Nancy G. Jensvold
Kaiser Permanente
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Featured researches published by Nancy G. Jensvold.
Circulation | 2005
Margaret C. Fang; Daniel E. Singer; Yuchiao Chang; Elaine M. Hylek; Lori E. Henault; Nancy G. Jensvold; Alan S. Go
Background—Previous studies provide conflicting results about whether women are at higher risk than men for thromboembolism in the setting of atrial fibrillation (AF). We examined data from a large contemporary cohort of AF patients to address this question. Methods and Results—We prospectively studied 13 559 adults with AF and recorded data on patients’ clinical characteristics and the occurrence of incident hospitalizations for ischemic stroke, peripheral embolism, and major hemorrhagic events through searching validated computerized databases and medical record review. We compared event rates by patient sex using multivariable log-linear regression, adjusting for clinical risk factors for stroke, and stratifying by warfarin use. We identified 394 ischemic stroke and peripheral embolic events during 15 494 person-years of follow-up off warfarin. After multivariable analysis, women had higher annual rates of thromboembolism off warfarin than did men (3.5% versus 1.8%; adjusted rate ratio [RR], 1.6; 95% CI, 1.3 to 1.9). There was no significant difference by sex in 30-day mortality after thromboembolism (23% for both). Warfarin use was associated with significantly lower adjusted thromboembolism rates for both women and men (RR, 0.4; 95% CI, 0.3 to 0.5; and RR, 0.6; 95% CI, 0.5 to 0.8, respectively), with similar annual rates of major hemorrhage (1.0% and 1.1%, respectively). Conclusions—Women are at higher risk than men for AF-related thromboembolism off warfarin. Warfarin therapy appears be as effective in women, if not more so, than in men, with similar rates of major hemorrhage. Female sex is an independent risk factor for thromboembolism and should influence the decision to use anticoagulant therapy in persons with AF.
The New England Journal of Medicine | 2013
Afshin Parsa; W.H. Linda Kao; Dawei Xie; Brad C. Astor; Man Li; Chi-yuan Hsu; Harold I. Feldman; Rulan S. Parekh; John W. Kusek; Tom Greene; Jeffrey C. Fink; Amanda H. Anderson; Michael J. Choi; Jackson T. Wright; James P. Lash; Barry I. Freedman; Akinlolu Ojo; Cheryl A. Winkler; Dominic S. Raj; Jeffrey B. Kopp; Jiang He; Nancy G. Jensvold; Kaixiang Tao; Michael S. Lipkowitz; Lawrence J. Appel
BACKGROUND Among patients in the United States with chronic kidney disease, black patients are at increased risk for end-stage renal disease, as compared with white patients. METHODS In two studies, we examined the effects of variants in the gene encoding apolipoprotein L1 (APOL1) on the progression of chronic kidney disease. In the African American Study of Kidney Disease and Hypertension (AASK), we evaluated 693 black patients with chronic kidney disease attributed to hypertension. In the Chronic Renal Insufficiency Cohort (CRIC) study, we evaluated 2955 white patients and black patients with chronic kidney disease (46% of whom had diabetes) according to whether they had 2 copies of high-risk APOL1 variants (APOL1 high-risk group) or 0 or 1 copy (APOL1 low-risk group). In the AASK study, the primary outcome was a composite of end-stage renal disease or a doubling of the serum creatinine level. In the CRIC study, the primary outcomes were the slope in the estimated glomerular filtration rate (eGFR) and the composite of end-stage renal disease or a reduction of 50% in the eGFR from baseline. RESULTS In the AASK study, the primary outcome occurred in 58.1% of the patients in the APOL1 high-risk group and in 36.6% of those in the APOL1 low-risk group (hazard ratio in the high-risk group, 1.88; P<0.001). There was no interaction between APOL1 status and trial interventions or the presence of baseline proteinuria. In the CRIC study, black patients in the APOL1 high-risk group had a more rapid decline in the eGFR and a higher risk of the composite renal outcome than did white patients, among those with diabetes and those without diabetes (P<0.001 for all comparisons). CONCLUSIONS Renal risk variants in APOL1 were associated with the higher rates of end-stage renal disease and progression of chronic kidney disease that were observed in black patients as compared with white patients, regardless of diabetes status. (Funded by the National Institute of Diabetes and Digestive and Kidney Diseases and others.).
