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1.
J Prim Care Community Health ; 5(3): 160-5, 2014 Jul.
Article in English | MEDLINE | ID: mdl-24399443

ABSTRACT

The gold standard for health information is the health record. Hospitalization and outpatient diagnoses provide health systems with data on which to project health costs and plan programmatic changes. Although health record information may be reliable and perceived as accurate, it may not include population-specific information and may exclude care provided outside a specific health care facility. Sole reliance on medical record information may lead to underutilization of health care services and inadequate assessment of population health status. In this study, we analyzed agreement, without assuming a gold standard, between self-reported and recorded chronic conditions in an American Indian/Alaska Native cohort. Self-reported health history was collected from 3821 adult participants of the Alaska EARTH study during 2004-2006. Participant medical records were electronically accessed and reviewed. Self-reported chronic conditions were underreported in relation to the medical record and both information sources reported the absence more reliably than the presence of conditions (across conditions, median positive predictive value = 64%, median negative predictive value = 94%). Agreement was affected by age, gender, and education. Differences between participant- and provider-based prevalence of chronic conditions demonstrate why health care administrators and policy makers should not rely exclusively on medical record-based administrative data for a comprehensive evaluation of population health.


Subject(s)
/statistics & numerical data , Chronic Disease/ethnology , Data Collection/methods , Indians, North American/statistics & numerical data , Medical Records/statistics & numerical data , Self Report , Adolescent , Adult , Age Factors , Aged , Alaska/epidemiology , Educational Status , Female , Health Status , Humans , Male , Middle Aged , Prevalence , Sex Factors , Socioeconomic Factors , Young Adult
2.
Adv Skin Wound Care ; 21(12): 576-81, 2008 Dec.
Article in English | MEDLINE | ID: mdl-19065084

ABSTRACT

OBJECTIVE: To examine whether a patient group with chronic venous disorders (CVDs) would show a different response to a pressure provocation test, such as skin perfusion pressure (SPP) of microcirculatory function. DESIGN: A cuff inflation technique was applied to the gaiter area of the lower legs to induce complete occlusion of the microcirculation. The cuff was then released to measure the pressure at which perfusion resumed, and SPP was measured with a laser Doppler flowmeter (LDF). The measurements at reperfusion were taken of skin of the lower legs of individuals with CVD and compared with the lower-leg skin of control participants. MAIN OUTCOME MEASURES: To establish whether a measurable difference in SPP exists between the group with CVD and the group without CVD, the means of 9 measurements taken were compared using the Student t test. The lowest value of the 9 measurements of minimum pressure (LMV) was used to estimate the pressure at which reperfusion occurred (SPP). The means of those estimates were then compared using the Student t test. MAIN RESULTS: The mean LMV measured in the CVD group was slightly higher than that measured in the group without CVD. Although this could be considered a clinically significant result, it was not statistically different. CONCLUSIONS: For this study, SPP was not significantly different for those with CVD compared with those without. These results suggest that SPP conducted with an LDF has little potential to detect "invisible" changes in the microcirculatory function of the skin affected by CVDs.


Subject(s)
Blood Pressure , Leg/blood supply , Skin/blood supply , Varicose Ulcer/prevention & control , Venous Insufficiency/physiopathology , Aged , Case-Control Studies , Chronic Disease , Female , Humans , Laser-Doppler Flowmetry , Male , Microcirculation , Predictive Value of Tests , Risk Assessment , Sphygmomanometers , Venous Insufficiency/diagnosis
3.
Diabetes Technol Ther ; 9(6): 523-34, 2007 Dec.
Article in English | MEDLINE | ID: mdl-18034607

