descriptive statistics of the PAT2.0. PAT2.0 – Psychosocial Assessment Tool 2.0. To achieve our second aim, we used Mplus version 7.4 to conduct LPA based on the observed response patterns across the remaining six domains of PAT2.0. To interpret which indicators are above and below the sample means clearly, we used the z-standardized mean scale scores. Five sequential latent profile models were identified. Relative model fit and accuracy of classification were examined using three fit statistics (Nylund et al., 2007; van de Schoot et al., 2017): (1) The Akaike Information Criterion (AIC) and the Bayesian Information Criterion (BIC), with lower AIC and BIC values indicating better fit; (2) The Vuong-Lo-Mendell-Rubin (VLMR) Adjusted Likelihood Ratio Test, and the Lo-Mendell-Rubin Adjusted Likelihood Ratio Test (LMR) where P-values <.05 were assumed to indicate that the larger profile solution was a better model fit; and (3) Entropy values closer to 1 indicating better class separation and values, with .80 being considered acceptable. After identifying the optimal latent profile solution, the three-step approach was conducted to test our third aim: demographic- and event-related predictors associated with membership in the profiles (Asparouhov & Muthén, 2014). This approach employed a classification-error corrected multinomial logistic regression to test differences between classes in demographic variables; child’s gender (1 = boys, 2 = girls), age (in years), ethnicity (1 = Jewish, 2 = Arab), illness etiology (i.e. acquired brain injury/ABI, spinal cord, orthopedic, other) and illness/injury phase. Information about the illness/injury phase was grouped into two categories based on previous research (Marsac et al., 2014; Rolland, 2005). The first category concerned the crisis phase (i.e. one-month post-illness/injury); the second category comprised the chronic or adaptation phase (i.e. families within the first year up to 4 years after the initial illness/injury phase).

Results

Bivariate analyses

Levels of PAT2.0 total score and PAT2.0 sub-domains in the sample

The whole sample had a mean PAT2.0 total score of 1.17 (SD = 0.77; i.e. targeted risk). Domain mean scores ranged from 0.00 to 1.00, with the highest risk level in the family beliefs domain. Descriptive statistics for the PAT2.0 domain scores are presented in Table 2. Out of the 374 families, 46.5% (n = 174; M = 0.53; 95% CI [0.49, 0.57]) corresponded with the universal risk category; 39% (n = 146; M = 1.42; 95% CI [1.37, 1.47]) with the targeted risk category; and 14.4% (n = 54; M = 2.58; 95% CI [2.46, 2.72]) with the clinical risk category. A one-sample t-test comparing PAT2.0 scores in our sample (M = 1.177, SD = 0.771) with previous studies revealed that our sample had significantly higher levels of psychosocial risk compared to specific clinical pediatric samples, such as pediatric cystic fibrosis (M = 1.00, SD = 0.77, N = 374) (Filigno et al., 2019) or pediatric cancer (M = 1.021, SD = 0.700, N = 396) (Kazak et al., 2020). However, the total risk score in our sample was relatively similar to that of children with medical complexities (CMC) (M = 1.170, SD = 0.740, N = 136) (Verma et al., 2020).

Latent profile analysis

Overall, based on fit statistics and parsimony of the class solution, a three-profile LPA model of psychosocial risk profiles provided the most theoretically interpretable and adequate fit to the data (Table 3 shows the fit indices for the latent profile models, one to five profiles). According to the VLMR and LMR, the two-profile and three-profile solution had an optimal fit to the data and meaningful profile sizes. All entropy values were acceptable, with the two- and five-profile models having the highest values. However, in the five-profile solution, the sample sizes of some of the profiles were too small (<1%), and the LMR value was non-significant.
Table 3.

Fit statistics for PAT2.0 domains latent profile analysis.

 AICBICSample size-adjusted BICVLMRLMREntropySample size by class based on most likely membership
1 Class6393.0606440.1516402.078   374
2 Classes6049.4036123.9646063.682357.657**349.235**0.967318/55
3 Classes5938.4686040.4995958.008124.935**121.993**0.890237/84/52
4 Classes5909.0466038.5465933.84743.42242.4000.897224/80/50/18
5 Classes5754.6125911.5825784.67388.13486.0580.935208/83/39/30/14

Note: AIC: Akaike Information Criterion; BIC: Bayesian Information Criterion; LMR: Lo-Mendell-Rubin Adjusted Likelihood Ratio Test; VLMR: Vuong-Lo-Mendell-Rubin Adjusted Likelihood Ratio Test; BLRT: Bootstrp likelihood ratio difference test. Bold row was chosen model.

