Controlled-release carvedilol in the management of systemic hypertension and myocardial dysfunction

Cardiovascular disease is the leading cause of death worldwide. Within the treatment armamentarium, beta-blockers have demonstrated efficacy across the spectrum of cardiovascular disease – from modification of a risk factor (ie, hypertension) to treatment after an acute event (ie, myocardial infarction). Recently, the use of beta-blockers as a first-line therapy in hypertension has been called into question. Moreover, beta-blockers as a class are saddled with a misperception of having poor tolerability. However, vasodilatory beta-blockers such as carvedilol have a different hemodynamic action that provides the benefits of beta-blockade with the addition of vasodilation resulting from alpha 1-adrenergic receptor blockade. Vasodilation reduces total peripheral resistance, which may produce an overall positive effect on tolerability. Recently, a new, controlled-release carvedilol formulation has been developed that provides the clinical efficacy of carvedilol but is indicated for once-daily dosing. This review presents an overview of the clinical and pharmacologic carvedilol controlled-release data

Influence of heart rate, blood pressure, and beta-blocker dose on outcome and the differences in outcome between carvedilol and metoprolol tartrate in patients with chronic heart failure: results from the COMET trial

Aims We studied the influence of heart rate (HR), systolic blood pressure (SBP), and beta-blocker dose on outcome in the 2599 out of 3029 patients in Carvedilol Or Metoprolol European Trial (COMET) who were alive and on study drug at 4 months after randomization (time of first visit on maintenance therapy). Methods and results By multivariable analysis, baseline HR, baseline SBP, and their change after 4 months were not independently related to subsequent outcome. In a multivariable analysis including clinical variables, HR above and SBP below the median value achieved at 4 months predicted subsequent increased mortality [relative risk (RR) for HR>68 b.p.m. 1.333; 95% confidence intervals (CI) 1.152-1.542; P120 mmHg 0.78; 95% CI 0.671-0.907; P<0.0013]. Achieving target beta-blocker dose was associated with a better outcome (RR 0.779; 95% CI 0.662-0.916; P<0.0025). The superiority of carvedilol as compared to metoprolol tartrate was maintained in a multivariable model (RR 0.767; 95% CI 0.663-0.887; P=0.0004) and there was no interaction with HR, SBP, or beta-blocker dose. Conclusion Beta-blocker dose, HR, and SBP achieved during beta-blocker therapy have independent prognostic value in heart failure. None of these factors influenced the beneficial effects of carvedilol when compared with metoprolol tartrate at the pre-defined target doses used in COME

Early mortality and loss to follow-up in HIV-infected children starting antiretroviral therapy in Southern Africa.

BACKGROUND: Many HIV-infected children in Southern Africa have been started on antiretroviral therapy (ART), but loss to follow up (LTFU) can be substantial. We analyzed mortality in children retained in care and in all children starting ART, taking LTFU into account. PATIENTS AND METHODS: Children who started ART before the age of 16 years in 10 ART programs in South Africa, Malawi, Mozambique, and Zimbabwe were included. Risk factors for death in the first year of ART were identified in Weibull models. A meta-analytic approach was used to estimate cumulative mortality at 1 year. RESULTS: Eight thousand two hundred twenty-five children (median age 49 months, median CD4 cell percent 11.6%) were included; 391 (4.8%) died and 523 (7.0%) were LTFU in the first year. Mortality at 1 year was 4.5% [95% confidence interval (CI): 2.8% to 7.4%] in children remaining in care, but 8.7% (5.4% to 12.1%) at the program level, after taking mortality in children and LTFU into account. Factors associated with mortality in children remaining in care included age [adjusted hazard ratio (HR) 0.37; 95% CI: 0.25 to 0.54 comparing > or =120 months with <18 months], CD4 cell percent (HR: 0.56; 95% CI: 0.39 to 0.78 comparing > or =20% with <10%), and clinical stage (HR: 0.12; 95% CI: 0.03 to 0.45 comparing World Health Organization stage I with III/IV). CONCLUSIONS: In children starting ART and remaining in care in Southern Africa mortality at 1 year is <5% but almost twice as high at the program level, when taking LTFU into account. Age, CD4 percentage, and clinical stage are important predictors of mortality at the individual level

