000 02778ntm a2200337 i 4500
003 MY-KuUP
005 20261006105515.0
006 t||||fr|||| 000 0
007 ta
008 261006t20262026my a|||fr|||| 000 0 eng d
020 _aTHE0010815 (Local)
_qHardback
040 _aUMPSA
_beng
_cUMPSA
_erda
090 _aFTKPM .M86 2026 r Thesis
100 _aSiti Munirah Muhammad Ali,
_eauthor.
245 1 0 _aPatient-specific lumped parameter models for cardiovascular simulations /
_cSiti Munirah Muhammad Ali
264 1 _aKuantan, Pahang :
_bUMPSA,
_c2026
264 4 _c© 2026
300 _axiv, 221 pages :
_billustrations (some color) ;
_c30 cm. +
_e1 CD-COM
336 _2rdacontent
_atext
337 _2rdamedia
_aunmediated
338 _2rdacarrier
_avolume
347 _2rda
_atext file
_bPDF
500 _aFaculty of Manufacturing and Mechatronic Engineering Technology
502 _aThesis (Doctor of Philosophy) -- Universiti Malaysia Pahang – 2026
504 _aIncludes bibliographical references
520 3 _aMost lumped parameter (LP) cardiovascular models currently rely on population-averaged parameters, as practical methodologies to estimate personalized parameter values from routinely available non-invasive data remain limited. This study addresses this methodological gap by developing a patient-specific framework that combines an LP cardiovascular model with a genetic algorithm (GA) to estimate individualized physiological parameters. The proposed framework reconstructs individual hemodynamic states using only standard clinical inputs, including heart rate and systolic and diastolic blood pressure. Influential model parameters were identified through sensitivity analysis and subsequently optimized via a genetic algorithm, using clinical blood pressures as calibration targets and cardiac index as a soft constraint to ensure physiological validity. Validation on clinical data from 40 patients demonstrated that the model accurately replicates patient-specific hemodynamic and distinguishes between normotensive and Stage 2 hypertensive profiles without requiring prior diagnostic labels. Statistical analysis confirmed significant differences in estimated parameters, such as systemic arterial resistance (Rsysar) and compliance (Csysar), aligning closely with clinical expectations. This research demonstrates a robust, data-efficient approach for personalizing cardiovascular simulations using universally assessable measurements, bridging the divide between mechanistic modelling and practical clinical applicability.
610 2 0 _aFaculty of Manufacturing and Mechatronic Engineering Technology
_xDissertations
650 0 _aUniversities and colleges
_xDissertations
650 0 _aThesis
_xDissertations
942 _2lcc
_cTHESIS
999 _c105674
_d105680