a Departments of Medicine
d Psychiatry
b Clinical Research Program, Children's Hospital Boston, Boston, Massachusetts
c Pediatrix/NeoGen, Bridgeville, Pennsylvania
| ABSTRACT |
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METHODS. Parents of 173 infants with false-positive screening results for a biochemical genetic disorder in the expanded newborn screening panel were compared with parents of 67 children with normal screening results. Parents completed an interview that elicited information about demographic features, child and parental health, and understanding of newborn screening. Parents also completed the parenting stress index.
RESULTS. Parents in the false-positive group attained higher total scores on the PSI than did parents in the normal-screened group, scoring higher on the parent-child dysfunction subscale and the difficult child subscale. Only approximately one third of parents in the false-positive group reported knowing the correct reason for repeat screening. Mothers who reported knowing the correct reason for their child's repeat screening test experienced less total stress than did mothers who were misinformed, were not informed, or did not remember.
CONCLUSIONS. False-positive screening results may affect parental stress and the parent-child relationship. Improved communication with parents regarding the need for repeat screening tests may reduce the negative impact of false-positive results.
Key Words: newborn screening false-positive parental stress vulnerable child nocebo phenomenon parent-child relationship
Abbreviations: PKUphenylketonuria PSIparenting stress index
Recent expansion of newborn screening for biochemical genetic disorders has led not only to an increase in positive identifications but also to a dramatic increase in false-positive test results. A false-positive result is an initial out-of-range screening result that does not indicate a metabolic disorder with additional evaluation of the child. Generally these results are not laboratory mistakes but rather are transient findings or indications of variant or carrier status. When needed, typically repeat specimens in expanded newborn screening are requested after an infant's discharge from the nursery.1 Expanded newborn screening with tandem mass spectrometry for >20 disorders has a 0.33% false-positive rate and an overall incidence of
1 case per 2400 infants.2 Therefore, of the >4 million infants born in the United States each year,
13000 are likely to receive a false-positive result, with at least 550 from New England alone.3 Apart from a "PKU anxiety syndrome" described in 1968 in relation to false-positive screening for phenylketonuria (PKU), little is known about the subsequent impact on parental stress, family relationships, and perceptions of the child's health.
This report describes parental responses to false-positive newborn screening results among a cohort of children born after February 1, 1999, when expanded newborn screening began in Massachusetts. This cohort represents a subset of children enrolled in an expanded newborn screening study for metabolic disorders that includes children identified with biochemical genetic disorders through expanded newborn screening, as well as parents in the false-positive cohort.4
| METHODS |
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6 months after the diagnosis of a metabolic disorder had been ruled out. Parents who did not "opt out" by returning a response card indicating a preference not to be contacted were called to participate in a telephone interview. Both the initial letter and the telephone call contained the elements of an informed consent form, including descriptions of the study, confidentiality measures, potential risks, and benefits. Although both parents were invited, it was acceptable if only 1 parent participated. On occasion, when the second parent wanted to participate but was unable to complete the telephone interview, questionnaires were returned by mail. The comparison group for the false-positive cohort consisted of parents of 6- to 12-month-old children with normal screening results, selected sequentially from the Commonwealth of Massachusetts Department of Public Health Birth Registry of Vital Records and Statistics. Birth registry data include only children born to married couples and contain the date of birth, birth weight, parents' names, birth hospital, and hometown. All recruitment occurred between February 1, 1999, and February 28, 2004. All parent participants were interviewed once. Additional follow-up interviews were not included in the study design.
Exclusions included parents of children who had died and parents of newborns whose birth weight was <2500 g. The latter exclusion avoided recruitment of parents of premature newborns, who frequently experience transient initial newborn screening abnormalities.5 Human studies approval for the study was obtained annually from the institutional review board of Children's Hospital Boston. By design, the number of false-positive participants exceeded the number of participants in the comparison group. Statistical methods that did not require balanced sample sizes were selected.