Interleukin‐6 and the Risk of Adverse Outcomes in Patients After an Acute Coronary Syndrome: Observations From the SOLID‐TIMI 52 (Stabilization of Plaque Using Darapladib—Thrombolysis in Myocardial Infarction 52) Trial

Background: Interleukin‐6 (IL‐6) is an inflammatory cytokine implicated in plaque instability in acute coronary syndrome (ACS). We aimed to evaluate the prognostic implications of IL‐6 post‐ACS. Methods and Results: IL‐6 concentration was assessed at baseline in 4939 subjects in SOLID‐TIMI 52 (Stabilization of Plaque Using Darapladib—Thrombolysis in Myocardial Infarction 52), a randomized trial of darapladib in patients ≤30 days from ACS. Patients were followed for a median of 2.5 years for major adverse cardiovascular events; cardiovascular death, myocardial infarction, or stroke) and cardiovascular death or heart failure hospitalization. Primary analyses were adjusted first for baseline characteristics, days from index ACS, ACS type, and randomized treatment arm. For every SD increase in IL‐6, there was a 10% higher risk of major adverse cardiovascular events (adjusted hazard ratio [adj HR] 1.10, 95% confidence interval [CI] 1.01‐1.19) and a 22% higher risk of cardiovascular death or heart failure (adj HR 1.22, 95% CI 1.11‐1.34). Patients in the highest IL‐6 quartile had a higher risk of major adverse cardiovascular events (adj HR Q4:Q1 1.57, 95% CI 1.22‐2.03) and cardiovascular death or heart failure (adj HR 2.29, 95% CI 1.6‐3.29). After further adjustment for biomarkers (high‐sensitivity C‐reactive protein, lipoprotein‐associated phospholipase A2 activity, high‐sensitivity troponin I, and B‐type natriuretic peptide), IL‐6 remained significantly associated with the risk of major adverse cardiovascular events (adj HR Q4:Q1 1.43, 95% CI 1.09‐1.88) and cardiovascular death or heart failure (adj HR 1.79, 95% CI 1.22‐2.63). Conclusions: In patients after ACS, IL‐6 concentration is associated with adverse cardiovascular outcomes independent of established risk predictors and biomarkers. These findings lend support to the concept of IL‐6 as a potential therapeutic target in patients with unstable ischemic heart disease

The management of iron deficiency in inflammatory bowel disease

__Background__ Iron deficiency is a common and undertreated problem in inflammatory bowel disease (IBD). __Aim__ To develop an online tool to support treatment choice at the patient-specific level. __Methods__ Using the RAND/UCLA Appropriateness Method (RUAM), a European expert panel assessed the appropriateness of treatment regimens for a variety of clinical scenarios in patients with non-anaemic iron deficiency (NAID) and iron deficiency anaemia (IDA). Treatment options included adjustment of IBD medication only, oral iron supplementation, high-/low-dose intravenous (IV) regimens, IV iron plus erythropoietin-stimulating agent (ESA), and blood transfusion. The panel process consisted of two individual rating rounds and three plenary discussion meetings. __Results__ The panel reached agreement on 71% of treatment indications. 'No treatment' was never considered appropriate, and repeat treatment after previous failure was generally discouraged. For 98% of scenarios, at least one treatment was appropriate. Adjustment of IBD medication was deemed appropriate in all patients with active disease. Use of oral iron was mainly considered an option in NAID and mildly anaemic patients without disease activity. IV regimens were often judged appropriate, with high-dose IV iron being the preferred option in 77% of IDA scenarios. Blood transfusion and IV+ESA were indicated in exceptional cases only. __Conclusions__ The RUAM revealed high agreement amongst experts on the management of iron deficiency in patients with IBD. High-dose IV iron was more often considered appropriate than other options. To facilitate dissemination of the recommendations, panel outcomes were embedded in an online tool, accessible via http://ferroscope.com/

Pharmacodynamic evaluation and safety assessment of treatment with antibodies to serum amyloid P component in patients with cardiac amyloidosis: an open-label Phase 2 study and an adjunctive immuno-PET imaging study.

