Joint screening and intervention managing system for newborn hearing and deafness susceptibility gene

Abstract

The invention relates to a joint screening and intervention managing system for newborn hearing and deafness susceptibility gene, and the joint screening and intervention managing system comprises two parts: the software system platform, comprising a home page information management module, a short message management module, a member management module, a medical record management module, a system management module and a short message receiving and sending program; a hardware network platform. The patient can login the PC machine for obtaining the screening result and the information related to the screening result for exchanging and consulting with the medical staff; the medical staff can login the PC machine for managing the joint screening and intervention information for newborn hearing and deafness susceptibility gene. The newborn parents can login the machine the through the Internet to obtain the related screening diagnosis result and precautionary measure record in the hospital; the medical staff can login the system for building the record for the patient for automatically reminding the medical staff for visiting the patient beforehand and automatically sending the short message for reminding the parents to come to visit with children.

Description

technical field [0001] The invention relates to a newborn hearing and deaf disease susceptibility gene joint screening and intervention management system. Background technique [0002] Hearing impairment is one of the common birth defects in newborns. In my country, hearing and speech disabilities rank first among the five types of disabilities. Hearing impairment seriously affects children's language, psychological and social communication skills, and brings a heavy burden to families and society. Early detection, early diagnosis, and early intervention of hearing-impaired children through hearing screening can maximize the approach to and reach the speech development level of normal children of the same age, so that they can be deaf but not dumb. In 2000, the Chinese government affirmed the significance and necessity of newborn hearing screening in the form of the Maternal and Child Health Law of the People's Republic of my country, and it was widely carried out nationwid...

AI Technical Summary

Problems solved by technology

[0003] The purpose of the present invention is to develop a combined screening and intervention management system for newborn hearing and deaf susceptibility genes, which can overcome the above-mentioned defects of joint screening and intervention management of newborn hearing and deaf susceptibility genes, and solve the problem of hearing screening. Failure to pass newborn tracking and follow-up difficulties, to meet the information management of newborn hearing screening data computer input, data analysis, result classification, information feedback, quality control, deafness intervention and language rehabilitation

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