ABSTRACT

BACKGROUND: The purpose of this study was to examine whether a web-based, on-line intravenous insulin (IVI) infusion calculator (IVIIC) program for the delivery of IVI therapy in coronary artery bypass graft (CABG) patients was superior to a prior IVI protocol used in the cardiothoracic intensive care unit at our institution. METHODS: The study included 97 CABG patients studied from October 2004 to February 2005 pre-protocol (type 2 diabetes) and October 2005 to February 2006 post-protocol (with or without type 2 diabetes). The IVIIC was programmed to resemble an algorithm whereby any patient with type 2 diabetes or a blood glucose (BG) greater than 120 mg/dL was started on IVI with an insulin sensitivity factor, a multiplier of 0.03. The calculator used the following mathematical formula: rate of insulin infusion/hour = (current BG - 60 mg/dL) x 0.03. RESULTS: Pre- and post-protocol groups for patients with type 2 diabetes were similar in all demographics measured, including initial age, mean age, percentage female, and percentage African-American. Significant differences were observed between pre- and post-protocol groups in mean BG recorded over a 48-h period (P < 0.0001), percentage not at target within 48 h (P < 0.0001), mean hours to first BG between 80 to 120 mg/dL (P < 0.0001), mean hours to target (three consecutive BGs 80-120 mg/dL) (P < 0.0001), and hyperglycemic index (P < 0.0001). The incidence of hypoglycemia (percentage BG < 70 mg/dL) was not significantly increased in the post-protocol groups (P = 0.2581). CONCLUSIONS: We conclude that the IVIIC is a safe nurse-driven protocol with excellent BG outcomes.


Subject(s)
Blood Glucose , Coronary Care Units/standards , Drug Dosage Calculations , Hypoglycemic Agents/administration & dosage , Insulin/administration & dosage , Aged , Algorithms , Coronary Artery Bypass , Female , Hospitals, University/standards , Humans , Infusions, Intravenous , Internet , Male , Middle Aged
4.
Biomaterials ; 26(27): 5433-43, 2005 Sep.
Article in English | MEDLINE | ID: mdl-15860200

ABSTRACT

The polymer poly-N-acetylglucosamine (pGlcNAc) containing fiber material is becoming increasingly important as a topical agent for hemostasis at wound sites. The pGlcNAc polymeric fiber provides hemostasis through redundant mechanisms that include platelet activation for fibrin network formation. The research presented here better defines the mechanism for the effect of pGlcNAc containing fibers on platelet-mediated processes. Adsorption experiments demonstrated that pGlcNAc fibers tightly bind most major plasma proteins and a specific sub-set of platelet surface proteins, including the integrin beta(3) subunit (CD61) and the von Willebrand receptor GP1b (CD42b). The result of this interaction is a platelet-dependent acceleration of fibrin gel formation. Accelerated fibrin polymerization is sensitive to factor XII inhibition by corn trypsin inhibitor and integrin inactivation with integrilin. Confocal microscopy studies show that when platelet integrins contact plasma protein-saturated pGlcNAc fibers, an increase in intracellular free calcium for platelet activation occurs to drive surface expression of phosphatidyl serine (PS). Thus, a catalytic surface for thrombin generation and accelerated fibrin clot formation results from the interaction of platelets with pGlcNAc. These findings, when considered with the observation that pGlcNAc fibers also induce red blood cell agglutination and vasoconstriction, provides an explanation for the ability of the pGlcNAc material to provide hemostasis in a wide variety of clinical applications.


Subject(s)
Acetylglucosamine/pharmacology , Complement Activation/physiology , Factor XII/metabolism , Hemostasis/physiology , Integrins/metabolism , Platelet Activation/physiology , Signal Transduction/physiology , Acetylglucosamine/chemistry , Blood Platelets/chemistry , Blood Platelets/drug effects , Blood Platelets/physiology , Cells, Cultured , Coagulants/pharmacology , Complement Activation/drug effects , Factor XII/chemistry , Factor XII/immunology , Hemostasis/drug effects , Humans , Integrins/chemistry , Integrins/immunology , Platelet Activation/drug effects , Protein Binding , Signal Transduction/drug effects
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