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1.
J Nurs Adm ; 47(9): 465-469, 2017 Sep.
Article in English | MEDLINE | ID: mdl-28834807

ABSTRACT

Collegial relationships, administrative champions, and persistence are key components to breaking down barriers to advanced practice RN (APRN) practice. This article addresses how Iowa APRNs in a state-sanctioned task force identified barriers for practicing at the top of their licensure in a full practice authority state including defending the right to control the scope of nursing practice in court.


Subject(s)
Advanced Practice Nursing/organization & administration , Licensure, Nursing/standards , Nurse Practitioners/organization & administration , Advanced Practice Nursing/standards , Humans , Iowa , Nurse Practitioners/standards
2.
J Pediatr Endocrinol Metab ; 25(3-4): 301-5, 2012.
Article in English | MEDLINE | ID: mdl-22768660

ABSTRACT

Nationally, newborn screening programs use 17-hydroxyprogesterone (17-OHP) as the biomarker to detect the rare but potentially fatal inherited disease, congenital adrenal hyperplasia. However, this biomarker is highly variable, with a high false-positive rate of detection, particularly in neonates born preterm. Several studies have examined various clinical and genetic factors to explain the variability of 17-OHP in preterm infants. The purpose of this study was to replicate previous clinical and genetic associations with 17-OHP in a well-characterized cohort of 762 preterm infants. We replicated previous findings that respiratory distress syndrome (p = 2 x 10(-3)) is associated with higher 17-OHP. Higher 17-OHP and false positives were significantly associated with lower gestational age and birth weight, as previously reported. Incorporating gestational age and birth weight together decreases the false-positive rate.


Subject(s)
17-alpha-Hydroxyprogesterone/blood , Adrenal Hyperplasia, Congenital/diagnosis , Neonatal Screening , Respiratory Distress Syndrome, Newborn/diagnosis , Adrenal Hyperplasia, Congenital/blood , Adrenal Hyperplasia, Congenital/genetics , Birth Weight , DNA/blood , DNA/genetics , Female , Gestational Age , Humans , Infant , Infant, Newborn , Infant, Premature , Prognosis , Prospective Studies , Respiratory Distress Syndrome, Newborn/blood , Respiratory Distress Syndrome, Newborn/genetics , Retrospective Studies
3.
J Pediatr ; 160(1): 19-24.e4, 2012 Jan.
Article in English | MEDLINE | ID: mdl-21885063

ABSTRACT

OBJECTIVE: To examine associations between rs9883204 in ADCY5 and rs900400 near LEKR1 and CCNL1 with birth weight in a preterm population. Both markers were associated with birth weight in a term population in a recent genome-wide association study of Freathy et al. STUDY DESIGN: A meta-analysis of mother and infant samples was performed for associations of rs900400 and rs9883204 with birth weight in 393 families from the US, 265 families from Argentina, and 735 mother-infant pairs from Denmark. Z-scores adjusted for infant sex and gestational age were generated for each population separately and regressed on allele counts. Association evidence was combined across sites by inverse-variance weighted meta-analysis. RESULTS: Each additional C allele of rs900400 (LEKR1/CCNL1) in infants was marginally associated with a 0.069 SD lower birth weight (95% CI, -0.159 to 0.022; P = .068). This result was slightly more pronounced after adjusting for smoking (P = .036). No significant associations were identified with rs9883204 or in maternal samples. CONCLUSIONS: These results indicate the potential importance of this marker on birth weight regardless of gestational age.


Subject(s)
Birth Weight/genetics , Genome-Wide Association Study , Female , Humans , Infant, Newborn , Infant, Premature , Male
4.
J Pediatr ; 159(1): 104-9, 2011 Jul.
Article in English | MEDLINE | ID: mdl-21353244

ABSTRACT

OBJECTIVE: To determine genetic and clinical risk factors associated with elevated systolic blood pressure (ESBP) in preterm infants after discharge from the neonatal intensive care unit (NICU). STUDY DESIGN: A convenience cohort of infants born at <32 weeks gestational age was followed after NICU discharge. We retrospectively identified a subgroup of subjects with ESBP (systolic blood pressure [SBP] >90th percentile for term infants). Genetic testing identified alleles associated with ESBP. Multivariate logistic regression analysis was performed for the outcome ESBP, with clinical characteristics and genotype as independent variables. RESULTS: Predictors of ESBP were cytochrome P450, family 2, subfamily D, polypeptide 6 (CYP2D6) (rs28360521) CC genotype (OR, 2.92; 95% CI, 1.48-5.79), adjusted for outpatient oxygen therapy (OR, 4.53; 95% CI, 2.23-8.81) and history of urinary tract infection (OR, 4.68; 95% CI, 1.47-14.86). Maximum SBP was modeled by multivariate linear regression analysis: maximum SBP=84.8 mm Hg + 6.8 mm Hg if cytochrome P450, family 2, subfamily D, polypeptide 6 (CYP2D6) CC genotype + 6.8 mm Hg if discharged on supplemental oxygen + 4.4 mm Hg if received inpatient glucocorticoids (P=.0002). CONCLUSIONS: ESBP is common in preterm infants with residual lung disease after discharge from the NICU. This study defines clinical factors associated with ESBP, identifies a candidate gene for further testing, and supports the recommendation to monitor blood pressure before age 3 years, as is suggested for term infants.


Subject(s)
Cytochrome P-450 CYP2D6/genetics , Hypertension/genetics , Infant, Premature , Cohort Studies , Female , Gene Frequency , Genotype , Glucocorticoids/therapeutic use , Humans , Hypertension/epidemiology , Infant, Newborn , Intensive Care Units, Neonatal , Male , Multivariate Analysis , Oxygen Inhalation Therapy , Patient Discharge , Polymorphism, Single Nucleotide , Retrospective Studies , Systole , Urinary Tract Infections/epidemiology
5.
Acta Paediatr ; 100(3): 347-51, 2011 Mar.
Article in English | MEDLINE | ID: mdl-20969622

ABSTRACT

AIM: To explore the association of serum bilirubin level and breast milk feeding with retinopathy of prematurity (ROP) in preterm infants. METHODS: We conducted a case-control study to examine the independent and combined effects of serum bilirubin and breast milk feeding on ROP risk in infants <32 weeks gestation or with birth weight <1500 g. Cases (66 infants with ROP) were matched with controls (66 infants without ROP) based on factors known to affect ROP risk. RESULTS: When analysed using the paired t-test, the peak bilirubin levels were lower in ROP cases than in controls (mean 7.2 vs. 7.9 mg/dL; p = 0.045). Using conditional logistic regression, we found a negative association between highest serum bilirubin level and risk of ROP (OR = 0.82 per 1-mg/dL change in bilirubin; p = 0.06). There was no significant association between breast milk feeding and risk of ROP. CONCLUSION: Bilirubin may help to protect preterm infants against ROP.


Subject(s)
Bilirubin/blood , Breast Feeding , Milk, Human , Retinopathy of Prematurity/prevention & control , Case-Control Studies , Female , Gestational Age , Humans , Infant, Newborn , Infant, Premature , Infant, Very Low Birth Weight , Male , Retinopathy of Prematurity/blood , Retrospective Studies , Risk Factors
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