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1.
J Am Med Dir Assoc ; 21(7): 919-923, 2020 Jul.
Article in English | MEDLINE | ID: mdl-32571651

ABSTRACT

OBJECTIVE: Bedside chest ultrasonography, when integrated with clinical data, is an accurate tool for improving the diagnostic process of many respiratory diseases. This study aims to evaluate the feasibility of a chest ultrasonographic screening program in nursing homes for detecting coronavirus disease-19 (COVID-19)-related pneumonia and improving the appropriateness of hospital referral of residents. DESIGN: Pragmatic, descriptive, feasibility study from April 2 to April 9, 2020. SETTING AND PARTICIPANTS: A total of 83 older residents (age 85 ± 8) presenting mild to moderate respiratory symptoms and not previously tested for COVID-19, residing in 5 nursing homes in Northern Italy. METHODS: Chest ultrasonography was performed at the bedside by a team of hospital specialists with certified expertise in thoracic ultrasonography, following a systematic approach exploring 4 different areas for each hemithorax, from the anterior and posterior side. Presence of ultrasonographic signs of interstitial pneumonia, including comet-tail artifacts (B-lines) with focal or diffuse distribution, subpleural consolidations, and pleural line indentation, was detected. The specialist team integrated ultrasonography data with clinical and anamnestic information, and gave personalized therapeutic advice for each patient, including hospital referral when needed. RESULTS: The most frequent reasons for ultrasonographic evaluation were fever (63% of participants) and mild dyspnea (40%). Fifty-six patients (67%) had abnormal ultrasonographic findings. The most common patterns were presence of multiple subpleural consolidations (32 patients) and diffuse B-lines (24 patients), with bilateral involvement. A diagnosis of suspect COVID-19 pneumonia was made in 44 patients, and 6 of them required hospitalization. Twelve patients had ultrasonographic patterns suggesting other respiratory diseases, and 2 patients with normal ultrasonographic findings were diagnosed with COPD exacerbation. CONCLUSIONS AND IMPLICATIONS: In nursing home residents, screening of COVID-19 pneumonia with bedside chest ultrasonography is feasible and may represent a valid diagnostic aid for an early detection of COVID-19 outbreaks and adequate patient management.


Subject(s)
Coronavirus Infections/epidemiology , Nursing Homes/organization & administration , Pneumonia, Viral/epidemiology , Point-of-Care Systems/organization & administration , Severe Acute Respiratory Syndrome/diagnostic imaging , Ultrasonography, Doppler/methods , Aged , Aged, 80 and over , COVID-19 , Disease Outbreaks/statistics & numerical data , Feasibility Studies , Female , Humans , Italy , Male , Outcome Assessment, Health Care , Pandemics , Pneumonia, Viral/diagnostic imaging , Severe Acute Respiratory Syndrome/epidemiology
2.
Intern Emerg Med ; 11(7): 905-16, 2016 Oct.
Article in English | MEDLINE | ID: mdl-27273018

ABSTRACT

Liver cirrhosis is a major cause of morbidity and mortality worldwide, mainly due to complications of portal hypertension. In this article, we review the current understanding on the pathophysiology, the diagnostic criteria and the available therapeutic options for patients with emerging hepatic syndromes in cirrhosis, namely the hepatorenal, hepato-adrenal and hepatopulmonary syndrome. The hepatorenal syndrome is a well-recognized complication of advanced cirrhosis and is usually associated with an accelerated course to death unless liver transplantation is performed. The hepatopulmonary syndrome is often missed in the evaluation of patients with cirrhosis; however, early recognition is essential for the efficient management of individual patients. The hepato-adrenal syndrome, although not fully characterized, offers an exciting field for research and potential therapeutic interventions.


Subject(s)
Hepatorenal Syndrome/complications , Hypertension, Portal/complications , Liver Cirrhosis/physiopathology , Acute Kidney Injury/etiology , Adrenal Insufficiency/complications , Adrenal Insufficiency/etiology , Ascites/complications , Ascites/etiology , Creatinine/urine , Evidence-Based Medicine/methods , Hepatorenal Syndrome/etiology , Hepatorenal Syndrome/physiopathology , Humans , Hypertension, Portal/physiopathology , Liver Cirrhosis/complications , Liver Cirrhosis/etiology , Liver Transplantation , Lypressin/analogs & derivatives , Lypressin/pharmacology , Lypressin/therapeutic use , Midodrine/pharmacology , Midodrine/therapeutic use , Norepinephrine/pharmacology , Norepinephrine/therapeutic use , Octreotide/pharmacology , Octreotide/therapeutic use , Plasma Substitutes/pharmacology , Plasma Substitutes/therapeutic use , Portasystemic Shunt, Transjugular Intrahepatic , Serum Albumin/pharmacology , Serum Albumin/therapeutic use , Terlipressin , Vasodilator Agents/pharmacology , Vasodilator Agents/therapeutic use , Vasopressins/pharmacology , Vasopressins/therapeutic use
3.
Curr Opin Allergy Clin Immunol ; 13(6): 677-85, 2013 Dec.
Article in English | MEDLINE | ID: mdl-24152740