*p < .05, **p < .01, ***p < .001.

Fit statistics for PAT2.0 domains latent profile analysis. Note: AIC: Akaike Information Criterion; BIC: Bayesian Information Criterion; LMR: Lo-Mendell-Rubin Adjusted Likelihood Ratio Test; VLMR: Vuong-Lo-Mendell-Rubin Adjusted Likelihood Ratio Test; BLRT: Bootstrp likelihood ratio difference test. Bold row was chosen model. *p < .05, **p < .01, ***p < .001. Additionally, although the four- and five-profiles had decreasing AIC and BIC values suggesting solutions with more profiles, the LMR and VLMR indicated that the improvement compared to the three- and four-profile (accordingly) was not statistically significant. Between the two-and-three-profiles, the three-profile solution was selected as the best fitting model as it had the lower BIC and AIC for the three-class solution compared to the two-class solution, which is considered the preferred fit index to rely on according to an expert panel (van de Schoot et al., 2017). The largest latent profile, labelled low family risk (n = 238, 63.53%), showed low average risk across all domains of PAT2.0 (Bs < −0.085). A smaller latent profile, labelled high caregiver stress, with above-average levels of family risk (n = 84, 22.5%), demonstrated moderate risk, above-average, across all psychosocial domains (Bs > 0.10), with particularly high risk, on average, in the caregiver stress reaction domain, B = 1.275, 95% CI [1.16, 1.39], and family belief domain, B = 0.648, 95% CI [0.53, 0.76]. The third profile, labelled sibling problems, with above-average levels of family risk (n = 52, 13.94%), demonstrated elevated risk, on average, across all psychosocial domains (Bs > 0.152) with particularly high risk, on average, in the sibling problems domain, B = 2.193, 95% CI [2.074, 2.312]. See Figure 1 for a graphical representation of group risk across domains.
Figure 1.

Mean domain score by PAT2.0 latent profile.

Mean domain score by PAT2.0 latent profile.

Predictors of profile membership

In Table 4, comparisons between classes in terms of demographic- and illness-related variables are summarised. Predictors of profile membership were examined via the three-step approach procedure (Asparouhov & Muthén, 2014). Correlates of profile membership included in the analysis comprised gender (1 = boys, 2 = girls), child’s age (0–18), ethnicity (1 = Israeli-Jewish, 2 = Israeli-Arab), illness/injury etiology (i.e. ABI, spinal cord, orthopedic, other), and illness/injury phase (i.e. crisis or chronic/adaptation). Ethnicity predicted membership in the sibling problems, above-average levels of family risk (profile 3), with Israeli-Arab ethnicity (vs. Israeli-Jewish ethnicity) related to the likelihood of being a member of the sibling problems, above-average levels of family risk (profile 3), compared to the low family risk (profile 1). Ethnicity did not predict membership in any other group, relative to the high caregiver stress, above-average levels of family risk (profile 2), or low family risk (profile 1).
Table 4.

Univariate associations with class membership.

 Low family risk(1)High caregiver stress, above average levels of family risk(2)High caregiver stress, above average levels of family risk(2)
 Versus High sibling problems, above average level of family risk (3)Versus low family risk (1)
Correlates of class membershipBSEpBSEpBSEp
Child gender (boy=1, girl=2)−0.4080.460.376−0.4320.522.408−0.3820.387.323
Child age (0–18)−0.0820.041.065−0.0340.045.4450.0540.034.111
Ethnicity (Israeli Jewish=1, Israeli Arab=2)1.207*0.574.035−0.0590.570.917−0.5390.523.303
Illness/injury etiology (acquired brain injury=1, spinal cord=2, orthopedic=3, other=4)0.9100.492.0641.426*0.551.0100.5910.408.147
Illness/injury phase (0=crisis phase 1=chronic adaptation phase)0.1310.4870.294−0.5780.551.2940.5910.408.147

Note: SE: standard error. Parameters comprise associations with the respective class (second row) in comparison to the reference class (first row). *Statistically significant difference between classes at p < .05.

