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    請使用永久網址來引用或連結此文件: https://ir.lib.ncu.edu.tw/handle/987654321/110165


    題名: 可攜式心血管監測系統之開發:從臨床驗證至居家血流動力學評估;可攜式心血管監測系統之開發:從臨床驗證至居家血流動力學評估
    作者: 盧威廷;LU, WEI-TING
    貢獻者: 生醫科學與工程學系生物醫學工程碩士班
    關鍵詞: 心血管;阻抗心動描記術;心輸出量;血流動力學;心搏量;Cardiovascular;Impedance Cardiography;Cardiac Output;Hemodynamic;Stroke Volume
    日期: 2026-08-29
    上傳時間: 2026-10-20 15:20:38 (UTC+8)
    出版者: 國立中央大學
    摘要: 本研究旨在開發一套可同步量測心電圖(Electrocardiogram, ECG)與阻抗心動描記術(Impedance Cardiography, ICG)之可攜式生理訊號量測系統,並透過公開資料庫與臨床資料驗證其應用於非侵入式血流動力學監測之可行性。血流動力學參數如心搏量(Stroke Volume, SV)與心輸出量(Cardiac Output, CO),對於心臟功能與循環狀態評估具有重要意義;然而,現有臨床量測方式受限於設備成本、操作需求與可攜性,較不利於長時間或居家化監測。

    本研究完成一套整合 ECG、ICG 訊號擷取、低雜訊電源管理、STM32U575 微控制器、SD 卡儲存與藍牙通訊之可攜式系統。以 10 Hz 正弦波進行同步性測試後,兩通道相對時間差約為 1.07 ms。訊號分析方面,以 ECG R peak 建立心搏時間基準,並結合 T peak 輔助 ICG 特徵點搜尋,由 dZ/dt 波形擷取 B、C、X 點及 Z_0、LVET 與 (dZ/dt)_max 等特徵,進一步估測 SV。

    演算法首先利用公開資料進行驗證。HeartCycle 資料庫中,各 case 平均估測 SV_ICG 與 NICCOMO SV 之相關係數為 R = 0.848;Radar Vital Signs Dataset 經 10-beat averaging 後,估測 SV_ICG 與 Task Force Monitor (TFM) SV 之相關係數為 R = 0.663。進一步於 ICU 臨床場域進行量測後,本研究估測 SV_ICG 與 FloTrac SV 於代表性 case 中呈現相似之時間變化趨勢,相關係數可達 R = 0.751。

    綜合上述結果,本研究所開發之可攜式 ECG–ICG 同步量測系統可於實際臨床環境中取得可供分析之訊號,且所建立之特徵擷取與 SV 估測方法於不同資料來源下皆能反映血流動力學變化,顯示其具有應用於非侵入式長時間血流動力學監測之潛力。;This study developed a portable system for synchronous electrocardiogram (ECG) and impedance cardiography (ICG) acquisition and evaluated its feasibility for non-invasive hemodynamic monitoring using public datasets and clinical measurements. Hemodynamic parameters such as stroke volume (SV) and cardiac output (CO) are important for assessing cardiac function; however, conventional clinical approaches are often limited by cost, operational requirements, and portability, making long-term monitoring difficult.

    The proposed system integrates ECG and ICG acquisition modules, low-noise power management, an STM32U575 microcontroller, SD-card storage, and Bluetooth communication. Synchronization was evaluated using a 10-Hz sinusoidal signal, resulting in an inter-channel time difference of approximately 1.07 ms. ECG R peaks were used as the primary timing reference, while T peaks assisted ICG feature localization. The B, C, and X points were identified from the dZ/dt waveform, and Z_0, LVET, and (dZ/dt)_max were extracted for SV estimation.

    The algorithm was validated using two public datasets. In the HeartCycle dataset, the correlation between case-averaged estimated SV_ICG and NICCOMO SV was R = 0.848. In the Radar Vital Signs Dataset, estimated SV_ICG correlated with Task Force Monitor (TFM) SV at R = 0.663 after 10-beat averaging. Clinical evaluation in an intensive care unit (ICU) showed similar temporal trends between estimated SV_ICG and FloTrac SV in a representative case, with R = 0.751.

    Overall, the proposed ECG–ICG system successfully acquired synchronized signals in a clinical environment, while the developed feature extraction and SV estimation method showed consistent relationships with reference SV measurements. These results support its potential for non-invasive and long-term hemodynamic monitoring.
    顯示於類別:[生物醫學工程研究所 ] 博碩士論文

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