BACKGROUND: In a Phase I study treatment with the serum amyloid P component (SAP) depleter miridesap followed by monoclonal antibody to SAP (dezamizumab) showed removal of amyloid from liver, spleen and kidney in patients with systemic amyloidosis. We report results from a Phase 2 study and concurrent immuno-positron emission tomography (PET) study assessing efficacy, pharmacodynamics, pharmacokinetics, safety and cardiac uptake (of dezamizumab) following the same intervention in patients with cardiac amyloidosis. METHODS: Both were uncontrolled open-label studies. After SAP depletion with miridesap, patients received ≤ 6 monthly doses of dezamizumab in the Phase 2 trial (n = 7), ≤ 2 doses of non-radiolabelled dezamizumab plus [89Zr]Zr-dezamizumab (total mass dose of 80 mg at session 1 and 500 mg at session 2) in the immuno-PET study (n = 2). Primary endpoints of the Phase 2 study were changed from baseline to follow-up (at 8 weeks) in left ventricular mass (LVM) by cardiac magnetic resonance imaging and safety. Primary endpoint of the immuno-PET study was [89Zr]Zr-dezamizumab cardiac uptake assessed via PET. RESULTS: Dezamizumab produced no appreciable or consistent reduction in LVM nor improvement in cardiac function in the Phase 2 study. In the immuno-PET study, measurable cardiac uptake of [89Zr]Zr-dezamizumab, although seen in both patients, was moderate to low. Uptake was notably lower in the patient with higher LVM. Treatment-associated rash with cutaneous small-vessel vasculitis was observed in both studies. Abdominal large-vessel vasculitis after initial dezamizumab dosing (300 mg) occurred in the first patient with immunoglobulin light chain amyloidosis enrolled in the Phase 2 study. Symptom resolution was nearly complete within 24 h of intravenous methylprednisolone and dezamizumab discontinuation; abdominal computed tomography imaging showed vasculitis resolution by 8 weeks. CONCLUSIONS: Unlike previous observations of visceral amyloid reduction, there was no appreciable evidence of amyloid removal in patients with cardiac amyloidosis in this Phase 2 trial, potentially related to limited cardiac uptake of dezamizumab as demonstrated in the immuno-PET study. The benefit-risk assessment for dezamizumab in cardiac amyloidosis was considered unfavourable after the incidence of large-vessel vasculitis and development for this indication was terminated. Trial registration NCT03044353 (2 February 2017) and NCT03417830 (25 January 2018)

Pharmacodynamic evaluation and safety assessment of treatment with antibodies to serum amyloid P component in patients with cardiac amyloidosis: an open-label Phase 2 study and an adjunctive immuno-PET imaging study.

