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1.
Medicina (Kaunas) ; 59(9)2023 Aug 31.
Artículo en Inglés | MEDLINE | ID: mdl-37763702

RESUMEN

Introduction: The post-COVID-19 syndrome is a clinical entity characterized by the manifestation of signs and symptoms that develop after the acute phase of COVID-19, which persist for a duration of more than 12 weeks and are not explained by any alternative diagnosis. It has been observed that individuals with pre-existing chronic diseases, including cardiovascular and pulmonary diseases, are at a greater risk of developing post-COVID-19 syndrome. The Charlson Comorbidity Index (CCI) is a useful tool employed to evaluate the burden of comorbidities and predict the prognosis of patients with post-COVID-19 syndrome. The present study aims to assess whether the burden of comorbidities, evaluated using the CCI, correlates with post-COVID-19 syndrome. Materials and Methods: Between 21 April 2020 and 15 May 2023, we enrolled all consecutive outpatients with previous COVID-19 admissions to a post-acute day-hospital service three months after a negative SARS-CoV-2 molecular test. We assessed age, sex, BMI, acute COVID-19 and post-COVID-19 signs, and symptoms and calculated CCI according to its current definition. Post-COVID-19 syndrome was defined as the persistence of at least one sign or symptom lasting more than 12 weeks after COVID-19 resolution and not explained by an alternative diagnosis. The relationship between post-COVID-19 and CCI was explored first with the chi-squared test, then with different binary logistic regression models. We considered significant values of p lower than 0.05. Results: We obtained a cohort of 3636 patients and observed a significant association between the number of post-COVID-19 symptoms and CCI. Patients developing post-COVID-19 were more commonly affected by a greater burden of comorbidities. Patients with at least one CCI point had an increased risk of post-COVID-19 syndrome (OR:2.961; 95%CI: 2.269-3.863; p < 0.0001), which increased further for CCI ≥ 4 (OR:6.062; 95%CI: 3.163-11.618; p < 0.0001). Conclusions: Patients affected by post-COVID-19 show a greater clinical complexity and a larger burden of comorbidities, synthesized by a higher CCI; moreover, a higher CCI seems to correlate with an increasing post-COVID-19 risk, being the presence of ≥1 or ≥4 CCI points associated with a 3-fold and 6-fold increased risk of post-COVID-19 syndrome, respectively.


Asunto(s)
COVID-19 , Humanos , COVID-19/complicaciones , COVID-19/epidemiología , Síndrome Post Agudo de COVID-19 , SARS-CoV-2 , Comorbilidad , Hospitalización
2.
J Clin Med ; 13(7)2024 Mar 28.
Artículo en Inglés | MEDLINE | ID: mdl-38610717

RESUMEN

Pulmonary embolism (PE) is a potentially life-threatening condition requiring prompt diagnosis and treatment. Recent advances have led to the development of newer techniques and drugs aimed at improving PE management, reducing its associated morbidity and mortality and the complications related to anticoagulation. This review provides an overview of the current knowledge and future perspectives on PE treatment. Anticoagulation represents the first-line treatment of hemodynamically stable PE, direct oral anticoagulants being a safe and effective alternative to traditional anticoagulation: these drugs have a rapid onset of action, predictable pharmacokinetics, and low bleeding risk. Systemic fibrinolysis is suggested in patients with cardiac arrest, refractory hypotension, or shock due to PE. With this narrative review, we aim to assess the state of the art of newer techniques and drugs that could radically improve PE management in the near future: (i) mechanical thrombectomy and pulmonary embolectomy are promising techniques reserved to patients with massive PE and contraindications or failure to systemic thrombolysis; (ii) catheter-directed thrombolysis is a minimally invasive approach that can be suggested for the treatment of massive or submassive PE, but the lack of large, randomized controlled trials represents a limitation to widespread use; (iii) novel pharmacological approaches, by agents inhibiting thrombin-activatable fibrinolysis inhibitor, factor Xia, and the complement cascade, are currently under investigation to improve PE-related outcomes in specific settings.

