ABSTRACT
BACKGROUND: Molecular testing with gene-expression profiling (GEP) and donor-derived cell-free DNA (dd-cfDNA) is increasingly used in the surveillance for acute cellular rejection (ACR) after heart transplant. However, the performance of dual testing over each test individually has not been established. Further, the impact of dual noninvasive surveillance on clinical decision-making has not been widely investigated. METHODS: We evaluated 2,077 subjects from the Surveillance HeartCare Outcomes Registry registry who were enrolled between 2018 and 2021 and had verified biopsy dataĀ and were categorized as dual negative, GEP positive/dd-cfDNA negative, GEP negative/dd-cfDNA positive, or dual positive. The incidence of ACR and follow-up testing rates for each group were evaluated. Positive likelihood ratios (LRs+) were calculated, and biopsy rates over time were analyzed. RESULTS: The incidence of ACR was 1.5% for dual negative, 1.9% for GEP positive/dd-cfDNA negative, 4.3% for GEP negative/dd-cfDNA positive, and 9.2% for dual-positive groups. Follow-up biopsies were performed after 8.8% for dual negative, 14.2% for GEP positive/dd-cfDNA negative, 22.8% for GEP negative/dd-cfDNA positive, and 35.4% for dual-positive results. The LR+Ā for ACR was 1.37, 2.91, and 3.90 for GEP positive, dd-cfDNA positive, and dual-positive testing, respectively. From 2018 to 2021, biopsies performed between 2 and 12-months post-transplant declined from 5.9 to 5.3 biopsies/patient, and second-yearĀ biopsyĀ rates declined from 1.5 to 0.9 biopsies/patient. At 2 years, survival was 94.9%, and only 2.7% had graft dysfunction. CONCLUSIONS: Dual molecular testing demonstrated improved performance for ACR surveillance compared to single molecular testing. The use of dual noninvasive testing was associated with lower biopsy rates over time, excellent survival, and low incidence of graft dysfunction.
Subject(s)
Graft Rejection , Heart Transplantation , Registries , Humans , Heart Transplantation/adverse effects , Graft Rejection/diagnosis , Graft Rejection/epidemiology , Male , Female , Middle Aged , Acute Disease , Adult , Incidence , Gene Expression Profiling , Biopsy , Cell-Free Nucleic Acids/blood , Follow-Up Studies , United States/epidemiologySubject(s)
Antibiotics, Antineoplastic/adverse effects , Breast Neoplasms/drug therapy , Cardiomyopathy, Dilated/chemically induced , Doxorubicin/adverse effects , Heart Failure/blood , Liver Neoplasms/drug therapy , Natriuretic Peptide, Brain/blood , Peptide Fragments/blood , Breast Neoplasms/pathology , Cardiomyopathy, Dilated/complications , Cardiomyopathy, Dilated/diagnosis , Dyspnea/etiology , Emergency Service, Hospital , Female , Heart Failure/diagnosis , Heart Failure/etiology , Humans , Liver Neoplasms/secondary , Middle AgedABSTRACT
Gene therapy approaches to enhance endothelial progenitor cell (EPC) homing may augment cell engraftment to ischemic tissue and lead to a greater therapeutic response. Therefore, we assessed the effects of ultrasound-mediated (UM) transfection of the chemokine stromal cell-derived factor-1 (SDF-1) on homing and engraftment of intravenously administered EPCs and the subsequent angiogenic response in chronically ischemic skeletal muscle. Bone marrow-derived EPCs were isolated from donor Fisher 344 rats, cultured and labeled in preparation for injection into recipient animals via a jugular vein. Using a model of chronic hindlimb ischemia in rats, we demonstrated that UM destruction of intravenous carrier microbubbles loaded with SDF-1 plasmid DNA resulted in targeted transfection of the vascular endothelium within ischemic muscle and greater local engraftment of EPCs. The combination of SDF-1gene therapy and EPCs lead to the greatest increase in tissue perfusion and microvascular density within ischemic muscle, compared to no treatment or either monotherapy alone. Our results demonstrate that UM transfection of SDF-1 improves EPC targeting to chronically ischemic tissue, enhancing vascular engraftment and leading to a more robust neovascularization response.