BACKGROUND: In a Phase I study treatment with the serum amyloid P component (SAP) depleter miridesap followed by monoclonal antibody to SAP (dezamizumab) showed removal of amyloid from liver, spleen and kidney in patients with systemic amyloidosis. We report results from a Phase 2 study and concurrent immuno-positron emission tomography (PET) study assessing efficacy, pharmacodynamics, pharmacokinetics, safety and cardiac uptake (of dezamizumab) following the same intervention in patients with cardiac amyloidosis. METHODS: Both were uncontrolled open-label studies. After SAP depletion with miridesap, patients received ≤ 6 monthly doses of dezamizumab in the Phase 2 trial (n = 7), ≤ 2 doses of non-radiolabelled dezamizumab plus [89Zr]Zr-dezamizumab (total mass dose of 80 mg at session 1 and 500 mg at session 2) in the immuno-PET study (n = 2). Primary endpoints of the Phase 2 study were changed from baseline to follow-up (at 8 weeks) in left ventricular mass (LVM) by cardiac magnetic resonance imaging and safety. Primary endpoint of the immuno-PET study was [89Zr]Zr-dezamizumab cardiac uptake assessed via PET. RESULTS: Dezamizumab produced no appreciable or consistent reduction in LVM nor improvement in cardiac function in the Phase 2 study. In the immuno-PET study, measurable cardiac uptake of [89Zr]Zr-dezamizumab, although seen in both patients, was moderate to low. Uptake was notably lower in the patient with higher LVM. Treatment-associated rash with cutaneous small-vessel vasculitis was observed in both studies. Abdominal large-vessel vasculitis after initial dezamizumab dosing (300 mg) occurred in the first patient with immunoglobulin light chain amyloidosis enrolled in the Phase 2 study. Symptom resolution was nearly complete within 24 h of intravenous methylprednisolone and dezamizumab discontinuation; abdominal computed tomography imaging showed vasculitis resolution by 8 weeks. CONCLUSIONS: Unlike previous observations of visceral amyloid reduction, there was no appreciable evidence of amyloid removal in patients with cardiac amyloidosis in this Phase 2 trial, potentially related to limited cardiac uptake of dezamizumab as demonstrated in the immuno-PET study. The benefit-risk assessment for dezamizumab in cardiac amyloidosis was considered unfavourable after the incidence of large-vessel vasculitis and development for this indication was terminated. Trial registration NCT03044353 (2 February 2017) and NCT03417830 (25 January 2018)

Tuberculosis in Pediatric Antiretroviral Therapy Programs in Low- and Middle-Income Countries: Diagnosis and Screening Practices

Background The global burden of childhood tuberculosis (TB) is estimated to be 0.5 million new cases per year. Human immunodeficiency virus (HIV)-infected children are at high risk for TB. Diagnosis of TB in HIV-infected children remains a major challenge. Methods We describe TB diagnosis and screening practices of pediatric antiretroviral treatment (ART) programs in Africa, Asia, the Caribbean, and Central and South America. We used web-based questionnaires to collect data on ART programs and patients seen from March to July 2012. Forty-three ART programs treating children in 23 countries participated in the study. Results Sputum microscopy and chest Radiograph were available at all programs, mycobacterial culture in 40 (93%) sites, gastric aspiration in 27 (63%), induced sputum in 23 (54%), and Xpert MTB/RIF in 16 (37%) sites. Screening practices to exclude active TB before starting ART included contact history in 41 sites (84%), symptom screening in 38 (88%), and chest Radiograph in 34 sites (79%). The use of diagnostic tools was examined among 146 children diagnosed with TB during the study period. Chest Radiograph was used in 125 (86%) children, sputum microscopy in 76 (52%), induced sputum microscopy in 38 (26%), gastric aspirate microscopy in 35 (24%), culture in 25 (17%), and Xpert MTB/RIF in 11 (8%) children. Conclusions Induced sputum and Xpert MTB/RIF were infrequently available to diagnose childhood TB, and screening was largely based on symptom identification. There is an urgent need to improve the capacity of ART programs in low- and middle-income countries to exclude and diagnose TB in HIV-infected childre

Dalla progettazione all’utilizzo di un sistema informativo geologico al servizio del rilevamento geologico: la banca dati della Regione Lombardia e la cartografia geologica derivata

