138 results about "Infected patient" patented technology

The invention provides a three-color fluorescent RT-PCR (Reverse Transcription-Polymerase Chain Reaction) combined detection method of enterovirus 71, Coxsackie virus A16 and other subtypes of enterovirus as well as a kit thereof. The method can rapidly and accurately detect the enterovirus 71, the Coxsackie virus A16 and the other subtypes of nucleic acids of enterovirus in a sample. The method comprises the following steps of: (1) acquiring and conveying a sample of an infected patient or a suspected patient; (2) preprocessing the sample and extracting RNA; (3) detecting the sample by adopting a one-step PCR-three-color fluorescent probe in-vitro amplification method; and (4) analyzing the corresponding sample according to the fluorescence intensity of each amplification reaction after the amplification reaction is finished, thereby judging the existence of the enterovirus 71, the Coxsackie virus A16 and the other subtypes of nucleic acids of the enterovirus in the acquired sample and being capable of carrying out accurate quantitation (a figure 3) on the enterovirus 71, the Coxsackie virus A16 and the other subtypes of nucleic acids of the enterovirus. The invention realizes the aim of carrying out rapid and accurate combined detection of the enterovirus 71, the Coxsackie virus A16 and the other subtypes of nucleic acids of the enterovirus.

An infection spread prevention support system includes an examination terminal and an infection spread prevention support server. The examination terminal includes an examination information acquisition unit that acquires examination information to examine the infection of an infectious disease in subjects and a transmission and reception unit that transmits the examination information to the infection spread prevention support server. The infection spread prevention support server includes a receiving unit that receives examination information, an infection determination unit that determines the presence or degree of infection of the infectious disease using the examination information, an activity regulation information generation unit that generates activity regulation information to regulate the an activity of the infected patient based on infection determination information, which is a determination result of the infection determination unit, and information regarding the subjects, and an output unit that outputs the activity regulation information.

Compounds, compositions, and methods of treatment and prevention of HIV infection are disclosed. The compounds are pyrrolo[2,3-b]pyridines and pyrrolo[2,3-b]pyrimidine JAK inhibitors. Combinations of these JAK inhibitors and additional antiretroviral compounds, such as NRTI, NNRTI, integrase inhibitors, entry inhibitors, protease inhibitors, and the like, are also disclosed. In one embodiment, the combinations include a combination of adenine, cytosine, thymidine, and guanine nucleoside antiviral agents, optionally in further combination with at least one additional antiviral agent that works via a different mechanism than a nucleoside analog. This combination has the potential to eliminate the presence of HIV in an infected patient.

A system identifies multiple medical conditions, observations, and laboratory test results using active sensors and predetermined rules to identify infected patients. An infection control and workflow management system includes a repository of worker information identifying healthcare workers for performing infection control tasks as well as worker associated communication data for use in informing healthcare workers of infection control tasks to be performed. A detection processor automatically detects infection in patients from multiple different sources including from at least one of, (a) a medical record evaluated upon admission of a patient to a hospital and (b) a laboratory test result. A workflow processor uses the worker information for automatically communicating a message to inform a healthcare worker of a task to be performed to initiate infection control tasks using communication data in response to detection of an infected patient.

The invention provides a polypeptide chip, which comprises a substrate and n polypeptides distributed on the substrate in an array, each polypeptide sequence has 10-20 amino acids, a group consistingof sequences of first to nth polypeptides covers at least 95% of a viral protein sequence, the adjacent polypeptides have an overlap of 3-8 amino acids, and n is 810-1370. According to the method, proteomics and system biology strategies are adopted, all coded protein sequences of COVID-19 are extracted from NCBI data, an SARS-CoV-2 virus proteome polypeptide chip is designed and prepared, and panoramic scanning of all SARS-CoV-2 virus antibodies in blood of a novel pneumonia virus infected patient is achieved.

