and LI Ning2
(1)
Radiology Department, Capital Medical University Beijing You’an Hospital, Beijing, China, People’s Republic
(2)
Capital Medical University Beijing You’an Hospital, Beijing, China, People’s Republic
Abstract
National sentinel hospitals for surveillance of influenza and laboratories network should continue their duties for the surveillance of influenza liked cases according to National Implementation Plan of Influenza Surveillance and Management Plan of Extending Network Projects on the Surveillance of Influenza, 2009 as well as the techniques requirements included in the appendices of the two official documents.
17.1 Surveillance of Epidemic
17.1.1 Sentinel Surveillance of Influenza Liked Cases
National sentinel hospitals for surveillance of influenza and laboratories network should continue their duties for the surveillance of influenza liked cases according to National Implementation Plan of Influenza Surveillance and Management Plan of Extending Network Projects on the Surveillance of Influenza, 2009 as well as the techniques requirements included in the appendices of the two official documents.
17.1.1.1 Definition of Monitored Cases
Influenza liked cases refer to patients with fever (body temperature above 38 °C) and accompanying cough or sore throat, with no evidence of laboratory diagnosis.
17.1.1.2 Surveillance Time
All national sentinel hospitals for surveillance of influenza liked cases and network laboratories should carry out the surveillance of influenza all the year round.
17.1.1.3 Establishment of Surveillance Clinics
1.
In urban comprehensive hospitals, internal medicine department, internal emergency room, fever clinic and/or internal pediatric clinic, internal pediatric emergency room have duties of monitoring influenza liked cases.
2.
In urban pediatric hospitals, the internal pediatric clinic, internal pediatric emergency room and fever clinics have the duties of monitoring influenza liked cases.
3.
Internal medicine clinics monitoring influenza liked cases should include all internal clinic consultation rooms.
4.
If the internal pediatric clinic in the sentinel hospitals has subdivided sections, all the internal pediatric clinic consultation rooms have duties in monitoring influenza liked cases.
17.1.1.4 Reporting Influenza Liked Cases
1.
According to the definition of influenza liked cases, medical staffs in monitoring consultation rooms of sentinel hospitals must record the number of influenza liked cases found in each age group and in each department. And the total number of cases found in clinics and emergency rooms should also be recorded. The department in charge in sentinel hospital should collect the data everyday and input the data into Chinese Surveillance System of Influenza on Mondays.
2.
The number of influenza liked cases and hospital total number of clinic/emergency room visits should have consistent source from each monitoring consultation rooms.
3.
The sentinel hospitals have rights to determine the department in charge.
17.1.1.5 Specimens Collection from Influenza Liked Cases
1.
Subjects of sampling: influenza liked cases who show symptoms within 3 days with no use of any anti-viral drugs.
2.
The sentinel hospital should collect 20–30 specimens per week. The collection time should be evenly distributed to avoid focused and sudden sampling. Sampling can be performed every other day, with 7–10 samples collected on the day. Sampling may also be performed each day, with 4–6 samples collected on the day. The specimens should be kept at the temperature of below 4 °C. For each week, samples should be sent to the network laboratories at least twice.
17.1.1.6 Laboratory Tests
1.
After influenza surveillance network laboratories receive the samples by routine collection from sentinel hospitals, it is required to process the samples and test the nucleic acid within 48 h. The samples with positive findings should be performed isolation and identification of Influenza A (H1N1) virus in laboratories with biological safety and testing conditions. All the influenza strains should be sent to provincial CDC for reservation and identification. The provincial CDC is required to send all Influenza A (H1N1) strains with HA titer no less than 8 (including seasonal flu viruses) to national influenza center and the virus culture fluid should be no less than 3 mL/strain. Within 4 weeks of samples collection, the virus strain should be sent out.
2.
The provincial CDC and other influenza surveillance network laboratories with required biological safety and testing conditions should isolate Influenza A (H1N1) virus from samples.
3.
The influenza surveillance network laboratories should send positive samples with unidentifiable virus types and subtypes to national influenza center within 48 h.
4.
After laboratory testing, the samples information, nucleic acid testing, virus isolation and identification must be input into the Chinese Influenza Surveillance Information System within 24 h.
5.
After influenza surveillance network laboratories receive samples from epidemic outbreaks, the samples should be processed for nucleic acid tests within 24 h. The Influenza A (H1N1) viruses should be isolated and identified in laboratories with biological safety and testing conditions. All the Influenza A (H1N1) virus strains with HA titer no less than 8 should be sent to national influenza center, with the virus culture fluid no less than 3 mL/strain. Within 4 weeks of samples collection, the virus strain should be sent out. At least five positive specimens should be performed virus isolation for each epidemic outbreak. If the collected specimens are less than five, all specimens should be performed virus isolation.
17.1.2 Surveillance of Epidemic Outbreak
17.1.2.1 Definition of Outbreak
Outbreak refers to abnormally increased cases of fever and acute respiratory infection in an area or unit within a short period of time, which is confirmed by laboratory tests to be epidemic seasonal influenza or Influenza A (H1N1).
17.1.2.2 Finding and Reporting of the Epidemic
1.
