System and method for determining a reference baseline record

Abstract

A system and method for determining a reference baseline record for use in automated patient care. One or more physiological measures are retrieved. Each of the measures relates to individual patient information recorded during an initial observation period from a patient care record. One or more reference measures are determined from the physiological measures. Each reference measure is representative of at least one of measured and derived patient information. The reference measures are stored into the patient care record indicating a reference baseline patient status.

Description

CROSS-REFERENCE TO RELATED APPLICATION [0001] This patent application is a continuation of U.S. patent application, Ser. No. 09 / 860,987, filed on May 18, 2001, pending, which is a continuation of U.S. Pat. No. 6,280,380, issued on Aug. 28, 2001, which is a continuation-in-part of U.S. Pat. No. 6,221,011, issued Apr. 24, 2001, the priority of filing dates of which are claimed, and the disclosures of which are incorporated by reference.FIELD OF THE INVENTION [0002] The present invention relates in general to automated data collection and analysis, and, in particular, to a system and method for determining a reference baseline record for use in automated patient care. BACKGROUND OF THE INVENTION [0003] A broad class of medical subspecialties, including cardiology, endocrinology, hematology, neurology, gastroenterology, urology, ophthalmology, and otolaryngology, to name a few, rely on accurate and timely patient information for use in aiding health care providers in diagnosing and trea...

AI Technical Summary

Benefits of technology

[0016] The present invention provides a meaningful, quantitative measure of patient wellness for use as a reference baseline in an automated system and method for continuous, remote patient care. The reference baseline increases the accuracy of remote patient care, particularly during the first few weeks of care, by providing a grounded starting assessment of the patient's health and well-being.

[0017] A collateral benefit of the reference baseline is the removal of physician “bias” which can occur when the apparent normal outward appearance of a patient belies an underlying condition that potentially requires medical attention. The reference baseline serves to objectify a patient's self-assessment of wellness.

[0018] The present invention also provides an objective approach to humanizing the raw measures recorded by medical devices, including implantable medical devices. Using known quality of life assessment instruments, a patient can be evaluated and scored for relative quality of life at a given point in time. The reference baseline of the present invention provides a means for correlating the quality of life assessment to machine-recorded measures, thereby assisting a physician in furthering patient care.

[0019] Finally, the present invention improves the chronicling of legal responsibility in patient care. A prescribed course of treatment can be traced back to a grounded point in time memorialized by the reference baseline. Thus, a medical audit trail can be generated with a higher degree of accuracy and certainty based on having an established originating point of reference.

Problems solved by technology

Bradycardia can cause symptoms such as fatigue, dizziness, and fainting.

Tachycardia can result in sudden cardiac death (SCD).

In addition, automated remote patient care poses a further challenge vis-a-vis evaluating quality of life issues.

Unlike in a traditional clinical setting, physicians participating in providing remote patient care are not able to interact with their patients in person.

Consequently, quality of life measures, such as how the patient subjectively looks and feels, whether the patient has shortness of breath, can work, can sleep, is depressed, is sexually active, can perform activities of daily life, and so on, cannot be implicitly gathered and evaluated.

However, these measures are limited in their usefulness and do not provide the scope of detailed medical information made available through implantable and external medical devices.

Moreover, such measures are generally obtained through manual means and do not ordinarily directly tie into quality of life assessments.

Further, a significant amount of time generally passes between the collection of sets of these measures.

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