Journal of the American Geriatrics Society | 2006
Margaret C. Fang; Alan S. Go; Elaine M. Hylek; Yuchiao Chang; Lori E. Henault; Nancy G. Jensvold; Daniel E. Singer
OBJECTIVES: To assess whether older age is independently associated with hemorrhage risk in patients with atrial fibrillation, whether or not they are taking warfarin therapy.
Journal of Asthma | 2003
Harold J. Farber; Angela M. Capra; Jonathan A. Finkelstein; Paula Lozano; Charles P. Quesenberry; Nancy G. Jensvold; Felicia W. Chi; Tracy A. Lieu
Objective. Nonadherence to regular inhaled anti-inflammatory medication use is a frequent contributor to poor control of persistent asthma and may result from misunderstanding of the preventive role of such medications. This studys aims are to 1) test the hypothesis that misunderstanding is associated with decreased adherence to its daily use and 2) identify factors associated with increased risk of misunderstanding. Study Design. A sample of parents of children with asthma insured by Medicaid and enrolled in managed care programs in Northern California, Washington, and Massachusetts were interviewed by telephone. This analysis focused on the subset that reported having an inhaled anti-inflammatory medication and whose medication use and symptom frequency in the 2 weeks before the interview suggested persistent asthma. Misunderstanding of the role of inhaled anti-inflammatory medication was defined as identifying it as being for treatment of symptoms after they begin and not for prevention of symptoms before they start. Results. A total of 1663 parents of children with asthma (63% response rate) were interviewed. Of those, 571 subjects (34%) reported use of an inhaled anti-inflammatory medication and met our criteria for persistent asthma. Among those with persistent asthma, 23% (131 parents) misunderstood the role of their childs inhaled anti-inflammatory. Misunderstanding of inhaled anti-inflammatory medication was associated with decreased adherence to its daily use (odds ratio [OR] 0.18, 95% confidence interval [CI], 0.11–0.29). The risk for misunderstanding was lower if the patient had seen a specialist (OR 0.42, 95% CI, 0.24–0.75) or had graduated high school (OR = 0.54, 95% CI, 0.34–0.84). Conclusion. Misunderstanding of the role of inhaled anti-inflammatory medication is associated with reduced adherence to its daily use.
Pediatric Research | 1998
Tracy A. Lieu; Paula Braveman; Gabriel J. Escobar; Allen F. Fischer; Nancy G. Jensvold; Angela M. Capra
A Randomized Study of Home vs. Clinic Follow-up Visits After Early Postpartum Discharge. • 655
The New England Journal of Medicine | 2003
Elaine M. Hylek; Alan S. Go; Yuchiao Chang; Nancy G. Jensvold; Lori E. Henault; Joe V. Selby; Daniel E. Singer
JAMA | 2003
Alan S. Go; Elaine M. Hylek; Yuchiao Chang; Kathleen A. Phillips; Lori E. Henault; Angela M. Capra; Nancy G. Jensvold; Joe V. Selby; Daniel E. Singer
Pediatrics | 2003
Elsie M. Taveras; Angela M. Capra; Paula Braveman; Nancy G. Jensvold; Gabriel J. Escobar; Tracy A. Lieu
Pediatrics | 2002
Tracy A. Lieu; Paula Lozano; Jonathan A. Finkelstein; Felicia W. Chi; Nancy G. Jensvold; Angela M. Capra; Charles P. Quesenberry; Joe V. Selby; Harold J. Farber
Journal of the American College of Cardiology | 2004
Bernice Ruo; Angela M. Capra; Nancy G. Jensvold; Alan S. Go