Method for providing information on hypotension and device using the same

Patent metadata

Field	Value
Publication number	US-2025246306-A1
Application number	US-202419007290-A
Country	US
Kind code	A1
Filing date	Dec 31, 2024
Priority date	Jan 26, 2024
Publication date	Jul 31, 2025
Grant date	—

Abstract

According to this specification, a method for providing information on hypotension implemented by a processor includes: receiving first clinical data and second clinical data for an individual; extracting a statistical value for the received first clinical data as a first feature; extracting an embedding vector for the received second clinical data as a second feature; and predicting whether the hypotension occurs in the individual within a first period by inputting the first feature and the second feature to a prediction model trained to predict whether the hypotension occurs using the first feature and the second feature as inputs.

First claim

What is claimed is:

1 . A method for providing information on hypotension implemented by a processor, comprising:
receiving first clinical data and second clinical data for an individual; extracting a statistical value for the received first clinical data as a first feature; extracting an embedding vector for the received second clinical data as a second feature; and predicting whether the hypotension occurs in the individual within a first period by inputting the first feature and the second feature to a prediction model trained to predict whether the hypotension occurs using the first feature and the second feature as inputs.

2 . The method of claim 1 , wherein the hypotension has a systolic blood pressure (SBP) of 90 mmHg or less and a mean arterial pressure (MAP) of 60 mmHg or less, which occur 5 times or more for about 10 minutes.

3 . The method of claim 1 , wherein the first clinical data includes at least one of heart rate, respiration (RESP), O2 saturation (SpO2), and non-invasive blood pressure (NBP), the second clinical data includes at least one of ECG lead II and photoplethysmography (PPG), and
the statistical value includes at least one of mean, variance, median, a min value, a max value, quantile, and an exponentially weighted moving average.

4 . The method of claim 1 , wherein the extracting of the statistical value as the first feature includes extracting as the first feature a first window having a size smaller than that of the first period from the received first clinical data by time-series interval movement (rolling windows) of the first window at a predetermined time interval.

5 . The method of claim 1 , wherein the extracting of the embedding vector as the second feature includes extracting as the second feature a first window having the size smaller than that of the first period from the received second clinical data by the rolling windows of the first window at the predetermined time interval, and
the extracting of the embedding vector as the second feature includes: extracting first extraction data having a size of the first window based on the first window from the received second clinical data; segmenting the extracted first extraction data into a predetermined size; extracting second extraction data for a portion of an initial period from the segmented first extraction data; sampling the extracted second extraction data so that the extracted second extraction data is transformed into an embedding feature in a digital form; and inputting the embedding feature to a transformer encoder and outputting the embedding feature as the embedding vector.

6 . The method of claim 5 , wherein the sampling further includes transforming the second extraction data into a two-dimensional or more embedding feature by inputting the extracted second extraction data to a transformation model trained to transform the second extraction data into the two-dimensional or more embedding feature using the second extraction data as input.

7 . The method of claim 1 , further comprising:
prior to the extracting, selecting a hypotension group from the received first clinical data and second clinical data; setting a first prediction window of the first period in the first clinical data of the selected hypotension group; setting a second prediction window of the first period in the second clinical data of the selected hypotension group; extracting a first learning feature and a second learning feature from each of the set first prediction window and second prediction window by rolling windows of a first window having a size smaller than that of the first period at a predetermined time interval; and training the prediction model based on the extracted first learning feature and second learning feature, and the setting of the first prediction window includes: setting a first event time for a first hypotension occurrence event time in the first clinical data of the selected hypotension group; setting a second event time before the first period from the first event time; and setting the first clinical data for the hypotension group from the second event time to the first event time as the first prediction window, and the setting of the second prediction window includes: setting an event time corresponding to the first event time in the second clinical data of the selected hypotension group as a third event time; setting a fourth event time before the first period from the third event time; and setting the second clinical data for a non-hypotension group from the fourth event time to the third event time as the second prediction window.

8 . The method of claim 1 , further comprising:
prior to the extracting, selecting a non-hypotension group from the received first clinical data and second clinical data; setting a third prediction window of the first period in the first clinical data of the selected non-hypotension group; setting a fourth prediction window of the first period in the second clinical data of the selected non-hypotension group; extracting a third learning feature and a fourth learning feature from each of the set third prediction window and fourth prediction window by rolling windows of a first window having a size smaller than that of the first period at a predetermined time interval; and training the prediction model based on the extracted third learning feature and fourth learning feature.

9 . The method of claim 8 , wherein the setting of the third prediction window includes:
setting a first event time for a first hypotension occurrence event time in the first clinical data of the selected non-hypotension group; setting a second event time before the first period from the first event time; and setting the first clinical data for the non-hypotension group from the second event time to the first event time as the third prediction window.

10 . The method of claim 9 , wherein the setting of the fourth prediction window includes:
setting an event time corresponding to the first event time in the second clinical data of the selected non-hypotension group as a third event time; setting a fourth event time before the first period from the third event time; and setting the second clinical data for the non-hypotension group from the fourth event time to the third event time as the fourth prediction window.

11 . A device for providing information on hypotension, comprising:
a communication unit configured to receive first clinical data and second clinical data for an individual; and a processor configured to communicate with the communication unit, wherein the processor is configured to extract a statistical value for the received first clinical data as a first feature; extract an embedding vector for the received second clinical data as a second feature; and predict whether the hypotension occurs in the individual within a first period by inputting the first feature and the second feature to a prediction model trained to predict whether the hypotension occurs using the first feature and the second feature as input.

12 . The device of claim 11 , wherein the hypotension has a systolic blood pressure (SBP) of 90 mmHg or less and a mean arterial pressure (MAP) of 60 mmHg or less which occur 5 times or more for about 10 minutes.

13 . The device of claim 11 , wherein the first clinical data includes at least one of heart rate, respiration (RESP), O2 saturation (SpO2), and non-invasive blood pressure (NBP),
the second clinical data includes at least one of ECG lead II and photoplethysmography (PPG), and the statistical value includes at least one of mean, variance, median, a mini

Assignees

• Univ Yonsei Iacf

Inventors

• Yoon Duk Yong
• Seo Ji Hoon
• Park Chan Min
• Han Chang Ho

Classifications

• A61B5/14551

  for measuring blood gases · CPC title

• A61B5/318

  Heart-related electrical modalities, e.g. electrocardiography [ECG] · CPC title

• A61B5/024

  Measuring pulse rate or heart rate · CPC title

• G06N3/08

  Learning methods · CPC title

• G16H50/20 Primary

  for computer-aided diagnosis, e.g. based on medical expert systems · CPC title