The present invention relates generally to a method of determining whether to perform a medical procedure based on the predictive outcome of the medical procedure and the effect on the patient after the medical procedure.
Management of various diseases or surgical problems has allowed patients a cure, partial treatment or palliation of their disease, injury, or acquired or genetic medical or surgical conditions. These therapies or the avoidance of these therapies impact the quality of life (“QOL”) of patients.
By gathering data from the patient in the pre-treatment arena (including QOL data, personal, medical and surgical histories, physical examination information, laboratory, organ and physical function, radiographic data, and other health, personal, psychological, and related data), acquiring information during and after any and all forms of medical and surgical therapy, and by determining medical, surgical, functional and psychological outcomes and QOL of the patient, these data can be studied and analyzed to predict QOL outcomes. Using statistical functions such a univariate and multivariate logistic regression model, Fisher's exact, Chi-square test, principal component analysis, and/or forward stepwise logistic regression, among others, the outcomes of therapies or the lack of therapy can be predicted via a mathematical equation or algorithm including the QOL. The more important variables will be weighted more significantly in this equation to allow for greater influence in the outcomes measure.
Thus, a predictive model has been developed to determine based on gathered information, whether a particular procedure will affect the quality of life of a patient.
Disclosed herein is a method for determining the risk of performing a procedure on a patient that includes the steps of taking a patient history from the patient who is a candidate for the procedure, performing a physical examination of the patient, determining the procedure to be performed, and predicting the quality of life of the patient after the procedure based on the patient history and the physical examination.
Additional features and advantages of the invention will be set forth in the detailed description which follows, and in part will be readily apparent to those skilled in the art from that description or recognized by practicing the invention as described herein, including the detailed description which follows, the claims, as well as the appended drawings.
It is to be understood that both the foregoing general description and the following detailed description of the present embodiments of the invention are intended to provide an overview or framework for understanding the nature and character of the invention as it is claimed. The accompanying drawings are included to provide a further understanding of the invention and are incorporated into and constitute a part of this specification. The drawings illustrate various embodiments of the invention and, together with the description, serve to explain the principles and operations of the invention.
Reference will now be made in detail to the present preferred embodiment(s) of the invention and with reference to the information illustrated in the accompanying drawings. Whenever possible, the same reference numerals will be used throughout the drawings to refer to the same or like parts.
As one example, inguinal hernia repair is one of the most common operations performed in the United States and throughout the world. However, patients undergoing repair have a 7-40% incidence of chronic pain lasting months or indefinitely. To better understand and predict QOL after inguinal hernia repair, patients undergoing inguinal hernia repair in a prospective trial from 2007 to 2011 were included in an analysis. Initially, peri-operative factors predictive of chronic discomfort or pain long-term were identified. As well, in this and other studies, patients with potential postoperative confounders can be excluded. Carolinas Comfort Scale (CCS), a treatment, QOL tool was used to compare postoperative symptoms outcomes at 1 year follow-up. A score of 2 or higher (mild but bothersome to severe) was considered symptomatic. Multivariate logistic regression model was used to calculate the adjusted odds ratios of factors contributing to chronic symptoms and develop a predictive mathematical algorithm. Of the 2,497 subjects, 1,718 patients (75.5%) were seen at one-year follow-up. A random sample of 80% of these patients was used for a chronic pain predictive model. The remaining 20% were used for predictive model validation.
Using the information from these patients, a univariate analysis was performed on the data from these patients to identify potential confounders of chronic pain at the one-year visit by comparing symptomatic to asymptomatic patients. The table in
The table in
Principal component analysis was performed on all pre-operative CCS responses (pain+movement questions). Forward stepwise logistic regression (FSLR) was then performed. Pertinent clinical variables and significant principle components were included as potential explanatory/predictor variables. The result was a predictive algorithm:
P=0.1190−(0.0306*age)+(0.5746*gender)−(0.3955*primary/recurrent)+(0.2343*bilateral/unilateral)+(0.1114*prin1),
where age is the age of the patient in years, gender is 1 for female and −1 for male, primary/recurrent is 1 for primary and −1 for recurrent procedure, and bilateral/unilateral is 1 for bilateral and −1 for unilateral, and prin1 is principal component analysis using preoperative pain and movement limitations.
The sensitivity and specificity of this predictive algorithm were 70% and 65% respectively. Eighty percent of the original group of patients was utilized to develop the algorithm or sophisticated mathematical equation above. The remaining 20% were then tested for predictive model validation and confirmed its predictive value with sensitivity and specificity of this predictive algorithm remaining between 60% and 70%.
As a result, a prediction can be made about the patient's response to the procedure that is being suggested. After taking a patient history that covers the confounders noted above, performing a physical examination of the
It will be apparent to those skilled in the art that various modifications and variations can be made to the present invention without departing from the spirit and scope of the invention. Thus, it is intended that the present invention cover the modifications and variations of this invention provided they come within the scope of the appended claims and their equivalents.
This application claims the benefit of application Ser. No. 61/601,797, filed on Feb. 22, 2012, which is hereby incorporated by reference in its entirety.
Number | Date | Country | |
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61601797 | Feb 2012 | US |