Marilyn G. Klug
University of North Dakota
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Publication
Featured researches published by Marilyn G. Klug.
Journal of Perinatal Medicine | 1999
Larry Burd; Robin Severud; Jacob Kerbeshian; Marilyn G. Klug
Abstract Aim: To identify pre- and perinatal risk factors for autism. Method: Case control study. We matched names of patients from North Dakota who met DSM criteria for autism, a pervasive developmental disorder, and autisticdisorder with their birth certificates. Five matched controls were selected for each case. Results: Univariate analysis of the 78 cases and 390 controls identified seven risk factors. Logistic modeling to control for confounding produced a five variable model. The model parameters were χ2 = 36.6 and p <0.001. The five variables in the model were decreased birth weight, low maternal education, later start of prenatal care, and having a previous termination of pregnancy. Increasing fathers age was associated with increased risk of autism. Conclusion: This methodology may provide an inexpensive method for clinics and public health providers to identify risk factors and to identify maternal characteristics of patients with mental illness and developmental disorders.
Congenital Heart Disease | 2007
Larry Burd; Eric Deal; Rodrigo Rios; Edward Adickes; Joshua Wynne; Marilyn G. Klug
OBJECTIVE Review of the prevalence of congenital heart defects (CHD) and fetal alcohol spectrum disorder (FASD). DESIGN We conducted a search of the Medline and Pubmed databases to identify papers reporting the association. We then searched the reference lists of the papers and reference books for additional sources. RESULTS We found 29 studies that met our inclusion criteria. In the 12 case series studies of subjects with FASD, the proportion of cases with a CHD (atrial [ASD] and ventricular [VSD] septal defects, other defects, or unspecified CHD) ranged from 33% to 100%. From the 14 retrospective studies, the rate of septal defects was 21%, other structural defects 6% and unspecified defects was 12%. For the 2 case-control studies, the odds of CHD ranged from 1.0 (subjects with fetal alcohol effect) to 18.0 (subjects with fetal alcohol syndrome). In the 1 prospective study of CHD the OR for a child to have CHD and FASD was 1.0. KEY CONCLUSION Pediatric cardiologists may have frequent contact with children with FASD and increased levels of attention to prenatal alcohol exposure as a potential etiology of CHD is indicated.
BMC Pediatrics | 2005
Larry Burd; Roger D. Freeman; Marilyn G. Klug; Jacob Kerbeshian
BackgroundTourette Syndrome (TS) is a neurodevelopmental disorder of childhood. Learning disabilities are frequently comorbid with TS. Using the largest sample of TS patients ever reported, we sought to identify differences between subjects with TS only and subjects with TS and a comorbid learning disability.MethodsWe used the Tourette Syndrome International Consortium database (TIC) to compare subjects with comorbid Tourette Syndrome and learning disabilities (TS + LD) to subjects who did not have a comorbid learning disability (TS - LD). The TIC database contained 5,500 subjects. We had usable data on 5,450 subjects.ResultsWe found 1,235 subjects with TS + LD. Significant differences between the TS + LD group and the TS - LD group were found for gender (.001), age onset (.030), age first seen (.001), age at diagnosis (.001), prenatal problems (.001), sibling or other family member with tics (.024), two or more affected family members (.009), and severe tics (.046). We used logistic modeling to identify the optimal prediction model of group membership. This resulted in a five variable model with the epidemiologic performance characteristics of accuracy 65.2% (model correctly classified 4,406 of 5,450 subjects), sensitivity 66.1%, and specificity 62.2%.ConclusionSubjects with TS have high prevalence rates of comorbid learning disabilities. We identified phenotype differences between the TS - LD group compared to TS + LD group. In the evaluation of subjects with TS, the presence of a learning disability should always be a consideration. ADHD may be an important comorbid condition in the diagnosis of LD or may also be a potential confounder. Further research on etiology, course and response to intervention for subjects with TS only and TS with learning disabilities is needed.
Journal of Child Neurology | 2003
Larry Burd; Marilyn G. Klug; Matthew J. Coumbe; Jacob Kerbeshian
The objective of this study was to use population-based data to estimate the prevalence and cost of treatment for attention-deficit hyperactivity disorder (ADHD). The North Dakota Department of Health Claims Database was used to estimate the administrative prevalence, annual cost of care per case, and total annual cost of care for subjects with ADHD compared with controls. The case population was 7745, and the mean prevalence rate was 3.9%, with a peak prevalence at 10 years of age. For children with ADHD, the annual cost of care was
Journal of Child Neurology | 2001
Larry Burd; Jacob Kerbeshian; Amy Barth; Marilyn G. Klug; Karilyn Avery; Becky Benz
649 compared with that of controls at
Journal of Perinatal Medicine | 1999
Larry Burd; Robin Severud; Marilyn G. Klug; Jacob Kerbeshian
495. Cost of care attributable to ADHD was
Journal of Perinatal Medicine | 1998
Mohammed M. Bagheri; Larry Burd; John T. Martsolf; Marilyn G. Klug
649 -
Journal of Wound Ostomy and Continence Nursing | 2003
Susan Hunter; Julie Anderson; Darlene Hanson; Patricia Thompson; Diane Langemo; Marilyn G. Klug
495 =
Journal of Clinical Oncology | 2003
Nathan L. Kobrinsky; Marilyn G. Klug; Peggy Jo Hokanson; Diane E. Sjolander; Larry Burd
154 (31%). Utilization by children with ADHD with publicly funded payers was increased 25 to 175% over that of children with privately funded coverage. In North Dakota, the annual cost of care for children with ADHD was
Journal of Child Neurology | 2009
Larry Burd; Qing Li; Jacob Kerbeshian; Marilyn G. Klug; Roger D. Freeman
5.1 million, 5.6% of all health care costs for children. The annual attributable cost of care was