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1.
Ann Epidemiol ; 18(5): 357-63, 2008 May.
Article in English | MEDLINE | ID: mdl-18395465

ABSTRACT

PURPOSE: The validity of parental occupation recalled by adult children is not established, yet it is commonly used to measure childhood socioeconomic status (SES). We investigated the feasibility of using data from historical records to validate recalled parental SES. METHODS: Data from death certificates and applications for Social Security numbers (parents' names, date and place of birth) were used to locate birth certificates and 1930 census records of 416 decedents in Forsyth County, NC, to verify parental occupation and childhood residence. RESULTS: Birth certificates and/or census records were located for 85% of decedents. Of 257 for whom both records were searched, both were found for 60%, only a census record for 10%, and only a birth certificate for 24%. Among those with father's occupation recorded on both records (n = 138), occupational category matched on 89% of records (kappa = 0.86). Place of residence/birth, which can be linked with census-based county socioeconomic indicators, was also highly concordant across records. CONCLUSIONS: These results demonstrate that birth and census records can be located for most decedents and that the childhood SES data contained therein is highly concordant. Thus they are an alternative to recalled childhood SES and a source of validation data in life course studies.


Subject(s)
Adult Children , Mental Recall , Occupations , Parents , Social Class , Atherosclerosis/economics , Atherosclerosis/epidemiology , Atherosclerosis/etiology , Databases, Factual , Feasibility Studies , Female , Humans , Male , Middle Aged , Monte Carlo Method , North Carolina/epidemiology , Pilot Projects , Records , Reproducibility of Results , Risk Factors
2.
BMC Health Serv Res ; 6: 46, 2006 Apr 04.
Article in English | MEDLINE | ID: mdl-16595013

ABSTRACT

BACKGROUND: Opioid misuse can complicate chronic pain management, and the non-medical use of opioids is a growing public health problem. The incidence and risk factors for opioid misuse in patients with chronic pain, however, have not been well characterized. We conducted a prospective cohort study to determine the one-year incidence and predictors of opioid misuse among patients enrolled in a chronic pain disease management program within an academic internal medicine practice. METHODS: One-hundred and ninety-six opioid-treated patients with chronic, non-cancer pain of at least three months duration were monitored for opioid misuse at pre-defined intervals. Opioid misuse was defined as: 1. Negative urine toxicological screen (UTS) for prescribed opioids; 2. UTS positive for opioids or controlled substances not prescribed by our practice; 3. Evidence of procurement of opioids from multiple providers; 4. Diversion of opioids; 5. Prescription forgery; or 6. Stimulants (cocaine or amphetamines) on UTS. RESULTS: The mean patient age was 52 years, 55% were male, and 75% were white. Sixty-two of 196 (32%) patients committed opioid misuse. Detection of cocaine or amphetamines on UTS was the most common form of misuse (40.3% of misusers). In bivariate analysis, misusers were more likely than non-misusers to be younger (48 years vs 54 years, p < 0.001), male (59.6% vs. 38%; p = 0.023), have past alcohol abuse (44% vs 23%; p = 0.004), past cocaine abuse (68% vs 21%; p < 0.001), or have a previous drug or DUI conviction (40% vs 11%; p < 0.001%). In multivariate analyses, age, past cocaine abuse (OR, 4.3), drug or DUI conviction (OR, 2.6), and a past alcohol abuse (OR, 2.6) persisted as predictors of misuse. Race, income, education, depression score, disability score, pain score, and literacy were not associated with misuse. No relationship between pain scores and misuse emerged. CONCLUSION: Opioid misuse occurred frequently in chronic pain patients in a pain management program within an academic primary care practice. Patients with a history of alcohol or cocaine abuse and alcohol or drug related convictions should be carefully evaluated and followed for signs of misuse if opioids are prescribed. Structured monitoring for opioid misuse can potentially ensure the appropriate use of opioids in chronic pain management and mitigate adverse public health effects of diversion.


Subject(s)
Analgesics, Opioid/therapeutic use , Disease Management , Health Services Misuse/statistics & numerical data , Pain/drug therapy , Patient Compliance/statistics & numerical data , Substance Abuse Detection , Academic Medical Centers , Adult , Aged , Aged, 80 and over , Analgesics, Opioid/administration & dosage , Analgesics, Opioid/urine , Chronic Disease , Cohort Studies , Crime , Diagnosis, Dual (Psychiatry) , Drug Monitoring , Drug and Narcotic Control , Female , Humans , Internal Medicine , Male , Middle Aged , North Carolina , Pain/diagnosis , Pain/prevention & control , Prospective Studies
3.
J Electrocardiol ; 38(2): 139-47, 2005 Apr.
Article in English | MEDLINE | ID: mdl-15892024

ABSTRACT

Although ventricular repolarization abnormalities reflect arrhythmic susceptibility, few reliable tools exist to identify their presence. We investigated the repeatability of the spatial T-wave axis and QT interval from standard 12-lead electrocardiograms in 63 asymptomatic volunteers. Certified technicians used a standardized protocol to digitally record 2 electrocardiograms per participant at each of 2 visits separated by 1 to 2 weeks. Absolute paired differences within and between visits were 0.19 degrees and 0.90 degrees for the T-wave axis and 1.08 and 1.55 milliseconds for the QT interval, respectively. The intraclass correlation coefficients for the T-wave axis and QT interval were 0.87 and 0.86, respectively. The impact of repeated measurements on the precision of the QT-interval measurements was evaluated for a hypothetical clinical trial aimed at detecting a drug-induced QT prolongation. We conclude that the spatial T-wave axis is as repeatable a measure of ventricular repolarization as the QT interval.


