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1.
Circ Cardiovasc Interv ; 10(12)2017 Dec.
Article de Anglais | MEDLINE | ID: mdl-29246918

RÉSUMÉ

BACKGROUND: The association of short-term readmissions after percutaneous coronary intervention (PCI) on healthcare costs has not been well studied. METHODS AND RESULTS: The Healthcare Cost and Utilization Project National Readmission Database encompassing 722 US hospitals was used to identify index PCI cases in patients ≥18 years old. Hierarchical regression analyses were used to examine the factors associated with risk of 30-day readmission and higher cumulative costs. We evaluated 206 869 hospitalized patients who survived to discharge after PCI from January through November 2013 and analyzed readmissions over 30 days after discharge. A total of 24 889 patients (12%) were readmitted within 30 days, with rates ranging from 6% to 17% across hospitals. Among the readmitted patients, 13% had PCI, 2% had coronary artery bypass surgery, and 3% died during the readmission. The most common reasons for readmission included nonspecific chest pain/angina (24%) and heart failure (11%). Mean cumulative costs were higher for those with readmissions ($39 634 versus $22 058; P<0.001). The multivariable analyses showed that readmission increased the log10 cumulative costs by 45% (ß: 0.445; P<0.001). There was no significant difference in cumulative costs by the type of insurance. CONCLUSIONS: In a national sample of inpatient PCI cases, 30-day readmissions were associated with a significant increase in cumulative costs. The majority of readmissions were because of low-risk chest pain that did not require any intervention. Ongoing effort is warranted to recognize and mitigate potentially preventable post-PCI readmissions.


Sujet(s)
Maladie coronarienne/économie , Maladie coronarienne/thérapie , Coûts hospitaliers , Réadmission du patient/économie , Intervention coronarienne percutanée/économie , /économie , Adolescent , Adulte , Sujet âgé , Angine de poitrine/économie , Angine de poitrine/épidémiologie , Loi du khi-deux , Maladie coronarienne/mortalité , Bases de données factuelles , Femelle , Mortalité hospitalière , Humains , Modèles linéaires , Modèles logistiques , Mâle , Medicare (USA)/économie , Adulte d'âge moyen , Modèles économiques , Analyse multifactorielle , Intervention coronarienne percutanée/effets indésirables , Intervention coronarienne percutanée/mortalité , Facteurs de risque , Facteurs temps , Résultat thérapeutique , États-Unis/épidémiologie , Jeune adulte
2.
Microsurgery ; 31(1): 59-65, 2011 Jan.
Article de Anglais | MEDLINE | ID: mdl-21207501

RÉSUMÉ

This study was designed to determine if cigarette smoking adversely affects functional recovery following ischemia/reperfusion (I/R) injury in peripheral nerves. Forty Wistar rats were divided evenly among four groups. Animals in groups A and B were exposed to cigarette smoke via a controlled smoking chamber for 20 minutes daily. On study day 14, all animals underwent a controlled I/R injury to one sciatic nerve. Recovery was assessed with walking track assessments, malondialdehyde (MDA) assay, and histology. Walking track results on study day 21 did not differ significantly between the smoking and nonsmoking animals. However, by study day 28, the nonsmoking animals showed a greater degree of functional recovery (SFI = -18.0 and -22.8, respectively, P = 0.03). MDA concentration in the smoking group was significantly higher than the nonsmoking group at the 28 day time point (P = 0.04). Exposure to cigarette smoke was associated with a slower functional recovery following peripheral nerve I/R injury.


Sujet(s)
Nerfs périphériques/vascularisation , Lésion d'ischémie-reperfusion/physiopathologie , Fumer/physiopathologie , Animaux , Cotinine/urine , Mâle , Malonaldéhyde/analyse , Stress oxydatif , Nerfs périphériques/anatomopathologie , Rats , Rat Wistar , Récupération fonctionnelle , Lésion d'ischémie-reperfusion/anatomopathologie , Nerf ischiatique/physiopathologie
3.
Plast Reconstr Surg ; 125(3): 866-71, 2010 Mar.
Article de Anglais | MEDLINE | ID: mdl-20195113

RÉSUMÉ

BACKGROUND: Calcium channel blockers have been shown experimentally to reverse many of the effects of nicotine. The purpose of this study was to assess the effect of calcium channel blockers on smoking-induced skin flap necrosis. METHODS: Forty male albino Wistar rats were divided into four groups. Groups A, B, and C were treated in a controlled smoking chamber for 20 minutes daily for 21 days. On day 14, caudally based dorsal skin flaps (3 x 10 cm) were created. On days 14 through 21, group B animals received verapamil (20 mg/kg/day) by gavage. Group C received nifedipine (10 mg/kg/day). On day 21, standardized photographs were taken and flap survival areas determined. Urine cotinine concentrations were measured on days 14 and 21. RESULTS: The mean cotinine level at surgery was 161 ng/ml in group A (smoking), 149 ng/ml in group B (verapamil), and 168 ng/ml in group C (nifedipine). These differences were not statistically significant. Cotinine concentration at surgery for group D (no smoking) was less than 10 ng/ml. The mean flap survival in group D was 79.1 percent, compared with 63.7 percent in group A (p = 0.003). The mean flap survival in group B (verapamil) was 72.8 percent, compared with 73.7 percent in group C (nifedipine). Both values were significantly greater than in group A (p = 0.04 and p = 0.008, respectively). CONCLUSIONS: In this study, enteral calcium channel blockers were associated with a statistically significant improvement in flap survival compared with untreated animals with an equivalent smoke exposure. Calcium channel blockers may reduce perioperative risk in active smokers who require skin flap surgery.


Sujet(s)
Inhibiteurs des canaux calciques/pharmacologie , Survie du greffon/effets des médicaments et des substances chimiques , Nifédipine/pharmacologie , Fumer/effets indésirables , Lambeaux chirurgicaux/anatomopathologie , Vérapamil/pharmacologie , Animaux , Inhibiteurs des canaux calciques/administration et posologie , Cotinine/urine , Mâle , Nécrose/induit chimiquement , Nicotine/effets indésirables , Nicotine/antagonistes et inhibiteurs , Nifédipine/administration et posologie , Rats , Rat Wistar , Fumer/anatomopathologie , Lambeaux chirurgicaux/vascularisation , Vasodilatation/effets des médicaments et des substances chimiques , Vérapamil/administration et posologie
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