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dc.contributor.authorMalik, M.S.
dc.contributor.authorAkoh, J.
dc.contributor.authorAroori, S.
dc.contributor.authorLatour, Jos
dc.date.accessioned2023-12-26T06:33:56Z
dc.date.available2023-12-26T06:33:56Z
dc.date.issued2022
dc.identifier.citationMalik, M.S. and Akoh, J. and Aroori, S. and Latour, J.M. 2022. Implantable Doppler Probe as a Vascular Monitoring Device in Kidney Transplant Patients: Investigation of Use at a Single Center. Experimental and Clinical Transplantation. 20 (4): pp. 355-361.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/94040
dc.identifier.doi10.6002/ect.2021.0500
dc.description.abstract

Objectives: Vascular complications account for 30% to 35% of total kidney grafts lost during the first 3 months posttransplant. Early detection of vascular complications allows an opportunity for prompt intervention, which is critical to reducing graft loss. In this study, we evaluated the usefulness of an implantable Doppler probe as a vascular monitoring device in kidney transplant patients. Materials and Methods: An implantable Doppler probe is used intermittently for postoperative monitoring of kidney transplant patients at our center. In this retrospective study, we analyzed prospectively maintained medical data in which we compared clinical outcomes of kidney transplant recipients who had postoperative implantable Doppler probe monitoring versus standard care clinical observation. Between January 2016 and October 2021, 324 kidney transplant patients were seen at our center. Patients were divided into 2 groups: group 1 (n = 194; 60%) included kidney transplant recipients with postoperative implantable Doppler probe monitoring and group 2 (n = 129; 40%) included kidney transplant recipients with standard care clinical observation. We compared number of vascular complications, number of departmental ultrasonographic scans required posttransplant, and graft loss at 3 months between the 2 groups. Results: Vascular complications were identified in 13.5% of total patients, with graft loss identified in 2.1%. Both groups were similar in demographical characteristics. Group 1 had more vascular complications (17.5% vs 9.3%; relative risk = 1.88), fewerultrasonographic scans during the first 24 hours posttransplant (71.1% vs 83.7%; relative risk = 0.84), and lower graft loss (1.5% vs 3.1%; relative risk = 0.48) than group 2. All probes were removed safely after 72 hours, and no complications related to the device were reported. Conclusions: The monitoring device may be used as an additional adjunct for graft monitoring in kidney transplant patients. Further controlled studies are warranted to evaluate this device in clinical practice.

dc.languageeng
dc.subjectHumans
dc.subjectKidney
dc.subjectKidney Transplantation
dc.subjectRetrospective Studies
dc.subjectRisk Factors
dc.subjectTreatment Outcome
dc.subjectKidney
dc.subjectHumans
dc.subjectTreatment Outcome
dc.subjectKidney Transplantation
dc.subjectRisk Factors
dc.subjectRetrospective Studies
dc.titleImplantable Doppler Probe as a Vascular Monitoring Device in Kidney Transplant Patients: Investigation of Use at a Single Center
dc.typeJournal Article
dcterms.source.volume20
dcterms.source.number4
dcterms.source.startPage355
dcterms.source.endPage361
dcterms.source.issn1304-0855
dcterms.source.titleExperimental and Clinical Transplantation
dc.date.updated2023-12-26T06:33:52Z
curtin.departmentCurtin School of Nursing
curtin.accessStatusOpen access via publisher
curtin.facultyFaculty of Health Sciences
curtin.contributor.orcidLatour, Jos [0000-0001-9677-8340] [0000-0002-8087-6461]
curtin.contributor.researcheridLatour, Jos [ABE-9521-2020]
dcterms.source.eissn2146-8427
curtin.contributor.scopusauthoridLatour, Jos [23019310400] [57218590755]
curtin.repositoryagreementV3


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