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1.
World J Pediatr Congenit Heart Surg ; 11(4): NP34-NP36, 2020 Jul.
Article in English | MEDLINE | ID: mdl-28673108

ABSTRACT

Transcatheter pulmonary valve placement is emerging as a standard therapy for dysfunctional right ventricular outflow tract conduits. The Melody transcatheter pulmonary valve is indicated for use in the management of pediatric and adult patients with right ventricular outflow tract conduits measuring at least 16 mm in diameter. This is the first reported case of placement in a patient with a left ventricular assist device. We outline the preprocedural evaluation process, the procedural methods, and the outcomes of a successful implantation in a complex patient. With a team-based approach including thoughtful preprocedural evaluation, and close monitoring, successful deployment of a transcatheter pulmonary valve is possible in complex patients in the setting of mechanical circulatory support.


Subject(s)
Cardiac Catheterization/methods , Heart Valve Prosthesis Implantation/methods , Heart Valve Prosthesis , Heart-Assist Devices , Pulmonary Valve Insufficiency/therapy , Pulmonary Valve/surgery , Adult , Echocardiography, Transesophageal , Female , Fluoroscopy , Humans , Pulmonary Valve/diagnostic imaging , Pulmonary Valve Insufficiency/diagnosis
2.
J Pain Symptom Manage ; 57(2): 330-340.e4, 2019 02.
Article in English | MEDLINE | ID: mdl-30447385

ABSTRACT

CONTEXT: Destination therapy (DT) patients face significant challenges as they transition from chronic left ventricular assist device (LVAD) support to comfort-oriented care. Integration of palliative medicine (PM) into the multidisciplinary team is important to facilitate advanced care planning (ACP) and improve quality of life (QoL). OBJECTIVES: We evaluated the impact of a structured programmatic approach to the end-of-life (EOL) process in DT patients as measured by QoL surveys and the utilization of ACP. METHODS: We instituted a four prong intervention approach: 1) delineated the path from implant to EOL by defining specific stages, including a transitional phase where care limits were agreed upon, 2) standardized the role of PM, 3) held transitional care meetings to support shared decision-making, and 4) held multidisciplinary team debriefings to facilitate communication. Preintervention and postintervention outcomes were measured for patients/caregivers by using the QUAL-E/QUAL-E (family) QoL instrument. Wilcoxon signed-ranks test compared nonparametric variables. RESULTS: All patients (n = 41)/caregivers (n = 28) reported improved QoL measures (patient P = 0.035/caregiver P = 0.046). Preparedness plans increased from 52% to 73% after implementation and advance directives increased from 71% to 83%. Fifty-nine percent of the patients completed an outpatient PM clinic visit; 51% completed/scheduled a second visit. Clinician outcomes improved including satisfaction with multidisciplinary team communication/expectations, ACP processes, and EOL management. CONCLUSION: A programmatic approach that standardizes the role of PM and delineates the patient's path from implant to EOL improved quality outcomes and increased implementation of ACP. A defined communication process allowed the multidisciplinary team to have a clear patient management approach.


Subject(s)
Palliative Care/standards , Terminal Care/standards , Advance Care Planning , Advance Directives , Aged , Aged, 80 and over , Caregivers , Female , Heart Failure/therapy , Heart-Assist Devices , Humans , Male , Middle Aged , Palliative Care/methods , Patient Care Team , Patients , Quality of Life , Terminal Care/methods
3.
ASAIO J ; 64(6): e161-e165, 2018.
Article in English | MEDLINE | ID: mdl-30199385