Univariate associations with class membership. Note: SE: standard error. Parameters comprise associations with the respective class (second row) in comparison to the reference class (first row). *Statistically significant difference between classes at p < .05. Etiology predicted membership in the high caregiver stress, above-average levels of family risk (profile 2), with ABI associated with higher odds of being in the high caregiver stress, above-average levels of family risk (profile 2), compared to the sibling problems, above-average levels of family risk (profile 3). Other etiologies did not predict membership in any other group, relative to sibling problems, above-average levels of family risk (profile 3), or high caregiver stress, above-average levels of family risk (profile 2). Child’s age, gender or illness/injury phase did not predict group membership relative to sibling problems, above-average levels of family risk (profile 3), or high caregiver stress, above-average levels of family risk (profile 2).

Discussion

The present study aimed to assess psychosocial risk and identify unique risk and protective factors of families admitted to pediatric rehabilitation following PTMEs. Our findings show that families of children in pediatric rehabilitation are prone to significant psychosocial risk, demonstrated by an average PAT2.0 score of 1.17 and a distribution of PAT2.0 scores of 46.5% universal vs. 39% targeted and 14.4% clinical. Previous research shows that, in generally, two-thirds of families in multiple samples fall within the universal range, about one-third fall within the targeted range, and 11% or less fall within the clinical range (Kazak et al., 2015; Law et al., 2019). Results suggest that there was a higher proportion of families in the targeted (39%) and clinical (14.4%) ranges in our sample compared to samples in previous studies (Filigno et al., 2019; Kazak et al., 2020). This difference can be attributed to the relatively high heterogeneity of etiologies in our sample, as compared to those found in more homogeneous samples (Filigno et al., 2019; Kazak et al., 2020). Furthermore, our results are in accordance with a recent study (Verma et al., 2020) among families of children with medical complexities (CMC). In the CMC sample, similar frequencies of families in the higher-risk categories (45% universal vs. 44% targeted and 11% clinical) were found. The authors suggested that the high proportion could have been attributable to the intense stressors among the CMC population, including prolonged hospitalisation, uncertainty of life expectancy, and time spent by caregivers advocating for resources (Verma et al., 2020). These stressors are also common among families with children hospitalised in pediatric rehabilitation departments post-TME and may partly explain the presence of high-risk families in our sample (Kaufman & Lahey, 2020). Other studies that found similar frequencies of families in the higher-risk categories suggest that socioeconomic considerations in these samples are important to recognise (Kazak et al., 2018; Reader et al., 2020). Specifically in terms of pediatric rehabilitation, these findings reinforce the need to examine the unique risk profiles that characterise families following PTMEs via the use of a complementary profile analysis method, such as LPA. Our second aim was to identify latent profiles of psychosocial risk using LPA, based on the sub-domains measured by the PAT2.0. LPA resulted in a three-profile solution. Low family risk (profile 1) (63.53%) was defined by generally low levels of risk across all PAT2.0 domains. High caregiver stress, above-average levels of family risk (profile 2) (22.5%), showed a high probability of caregiver’s stress reactions – which diverged substantially from the third group (12.7%, 5.17%, respectively) – and negative family beliefs (6.48%, 1.5%, respectively). Sibling problems, above-average levels of family risk (profile 3) (13.94%), depicted an overall high probability of reports of all domains with a characterising feature of sibling problems. This tendency toward divergence might support a multidimensional, qualitative-based conceptualisation of psychosocial risk patterns among families of children admitted to pediatric settings (Spurk et al., 2020). Parents’ stress reactions post-PTME and parents’ beliefs (also known as cognitive appraisals/perceptions) regarding their child’s recovery are known to be interrelated (Schilpzand et al., 2018). Parents who are more symptomatic and overwhelmed tend to perceive their child’s PTME as more severe and/or as posing significant limitations on the child’s and family’s current and future functioning (Salvador et al., 2015). Compared to other psychosocial risk domains, both factors (i.e. parental stress and parental beliefs) are seen to be more event-related appraisals. As such, examining demographic and PTME variables that might predict membership in the high caregiver stress, above-average levels of family risk (profile 2), could further enhance our understanding of this group’s specific risk factors. Sibling problems, above-average levels