Subject(s)
Chemokine CXCL12/metabolism , Endothelial Cells/metabolism , Ischemia/therapy , Muscle, Skeletal/blood supply , Neovascularization, Physiologic , Stem Cells/metabolism , Animals , Cell Movement/genetics , Cells, Cultured , Chemokine CXCL12/genetics , Endothelium, Vascular/physiopathology , Genetic Therapy , Hindlimb/blood supply , Ischemia/genetics , Ischemia/metabolism , Ischemia/physiopathology , Rats , Rats, Inbred F344 , Transfection , TransplantsABSTRACT
BACKGROUND: Heart failure (HF) affects many patients who are older and frail, presenting multiple physical barriers to accessing specialty care in a traditional ambulatory clinic model. Here, we present an assisted virtual care model in which a home visiting nurse facilitated video visits with a HF cardiologist to follow homebound, frail, and older patients with HF. METHODS: This is a pragmatic, quasi-experimental, pre-post, single-centre study. It included homebound, frail, and older patients with HF from 2015 to 2019 who were followed for 1 year; in-person clinic visits were completely replaced by nurse-facilitated virtual video visits. Outcomes evaluated included annualized hospitalization rate, number of hospitalization days, and number of emergency department visits. RESULTS: A total of 49 patients were included, with a median age of 86 (83-93) years, and were followed for 1 year after enrollment. Among patients enrolled, HF with preserved ejection fraction was the most common subtype (57%). Compared to the year prior to enrollment, patients had a lower mortality-adjusted all-cause annualized hospitalization rate in the year following enrollment (2.57 vs 1.78, P < 0.0001). Compared to the year prior, the number of mortality-adjusted all-cause hospitalization days was significantly lower in the year following enrollment (27.2 vs 21.4, P < 0.0001). There was a reduction in the number of all-cause annualized emergency department visits (3.10 vs 2.27, PĀ = 0.003). CONCLUSIONS: Nurse-assisted virtual visits may be a preferable strategy for homebound, frail, and older patients with HF to receive longitudinal care. This approach may represent a plausible strategy to care for other patients with significant barriers to accessing specialized cardiac care.
CONTEXTE: L'insuffisance cardiaque (IC) touche de nombreux patients Ć¢gĆ©s et fragiles, et dresse maints obstacles physiques Ć l'accĆØs aux soins spĆ©cialisĆ©s au sein d'un modĆØle classique de soins cliniques ambulatoires. Dans le prĆ©sent article, nous exposons un modĆØle de soins virtuels assistĆ©s oĆ¹ une infirmiĆØre visiteuse assure par vidĆ©oconsultation, avec un cardiologue, le suivi de patients Ć¢gĆ©s et fragiles atteints d'IC confinĆ©s Ć la maison. MĆTHODOLOGIE: Une Ć©tude monocentrique et pragmatique, quasi expĆ©rimentale de type Ā« avant-aprĆØs Ā¼, a Ć©tĆ© menĆ©e de 2015 Ć 2019 auprĆØs de patients Ć¢gĆ©s et fragiles atteints d'IC confinĆ©s Ć la maison. Les patients ont Ć©tĆ© suivis durant un an; les consultations en personne ont Ć©tĆ© entiĆØrement remplacĆ©es par des vidĆ©oconsultations effectuĆ©es par une infirmiĆØre. Les paramĆØtres Ć©valuĆ©s comprenaient le taux annualisĆ© d'hospitalisation, le nombre de jours d'hospitalisation et le nombre de consultations aux urgences. RĆSULTATS: Au total, 49 patients dont l'Ć¢ge mĆ©dian Ć©tait de 86 ans (83-93 ans) ont Ć©tĆ© suivis durant un an Ć compter de leur admission Ć l'Ć©tude. L'IC Ć fraction d'Ć©jection prĆ©servĆ©e Ć©tait le sous-type d'IC le plus frĆ©quent (57 %) chez les patients participant Ć l'Ć©tude. Par comparaison Ć l'annĆ©e prĆ©cĆ©dente, le taux annualisĆ© d'hospitalisation toutes causes confondues ajustĆ© en fonction de la mortalitĆ© a Ć©tĆ© plus faible chez les patients au cours de l'annĆ©e oĆ¹ ils ont Ć©tĆ© suivis dans le cadre de l'Ć©tude (2,57 vs 1,78, P < 0,0001). Toujours par comparaison Ć l'annĆ©e prĆ©cĆ©dente, le nombre de jours d'hospitalisation toutes causes confondues ajustĆ© en fonction de la mortalitĆ© a Ć©tĆ© significativement infĆ©rieur chez les patients au cours de l'annĆ©e oĆ¹ ils ont Ć©tĆ© suivis dans le cadre de l'Ć©tude (27,2 vs 21,4, P < 0,0001). Le nombre annualisĆ© de consultations aux urgences toutes causes confondues a quant Ć lui diminuĆ© (3,10 vs 2,27, PĀ = 0,003). CONCLUSIONS: Les consultations virtuelles assistĆ©es par une infirmiĆØre peuvent constituer une stratĆ©gie Ć privilĆ©gier dans la prestation de soins longitudinaux Ć des patients Ć¢gĆ©s et fragiles atteints d'IC qui sont confinĆ©s Ć la maison. Cette approche pourrait reprĆ©senter une stratĆ©gie plausible pour prodiguer des soins Ć d'autres patients qui sont confrontĆ©s Ć d'importants obstacles limitant leur accĆØs Ć des soins spĆ©cialisĆ©s en cardiologie.