In questa Tesi è descritto il processo di creazione di un Sistema Informativo Geologico e degli strumenti informatici per la gestione dell’informazione su base geografica, o più semplicemente GIS (Geographic Information System), al servizio delle attività di rilevamento geologico, finalizzato alla raccolta dei dati ed alla loro rappresentazione cartografica nell'ambito di un Sistema Informativo Territoriale (SIT). Un SIT è definibile come l'insieme di uomini, strumenti e procedure che, nell’ambito di una organizzazione, permettono l’acquisizione e la distribuzione dei dati relativi alla conoscenza dei fenomeni e degli attori presenti su territorio; tutto questo è facilitato in gran parte dalle capacità e funzionalità dei GIS. Il Sistema Informativo Territoriale orientato alla Geologia (SIG – Sistema Informativo Geologico) della Regione Lombardia è costituito da un gruppo di lavoro composto da geologi, informatici e geologi-informatici dell’Ente regionale e della società Lombardia Servizi (Gruppo Lombardia Informatica). Ho fatto parte del team di consulenza tecnico-scientifica incaricato da Lombardia Servizi per la realizzazione del SIG regionale. I compiti del gruppo di lavoro sono: - definizione di ruoli e metodi per la costituzione del SIG; - definizione delle logiche per la creazione di strumenti finalizzati all’archiviazione del dato geologico in una banca dati geologica e loro manutenzione; Il progetto è inserito nel più ampio processo di aggiornamento della Cartografia Geologica nazionale (progetto CARG). Il SIG ha come principali obiettivi: - la pianificazione ed esecuzione del rilevamento geologico di dettaglio (scala 1:10.000) del territorio lombardo; - la costruzione di un database della geologia di superficie (ma anche del sottosuolo per le aree di pianura) interrogabile e aggiornabile ; - il supporto ai processi di analisi finalizzati alla descrizione della geologia superficiale e ricostruzione degli eventi che hanno creato il paesaggio attuale; - la rappresentazione cartografica dell’ambiente geologico a partire dal database creato. - la distribuzione dell’informazione geologica archiviata in vari formati (cartaceo e digitale); Sono qui descritte ed analizzate criticamente la filosofia di costruzione delle procedure e le soluzioni tecniche e metodologiche adottate per realizzare gli obiettivi prefissi. L’APAT (Agenzia per la Protezione dell'Ambiente e per i servizi Tecnici nazionali) ha ereditato dal Servizio Geologico il compito di rilevare, aggiornare e pubblicare la Carta Geologica d'Italia (progetto nazionale CARG) quale organo cartografico dello Stato in base alla legge 68/60. Nel 1976 era stato completato il rilevamento della Carta geologica d'Italia alla scala 1:100.000 costituita da 278 fogli a copertura del territorio nazionale; per il suo aggiornamento sono stati definiti strumenti normativi idonei a garantire l'omogeneità dei contenuti e della rappresentazione cartografica; la definizione delle norme discende dall'applicazione di linee guida, frutto dell'attività di Commissioni e Gruppi di lavoro, pubblicate nei Quaderni della serie III (ed. APAT). L’Ente Regione Lombardia, per rispondere all’impegno istituzionale di aggiornamento della Carta Geologica, all’interno del più ampio e strutturato Sistema Informativo Territoriale regionale, ha dunque creato il Sistema Informativo Geologico (SIG) regionale. Il rapido evolversi delle ricerche nel campo delle Scienze della Terra e l'importanza che riveste la cartografia geologica nella gestione del territorio, hanno spinto la Regione Lombardia a progettare un rilevamento geologico di dettaglio per dotarsi di una banca dati geologica dalla quale derivare la propria cartografia geologica (alla scala 1:10.000). Sono stati quindi definiti standard specifici rispondenti a questa esigenza di maggior dettaglio (rispetto a quanto indicato dal progetto nazionale CARG) ed è stato pianificato e in gran parte realizzato un rilevamento ex-novo finalizzato