3.
Antibiotics (Basel) ; 11(12)2022 Dec 13.
Artículo en Inglés | MEDLINE | ID: mdl-36551468

RESUMEN

The proper posology of antibiotics in the critically ill in CRRT is difficult to assess. We therefore performed a prospective observational cohort study to make clear hints in this topic. Our results reveal a high Sieving Coefficient for all antibiotics, equal to or higher than those described in previous papers. CVVH clearance in relation to total body clearance was significant, (i.e., >than 25% for all classes). A strong correlation between the antibiotic concentrations obtained in plasma and ultrafiltrate was found both at the peak and in the valley, with the determination of two equations that allow a new method for calculating the amount of antibiotic lost in CVVH both for trough levels and peak. Based on the results of our study and considering the limitations we believe that we can extrapolate the following final considerations: (1) it is likely to carry out a loading dose for the main antibiotics (2) subsequent administrations must take into account the daily loss identified by the linear regression equation. This angular coefficient gives the idea that the average daily loss of given antibiotic is about 25%; this implies that on the basis of the linear regression equation that correlates ultrafiltered/plasma antibiotic concentration, the dosage should be increased by 25% every day, while still ensuring a daily plasma TDM of the drug.

4.
Sci Data ; 9(1): 537, 2022 09 01.
Artículo en Inglés | MEDLINE | ID: mdl-36050312

RESUMEN

We present a multi-device and multi-modal dataset, called WEEE, collected from 17 participants while they were performing different physical activities. WEEE contains: (1) sensor data collected using seven wearable devices placed on four body locations (head, ear, chest, and wrist); (2) respiratory data collected with an indirect calorimeter serving as ground-truth information; (3) demographics and body composition data (e.g., fat percentage); (4) intensity level and type of physical activities, along with their corresponding metabolic equivalent of task (MET) values; and (5) answers to questionnaires about participants' physical activity level, diet, stress and sleep. Thanks to the diversity of sensors and body locations, we believe that the dataset will enable the development of novel human energy expenditure (EE) estimation techniques for a diverse set of application scenarios. EE refers to the amount of energy an individual uses to maintain body functions and as a result of physical activity. A reliable estimate of people's EE thus enables computing systems to make inferences about users' physical activity and help them promoting a healthier lifestyle.


Asunto(s)
Metabolismo Energético , Dispositivos Electrónicos Vestibles , Composición Corporal , Ejercicio Físico , Humanos , Muñeca
5.
Materials (Basel) ; 14(15)2021 Jul 27.
Artículo en Inglés | MEDLINE | ID: mdl-34361356

RESUMEN

Climate change (CC) is predominantly connected to greenhouse gas (GHG) emissions from the construction sector. It is clear how it is necessary to rethink construction materials in order to reduce GHG emissions. Among the various strategies proposed, recent research has investigated the potential of smart materials. This study in particular aims to develop an innovative building component that combines high energy performance with reduced thickness and weight. For this reason, the potential of Phase Change Materials (PCM) in cement-based mixes is investigated, comparing the performance of a traditional mix with two innovative mixes made with the addition of 3% and 7% PCM. This work characterizes the new material, analyzing its mechanical and thermal performance, highlighting how the mix strength decreases as the PCM ratio increases; however, both mixes may be considered suitable for masonry structures and may be classified as M5 and M15. Furthermore, from the analysis of the thermal performance, it emerges that the mix presents good behavior in terms of insulating properties.

6.
Nutrients ; 13(6)2021 Jun 08.
Artículo en Inglés | MEDLINE | ID: mdl-34201106

RESUMEN

Ischemic stroke (IS) is still among the leading causes of death and disability worldwide. The pathogenic mechanisms beyond its development are several and are complex and this is the main reason why a functional therapy is still missed. The beneficial effects of natural compounds against cardiovascular diseases and IS have been investigated for a long time. In this article, we reviewed the association between the most studied polyphenols and stroke protection in terms of prevention, effect on acute phase, and rehabilitation. We described experimental and epidemiological studies reporting the role of flavonols, phenolic acid, and stilbens on ischemic mechanisms leading to stroke. We analyzed the principal animal models used to evaluate the impact of these micronutrients to cerebral blood flow and to molecular pathways involved in oxidative stress and inflammation modulation, such as sirtuins. We reported the most significant clinical trials demonstrated as the persistent use of polyphenols is clinically relevant in terms of the reduction of vascular risk factors for IS, such as Atrial Fibrillation. Interestingly, different kinds of polyphenols provide brain protection by activating different pathways and mechanisms, like inducing antithrombotic effect, such as Honokiol. For this reason, we discussed an appropriate integrative use of them as a possible therapeutic alternative against stroke.