ABSTRACT
Background: Coronavirus disease 2019 (COVID-19) has resulted in a reduction in patients seeking timely consultation for illnesses that are not related to COVID-19. Previously, we reported a decline in the number of emergency department (ED) visits and hospitalizations for acute decompensated heart failure (ADHF) during the 2020 COVID-19 pandemic vs that in 2019. We aimed to determine the consequences of these early trends on ADHF-patient morbidity and mortality. Methods: We compared consecutive patients presenting with ADHF to 3 academic medical centres in Toronto, Canada from March 1-September 28, 2020, vs those from the same time period in 2019. We used multivariate logistic regression models to evaluate whether the odds of hospitalization after presenting to the ED, recurrent ED visits or readmission within 30 days, and in-hospital all-cause mortality differed by timeframe. Results: We observed that, during the COVID-19 pandemic, a lower total number of patients presented to the hospital with ADHF, vs that in 2019. Despite this difference, the probability of being admitted to the hospital did not differ for patients seen in 2020 vs 2019. Among ADHF patients admitted to the hospital, however, we observed a significantly higher proportion being admitted to the intensive care unit, and a relative 66% increase in in-hospital mortality during the 2020 COVID-19 era, compared to that inĀ 2019. Conclusions: Our findings suggest that improved messaging may be needed for patients living with chronic health conditions, including HF, during the pandemic, to educate and encourage them to present to hospital services when in need.
Contexte: La maladie Ć coronavirus 2019 (COVID-19) s'est traduite par une diminution du nombre de patients demandant des consultations mĆ©dicales pour des Ć©tats de santĆ© sans lien avec la COVID-19. Nous avons prĆ©cĆ©demment dĆ©crit une diminution du nombre de consultations aux urgences et d'hospitalisations en raison d'une insuffisanceĀ cardiaque aiguĆ« dĆ©compensĆ©e (ICAD) au cours de la pandĆ©mie de COVID-19 en 2020, par rapport Ć 2019. Nous avons voulu dĆ©terminer les consĆ©quences de ces tendances prĆ©coces sur la morbiditĆ© et la mortalitĆ© chez les patients atteints d'ICAD. MĆ©thodologie: Nous avons comparĆ© les donnĆ©es pour les patients consĆ©cutifs atteints d'ICAD de trois centres mĆ©dicaux hospitaliers de Toronto (Canada) traitĆ©s entre le 1er mars et le 28 septembre 2020 et durant la mĆŖme pĆ©riode en 2019. Ć l'aide de modĆØles de rĆ©gression logistique multivariĆ©e, nous avons Ć©valuĆ© les diffĆ©rences entre les probabilitĆ©s d'hospitalisation aprĆØs une consultation aux urgences, de consultations rĆ©currentes aux urgences ou de rĆ©admission dans les 30 jours suivant la visite initiale, ainsi que de mortalitĆ© hospitaliĆØre toutes causes confondues pour les patients vus durant ces deux pĆ©riodes. RĆ©sultats: Durant la pandĆ©mie de COVID-19, le nombre total de patients atteints d'ICAD s'Ć©tant prĆ©sentĆ©s Ć l'hĆ“pital a Ć©tĆ© plus faible que celui relevĆ© pour l'annĆ©e 2019. MalgrĆ© cet Ć©cart, la probabilitĆ© d'admission Ć l'hĆ“pital ne diffĆ©rait pas pour les patients vus en 2020 et en 2019. Parmi les patients atteints d'ICAD admis Ć l'hĆ“pital, nous avons toutefois observĆ© une proportion significativement plus Ć©levĆ©e de sĆ©jours aux soins intensifs et une hausse relative de 66 % du taux de mortalitĆ© hospitaliĆØre, en comparant les donnĆ©es de 2020 (pandĆ©mie de COVID-19) et celles deĀ 2019. Conclusions: Nos observations indiquent qu'il pourrait ĆŖtre nĆ©cessaire d'amĆ©liorer la communication avec les patients atteints de problĆØmes de santĆ© chroniques (y compris l'IC) en situation de pandĆ©mie de faƧon Ć mieux les informer et Ć les encourager Ć consulter les services hospitaliers lorsque nĆ©cessaire.