Within 1 week, occurrence of five or more cases of clustering acute fever and respiratory infection that is associated with epidemiology in the places where the same group of people clustering (such as schools, kindergartens, hospitals, homes for the aged, factory and construction sites) should be reported within 2 h to county CDC. The outbreak in rural areas can also be reported to the local village or town hospitals.
2.
Once county (district) CDC receives the epidemic report, it has the responsibilities to organize preliminary investigation and verification immediately, followed by collection of the patients’ samples, tests of the samples in appropriate laboratories to detect seasonal flu viruses and Influenza A (H1N1) viruses. The amount of samples collected should be enough for laboratory diagnosis of the epidemic. Generally, for clustering epidemic of less than 20 cases, samples from all cases should be collected; for clustering epidemic of more than 20 cases, only samples from no more than 20 cases should be collected. Patients with acute fever and respiratory infection but no definitive laboratory diagnosis in the same epidemic event can be diagnosed as clinical cases when other diseases causing flu liked symptoms are excluded.
3.
The definitively diagnosed cases of seasonal flu or Influenza A (H1N1) meet the following at least one criterion should be reported in the forms of Information Report of Sudden Public Health Events and Epidemic Outbreak Report of Seasonal Flu and Influenza A (H1N1) by county (district) CDC in 2 h. Direct internet reporting may also be performed in Sudden Public Health Events Reporting System. The province (district or city) can adjust reporting standards according to local epidemic situation. The direct internet reporting of Reporting Form for Epidemic Outbreak Surveillance for Flu Liked Cases has been terminated.
Within 1 week, more than ten cases of seasonal flu or Influenza A (H1N1) occur;
Within 1 week, more than two cases of seasonal flu or severe cases of Influenza A (H1N1);
Within 1 week, more than one case of seasonal flue or death from Influenza A (H1N1).
4.
The definitively diagnosed cases in the outbreak event should be relevant to individual case in Disease Surveillance Information Reporting Management System. The definitively diagnosed cases that have not reported in the system should be supplementary reported.
The network laboratories responsible to laboratory tests should input the laboratory testing results into Chinese Influenza Surveillance Information System. The CDC reporting the epidemic should relate the samples information to the individual case of Disease Surveillance Information Reporting Management System.
5.
During the process of investigation and management of epidemic outbreak, various levels of CDC should timely revise the initial report in Outbreak Reporting Form of Seasonal Flu and Influenza A (H1N1). The progress reports and final reports should be well finished according to the requirements in Management Standards of National Sudden Public Health Events Information Reporting.
17.1.3 Surveillance of Other Influenza Liked Cases
1.
In clinic, emergency and admitted patients diagnosed as suspected severe or critical Influenza A (H1N1) should be performed samples collection and laboratory testing as early as possible, with following direct internet reporting. The patients with positive findings should be revised as definitively diagnosed cases. Within 24 h of discharge or death, the hospital should be responsible to finish Questionnaire for Severe Cases of Influenza A (H1N1) and to input the information into Information Management System for Influenza A (H1N1). The samples with positive results should be sent to network laboratories for further analysis. Samples from other flu liked cases in clinics and emergency departments should not be tested by network laboratories.
For the death cases occurring outside the hospitals, the county CDC is responsible to collect questionnaire information within 24 h after death. And the information should be input into Information Management System for Influenza A (H1N1).
2.
As for the cases with definitive diagnosis of other diseases or definitive exclusion of Influenza A (H1N1), the diagnosis should be timely revised to the definitively diagnosed disease or other disease with no known causes. For cases diagnosis revised from suspected or clinical to definitive, the reporting unit should revise the diagnosis after the laboratory testing results are informed.
3.
Any responsible medical or administrative staff should fill in the Infectious Diseases Report of Influenza A (H1N1) Cases according to the guidelines for diagnosis and treatment of Influenza A (H1N1). The corresponding cases classification should be checked at slight cases, severe cases, critical cases. Admission should also be filled in (Infectious Diseases Reporting Card has been revised).
4.
Except for the definitively diagnosed severe and critical cases and death cases, other cases with Influenza A (H1N1) should not be reported in Individual Cases Inventory.
17.2 Report of Epidemic
The infectious diseases reporting in China began from 1950s and has more than 50 years of history. Since the acts of China Infectious Disease Prevention and Cure Statute was issued and implemented in 1989, the infectious diseases reporting is recruited into legal management in China. In the fight against Influenza A (H1N1) epidemic, the infectious diseases reporting system played an indispensable role.
17.3 Control of Infectious Source
Infectious sources are persons or animals who have pathogen survival and reproduction in their bodies, and are capable of discharging pathogen out of their bodies. The objective of infectious sources control is to avoid continued spreading. The infectious source of Influenza A (H1N1) is predominantly patients with the disease. The principles for controlling Influenza A (H1N1) patients are early finding, early reporting, early quarantine and early treatment.
17.4 Management of Contacts
17.4.1 Close Contacts
Persons with close contact history refers to high risk populations who had contacts with Influenza A (H1N1) patients in their infectious phase with no protective measures. Persons with following at least one condition can be regarded as the closely contacted:
1.
Personnels diagnosing, treating, nursing or visiting patients with Influenza A (H1N1).