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1.
Respir Med ; 206: 107066, 2023 01.
Artigo em Inglês | MEDLINE | ID: mdl-36470050

RESUMO

BACKGROUND: Pulmonary arterial hypertension (PAH) is a life limiting disease with substantial symptom burden and healthcare utilization. Palliative care alleviates physical and emotional symptoms for patients with serious illness, and has been underutilized for these patients. OBJECTIVE: To characterize patients with PAH referred to palliative care and identify predictors of referral. METHODS: We conducted an observational study of adult patients enrolled in the Pulmonary Hypertension Association Registry from January 2015 through June 2021, performing descriptive statistics on patient characteristics at baseline for all patients and the subset referred to palliative care. These characteristics were modeled in a backwards elimination Cox regression with time to referral to palliative care as the primary outcome. RESULTS: 92 of 1,578 patients were referred to palliative care (5.8%); 43% were referred at their last visit prior to death. Referrals were associated with increasing age per decade (hazard ratio 1.35 [95% confidence interval 1.16-1.58]), lower body mass index (hazard ratio 0.97 [95% confidence interval 0.94-0.998]), supplemental oxygen use (hazard ratio 2.01 [95% confidence interval 1.28-3.16]), parenteral prostanoid use (hazard ratio 2.88 [95% confidence interval 1.84-4.51]), and worse quality of life, measured via lower physical (hazard ratio 0.97 [95% confidence interval 0.95-0.99]) and mental (hazard ratio 0.98 [95% confidence interval 0.96-0.995]) scores on the 12-item Short Form Health Survey. CONCLUSION: Patients with PAH are infrequently referred to palliative care, even at centers of excellence. Referrals occur in sicker patients with lower quality of life scores, often close to the end of life.


Assuntos
Hipertensão Pulmonar , Hipertensão Arterial Pulmonar , Adulto , Humanos , Hipertensão Pulmonar/epidemiologia , Hipertensão Pulmonar/terapia , Cuidados Paliativos , Qualidade de Vida , Hipertensão Pulmonar Primária Familiar , Encaminhamento e Consulta , Sistema de Registros
2.
3.
BMJ Open ; 10(6): e034145, 2020 06 03.
Artigo em Inglês | MEDLINE | ID: mdl-32499261

RESUMO

OBJECTIVE: To determine whether maternal cardiovascular disease (CVD) risk factors predict preterm birth. DESIGN: Case control. SETTING: California hospitals. PARTICIPANTS: 868 mothers with linked demographic information and biospecimens who delivered singleton births from July 2009 to December 2010. METHODS: Logistic regression analysis was employed to calculate odds ratios for the associations between maternal CVD risk factors before and during pregnancy (including diabetes, hypertensive disorders and cholesterol levels) and preterm birth outcomes. PRIMARY OUTCOME: Preterm delivery status. RESULTS: Adjusting for the other maternal CVD risk factors of interest, all categories of hypertension led to increased odds of preterm birth, with the strongest magnitude observed in the pre-eclampsia group (adjusted OR (aOR), 13.49; 95% CI 6.01 to 30.27 for preterm birth; aOR, 10.62; 95% CI 4.58 to 24.60 for late preterm birth; aOR, 17.98; 95% CI 7.55 to 42.82 for early preterm birth) and chronic hypertension alone for early preterm birth (aOR, 4.58; 95% CI 1.40 to 15.05). Diabetes (types 1 and 2 and gestational) was also associated with threefold increased risk for preterm birth (aOR, 3.06; 95% CI 1.12 to 8.41). A significant and linear dose response was found between total and low-density lipoprotein (LDL) cholesterol and aORs for late and early preterm birth, with increasing cholesterol values associated with increased risk (likelihood χ2 differences of 8.422 and 8.019 for total cholesterol for late and early, and 9.169 and 10.896 for LDL for late and early, respectively). Receiver operating characteristic curves using these risk factors to predict late and early preterm birth produced C statistics of 0.601 and 0.686. CONCLUSION: Traditional CVD risk factors are significantly associated with an increased risk of preterm birth; these findings reinforce the clinical importance of integrating obstetric and cardiovascular risk assessment across the healthcare continuum in women.


Assuntos
Complicações Cardiovasculares na Gravidez/epidemiologia , Nascimento Prematuro/epidemiologia , California , Estudos de Casos e Controles , Correlação de Dados , Feminino , Humanos , Hipercolesterolemia/epidemiologia , Hipertensão Induzida pela Gravidez/epidemiologia , Recém-Nascido , Razão de Chances , Gravidez , Complicações Cardiovasculares na Gravidez/diagnóstico , Gravidez em Diabéticas/epidemiologia , Fatores de Risco
4.
Nanomaterials (Basel) ; 4(1): 69-86, 2014 Jan 08.
Artigo em Inglês | MEDLINE | ID: mdl-28348286

RESUMO

We report a one-pot solvothermal synthesis of sub-10 nm, dominant ultraviolet (UV) emissive upconverting nanocrystals (UCNCs), based on sodium-codoped LaF3 and BaLaF5 (0.5%Tm; 20%Yb) and their corresponding core@shell derivatives. Elemental analysis shows a Na-codopant in these crystal systems of ~20% the total cation content; X-ray diffraction (XRD) data indicate a shift in unit cell dimensions consistent with these small codopant ions. Similarly, X-ray photoelectron spectroscopic (XPS) analysis reveals primarily substitution of Na⁺ for La3+ ions (97% of total Na⁺ codopant) in the crystal system, and interstitial Na⁺ (3% of detected Na⁺) and La3+ (3% of detected La3+) present in (Na)LaF3 and only direct substitution of Na⁺ for Ba2+ in Ba(Na)LaF5. In each case, XPS analysis of La 3d lines show a decrease in binding energy (0.08-0.25 eV) indicating a reduction in local crystal field symmetry surrounding rare earth (R.E.3+) ions, permitting otherwise disallowed R.E. UC transitions to be enhanced. Studies that examine the impact of laser excitation power upon luminescence intensity were conducted over 2.5-100 W/cm² range to elucidate UC mechanisms that populate dominant UV emitting states. Low power saturation of Tm3+ ³F3 and ³H4 states was observed and noted as a key initial condition for effective population of the ¹D2 and ¹I6 UV emitting states, via Tm-Tm cross-relaxation.

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