ABSTRACT
The Fontan circulation has inherent long-term vulnerabilities such that adult Fontan patients now comprise the largest, most rapidly growing subgroup of adult congenital heart disease referred for transplant assessment. Almost all have Fontan Associated Liver Disease (FALD). There is an absence of mid to late hepatic outcome data after heart transplant alone. Therefore, we analyzed outcomes of survivors of heart only transplant in patients with failing Fontan circulation. Including all 10 of our adult Fontan patients surviving >1 year after isolated heart transplant, we report evolution of their clinical features, bloodwork, hemodynamic data, and liver ultrasound findings over a median of 4.7 years. Nonprogression of FALD, resolution of ascites and freedom from hepatocellular carcinoma in the mid-term highlight the outcomes in this selected group once normal cardiac output and venous pressures are established by heart transplant.
Subject(s)
Fontan Procedure , Heart Defects, Congenital/surgery , Heart Transplantation , Liver Diseases/epidemiology , Postoperative Complications/epidemiology , Adult , Female , Humans , Male , Middle Aged , Retrospective Studies , Treatment Failure , Treatment OutcomeABSTRACT
Background: The COVID-19 pandemic has reduced access to endomyocardial biopsy (EMB) rejection surveillance in heart transplant (HT) recipients. This study is the first in Canada to assess the role for noninvasive rejection surveillance in personalizing titration of immunosuppression and patient satisfaction post-HT. Methods: In this mixed-methods prospective cohort study, adult HT recipients more than 6 months from HT had their routine EMBs replaced by noninvasive rejection surveillance with gene expression profiling (GEP) and donor-derived cell-free DNA (dd-cfDNA) testing. Demographics, outcomes of noninvasive surveillance score, hospital admissions, patient satisfaction, and health status on the medical outcomes study 12-item short-form health survey (SF-12) were collected and analyzed, using t tests and χ2 tests. Thematic qualitative analysis was performed for open-ended responses. Results: Among 90 patients, 31 (33%) were enrolled. A total of 36 combined GEP/dd-cfDNA tests were performed; 22 (61%) had negative results for both, 10 (27%) had positive GEP/negative dd-cfDNA results, 4 (11%) had negative GEP/positive dd-cfDNA results, and 0 were positive on both. All patients with a positive dd-cfDNA result (range: 0.19%-0.81%) underwent EMB with no significant cellular or antibody-mediated rejection. A total of 15 cases (42%) had immunosuppression reduction, and this increased to 55% in patients with negative concordant testing. Overall, patients' reported satisfaction was 90%, and on thematic analysis they were more satisfied, with less anxiety, during the noninvasive testing experience. Conclusions: Noninvasive rejection surveillance was associated with the ability to lower immunosuppression, increase satisfaction, and reduce anxiety in HT recipients, minimizing exposure for patients and providers during a global pandemic.
Contexte: La pandĆ©mie de COVID-19 a rĆ©duit l'accĆØs Ć la biopsie endomyocardique pour surveiller le risque de rejet aprĆØs une greffe du cĆ Āur. Cette Ć©tude est la premiĆØre Ć ĆŖtre menĆ©e au Canada pour Ć©valuer le rĆ“le de la surveillance non invasive du risque de rejet en personnalisant le titrage de l'immunosuppression et la satisfaction du patient aprĆØs la greffe cardiaque. MĆ©thodologie: Dans le cadre de cette Ć©tude de cohorte prospective Ć mĆ©thodes mixtes, des adultes ayant reƧu une greffe cardiaque depuis plus de six mois ont vu leurs biopsies endomyocardiques rĆ©guliĆØres remplacĆ©es par une surveillance non invasive du risque de rejet qui consiste Ć Ć©tablir le profil de l'expression gĆ©nique et Ć analyser l'ADN acellulaire dĆ©rivĆ© du donneur. Les donnĆ©es dĆ©mographiques, les rĆ©sultats du score de surveillance non invasive, les admissions Ć l'hĆ“pital, la satisfaction des patients et l'Ć©tat de santĆ© tirĆ©s du questionnaire SF-12 (questionnaire abrĆ©gĆ© sur la santĆ© comprenant 12 items) de l'Ć©tude sur les issues mĆ©dicales ont Ć©tĆ© colligĆ©s et analysĆ©s au moyen des tests T et des tests χ2. Les rĆ©ponses ouvertes ont fait l'objet d'une analyse qualitative thĆ©matique. RĆ©sultats: Parmi 90 patients, 31 (33 %) ont Ć©tĆ© recrutĆ©s. Au total, 36 tests combinĆ©s de profilages de l'expression gĆ©nique et d'ADN acellulaire dĆ©rivĆ© du donneur ont Ć©tĆ© rĆ©alisĆ©s; les rĆ©sultats ont Ć©tĆ© nĆ©gatifs pour les deux tests dans 22 cas (61 %), positifs pour le profilage deĀ l'expression gĆ©nique et nĆ©gatifs pour l'ADN acellulaire dans 10 cas (27Ā %), nĆ©gatifs pour le profilage de l'expression gĆ©nique et positifs pour l'ADN acellulaire dans quatre cas (11 %) et aucun cas n'a