Data Collection Instruments
Parents first completed a structured interview, which consisted of questions related to child and parental health, understanding of the newborn screening process, and background information. Parents provided short answers or ratings on a 5-point Likert scale. The same interview was given to both groups of parents, and parents in the false-positive group were asked additional questions about the repeat screen.
Parents next completed the parenting stress index (PSI), short form.6 This is a 36-item questionnaire that provides a total stress score and 3 subscale scores, namely, parental distress, parent-child dysfunctional interaction, and difficult child. The normal range for total stress scores is 55 to 85, with scores of >85 considered to be in the clinical range in which treatment may be necessary.6 The PSI also provides a defensive responding index, which is an internal index of validity based on the parent's responses. Scores of
10 for this index indicate that the validity of the total stress and subscale scores is questionable. The
reliability coefficients are .91 for the total stress score and .80 to .87 for the scaled scores.6 The short-form PSI has a correlation of .95 with the full-length PSI.6
Parents completed the interview separately. Copies of the PSI and a short form of the interview, which included questions related to child health, were mailed to second parents unable to complete a telephone interview.
Content analysis of the interview by 2 independent raters was used to derive 3 categories based on parents' suggestions for making the newborn screening process a more positive experience.7 Categories included adequacy of information about newborn screening and test results, reactions regarding newborn screening, and the length of time to receive confirmation of the false-positive result. The percentage of agreement between 2 independent raters was 95% for a total of 132 comments.
The Hollingshead scale was used to derive socioeconomic status.8 The scale incorporates level of education and occupational status (each coded from 1 to 7) to predict overall socioeconomic status (coded from 1 to 5).8 Low scores indicate higher educational levels, occupational status, and social position.
Data Analyses
For parental responses regarding characteristics of the child and family, information from the mother's interview was analyzed unless it was unavailable, in which case information from the father's interview was used. For the parent-specific indices, results were calculated separately for mothers and fathers.
The characteristics of children, parents, and families in the false-positive group were compared with those in the normal-screened group by using the Wilcoxon rank sum test for continuous and scale variables and Fisher's exact test for dichotomous variables. The number of hospitalizations occurring before 6 months of age was compared for the 2 groups by using Poisson regression.
For the PSI, subjects who failed the defensive responding index (scores of
10) were dropped from the analyses. To illuminate the unadjusted comparisons of PSI scores for the false-positive and normal-screened groups, linear regression analysis was used to estimate differences in PSI scores between the 2 groups, with adjustment for demographic characteristics in which the groups differed. Adjusted P values for these differences were estimated with the Van Elteren test, which is a stratified extension of the Wilcoxon rank sum test. All P values were 2-sided, and values of <.05 were considered significant.
| RESULTS |
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As noted in Table 1, the false-positive group was similar to the comparison group in terms of gender, birth order, ethnicity, primary language spoken in the home, and percentage of families with other children with medical problems. The source for normal-screened children contained only married parents, whereas some children in the false-positive group came from single-parent families (P < .001). In the false-positive group, children were older at the time of evaluation (mean: 13.3 months; SD: 3.7 months), compared with the normal-screened group (mean: 6.4; SD: 0.9 months; P < .001). The false-positive group was of lower socioeconomic status (mean: 3.0; SD: 1.1), compared with the normal-screened group (mean: 2.3; SD: 0.9; P < .001).
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As shown in Table 2, mothers in the false-positive group reported higher overall stress on the PSI than did mothers in the normal-screened group. Seventeen mothers in the false-positive group (11%) but no mothers in the normal-screened group scored in the clinical range (P = .008). The differences between groups were more pronounced on the total score, difficult child, and parent-child dysfunctional interaction subscales (P < .001) than on the parental distress subscale (P = .08). Fathers in the false-positive group also registered higher overall stress on the PSI than did fathers in the normal-screened group (Table 2), especially on the total score (P = .02), difficult child (P = .05), and parent-child dysfunctional interaction subscales (P = .004).
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.35 for fathers on the total score and all subscales with the Kruskal-Wallis test).