ABSTRACT

International normalized ratio (INR) measurements manage risks of bleeding and clotting sequelae in the population with left ventricular assist device (LVAD). Studies suggest that point-of-care (POC) INR does not significantly differ from plasma INR (P-INR) values in other patient populations, although this has not been validated in a multicenter LVAD study. We sought to determine whether POC-INR and P-INR values differ significantly in the LVAD population and reviewed patients with permanent LVAD implantation at seven institutions internationally. Our cohort comprised of 279 paired POC-INR and P-INR checks in patients supported on average 630 ± 598 days postimplant with predominately HeartWare, HeartMate II, and HeartMate III devices. The population averaged 57.9 years of age, and there were 86.7% male. We found no statistically significant difference between POC-INR and P-INR values. International normalized ratio accuracy correlated weakly with the time between INR measurements (p < 0.001). When the time difference was less than 4 hours, the difference between INR pairs was significantly lower than measurements greater than 8 hours (p = 0.006). There was no statistically significant difference when comparing paired INR values and time after implant to INR check (p = 0.43), age (p = 0.12), known coagulopathy (p = 0.12), bleeding history (p = 0.22), or thrombosis history (p = 0.34). This is the first large multicenter international study comparing POC-INR and P-INR measurements in patients with LVAD and found no statistically significant difference between either methods, particularly when measured within less than 4 hours of each other.


Subject(s)
Heart-Assist Devices/adverse effects , International Normalized Ratio/methods , Point-of-Care Systems , Aged , Cohort Studies , Female , Humans , Male , Middle Aged , Thrombosis/prevention & control
4.
Clin Infect Dis ; 64(2): 222-228, 2017 Jan 15.
Article in English | MEDLINE | ID: mdl-27986679

ABSTRACT

There are currently no guidelines for the management of infection and its prevention in mechanical circulatory support (MCS) device recipients. The International Society of Heart and Lung Transplantation (ISHLT) has initiated a multidisciplinary collaboration for the creation of a consensus document to guide clinicians in infection prevention and management in MCS patients. Most medical centers use local protocols that are based on expert opinion. MCS recipients are debilitated and have some immunological dysfunction. Over the years there have been technical advancements with smaller devices and drivelines with improved durability. The pulsatile devices have been replaced with newer-generation continuous-flow devices. Patient are living longer with MCSs for bridge to transplant (BTT) and destination therapy (DT). MCS centers have improved patient management by introducing standardized driveline protocols, leading to reduced infection rates among MCS recipients.


Subject(s)
Heart-Assist Devices/adverse effects , Prosthesis-Related Infections/etiology , Prosthesis-Related Infections/prevention & control , Antibiotic Prophylaxis , Combined Modality Therapy , Disease Management , Heart-Assist Devices/classification , Humans , Infection Control , Prophylactic Surgical Procedures , Prosthesis-Related Infections/diagnosis , Prosthesis-Related Infections/epidemiology , Risk Factors
5.
Surg Innov ; 23(5): 469-73, 2016 Oct.
Article in English | MEDLINE | ID: mdl-26839214

ABSTRACT

Objectives Increasing number of mechanical circulatory assist devices (MCADs) are being placed in heart failure patients. Morbidity from device placement is high and the outcome of patients who require noncardiac surgery after, is unclear. As laparoscopic interventions are associated with decreased morbidity, we examined the impact of such procedures in these patients. Methods A retrospective review was conducted on 302 patients who underwent MCAD placement from 2005 to 2012. All laparoscopic abdominal surgeries were included and impact on postoperative morbidity and mortality studied. Results Ten out of 16 procedures were laparoscopic with 1 conversion to open. Seven patients had a HeartMate II, 2 had Total Artificial Hearts, and 1 had CentriMag. Four patients had devices for ischemic cardiomyopathy and 6 cases were emergent. Surgeries included 6 laparoscopic cholecystectomies, 2 exploratory laparoscopies, 1 laparoscopic colostomy takedown, and 1 laparoscopic ventral hernia repair with mesh. Median age of the patients was 63 years (range, 29-79 years). Median operative time was 123 minutes (range, 30-380 minutes). Five of 10 patients were on preoperative anticoagulation with average intraoperative blood loss of 150 mL (range, 20-700 mL). There were 3 postoperative complications; acute respiratory failure, acute kidney injury and multisystem organ failure resulting in death not related to the surgical procedure. Conclusion The need for noncardiac surgery in post-MCAD patients is increasing due to limited donors and due to more durable and longer support from newer generation assist devices. While surgery should be approached with caution in this high-risk group, laparoscopic surgery appears to be a safe and successful treatment option.