donnĆ© de rĆ©sultats positifs pour les deux types de tests. Tous les patients qui ont donnĆ© des rĆ©sultats positifs Ć l'analyse de l'ADN acellulaire dĆ©rivĆ© du donneur (fourchette : 0,19 % Ć 0,81 %) ont subi une biopsie endomyocardique n'ayant rĆ©vĆ©lĆ© aucun rejet cellulaire ou Ć mĆ©diation par anticorps important. Au total, 15 cas (42 %) affichaient une immunosuppression rĆ©duite, proportion qui a grimpĆ© Ć 55 % chez les patients dont les tests de concordance ont donnĆ© des rĆ©sultats nĆ©gatifs. Dans l'ensemble, le niveau de satisfaction rapportĆ© par les patients Ć©tait de 90 % et, Ć l'analyse thĆ©matique, ils Ć©taient plus satisfaits et moins anxieux pendant les tests non invasifs. Conclusions: La surveillance non invasive du risque de rejet a Ć©tĆ© associĆ©e Ć la capacitĆ© de diminuer l'immunosuppression, d'augmenter la satisfaction et de rĆ©duire l'anxiĆ©tĆ© chez les patients qui ont reƧu une greffe cardiaque, en plus de rĆ©duire l'exposition des patients et du personnel mĆ©dical dans le contexte d'une pandĆ©mie.
ABSTRACT
INTRODUCTION: Heart failure (HF) symptoms improve through self-care, for which adherence remains low among patients despite the provision of education for these behaviours by clinical teams. Open Access Digital Community Promoting Self-Care, Peer Support and Health Literacy (ODYSSEE-vCHAT) combines automated digital counselling with social network support to improve mortality and morbidity, engagement with self-care materials, and health-related quality of life. METHODS AND ANALYSIS: Use of ODYSSEE-vCHAT via Internet-connected personal computer by 162 HF patients will be compared with a control condition over 22 months. The primary outcome is a composite index score of all-cause mortality, all-cause emergency department visits, and HF-related hospitalisation at trial completion. Secondary outcomes include individual components of the composite index, engagement with self-care materials, and patient-reported measures of physical and psychosocial well-being, disease management, health literacy, and substance use. Patients are recruited from tertiary care hospitals in Toronto, Canada and randomised on a 1:1 ratio to both arms of the trial. Online assessments occur at baseline (t=0), months 4, 8 and 12, and trial completion. Ordinal logistic regression analyses and generalised linear models will evaluate primary and secondary outcomes. ETHICS AND DISSEMINATION: The trial has been approved by the research ethics boards at the University Health Network (20-5960), Sunnybrook Hospital (5117), and Mount Sinai Hospital (21-022-E). Informed consent of eligible patients occurs in person or online. Findings will be shared with key stakeholders and the public. Results will allow for the preparation of a Canada-wide phase III trial to evaluate the efficacy of ODYSSEE-vCHAT in improving clinical outcomes and raising the standard of outpatient care. TRIAL REGISTRATION NUMBER: NCT04966104.
Subject(s)
Heart Diseases , Heart Failure , Humans , Quality of Life , Counseling , Social Networking , Randomized Controlled Trials as TopicABSTRACT
BACKGROUND: There is a complex relationship between heart failure (HF) clinic services and health outcomes. We hypothesized that ambulatory clinic activity may be associated with both hospital admission and also with avoidance of admission. METHODS: A retrospective comparative cohort study was conducted examining activity in an ambulatory HF Clinic. Consecutive clinic visits in 2013 were recorded (nĀ = 1728) and periods of high-intensity utilization (HIU) were identified (nĀ = 128). A HIU period was defined by ≥2 consecutive clinic visits within 30 days, ending after 30 days passed without an additional clinic visit. For each HIU period identified, patient characteristics (nĀ = 107) and all clinic visits (nĀ = 324) were examined. HIU periods were then classified by association with hospital admission (Ā±30 days). RESULTS: In 2013, 18.8% of all clinic visits occurred during HIU periods, involving 13.7% of the clinic population. Thirty-eight percent of HIU periods were associated with 62 total hospital admissions (Ā±30 days), of which 58% (nĀ = 36) were for a primary diagnosis of HF. In addition,17 HIU periods met criteria for admission avoided, and 7 HIU periods occurring after hospital discharge also met criteria for admission avoided. CONCLUSIONS: We identified periods of intensive ambulatory clinic activity dedicated to patients with high burdens of comorbidities and both HF and non-HF-related admissions. These periods were also associated with episodes of successful decongestion with oral diuretics, resulting in avoidance of admission. Identifying HF patients who can be treated successfully or who are likely to require admission may be helpful for allocating clinic resources.