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| DISCUSSION |
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The PKU anxiety syndrome that was described as a typical reaction to a false- positive PKU test is characterized by acute or chronic anxiety, expressed by parents as uncertainties about the test results and worry regarding their child's health.911 Among parents of infants with false-positive hypothyroidism results, sleep disturbances, maternal crying, shock, and infant feeding problems were reported.1012 According to Essex et al,13 contact with maternal stress during infancy may increase the susceptibility of the infant's hypothalamic-pituitary-adrenal system to later stress exposure.
Increased parental stress and altered parent-child relationships were also documented in studies screening for cystic fibrosis, hearing problems, diabetes mellitus, and metabolic disorders.1417 Those studies suggested that parents were more overprotective and more focused on physical symptoms of their child when a false-positive result occurred. This might explain a trend toward an increase in child hospitalizations during the first 6 months of life among false-positive children in our study (mean: 0.17 hospitalization vs 0.08 hospitalization; P = .09). Another recent study identified insecure attachment relationships among infants with false-positive cystic fibrosis results from newborn screening, even when evaluated 12 to 18 months after the child's birth.18 Stress resulting from a false-positive newborn screen might alter parental ability or readiness to heed infant signals and needs, which might affect the quality of the parent-child relationship.10,11 This might account for lower maternal health scores and for the high level of parent-child dysfunctional interaction noted in our study. In addition, high scores on the parent-child dysfunctional interaction subscale suggest that the parent-child bond either is threatened or has never been established adequately.7
Parents also may experience a false-positive screening result as a significant threat to the child's well-being.11,19 Earlier studies on the impact of acute illnesses among children identified the "vulnerable child syndrome."20 Other studies applied the vulnerable child syndrome to include (1) a condition or even a "nondisease" (eg, false-positive result) in a child, (2) parents who misinterpret that condition or its sequelae, and (3) parents who exhibit sustained unjustifiable anxiety about the child's vulnerability to future events.21 Parents whose child received a false-positive test result continued to fear that their child might be developmentally delayed, even after subsequent negative test results.21 Similarly, in our study, mothers who did not know the reason for the repeat screen reported higher stress levels on the PSI than did mothers who knew the correct reason for the repeat screen.
In addition, the delivery of the false-positive result may create a "nocebo phenomenon."22 Although not widely known, this heuristic may explain the reactions of parents to a false-positive newborn screening result. The nocebo phenomenon occurs when "expectations of sickness" and the emotional responses to such expectations cause illness or distress.22 Nocebos can be triggered through unfavorable messages from the health care system or from the patient's psychological and social environment.23 In newborn screening, the delivery of a false-positive screening result may engender stress among parents by creating expectations of illness for an otherwise healthy child. This may also account for the increased worries about their child's future among parents in the false-positive group.
This study has some limitations because of potential sample differences. The disparity in the children's ages between the false-positive and normal-screened groups could have biased results. However, the instrument used to measure parental stress, the PSI, is considered age independent for small increments of age. Test-retest reliability coefficients were reported to remain stable after a 1-year interval.24
Although the false-positive group was recruited primarily from Pennsylvania and the normal-screened group from Massachusetts, these groups did not differ in characteristics of birth order, ethnicity, and employment status. The differences in socioeconomic and marital status were considered as possible confounders but were determined not to account for the observed differences in PSI scores.
This study suggests that false-positive results may lead to increased parental stress. This is especially true for parents who have not received adequate information about newborn screening. Therefore, the negative effects of false-positive newborn screening results might be mitigated through improved parental education. The timing of parental education about expanded screening and the speed with which a metabolic disorder can be ruled out also may be important. Specific communication plans for informing parents, fact sheets, and better distribution of newborn screening information materials during the prenatal and postnatal periods might be initiatives to consider to alleviate parental stress regarding false-positive results.
| ACKNOWLEDGMENTS |
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| FOOTNOTES |
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Address correspondence to Elizabeth A. Gurian, BS, Department of Medicine, Children's Hospital Boston, 1 Autumn St, Room 526, Boston, MA 02115. E-mail: elizabeth.gurian{at}childrens.harvard.edu
The authors have indicated they have no financial relationships relevant to this article to disclose.
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