The invention relates to the technical field of medical detection, and in particular, relates to a primer and probe combination and a kit for detecting human pathogenic bacteria. The kit comprises theprimer and probe combination for detecting pseudomonas aeruginosa, escherichia coli, klebsiella pneumoniae, staphylococcus epidermidis, staphylococcus aureus, enterococcus faecium, human staphylococcus and acinetobacter baumannii. According to the kit, the primer and probe combination is adopted, multiple digital PCR is combined, the pathogenic bacteria types and the target nucleic acid copy number in the detection range can be rapidly and accurately identified, the detection method has high sensitivity, and positive detection of low-copy nucleic acid fragments of pathogenic bacteria is guaranteed; meanwhile, the variety of the pathogenic bacteria or the change of the copy number of the target nucleic acid fragment in the body of a pathogenic bacteria infected patient can be dynamically monitored, the treatment effect is assisted and evaluated in time, and reference is provided for optimization of a doctor clinical scheme.

The present invention relates to in vitro methods of determining a susceptibility to non-response to a hepatitis C treatment or a susceptibility to spontaneous hepatitis C clearance in a subject infected with hepatitis C.

The invention relates to the filed of drug detection, and particularly relates to a method and system for detecting drug resistance of beta-lactam antibiotics and application of beta-lactam antibiotics. The method comprises steps of mixing turbid liquid of microorganism to be tested with standard liquid of beta-lactam antibiotics, then removing the microorganism to be tested so as to obtain the liquid to be tested; obtaining liquid chromatogram of the liquid to be tested; judging the tolerance of the microorganism to be tested to the beta-lactam antibiotic according to the liquid chromatogram. The detection is not affected by concentration and purity of the microorganism and operation technique of an operator, so that the method has the advantages of high sensitivity, high accuracy, high detection speed and short detection time, and can be implemented within two hours. The detection method uses fewer microorganisms, does not need subculture for many times, greatly shortens the time of the whole experiment, provides prompt basis for rapid and early clinical drug use, especially for seriously infected patients; and since the detection time is greatly shortened, the consumable cost is low.

The invention discloses a plasmodium vivax PvMSP1 recombinant antigenic protein, which is protein of which the amino acid sequence is shown in SEQ ID NO:1 which has glycophosphatidylinositol (GPI) anchor and epidermal growth factor-like (EGF-like) structure domain. Furthermore, the invention also discloses a preparation method of the recombinant antigenic protein, which comprises the steps of amplifying a plasmodium vivax PvMSP1 gene sequence, constructing and identifying recombinant plasmid, inducibly expressing and purifying recombinant protein and the like. Experiments prove that the PvMSP1 recombinant antigenic protein has the advantages of high sensitivity, strong specificity and the like to assay of the serum antibody of a plasmodium vivax infected patient, and has a wide application prospect in the aspect of plasmodium vivax epidemiological investigation.

The invention discloses serratia marcescens ZJH20098. The officinal bacterium prodigiosum lipopolysaccharide produced at present has serious side effects, such as pyrogen and allergic phenomena. Besides the unspecified process, the main reasons are as follows: the strain is not explicitly stipulated, the mutation is generated by instability, and the functional component change is caused by extraction. The strain provided by the invention is preserved in the China General Microbiological Culture Collection Center (CGMCC) with the preservation number of CGMCC No.4010; and as the strain is collected from the bodies of clinical infected patients, and is a high-activity strain obtained through separation, purification, physical mutagism and optimization, the serratia marcescens ZJH20098 provided by the invention is used as a raw material for producing 'bacterium prodigiosum lipopolysaccharide' for human or livestock use.

The invention discloses an early prediction method and system for prognosis risk degree of a patient infected with COVID-19. According to the method and the system, an early prediction model of the prognosis risk degree of the patient infected with COVID-19 is established based on the admission information and the dynamic change of the COVID-19 infected patient, and the prediction model can provide important risk indexes for early identification of important critical patients, so that in the prevalence period of report case increase and medical resource shortage, severe COVID-19 cases can be recognized more accurately and quickly, and the treatment effect of the patient is improved.