CONTEXTE: Il existe un lien complexe entre les services cliniques relatifs Ć l'insuffisance cardiaque (IC) et les rĆ©sultats liĆ©s Ć la santĆ©. Nous avons posĆ© l'hypothĆØse que l'activitĆ© dans les unitĆ©s de soinsĀ ambulatoires pourrait avoir une influence Ć la fois sur les hospitalisations et sur l'Ć©vitement des hospitalisations. MĆTHODOLOGIE: Une Ć©tude de cohorte comparative rĆ©trospective a Ć©tĆ© menĆ©e afin d'examiner l'activitĆ© dans une unitĆ© de soins ambulatoires auprĆØs de patients atteints d'IC. Les visites consĆ©cutives effectuĆ©es Ć l'unitĆ© de soins en 2013 ont Ć©tĆ© compilĆ©es (nĀ = 1728) et les pĆ©riodes d'utilisation intensive des services (UIS) ont Ć©tĆ© relevĆ©es (nĀ = 128). Une pĆ©riode d'UIS Ć©tait dĆ©finie par au moins 2 visites consĆ©cutives Ć l'unitĆ© de soins ambulatoires en l'espace de 30 jours; la pĆ©riode Ć©tait considĆ©rĆ©e comme terminĆ©e aprĆØs 30 jours sans nouvelle visite. Pour chaque pĆ©riode d'UIS relevĆ©e, les caractĆ©ristiques des patients (nĀ = 107) et toutes les visites Ć l'unitĆ© de soins (nĀ = 324) ont Ć©tĆ© examinĆ©es. Les pĆ©riodes d'UIS ont ensuite Ć©tĆ© classĆ©es en fonction de leur association avec une hospitalisation (Ā± 30 jours). RĆSULTATS: En 2013, 18,8 % de toutes les visites Ć l'unitĆ© de soins ambulatoires Ć©taient rattachĆ©es Ć une pĆ©riode d'UIS et concernaient 13,7 % des patients de l'unitĆ©. Au total, 38 % des pĆ©riodes d'UIS ont Ć©tĆ© associĆ©es Ć 62 hospitalisations (Ā± 30 jours), dont 58 % (nĀ = 36) Ć©taient liĆ©es Ć un diagnostic primaire d'IC. En outre, 17 pĆ©riodes d'UIS rĆ©pondaient aux critĆØres dĆ©finissant une hospitalisation Ć©vitĆ©e, et 7 pĆ©riodes d'UIS survenues aprĆØs que le patient soit sorti de l'hĆ“pital rĆ©pondaient aussi aux critĆØres dĆ©finissant une hospitalisation Ć©vitĆ©e. CONCLUSIONS: Nous avons relevĆ© des pĆ©riodes d'activitĆ© intensive de l'unitĆ© de soins ambulatoires consacrĆ©es Ć des patients prĆ©sentant un lourd fardeau de comorbiditĆ©, ainsi que les hospitalisations liĆ©es Ć l'IC et non liĆ©es Ć l'IC. Ces pĆ©riodes Ć©taient aussi associĆ©es Ć des Ć©pisodes de congestion soulagĆ©e grĆ¢ce Ć des diurĆ©tiques oraux, ce qui a permis d'Ć©viter des hospitalisations. Le repĆ©rage des patients atteints d'IC qui peuvent ĆŖtre traitĆ©s efficacement en consultation externe et de ceux qui risquent de devoir ĆŖtre hospitalisĆ©s pourrait permettre d'optimiser l'affectation des ressources des unitĆ©s de soins.
ABSTRACT
Coronavirus disease 2019 (COVID-19) has resulted in public health measures and health care reconfigurations likely to have impact on chronic disease care. We aimed to assess the volume and characteristics of patients presenting to hospitals with acute decompensated heart failure (ADHF) during the 2020 COVID-19 pandemic compared with a time-matched 2019 cohort. Patients presenting to hospitals with ADHF from March 1, to April 19, 2020 and 2019 in an urban hospital were examined. Multivariable logistic-regression models were used to evaluate the difference in probability of ADHF-related hospitalization between the 2 years. During the COVID-19 pandemic, a total of 1106 emergency department (ED) visits for dyspnea or peripheral edema were recorded, compared with 800 ED visits in 2019. A decrease in ADHF-related ED visits of 43.5% (14.8%-79.4%, PĀ = 0.002) and ADHF-related admissions of 39.3% (8.6%-78.5%, PĀ = 0.009) was observed compared with 2019. Patients with ADHF presenting to hospitals (nĀ = 128) were similar in age, sex, and comorbidities compared with the 2019 cohort (nĀ = 186); however, a higher proportion had recent diagnoses of heart failure. Upon ED presentation, the relative probability of hospitalization or admission to intensive care was not statistically different. There was a trend toward higher in-hospital mortality in 2020. The decline in ADHF-related hospitalizations raises the timely question of how patients with heart failure are managing beyond the acute-care setting and reinforces the need for public education on the availability and safety of emergency services throughout the COVID-19 pandemic.
