Quick results:Rapid detection reagents can yield results in a short time, usually within 15 – 30 minutes. Compared with traditional detection methods such as virus culture, this significantly shortens the diagnosis time. It is conducive to the timely isolation and treatment of patients, effectively controlling the spread of the epidemic.
Simple operation:Generally, it does not require complex equipment or highly specialized personnel. People with basic training can operate it, enabling wide application in scenarios such as primary medical institutions and on – site testing. For example, it can be quickly deployed in community screenings and border port inspections.
High sensitivity and specificity:High – quality rapid detection reagents have high sensitivity and specificity for the monkeypox virus. They can accurately identify the monkeypox virus, effectively reducing the occurrence of false – positive and false – negative results, providing a reliable basis for clinical diagnosis and epidemic prevention and control.
On – site testing available:Testing can be directly carried out at the patient’s bedside, in isolation wards, or at the epidemic site. There is no need to send samples to a specialized laboratory, reducing the risks and time costs during sample transportation and improving the detection efficiency.
Applicable to diverse sample types:It can detect a variety of sample types, such as skin lesion swabs, blood, saliva, etc. This makes it convenient to collect samples according to different situations and requirements, enhancing the feasibility and convenience of detection.
Disadvantages
Accuracy affected by multiple factors:The accuracy of test results may be influenced by various factors such as the time of sample collection, collection site, sample storage conditions, and the operation process. For example, if the sample is collected too early or too late, the low viral load may lead to false – negative results. Improper sample collection, insufficient sample volume, or contamination can also affect the test results.
Possible cross – reactions:Although the specificity is relatively high, in some cases, cross – reactions with other similar viruses or pathogens may occur, resulting in false – positive results. For instance, due to certain antigenic similarities with the smallpox virus, misjudgments may occur in the detection, and further verification by more precise methods is required.
Limited detection scope:Some rapid detection reagents can only detect a specific antigen or gene segment of the monkeypox virus. There may be a situation where they cannot detect mutant strains of the virus. With the continuous mutation of the monkeypox virus, the effectiveness of the detection reagents may be reduced.
Subjectivity in result interpretation:The result interpretation of some rapid detection reagents requires manual operation, such as observing the color development on the test strip. This may be subjective, and different operators may have different judgments, affecting the accuracy and consistency of the results.
Inability to type the virus:Rapid detection reagents generally can only determine whether the monkeypox virus is present, but cannot type the virus. However, virus typing is of great significance for understanding the transmission characteristics of the virus and formulating targeted prevention and control strategies. In this regard, rapid detection reagents are insufficient.