Epidural labour analgesia-related fever
Conditions
Interventions
Observation group:None
Sponsors
Tianjin Central Hospital of Gynecology Obstetrics
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: 1.Hospital delivery from 1 January 2024 to 31 December 2025, singleton, cephalic pregnancy; 2.Gestational age =37 weeks and =42 weeks (full-term delivery); 3.Voluntarily undergo epidural analgesia for labour, with successful implementation (block level reaches below T10, satisfactory analgesic effect, NRS pain score =3); 4.Complete clinical data (including general information, obstetric information, analgesia-related information, temperature monitoring data, maternal and neonatal outcome data, etc.); 5.No history of severe liver and kidney dysfunction, coagulation disorders, or infectious diseases;
Exclusion criteria
Exclusion criteria: 1.Those who experience failure of epidural labour analgesia or abandon analgesia midway; 2.Those who have a fever (temperature =38.0°C) or clear signs of infection (such as chorioamnionitis, upper respiratory tract infection, Group B streptococcus infection, etc.) before delivery (prior to epidural analgesia); 3.Those with multiple pregnancies, abnormal fetal positions (breech, transverse, etc.), preterm labour, or post-term pregnancies; 4.Those with severe pregnancy complications (such as severe preeclampsia, eclampsia, severe gestational diabetes, heart failure, etc.); 5.People allergic to epidural analgesics (such as ropivacaine, sufentanil, etc.); 6.Clinical data is severely lacking, making it impossible to complete data extraction and analysis;
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Body temperature; | — |
Secondary
| Measure | Time frame |
|---|---|
| maternal and fetal outcome;severity of fever; | — |
Countries
China
Contacts
Public ContactDong Hui
Tianjin Central Hospital of Gynecology Obstetrics
Outcome results
None listed