Subject(s)
Abdomen/surgery , Digestive System Surgical Procedures/methods , Heart-Assist Devices , Laparoscopy/methods , Patient Safety , Adult , Aged , Cohort Studies , Digestive System Surgical Procedures/adverse effects , Feasibility Studies , Female , Follow-Up Studies , Humans , Laparoscopy/adverse effects , Length of Stay , Male , Middle Aged , Postoperative Complications/epidemiology , Postoperative Complications/physiopathology , Retrospective Studies , Risk Assessment , Treatment Outcome
6.
Curr Diab Rep ; 15(10): 76, 2015 Oct.
Article in English | MEDLINE | ID: mdl-26294335

ABSTRACT

Approximately 366 million people worldwide have been diagnosed with type-2 diabetes (T2D). Chronic insulin resistance, decreased functional ß-cell mass, and elevated blood glucose are defining characteristics of T2D. Great advances have been made in understanding the pathogenesis of T2D with respect to the effects of dietary macronutrient composition and energy intake on ß-cell physiology and glucose homeostasis. It has been further established that obesity is a leading pathogenic factor for developing insulin resistance. However, insulin resistance may not progress to T2D unless ß-cells are unable to secret an adequate amount of insulin to compensate for decreased insulin sensitivity. Therefore, pancreatic ß-cell dysfunction plays an important role in the development of overt diabetes. This paper reviews recent research findings on the effects of several micronutrients (zinc, vitamin D, iron, vitamin A), leucine, and the phytochemical, genistein on pancreatic ß-cell physiology with emphasis on their effects on insulin secretion, specifically in the context of T2D.


Subject(s)
Diet , Insulin-Secreting Cells , Insulin/metabolism , Nutritional Status , Animals , Diabetes Mellitus, Type 2/metabolism , Diabetes Mellitus, Type 2/physiopathology , Humans , Insulin Secretion , Insulin-Secreting Cells/drug effects , Insulin-Secreting Cells/metabolism , Iron/blood , Vitamin A/blood , Vitamin D/blood , Zinc/blood
7.
Innovations (Phila) ; 10(3): 188-94, 2015.
Article in English | MEDLINE | ID: mdl-26181585

ABSTRACT

OBJECTIVE: The portable Freedom Drive (SynCardia Inc, Tucson, AZ USA) for total artificial heart (TAH-t) support was approved for an investigational device exemption study in March 2010. We review our center's experience with the portable driver. METHODS: A retrospective review was conducted of patients who underwent TAH-t implantation and transfer to portable driver from September 2008 to June 2012, with follow-up through December 2012. RESULTS: A total of 30 patients underwent TAH-t implantation during this time period, with 11 patients successfully transferred to the Freedom Driver. Transfer to Freedom Driver after TAH-t implant was a median of 46 days (range, 225-86 days). Ninety-one percent (10) of 11 patients transferred to Freedom Driver were bridged to transplantation. One patient died on support. Five (45.5%) of 11 patients were discharged home and 5 (45.5%) remained in-patient on the portable driver before transplantation. Four patients (80%) successfully discharged home required at least 1 hospital readmission (range, 1-5 admissions per patient). Six patients (55%) transferred to the portable driver required a return to a main driver console. Two patients were temporarily maintained on the main driver then returned to the Freedom Driver for bridge to transplantation. CONCLUSIONS: Patients with TAH-t can be considered for transfer to the portable Freedom Driver while awaiting transplantation. Issues that complicated this patient population included inadequate social support, hemodynamic instability, and concurrent morbidities. The potential benefits of the portable driver are currently undergoing assessment. These may include increased mobility and improved quality of life, opportunity for discharge home, and decreased overall medical costs.