of family risk (profile 3) (13.94%), was differentiated by relatively high levels of risk in four out of six PAT2.0 domains (i.e. family’s structure/resources, parental problems, and child’s problems), with a specific increased risk pattern defined by an elevated score in the sibling problems domain. Our findings bolster findings from previous studies indicating that siblings’ distress may have an adverse impact on the whole family (Gill, 2020). Research in the field suggests that siblings’ emotional challenges might contribute to increased family stress and conflict (Velleman et al., 2016). When their unique needs are not adequately addressed, siblings may be at risk for adverse developmental and psychological outcomes (Gill, 2020), contributing to the elevated risk among families in the sibling problems, above-average levels of family risk. Sharkey et al. (2020) suggested that families in any of the three risk groups could experience an escalation of risk due to the change in one domain and the established links between the different domains. For example, research shows that siblings who receive emotional and social support display improved behaviour, emotional well-being, and illness knowledge, resulting in better family functioning and greater patient and family satisfaction (Besier et al., 2010). These results align with research in the pediatric field that emphasises the importance of evaluating the relationship between risk factors in various domains of the family in order to target specific sources of psychosocial risk (Christofferson et al., 2020; Muscara et al., 2017; Sadeh et al., 2020; Sharkey et al., 2020). Incorporating trauma-informed and family-centred care requires recognition that these events can be traumatic for all members of the family (Christofferson et al., 2020). As for our third aim, several characteristics were identified as predictors of group membership. The present findings indicate that families affected by PTMEs experience different cross-cultural patterns of psychosocial risk. Israeli-Arab ethnicity (vs. Israeli-Jewish ethnicity) was related to elevated risk of being a member of sibling problems, above-average levels of family risk (profile 3) – compared to low family risk (profile 1) – which was characterised by relatively high levels of risk in four out of six domains. These findings may be understood in light of previous findings indicating that Israeli-Arab citizens often have lower SES, and that schools have lower budgets and fewer available resources (Hobfoll et al., 2007). When further resources are threatened, minority groups who are already discriminated against might be exposed to an increased risk for psychological distress. In addition, perceived discrimination may prevent individuals from seeking support and using social resources that are perceived to be available only to the majority group (Wolmer et al., 2014). Acknowledging the health disparities faced by ethnicity groups worldwide (Kazak et al., 2020) and in Israel in particular (Hussien et al., 2021) is in line with the recent Sustainable Development Goals identified by the United Nations for a better future for all (Daelmans et al., 2017). Health services tailored to cultural values and needs may help bridge the gap between families and the pediatric healthcare system (Williams et al., 2014). Among the other risk factors, etiology predicted membership in high caregiver stress, above-average levels of family risk (profile 2), with ABI being associated with higher odds of being in that group compared to sibling problems, above-average levels of family risk (profile 3). High caregiver stress, above-average levels of family risk (profile 2), was characterised by high levels of caregiver stress reactions and negative family beliefs. In our sample, a relatively high percentage of children were diagnosed with an ABI (56.7%). Thus, our findings may be understood in light of the wide range of cognitive and neuro-behavioural impairments associated with ABIs (Renaud et al., 2020), which may add additional burden compared to other etiologies (Brown et al., 2013). The current study had several limitations. The first limitation of this study was that no follow-up or comparison data were collected, which made it impossible to determine whether the risk profiles presently identified are associated with later psychosocial distress. Second, because of the removal of social support from all analyses due to high levels of skewness, the relationship between social support difficulties and risk was not established. We suggest that future studies should examine confirmatory factor analysis in a larger sample to determine whether all subscales represent themselves as theoretically hypothesised (Sint Nicolaas et al., 2016). Furthermore, due to the important impact of sibling’s and parent’s distress on the entire family, additional information regarding the family (e.g. how many of the families included siblings, history of prior traumatic experiences, whether more than one family member have been injured, whether the caregiver witnessed or been part of the accident) is needed.