Subject(s)
Electrocardiography , Electrocardiography/methods , Female , Humans , Long QT Syndrome/diagnosis , Male , Middle Aged , Models, Theoretical , Reproducibility of Results , Signal Processing, Computer-Assisted
4.
BMC Health Serv Res ; 5(1): 3, 2005 Jan 13.
Article in English | MEDLINE | ID: mdl-15649331

ABSTRACT

BACKGROUND: Chronic non-cancer pain is a common problem that is often accompanied by psychiatric comorbidity and disability. The effectiveness of a multi-disciplinary pain management program was tested in a 3 month before and after trial. METHODS: Providers in an academic general medicine clinic referred patients with chronic non-cancer pain for participation in a program that combined the skills of internists, clinical pharmacists, and a psychiatrist. Patients were either receiving opioids or being considered for opioid therapy. The intervention consisted of structured clinical assessments, monthly follow-up, pain contracts, medication titration, and psychiatric consultation. Pain, mood, and function were assessed at baseline and 3 months using the Brief Pain Inventory (BPI), the Center for Epidemiological Studies-Depression Scale scale (CESD) and the Pain Disability Index (PDI). Patients were monitored for substance misuse. RESULTS: Eighty-five patients were enrolled. Mean age was 51 years, 60% were male, 78% were Caucasian, and 93% were receiving opioids. Baseline average pain was 6.5 on an 11 point scale. The average CESD score was 24.0, and the mean PDI score was 47.0. Sixty-three patients (73%) completed 3 month follow-up. Fifteen withdrew from the program after identification of substance misuse. Among those completing 3 month follow-up, the average pain score improved to 5.5 (p = 0.003). The mean PDI score improved to 39.3 (p < 0.001). Mean CESD score was reduced to 18.0 (p < 0.001), and the proportion of depressed patients fell from 79% to 54% (p = 0.003). Substance misuse was identified in 27 patients (32%). CONCLUSIONS: A primary care disease management program improved pain, depression, and disability scores over three months in a cohort of opioid-treated patients with chronic non-cancer pain. Substance misuse and depression were common, and many patients who had substance misuse identified left the program when they were no longer prescribed opioids. Effective care of patients with chronic pain should include rigorous assessment and treatment of these comorbid disorders and intensive efforts to insure follow up.


Subject(s)
Analgesics, Opioid/therapeutic use , Disease Management , Pain/drug therapy , Primary Health Care/standards , Adult , Aged , Analgesics, Opioid/adverse effects , Chronic Disease , Cohort Studies , Comorbidity , Depression/etiology , Diagnosis, Dual (Psychiatry) , Drug Utilization/statistics & numerical data , Family Practice , Female , Humans , Male , Middle Aged , Pain/diagnosis , Pain/psychology , Pain Measurement , Program Evaluation , Psychiatry , Retrospective Studies , Substance-Related Disorders/diagnosis , United States
5.
Ann Neurol ; 54(5): 647-54, 2003 Nov.
Article in English | MEDLINE | ID: mdl-14595654

ABSTRACT

Spinal muscular atrophy (SMA) is an inherited motor neuron disease caused by mutation of the telomeric copy of the survival motor neuron gene (SMN1). Although a centromeric copy of the survival motor neuron gene (SMN2) is retained in all patients with SMA, it differs from SMN1 at a critical nucleotide such that the majority of SMN2 transcripts lack exon 7 and encode an unstable, truncated protein. Here, we show that valproic acid increases levels of exon 7-containing SMN transcript and SMN protein in type I SMA patient-derived fibroblast cell lines. Valproic acid may increase SMN levels both by activating the SMN promoter and by preventing exon 7 skipping in SMN transcripts. Valproic acid and related compounds warrant further investigation as potential treatment for SMA.


Subject(s)
Anticonvulsants/pharmacology , Fibroblasts/drug effects , Nerve Tissue Proteins/drug effects , Spinal Muscular Atrophies of Childhood/genetics , Valproic Acid/pharmacology , Cell Line , Child, Preschool , Cyclic AMP Response Element-Binding Protein , Dose-Response Relationship, Drug , Fibroblasts/physiology , Humans , Immunoblotting , Immunohistochemistry , Infant , Infant, Newborn , Nerve Tissue Proteins/biosynthesis , Promoter Regions, Genetic , RNA-Binding Proteins , Reverse Transcriptase Polymerase Chain Reaction , SMN Complex Proteins , Survival of Motor Neuron 1 Protein , Survival of Motor Neuron 2 Protein , Time Factors , Transcription, Genetic/drug effects , Transcription, Genetic/genetics
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