Subject(s)
Betacoronavirus , Coronavirus Infections/epidemiology , Emergency Service, Hospital/statistics & numerical data , Heart Failure/epidemiology , Pandemics/statistics & numerical data , Patient Admission/statistics & numerical data , Pneumonia, Viral/epidemiology , COVID-19 , Hospitalization/statistics & numerical data , Hospitals/statistics & numerical data , Humans , Ontario/epidemiology , SARS-CoV-2 , Urban Population/statistics & numerical dataABSTRACT
BACKGROUND: Patients with heart failure (HF) are at the highest risk for hospital readmissions during the first few weeks after discharge when patients are transitioning from hospital to home. Telemonitoring (TM) for HF management has been found to reduce mortality risk and hospital readmissions if implemented appropriately; however, the impact of TM targeted for patients recently discharged from hospital, for whom TM might have the biggest benefit, is still unknown. Medly, a mobile phone-based TM system that is currently being used as a standard of care for HF at a large Canadian hospital, may be an effective tool for the management of HF in patients recently discharged from hospital. OBJECTIVE: The objective of the Medly-After an Incidence of acute Decompensation (Medly-AID) trial is to determine the effect of Medly on the self-care and quality of life of patients with HF who have been recently discharged from hospital after an HF-related decompensation. METHODS: A multisite multimethod randomized controlled trial (RCT) will be conducted at 2 academic hospitals and at least one community hospital to evaluate the impact of Medly-enabled HF management on the outcomes of patients with HF who had been hospitalized for HF-related decompensation and discharged during the 2 weeks before recruitment. The trial will include 144 participants with HF (74 in each control and intervention groups). Control patients will receive standard of care, whereas patients in the intervention group will receive standard of care and Medly. Specifically, patients in the intervention group will record daily weight, blood pressure, and heart rate and answer symptom-related questions via the Medly app. Medly will generate automated patient self-care messages such as to adjust diuretic medications, based on the rules-based algorithm personalized to the individual patient, and send real-time alerts to their health care providers as necessary. All patients will be followed for 3 months. Primary outcome measures are self-care and quality of life as measured through the validated questionnaires Self-Care of Heart Failure Index, EQ-5D-5L, and the Kansas City Cardiomyopathy Questionnaire-12. Secondary outcome measures for this study include cost of health care services used and health outcomes. RESULTS: Patient recruitment began in November 2018 at the Sunnybrook Health Sciences Centre, with a total of 35 participants recruited by July 30, 2019 (17 in the intervention group and 18 in the control group). The final analysis is expected to occur in the fall of 2020. CONCLUSIONS: This RCT will be the first to assess the effectiveness of the Medly TM system for use following discharge from hospital after a HF-related decompensation. TRIAL REGISTRATION: ClinicalTrials.gov NCT03358303; https://clinicaltrials.gov/ct2/show/NCT03358303. INTERNATIONAL REGISTERED REPORT IDENTIFIER (IRRID): DERR1-10.2196/15753.
ABSTRACT
Ethnic disparities in cardiovascular outcomes have been increasingly recognized in the medical literature. In a recent paper in this journal, Peled et al. provide evidence that Arab Israelis may have worse outcome after cardiac transplant than their Jewish counterparts. This commentary explores possible explanations for the differing outcomes and suggests potential solutions that may improve outcomes for cardiac transplant recipients regardless of ethnicity.
Subject(s)
Heart Transplantation , Arabs , Humans , Israel , Jews , White PeopleABSTRACT
Over the past few decades, left ventricular assist device (LVAD) support has extended the lives of many patients with end-stage heart failure. The most common devices are continuous-flow (CF) LVADs. The use of the CF-LVADs has required that clinicians learn the physiological and clinical consequences of long-term continuous blood flow. While this alteration in the normal physiology still offers advantages from mechanical circulatory support, the lack of pulsatility may also increase the likelihood of adverse events. However, it is currently unknown whether newly evolved devices should incorporate pulsatility. In this article, we discuss the possible benefits of incorporating pulsatility, while maintaining the benefits of the CF-LVAD, to maximize the treatment of patients.