Subject(s)
Heart Transplantation/instrumentation , Heart, Artificial , Adult , Aged , Cardiomyopathies/surgery , Female , Heart Failure/surgery , Humans , Male , Middle Aged , Patient Discharge/economics , Patient Discharge/statistics & numerical data , Quality of Life , Retrospective Studies , Treatment Outcome
9.
J Heart Lung Transplant ; 30(6): 618-23, 2011 Jun.
Article in English | MEDLINE | ID: mdl-21239189

ABSTRACT

Emergent mechanical support with transfer of patients in acute cardiopulmonary shock to specialty centers for definitive management is often required at non-transplant centers. An alternative approach to the traditional "hub and spoke" model is presented. A team of health care specialists from our hospital is deployed to the community hospital for stabilization, possible implantation, and transfer of patients to our tertiary care facility. Patient assessment can be made with intervention, allowing stabilization and safe transfer by our team to our institution. This method provides tertiary level care at the referring hospital and may improve survival for a sub-set of patients in the community hospital setting.


Subject(s)
Heart-Assist Devices , Patient Care Team/organization & administration , Patient Transfer/organization & administration , Respiratory Distress Syndrome/therapy , Shock, Cardiogenic/therapy , Adolescent , Adult , Aged , Extracorporeal Membrane Oxygenation , Female , Hospitals, Community , Humans , Male , Middle Aged , Outcome and Process Assessment, Health Care , Referral and Consultation , Young Adult
10.
Prog Transplant ; 20(2): 118-24, 2010 Jun.
Article in English | MEDLINE | ID: mdl-20642168

ABSTRACT

OBJECTIVE: Patients in acute cardiogenic shock are the most challenging patients to manage. Unless a mechanical circulatory assist device is placed, maintaining end-organ function can be difficult. Transporting cardiogenic shock patients to tertiary care centers for higher level care also is difficult. The Mayo Clinic Arizona uses a SWAT team approach to deploy a specialized medical or surgical multidisciplinary team to implant mechanical circulatory assist devices at referring hospitals and transport patients back to Mayo Clinic Arizona. RESULTS: The cardiac transport team at Mayo Clinic Arizona got 23 referrals from 15 local community hospitals from February 2006 to September 2009. The medical team deployed for transfers of 6 patients, 3 of whom survived to hospital discharge. The surgical transport team deployed for transfers of 17 patients (6 with left ventricular assist devices, 2 with right ventricular assist devices, 5 with biventricular assist devices, and 4 with extracorporeal membrane oxygenation), of whom 8 survived to hospital discharge. Ten of the 17 referrals (59%) required a surgeon to place a mechanical circulatory assist device at the referring hospital. CONCLUSION: The SWAT team approach allows cardiogenic shock patients to be stabilized at the referring hospital by heart failure and cardiac surgical specialists. If necessary, a surgeon from Mayo Clinic Arizona places a mechanical circulatory assist device at the referring hospital to stabilize the patient. Doing so allows safe transport back to the tertiary care center for higher level care and possible transplant evaluation with placement of a long-term durable device.


Subject(s)
Heart-Assist Devices , Patient Care Team/organization & administration , Patient Transfer/organization & administration , Shock, Cardiogenic/surgery , Transportation of Patients/organization & administration , Arizona , Humans
11.
Ann Thorac Surg ; 88(4): 1324-6, 2009 Oct.
Article in English | MEDLINE | ID: mdl-19766830

ABSTRACT

End-stage renal failure is often considered a relative contraindication for total artificial heart implantation due to the increased risk of mortality after transplantation. We report the successful treatment of a patient having heart and renal failure with the CardioWest (SynCardia Inc, Tucson, AZ) total artificial heart for bridge-to-cardiac transplantation of a heart and kidney.


Subject(s)
Heart Failure/surgery , Heart Transplantation/methods , Heart, Artificial , Kidney Failure, Chronic/surgery , Kidney Transplantation/methods , Follow-Up Studies , Heart Failure/complications , Humans , Kidney Failure, Chronic/complications , Male , Middle Aged , Prosthesis Design
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