ABSTRACT

PURPOSE OF REVIEW: Most asthma patients are easily managed with a standard combination of therapies consisting of inhaled controller and reliever drugs, but there remains a large unmet need at the severe end of the disease spectrum. For these patients, development of safer and more effective therapies for asthmatic patients with severe refractory disease remains a top priority. Here, drugs in development for the severe asthma sufferers and their specific mechanism-based pharmacological rationale will be reviewed with a focus on biologics. A systematic search of the literature was made using Medline, and publications were selected on the basis of their relevance to the topic. Here, the authors will review the existing efficacy and safety data from clinical trials of some of the new biologic therapies that are in development for severe asthma. RECENT FINDINGS: Despite strong preclinical data for many of the more recently identified asthma targets, especially those relating to the T-helper 2 allergic pathway, clinical trials with specific biologics have been largely disappointing. However, there is scope for their specific role in distinctively targeted subpopulations of severe asthmatic patients. SUMMARY: It is clear that more efforts should be devoted towards establishing new and more efficient key targets. A closer interaction between industry, academia and health workers will be required to achieve this goal effectively.


Subject(s)
Asthma/immunology , Asthma/therapy , Biological Therapy/methods , Th2 Cells/immunology , Biological Therapy/trends , Clinical Trials as Topic , Humans , MEDLINE
4.
Expert Opin Ther Targets ; 17(7): 761-72, 2013 Jul.
Article in English | MEDLINE | ID: mdl-23642090

ABSTRACT

INTRODUCTION: Adenosine receptors (ARs) and their differential pattern of expression modulate a series of pleiotropic activities that are known to contribute to the control of inflammation, remodeling, and tissue repair. Consequently, pharmacological manipulation of adenosine signaling pathway is of great interest and is currently exploited as a therapeutic target for a number of respiratory diseases with several molecules with agonist and antagonist activities against known ARs being developed for the treatment of different conditions of the respiratory system. AREAS COVERED: Herein, we will review the rational basis leading to the development of novel therapies for asthma, chronic obstructive pulmonary disease (COPD), interstitial lung disease (ILD), pulmonary arterial hypertension (PAH), and cystic fibrosis. Their most recent clinical development will be also discussed. EXPERT OPINION: Advances in our understanding of the pathogenetic role of adenosine in respiratory diseases may be soon translated into effective treatment options. In consideration of the complex interplay driven by the different pattern of receptor distribution and/or affinity of the four known AR subtypes in specific cell types at different stages of the disease, it is likely that combination of selective antagonist/agonists for different AR subtypes will be required to obtain reasonable clinical efficacy. Alternatively, controlling the factors involved in driving adenosine concentrations in the tissue may be also of great significance.


Subject(s)
Receptors, Purinergic P1/metabolism , Respiratory Tract Diseases/metabolism , Adenosine/metabolism , Animals , Humans , Signal Transduction
5.
Expert Opin Biol Ther ; 13(3): 393-402, 2013 Mar.
Article in English | MEDLINE | ID: mdl-23289846

ABSTRACT

INTRODUCTION: Patients with severe asthma have a significant unmet need with persistent symptoms and/or frequent exacerbations despite high intensity treatment. These severe unrelenting symptoms have a huge impact on heathcare resources due to frequent hospital admissions and requirement for intensive and expensive medications. There is a compelling need for more effective and safer therapies to help severe asthma sufferers to achieve adequate control of their disease. AREAS COVERED: Expanding knowledge of innate and adaptive immune responses has led to development of new biologic approaches for severe asthma. Here, the authors will review the existing efficacy and safety data from clinical trials of some of the new biologic therapies that are in development for severe asthma. Their specific role in distinctively targeted subpopulations of severe asthmatics will be also discussed. EXPERT OPINION: Defining and phenotyping severe asthma patients will become increasingly important as some patients who were previously classified as having severe asthma may become well-controlled with a targeted phenotype-specific treatment. However, pharmacoeconomic concerns should also be taken into account given the elevated acquisition costs of recombinant human monoclonals and of the diagnostic screening procedures for the identification of potential responders.


Subject(s)
Anti-Asthmatic Agents/therapeutic use , Asthma/drug therapy , Biological Products/therapeutic use , Inflammation/prevention & control , Signal Transduction/drug effects , Humans , Treatment Outcome
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