alla pubblicazione del dato alla scala del rilevamento e per la sua generalizzazione alle scale 1:25.000 e 50.000. Alla fine del processo saranno stati realizzati 14 fogli del territorio lombardo relativamente alle aree alpine e di passaggio alla pianura (Bergamo, Bormio, Breno, Clusone, Lecco, Iseo, Malonno, Ponte di Legno, Sondrio, Vimercate, Milano, Bagolino, Seregno, Voghera). In tale progetto sono anche coinvolti le Università di Milano, di Pavia e di Bolona, il Politecnico di Milano e il CNR - Centro di Studio per la Geodinamica Alpina e Quaternaria di Milano. L’attività di rilevamento geologico è di competenza dei funzionari regionali della Struttura Sistema Informativo Territoriale della Direzione Generale Territorio e Urbanistica che, coadiuvati da geologi rilevatori, realizzano tutte le fasi del lavoro, dalla raccolta del dato fino alla sua pubblicazione. L’ambiente informatico GIS sviluppato, denominato CARGeo (Cartografia Geologica), permette di inserire i dati raccolti da geologi rilevatori in un database appositamente predisposto, mediante interfacce grafiche semplificate e procedure standard di archiviazione e controllo di correttezza formale. La banca dati è costruita in modo da facilitare l’archiviazione della maggior parte dei dati che normalmente il geologo registra nella carta e nei taccuini di terreno e, allo stesso tempo, guidarlo nella raccolta organica dell’informazione geologica. Nella strutturazione del database è stata privilegiata la possibilità di inserire attributi direttamente associabili agli elementi geometrici anziché attraverso schede associate a punti di osservazione. Il geologo rilevatore interviene per correggere errori di digitalizzazione o di attribuzione con un processo ciclico, fino ad ottenere una banca dati corretta secondo gli standard predefiniti. Gli strumenti di creazione della banca dati permettono anche di: - disegnare gli schemi accessori (sezioni geologiche, schemi stratigrafici e strutturali etc.); - eseguire lo “sfoltimento” e posizionamento delle annotazioni sulla mappa (sigle di unità litologiche e parametri di inclinazione delle giaciture) secondo criteri di leggibilità della carta - creare le legende; - creare banche dati a scala inferiore (1:25.000 e 50.000); - stampare e pubblicare carte geologiche complete di schemi e legende. Il sistema contiene gli strumenti necessari alla migrazione della banca dati dalla struttura proprietaria CARG-Regione Lombardia a quella CARG-APAT secondo la struttura definita nei Quaderni della serie III Il Sistema nel corso del biennio 2006-2007 ha raggiunto la fase di consegna dei dati (derivazione e generalizzazione della banca dati CARG-APAT 1.50.000 da quella 1:10.000 CARG-Regione Lombardia) dei primi fogli completati (ISEO, MALONNO, LECCO e SONDRIO) con ritardo rispetto alla programmazione. Sono state analizzate le cause che hanno portato a questo rallentamento del flusso di lavoro, quindi apportate le necessarie modifiche al Sistema. Sono qui descritti i problemi e le soluzioni trovate per migliorare l'efficienza del sistema. Attualmente il Sistema Informativo Geologico è in una fase di ristrutturazione, che vede la migrazione verso un’architettura informatica basata sulla piattaforma ARCGis® 9.x. Attraverso il Sistema Informativo Geologico viene tentata una sintesi fra le logiche metodologiche dei due ambiti tecnico-scientifici coinvolti (Geologia e Informatica), in un ambiente dove ricercatori e tecnici lavorano sperimentando l’interazione tra le conoscenze e le metodologie conoscitive tipiche delle Scienze Geologiche e le tecnologie e processi logici delle Scienze Informatiche. Con questa Tesi è documentato tutto il percorso di costruzione della banca dati geologica attraverso e all’interno del sistema realizzato assieme gruppo di lavoro composto da geologi e tecnici informatici, cui ho partecipato, riassumendo gli oltre 9 anni di lavoro dall’ideazione del progetto CARGeo, anche in funzione del suo miglioramento