The Road to Destination Therapy: Optimizing Long-Term Mechanical Cardiopulmonary Support for Pulmonary Hypertension
The Road to Destination Therapy: Optimizing Long-Term Mechanical Cardiopulmonary Support for Pulmonary Hypertension
批准号:
10205153
负责人:
Matthew Dominic Bacchetta
金额:
$56.86万
依托单位国家:
美国
项目类别:
财政年份:
2018
资助国家:
美国
项目状态:
已结题
起止时间:
2018-08-15 至 2023-06-30
关键词:
AnticoagulationAortaBloodBlood CellsBlood VesselsBlood flowCannulationsCarbon DioxideCardiacCardiac OutputCardiopulmonaryCaringChronicClinicalCoagulation ProcessDestinationsDeteriorationDevicesDiseaseEffectivenessEnsureFDA approvedFailureFunctional disorderGasesGoalsHeart failureHematologyHomeHospitalsHourIndividualInternal jugular vein structureLeft atrial structureLiquid substanceLongevityLungLung TransplantationMagnetismMechanicsMethodsModelingNatureOrganOxygenatorsPatientsPerfusionPharmaceutical PreparationsPhasePhysiologic intraventricular pressurePrevalencePrognosisPulmonary HypertensionPulmonary artery structurePumpQuality of lifeRecoveryResistanceRespiration DisordersRespiratory FailureRight Ventricular FunctionRight atrial structureSelf-Help DevicesSheepStructure of brachiocephalic arteryStructure of subclavian arterySurfaceSurvival RateSystemTestingTransfusionTransplantationVentricularVentricular RemodelingWait Timebasebiomaterial compatibilityblood damagedesignexperiencehemodynamicsidiopathic pulmonary fibrosisimprovedimproved mobilityinnovationmortalityportabilitypressurepreventpulmonary arterial hypertensionrespiratoryrespiratory hypoxiashear stresssheep modeltreatment optimization
中文摘要
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英文摘要
Project Abstract:
The goal of this proposal is to develop long-term cardiopulmonary support for patients with chronic, severe
pulmonary arterial hypertension (PAH) and associated RV failure. Patients with severe PAH will die of RV
failure without lung transplant. Unfortunately many of these patients experience long waiting times, are
unstable, and become transplant ineligible, due to poor cardiac output and end-organ dysfunction. To prevent
this, our team has used innovative modes of venoarterial (VA) ECMO as a temporary bridge to recovery (BTR)
or transplantation (BTT) to support the RV, facilitate ambulation, and ensure uniform perfusion of the whole
body. Our approach has led to excellent survival rates, but it would be better to intervene prior to RV failure, to
support patients for longer periods, and to offer support to non-transplant eligible patients. The goal of this
proposal is to extend and improve our successful approach for temporary ECMO support for PAH patients
toward permanent, destination therapy support. To accomplish this, we need more compact portable ECMO
systems for enhanced mobility, with oxygenators that have slower clot formation, greater durability, and limited
blood damage to eliminate the need for transfusions. We plan to test a new pulmonary assist device (PAD)
being developed by our group in a sheep pulmonary hypertension (PH)/RV failure model. The PAD consists of
two parallel, highly biocompatible gas exchanger modules that can be driven by conventional magnetically
levitated pumps for BTR or BTT or a small, VAD-quality pump for destination therapy. The fluid mechanical
design and surface treatments of the device slow clot formation and reduce shear stress damage of blood
cells, allowing for longer-term support with minimal systemic anticoagulation, no transfusions, and minimized
end-organ dysfunction. Patients could potentially be supported initially in the hospital, transitioned to home,
and return for gas exchanger replacements every 2-3 months. For Aim 1, we will determine the mode of ECMO
attachment that provides optimal RV support in a sheep model of chronic PH/RV failure. Attachment modes
include: 1) pumped right atrium (RA) to pulmonary artery (PA), 2) pumped RA to left atrium (LA), 3) pumpless
PA to LA, 4) pumped RA – innominate artery, and 5) pumped venovenous (negative control). In each case, the
support will be maintained for 4 hours while examining the effect of PAD flow rate on hemodynamics, RV
function, and PAD function. These results will inform which mode(s) could be most beneficial to PAH patients.
For Aim 2, we will examine changes in RV function and durability of the PAD system over a month of support.
Either the PAD system or a Maquet Cardiohelp (MC) system will be attached in sheep with chronic PH/RV
failure for one month. The PAD will be attached in the optimal configuration determined from Aim 1, while the
MC system will use the optimal pumped configuration, since its high resistance precludes PA-LA use. We
hypothesize that the PAD will improve longevity, portability and create less blood damage than the MC and will
improve quality of life and survival when used clinically in an optimally determined study.
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DOI:
10.1097/hep.0000000000000357
发表时间:
2023-09-01
期刊:
HEPATOLOGY
影响因子:
13.5
作者:
[Wu, Wei Kelly, Ukita, Rei, Patel, Yatrik J., Cortelli, Michael, Trinh, Vincent Q., Ziogas, Ioannis A., Francois, Sean A., Mentz, Meredith, Cardwell, Nancy L., Talackine, Jennifer R., Grogan, William M., Stokes, John W., Lee, Youngmin A. A., Kim, Jinho, Alexopoulos, Sophoclis P., Bacchetta, Matthew]
通讯作者:
Bacchetta, Matthew
DOI:
10.3791/62694
发表时间:
2021-07-15
期刊:
JOVE-JOURNAL OF VISUALIZED EXPERIMENTS
影响因子:
1.2
作者:
[Ukita, Rei, Stokes, John W., Wu, W. Kelly, Talackine, Jennifer, Cardwell, Nancy, Patel, Yatrik, Benson, Clayne, Demarest, Caitlin T., Rosenzweig, Erika B., Cook, Keith, Tsai, Emily J., Bacchetta, Matthew]
通讯作者:
Bacchetta, Matthew
DOI:
10.1097/mat.0000000000001417
发表时间:
2022-02-01
期刊:
ASAIO journal (American Society for Artificial Internal Organs : 1992)
影响因子:
--
作者:
[Ukita R, Tumen A, Stokes JW, Pinelli C, Finnie KR, Talackine J, Cardwell NL, Wu WK, Patel Y, Tsai EJ, Rosenzweig EB, Cook KE, Bacchetta M]
通讯作者:
Bacchetta M
DOI:
10.1097/mat.0000000000001197
发表时间:
2021-01-01
期刊:
ASAIO journal (American Society for Artificial Internal Organs : 1992)
影响因子:
--
作者:
[Ukita R, Tipograf Y, Tumen A, Donocoff R, Stokes JW, Foley NM, Talackine J, Cardwell NL, Rosenzweig EB, Cook KE, Bacchetta M]
通讯作者:
Bacchetta M
The Road to Destination Therapy: Optimizing Long-Term Mechanical Cardiopulmonary Support for Pulmonary Hypertension
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批准号:9762967
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项目类别:
-
资助金额:$72.06万
-
财政年份:2018
-
负责人:Matthew Dominic Bacchetta
-
依托单位:
海外基金