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1.
Psychiatr Serv ; 70(10): 881-887, 2019 10 01.
Article in English | MEDLINE | ID: mdl-31215355

ABSTRACT

OBJECTIVE: Youths are using emergency departments (EDs) for behavioral health services in record numbers, even though EDs are suboptimal settings for service delivery. In this article, the authors evaluated a mobile crisis service intervention implemented in Connecticut with the aim of examining whether the intervention was associated with reduced behavioral health ED use among those in need of services. METHODS: The authors examined two cohorts of youths: 2,532 youths who used mobile crisis services and a comparison sample of 3,961 youths who used behavioral health ED services (but not mobile crisis services) during the same fiscal year. Propensity scores were created to balance the two groups, and outcome analyses were used to examine subsequent ED use (any behavioral health ED admissions and number of behavioral health ED admissions) in an 18-month follow-up period. RESULTS: A pooled odds ratio of 0.75 (95% confidence interval [CI]=0.66-0.84) indicated that youths who received mobile crisis services had a significant reduction in odds of a subsequent behavioral health ED visit compared with youths in the comparison sample. The comparable result for the continuous outcome of number of behavioral health ED visits yielded an incidence risk ratio of 0.78 (95% CI=0.71-0.87). CONCLUSIONS: Using comparison groups, the authors provided evidence suggesting that community-based mobile crisis services, such as Mobile Crisis, reduce ED use among youths with behavioral health service needs. Replication in other years and locations is needed. Nevertheless, these results are quite promising in light of current trends in ED use.


Subject(s)
Community Mental Health Services/methods , Crisis Intervention/methods , Emergency Services, Psychiatric/methods , Mental Disorders/therapy , Suicide Prevention , Adolescent , Child , Community Mental Health Services/statistics & numerical data , Connecticut , Crisis Intervention/statistics & numerical data , Emergency Service, Hospital , Female , Humans , Logistic Models , Male , Mental Disorders/diagnosis , Mobile Health Units , Non-Randomized Controlled Trials as Topic , Psychiatric Department, Hospital , Psychiatric Status Rating Scales , Suicide/psychology , Treatment Outcome
2.
Birth Defects Res A Clin Mol Teratol ; 88(7): 535-7, 2010 Jul.
Article in English | MEDLINE | ID: mdl-20564431

ABSTRACT

INTRODUCTION: Nonsyndromic cleft lip with or without cleft palate (NSCL/P) is one of the most common of all birth defects. NSCL/P has a multifactorial etiology that includes both genetic and environmental factors. The IRF6 gene and three further susceptibility loci at 8q24, 10q25, and 17q22, which were identified by a recent genome-wide association scan (GWAS), are confirmed genetic risk factors for NSCL/P in patients of European descent. METHODS: A case-control association study was performed to investigate whether these four risk loci contribute to NSCL/P in a Mesoamerican population using four single nucleotide polymorphisms to represent IRF6 and the three novel susceptibility loci. A total of 149 NSCL/P patients and 303 controls of Mayan origin were included. RESULTS: Single marker analysis revealed a significant association between NSCL/P and risk variants in IRF6 and the 8q24 and 10q25 loci. In contrast to previous findings, the association at the 8q24 locus was driven solely by homozygote carriers of the risk allele. This suggests that this locus might act in a recessive manner in the Mayan population. No evidence for association was found at the 17q22 locus. This may have been attributable to the limited power of the sample. CONCLUSION: These results suggest that IRF6 and the 10q25 and 8q24 loci confer a risk for the development of NSCL/P in persons of Mayan origin.


Subject(s)
Chromosome Aberrations , Chromosomes, Human, Pair 10/genetics , Chromosomes, Human, Pair 8/genetics , Cleft Lip/genetics , Cleft Palate/genetics , Indians, Central American/genetics , Interferon Regulatory Factors/genetics , Case-Control Studies , Genome-Wide Association Study , Humans , Risk Factors
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