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1.
J Perinatol ; 37(3): 270-276, 2017 03.
Article in English | MEDLINE | ID: mdl-27977012

ABSTRACT

OBJECTIVES: To assess progress of neonatal intensive care units (NICUs) participating in the Vermont Oxford Network iNICQ 2015: Alarm Safety Collaborative in achieving Joint Commission 2014 alarm safety goals with respect to oximeters, and to compare patient-level oxygen saturation (SpO2) and oximeter alarm data to local policies. STUDY DESIGN: Prospective multicenter audits in February and August 2015 assessed implementation of policies addressing Joint Commission 2014 Alarm Safety goals, and ascertained SpO2 targets, oximeter alarm settings and compliance with policy-specified SpO2 targets and alarms. RESULTS: Eighty-six NICUs completed both audits. Of 13 policies addressing mandated goals, median (interquartile range) 8 (5, 9) policies were implemented at audit 1 and 9 (6, 11) at audit 2 (P=0.004). At audit 1, 28 NICUs had implemented ⩾9 policies versus 47 at audit 2. For 794 infants <31 weeks gestation, <36 weeks postmenstrual age, and on supplemental oxygen, median SpO2 target lower limit was 88% (interquartile range 87%, 90%; range 75% to 94%), upper limit 95% (interquartile range 94%, 96%; range 85% to 100%). High oximeter alarm was set according to local policy for 63% of infants, for whom SpO2 >97% was less frequent than when high alarm was not set to policy (10.1% vs 21.5%, P=0.006). CONCLUSIONS: Participating NICUs showed significant progress between audits in their implementation of Joint Commission Alarm Safety goals for oximeter monitoring. Oximeter high alarm not set per local policy is associated with increased hyperoxemia in preterm infants. Recommendations to standardize oxygen saturation targets for infants at risk for oxygenation-related outcomes have not been widely adopted.


Subject(s)
Clinical Alarms/standards , Infant, Premature/blood , Intensive Care Units, Neonatal/standards , Oxygen/blood , Patient Safety , Gestational Age , Humans , Hyperoxia/prevention & control , Hypoxia/prevention & control , Infant, Newborn , Logistic Models , Monitoring, Physiologic , Oximetry/methods , Prospective Studies , Vermont
2.
Am J Physiol Lung Cell Mol Physiol ; 309(10): L1199-207, 2015 Nov 15.
Article in English | MEDLINE | ID: mdl-26386118

ABSTRACT

Here, we tested the hypothesis that a promiscuous bacterial cyclase synthesizes purine and pyrimidine cyclic nucleotides in the pulmonary endothelium. To test this hypothesis, pulmonary endothelial cells were infected with a strain of the Gram-negative bacterium Pseudomonas aeruginosa that introduces only exoenzyme Y (PA103 ΔexoUexoT::Tc pUCPexoY; ExoY(+)) via a type III secretion system. Purine and pyrimidine cyclic nucleotides were simultaneously detected using mass spectrometry. Pulmonary artery (PAECs) and pulmonary microvascular (PMVECs) endothelial cells both possess basal levels of four different cyclic nucleotides in the following rank order: cAMP > cUMP ≈ cGMP ≈ cCMP. Endothelial gap formation was induced in a time-dependent manner following ExoY(+) intoxication. In PAECs, intercellular gaps formed within 2 h and progressively increased in size up to 6 h, when the experiment was terminated. cGMP concentrations increased within 1 h postinfection, whereas cAMP and cUMP concentrations increased within 3 h, and cCMP concentrations increased within 4 h postinfection. In PMVECs, intercellular gaps did not form until 4 h postinfection. Only cGMP and cUMP concentrations increased at 3 and 6 h postinfection, respectively. PAECs generated higher cyclic nucleotide levels than PMVECs, and the cyclic nucleotide levels increased earlier in response to ExoY(+) intoxication. Heterogeneity of the cyclic nucleotide signature in response to P. aeruginosa infection exists between PAECs and PMVECs, suggesting the intracellular milieu in PAECs is more conducive to cNMP generation.


Subject(s)
Endothelial Cells/metabolism , Nucleotides, Cyclic/physiology , Pseudomonas aeruginosa/enzymology , Capillary Permeability , Cells, Cultured , Endothelial Cells/microbiology , Host-Pathogen Interactions , Microvessels/cytology , Pulmonary Artery/cytology
3.
J Consult Clin Psychol ; 63(1): 163-7, 1995 Feb.
Article in English | MEDLINE | ID: mdl-7896985

ABSTRACT

One in every 6 couples is infertile, and the literature suggests that a number of individuals experience psychological distress associated with infertility. The purpose of this study was to investigate predictors of psychological distress among infertility clinic patients. Analyses indicated that infertile men (n = 86) and women (n = 120) reported greater psychological distress than normative data from the general population. Separate hierarchical multiple regressions revealed that self-blame and avoidance coping was the best predictor of psychological distress among men and women. Increased age and not already having biological children added to the prediction among men but not among women. The limitations and implications of the findings are presented.


Subject(s)
Infertility, Female/psychology , Infertility, Male/psychology , Adaptation, Psychological , Adult , Female , Humans , Male , Severity of Illness Index , Sex Factors , Surveys and Questionnaires
4.
Arthritis Care Res ; 7(2): 58-63, 1994 Jun.
Article in English | MEDLINE | ID: mdl-7857994

ABSTRACT

The clinical implications of depression in the context of rheumatoid arthritis are described. An overview of the diagnostic criteria for depression is provided, with specific focus on major depression and the associated subtypes. The neurobiological literature on major depression is briefly reviewed and the implications of the depression literature for the care of persons with rheumatoid arthritis are discussed.


Subject(s)
Arthritis, Rheumatoid/psychology , Depressive Disorder , Depressive Disorder/classification , Depressive Disorder/diagnosis , Depressive Disorder/etiology , Depressive Disorder/psychology , Depressive Disorder/therapy , Humans , Neurobiology
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