Subject(s)
Heart Failure/therapy , Heart-Assist Devices , Hemodynamics/physiology , Ventricular Function, Left/physiology , Heart Failure/physiopathology , HumansABSTRACT
Quality improvement (QI) initiatives have become an integral part of patient-centered care. In this primer, we outline 6 steps for initiating, implementing, and monitoring improvement in heart failure care. These steps include acknowledging that improvement is needed and setting a culture for improvement; forming a QI team; understanding the local problem; generating improvement strategies that will fit with the local problem; monitoring; testing; and refining improvements, analysis of data, and interpretation of run charts. This primer provides tools and resources for clinicians who want to learn how to perform QI specifically in the field of heart failure. We will illustrate the application of these steps using a hypothetical example for a congestive heart failure postdischarge clinic.
Subject(s)
Clinical Competence , Delivery of Health Care/standards , Heart Failure/therapy , Physicians/standards , Quality Improvement , HumansABSTRACT
Over the past 5 years, researchers have examined the utility of many experimental heart failure biomarkers that are not yet widely adopted clinically, to complement the role of B-type natriuretic peptide and its precursor. Candidate biomarkers have been identified from several different pathophysiologic categories, including markers of inflammation, myocyte necrosis, renal dysfunction, neurohumoral activation, oxidative stress and raised intracardiac pressure. Indeed, some biomarkers provide prognostic information that is independent of information obtained from conventional clinical and biomarker assessment. Moreover, some biomarkers studied help to identify dominant pathology that may predict responsiveness to specific therapies. Preliminary data also suggest a potential role for the development of comprehensive biomarker profiling models, integrating biomarkers from several categories to refine risk assessment.
Subject(s)
Heart Failure/metabolism , Animals , Biomarkers/blood , Biomarkers/metabolism , Heart Failure/immunology , Heart Failure/pathology , Heart Failure/physiopathology , Humans , Myocytes, Cardiac/immunology , Myocytes, Cardiac/metabolism , Myocytes, Cardiac/pathology , Necrosis , Oxidative Stress , Renal Insufficiency/etiology , Ventricular Dysfunction/etiology , Ventricular Pressure , Ventricular RemodelingABSTRACT
OBJECTIVES: This study was designed to compare the efficacy of angiogenic gene delivery by ultrasound-mediated (UM) destruction of intravenous carrier microbubbles to direct intramuscular (IM) injections. BACKGROUND: Current trials of gene therapy for angiogenesis remain limited by suboptimal, invasive delivery techniques. METHODS: Hind-limb ischemia was produced by iliac artery ligation in 99 rats. In 32 rats, UM delivery of green fluorescent protein (GFP)/vascular endothelial growth factor-165 (VEGF(165)) plasmid deoxyribonucleic acid was performed. Thirty-five animals received IM injections of VEGF(165)/GFP plasmid. Remaining rats received no treatment. Before delivery (day 14 after ligation) and at days 17, 21, and 28 and week 8 after ligation, microvascular blood volume and microvascular blood flow to the proximal hind limbs were assessed by contrast-enhanced ultrasound (n = 8 per group). Total transfection was assessed by reverse transcriptase-polymerase chain reaction, and localization of transfection was determined by immunohistochemistry. RESULTS: By day 28, both IM and UM delivery of VEGF(165) produced significant increases in microvascular blood volume and microvascular blood flow. Whereas increases in microvascular blood volume were similar between treatment groups, microvascular blood flow was greater (p < 0.005) in UM-treated animals as compared with IM-treated animals, persisting to week 8. The VEGF(165)/GFP messenger ribonucleic acid expression was greater (p < 0.05) for IM-treated animals. A strong GFP signal was detected for both groups and was localized to focal perivascular regions and myocytes around injection sites for IM and to the vascular endothelium of arterioles/capillaries in a wider distribution for UM delivery. CONCLUSIONS: Despite lower transfection levels, UM delivery of VEGF(165) is as effective as IM injections. The UM delivery results in directed vascular transfection over a wider distribution, which may account for the more efficient angiogenesis.
Subject(s)
Gene Transfer Techniques , Genetic Therapy/methods , Neovascularization, Pathologic/therapy , Vascular Endothelial Growth Factor A/administration & dosage , Animals , Disease Models, Animal , Hindlimb/blood supply , Immunohistochemistry , Injections, Intramuscular , Ischemia/diagnostic imaging , Ischemia/drug therapy , Ischemia/pathology , Microbubbles , Microcirculation/drug effects , Neovascularization, Pathologic/diagnostic imaging , Rats , Rats, Sprague-Dawley , Transfection , UltrasonographyABSTRACT
A 48-year-old female hemodialysis patient with gram-positive mitral endocarditis developed progressive hemodynamic collapse. Echocardiography revealed a mitral annular abscess, which expanded rapidly due to connection with and pressure from the left ventricle. The mitral annular abscess had enlarged sufficiently to obstruct the mitral orifice, resulting in acute cardiogenic shock. The patient underwent and survived emergency surgical repair, and remained well on follow-up.