The invention provides a combination of cefoperazone sodium and sulbactam sodium. The combination consists of the cefoperazone sodium and the sulbactam sodium, and the weight ratio of which is 3 to 1. The combination of cefoperazone sodium and sulbactam sodium of the invention has the comparative curative effect at the aspect of antibacterial effect with a compound preparation of 1 to 1 or 2 to 1 of the cefoperazone sodium/the sulbactam sodium in markets. The invention reduces the corresponding content of the sulbactam sodium in the combination, so the invention has wider clinical application range and can reduce the production cost of the drug. Compared with the prior compound preparation of the cefoperazone sodium/the sulbactam sodium, the invention is characterized by being fit for the anti-infection remedy of the patient with the renal dysfunction and the remedy of the seriously infected patient.

The present invention provides for novel HCV replicon shuttle vectors useful for cloning in HCV polynucleotide sequences from samples of HCV-infected patients and testing the resulting replicons for drug susceptibility.

The invention discloses an application of a substance for detecting the content of a serum angiopoetin-like protein 2 (angptl2) in preparation of a product for detecting hepatitis and fibrosis degree. Experiments find out that the content of the angptl2 in serum has correlation with the hepatitis degree and fibrosis degree of a chronic hepatitis B virus infected patient, the content of the angptl2 can be used as a noninvasive single indicator for judging the hepatitis degree and fibrosis degree, the substance for detecting the content of the serum angptl2 or a substance for detecting other common clinical indicators of hepatopath can be combined together to prepare the product for detecting the human hepatitis degree and/or fibrosis degree, a product for diagnosing or auxiliarily diagnosing whether patients with hepatopathy need liver biopsy detection or a product for screening or auxiliarily screening the patients with hepatopathy who need or do not need liver biopsy.

A novel means by which HCMV infection can be detected with a high sensitivity and whose practicality is high is disclosed. The present inventors synthesized as many as 15 kinds of HCMV proteins in their full length forms, and intensively studied their reactivities with sera from HCMV-infected patients to find that all the infected patients can be detected without fail when using the pp28 full length protein as an antigen. The pp28 full length protein can be synthesized and purified as a recombinant protein in a large scale by using Escherichia coli, and can be commercially used as an antigen for HCMV tests.

The invention relates to application of IFN-lambda in preparation of a drug for treating a patient infected with a novel coronavirus. The level of the novel coronavirus in the infected patient can be effectively reduced, and the IFN-lambda shows more excellent performance in the aspects of controlling cytokine storm caused in the treatment process and relieving respiratory distress syndrome caused by the cytokine storm.

The invention discloses tea-seed oil fat emulsion injection and a preparing method and application thereof. Each liter of injection water of the tea-seed oil fat emulsion injection is prepared from following components: 0.01-30kg of tea-seed oil, 0.01-20kg of injection long chain oil, 0.5-10kg of emulsifier, 0.1-15kg of isoosmotic adjusting agent and 0-0.50kg of antioxygen and an adjusted pH is 5.5-9.50. By reducing the proportion of omega-6 polyunsaturated fatty acids while increasing the proportion of omega-3 polyunsaturated fatty acids, compatibility of various fats is optimized, a lipid metabolism level is accelerated, and organism material metabolism and synthesis of protein are helped. The injection can be widely used for various patients of parenteral nutrition treatment and particularly suitable for the low-immunity and various infected patients.

The invention provides a compound and a preparation method thereof. The compound has a structure shown in a structural formula (I), wherein MRAS-expressed beta-lactamase can activate photosensitive groups in the compound provided by the invention, so as to generate active oxygen for exterminating MRAS without influencing a microbe and normal tissue which have unexpressed beta-lactamase, and therefore, the compound provided by the invention can achieve the beneficial effects of high efficiency, high specificity and less side effect, can be used as a photosensitizer for PACT treatment of MRSA infection and can provide a powerful tool for treating clinical patients with MRSA injection.