Clinical implications

The current study provides greater information on the applicability of the PAT2.0 and its use across different cultures and within various medical settings. This study is aligned with global collaboration aims for traumatic stress (Olff et al., 2020) supporting the global effort to evaluate cross-cultural differences in trauma-related outcomes. By examining family’s psychosocial risk as a multidimensional phenomenon, with unique and qualitatively differentiated profiles, our findings have important implications regarding enhancing the need for tailored assessments and interventions for children and families post-TMEs. ⁠For example, our second profile suggests that families who display more difficulties regarding stress reactions also display difficulties in their personal beliefs about their child’s TMEs, with ABIs being associated with higher odds of being in that group. These families may face many difficulties due to their embedded emotional reactions following the diagnosis of their child; therefore, interventions in support of resolution (i.e. coming to terms) with a child’s diagnosis could be a central aspect of parenting such children. Parents having unresolved concerns related with grief or despair may continue to be overwhelmed or show displaced anger, potentially putting these families at an even higher risk over the years (Yehene et al., 2021). Together with other more traditional approaches, LPA may provide a new approach for exploring and understanding the impact of pediatric severe and chronic conditions on the needs of families (Colliva et al., 2020). In light of these findings, we should try to develop and implement interventions that directly target the most significant domains, while expecting improvements in the other domains as well. Additionally, the current findings point to the importance of family-centred and trauma-informed design and delivery of pediatric care. It is essential for providers to understand and identify the impact of trauma symptoms on child, parents, and siblings (Christofferson et al., 2020).
  46 in total

1.  Statistical and substantive checking in growth mixture modeling: comment on Bauer and Curran (2003).

Authors:  Bengt Muthén
Journal:  Psychol Methods       Date:  2003-09

2.  Feasibility of clinical psychosocial screening in pediatric oncology: Implementing the PAT2.0.

Authors:  Maria C McCarthy; Claire E Wakefield; Sharon DeGraves; Madeleine Bowden; Deborah Eyles; Lauren K Williams
Journal:  J Psychosoc Oncol       Date:  2016-07-11

3.  Family psychosocial risk screening guided by the Pediatric Psychosocial Preventative Health Model (PPPHM) using the Psychosocial Assessment Tool (PAT).

Authors:  Anne E Kazak; Stephanie Schneider; Stephen Didonato; Ahna L H Pai
Journal:  Acta Oncol       Date:  2015-03-09       Impact factor: 4.089

4.  Screening Family and Psychosocial Risk in Pediatric Migraine and Tension-Type Headache: Validation of the Psychosocial Assessment Tool (PAT).

Authors:  Emily F Law; Scott W Powers; Heidi Blume; Tonya M Palermo
Journal:  Headache       Date:  2019-07-18       Impact factor: 5.887

5.  Screening for caregiver psychosocial risk in children with medical complexity: a cross-sectional study.

Authors:  Rahul Verma; Yasna Mehdian; Neel Sheth; Kathy Netten; Jean Vinette; Ashley Edwards; Joanna Polyviou; Julia Orkin; Reshma Amin
Journal:  BMJ Paediatr Open       Date:  2020-07-27

Review 6.  Implementing a Trauma-Informed Approach in Pediatric Health Care Networks.

Authors:  Meghan L Marsac; Nancy Kassam-Adams; Aimee K Hildenbrand; Elizabeth Nicholls; Flaura K Winston; Stephen S Leff; Joel Fein
Journal:  JAMA Pediatr       Date:  2016-01       Impact factor: 16.193

7.  Development and Evaluation of the Thinking About Recovery Scale: Measure of Parent Posttraumatic Cognitions Following Children's Exposure to Trauma.

Authors:  Elizabeth J Schilpzand; Rowena Conroy; Vicki Anderson; Eva Alisic
Journal:  J Trauma Stress       Date:  2018-01-31

Review 8.  Psychosocial Assessment as a Standard of Care in Pediatric Cancer.

Authors:  Anne E Kazak; Annah N Abrams; Jaime Banks; Jennifer Christofferson; Stephen DiDonato; Martha A Grootenhuis; Marianne Kabour; Avi Madan-Swain; Sunita K Patel; Sima Zadeh; Mary Jo Kupst
Journal:  Pediatr Blood Cancer       Date:  2015-12       Impact factor: 3.167

9.  The Psychosocial Assessment Tool (PAT2.0): psychometric properties of a screener for psychosocial distress in families of children newly diagnosed with cancer.

Authors:  Ahna L H Pai; Anna Maria Patiño-Fernández; Mary McSherry; David Beele; Melissa A Alderfer; Anne T Reilly; Wei-Ting Hwang; Anne E Kazak
Journal:  J Pediatr Psychol       Date:  2007-07-03

10.  Psychological wellbeing and quality-of-life among siblings of paediatric CFS/ME patients: A mixed-methods study.

Authors:  Sophie Velleman; Simon M Collin; Lucy Beasant; Esther Crawley
Journal:  Clin Child Psychol Psychiatry       Date:  2015-09-22       Impact factor: 2.544

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