Asunto(s)
Isquemia Encefálica/tratamiento farmacológico , Isquemia Encefálica/prevención & control , Polifenoles/uso terapéutico , Accidente Cerebrovascular/tratamiento farmacológico , Accidente Cerebrovascular/prevención & control , Animales , Isquemia Encefálica/complicaciones , Isquemia Encefálica/fisiopatología , Modelos Animales de Enfermedad , Humanos , Estrés Oxidativo/efectos de los fármacos , Polifenoles/farmacología , Accidente Cerebrovascular/complicaciones , Accidente Cerebrovascular/fisiopatología , Rehabilitación de Accidente Cerebrovascular
7.
Acta Diabetol ; 51(2): 219-24, 2014 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-23818012

RESUMEN

Erythrocyte glutathione transferase (e-GST) displays increased activity in patients with renal damage and positive correlation with homocysteine (Hcy) in patients under maintenance hemodialysis. Here, we determined e-GST, Hcy, and erythrocyte catalase (e-CAT) in 328 patients affected by type 2 diabetes mellitus (T2DM), 61 diabetic non-nephropathic patients and 267 affected by diabetes and by chronic kidney disease (CKD) under conservative therapy subdivided into four stages according to K-DOQI lines. e-GST activity was significantly higher in all T2DM patients compared to the control group (7.90 ± 0.26 vs. 5.6 ± 0.4 U/g(Hb)), and we observed an enhanced activity in all subgroups of CKD diabetic patients. No significant correlation or increase has been found for e-CAT in all patients tested. Mean Hcy in diabetic patients is higher than that in healthy subjects (33.42 ± 1.23 vs. 13.6 ± 0.8 µM), and Hcy increases in relation to the CKD stage. As expected, a significant correlation was found between e-GST and Hcy levels. These findings suggest that e-GST hyperactivity is not caused directly by diabetes but by its consequent renal damage. e-GST, as well as Hcy, may represent an early biomarker of renal failure.


Asunto(s)
Diabetes Mellitus Tipo 2/enzimología , Neuropatías Diabéticas/enzimología , Eritrocitos/enzimología , Glutatión Transferasa/sangre , Fallo Renal Crónico/enzimología , Uremia/enzimología , Adulto , Anciano , Biomarcadores/sangre , Catalasa/sangre , Diabetes Mellitus Tipo 2/sangre , Neuropatías Diabéticas/sangre , Femenino , Homocisteína/sangre , Humanos , Fallo Renal Crónico/sangre , Masculino , Persona de Mediana Edad , Uremia/sangre
8.
Metabolism ; 58(3): 361-7, 2009 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-19217452

RESUMEN

In overweight patients (OW), the increased peripheral activity of the endocannabinoid system in visceral adipose tissue (VAT) may be mediated by cannabinoid type 1 (CB1) receptor expression. We determined whether CB1 receptor splice variants and messenger RNA (mRNA) levels in perirenal and subcutaneous adipose tissues are associated with obesity and metabolic syndrome (MetS). Gene expression with multiple-primers real-time polymerase chain reaction (TaqMan; Applied Biosystem, Weiterstadt, Germany) was performed to study VAT and paired subcutaneous adipose tissue (SAT) mRNA from 36 consecutive patients undergoing nephrectomy. Cannabinoid type 1A and CB1E mRNAs variants with the longer version of exon 4 were expressed. The CB1 expression in perirenal VAT significantly correlated with body mass index (BMI). Paired subcutaneous/perirenal samples from normal-weight patients (BMI < 25 kg/m(2)) showed higher CB1 expression in SAT (P = .002), whereas in OW (BMI > or = 25 kg/m(2)), the higher CB1 expression was in VAT (P = .038). In unpaired samples, SAT of normal-weight patients had significantly higher CB1 mRNA levels compared with SAT of OW, whereas higher CB1 expression (P = .009) was found in VAT of OW (n = 25). Overweight patients with increased visceral CB1 expression had higher waist circumference (P < .01), insulin (P < .01), and homeostasis model assessment index (P < .01). In addition, patients with the MetS (n = 22) showed higher CB1 expression in perirenal adipose tissues (P = .007). Visceral adipose CB1 expression correlated with BMI. Overweight patients and those with MetS showed a CB1 expression pattern supporting a CB1-mediated overactivity of the endocannabinoid system in human VAT.


Asunto(s)
Tejido Adiposo/fisiopatología , Índice de Masa Corporal , Enfermedades Metabólicas/fisiopatología , Sobrepeso/fisiopatología , Receptor Cannabinoide CB1/genética , Empalme Alternativo , Peso Corporal/genética , ADN de Cadena Simple/genética , Exones , Regulación de la Expresión Génica , Variación Genética , Humanos , Neoplasias Renales/genética , Neoplasias Renales/patología , Enfermedades Metabólicas/genética , Síndrome Metabólico/genética , Obesidad/genética , Sobrepeso/genética , ARN Mensajero/genética
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