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Viral illness and the postpericardiotomy syndrome. A prospective study in children
Insights
Post-pericardiotomy syndrome (PPS) following heart surgery is often triggered by viral infections, leading to an immune response. This study found that antiviral antibodies and antiheart antibodies appear concurrently in patients with PPS.
Area of Science:
- Pediatric Cardiology
- Immunology
- Infectious Diseases
Background:
- Post-pericardiotomy syndrome (PPS) is a common complication after cardiac surgery involving pericardial entry.
- The exact cause of PPS, whether viral or immunological, remains debated.
Purpose of the Study:
- To investigate the viral versus immunologic etiology of post-pericardiotomy syndrome (PPS).
- To evaluate the role of viral infections and antiheart antibody (AHA) development in PPS.
Main Methods:
- Prospective, triple-blind study of pediatric patients undergoing intrapericardial surgery.
- Serial measurement of antiheart antibody (AHA) and antiviral antibody (AVA) titers.
- Clinical evaluation for PPS and correlation with serological findings.
Main Results:
- Overall PPS incidence was 27%, significantly lower (3.5%) in infants under 2 years.
- High-titer AHA was present in all PPS patients.
- A significant rise in AVA titers was observed in 70% of PPS patients, suggesting a viral trigger.
Conclusions:
- Concurrent viral illness, either fresh or reactivated, likely triggers the immunologic response characteristic of PPS.
- The findings suggest a dual viral and immunologic basis for post-pericardiotomy syndrome.
Abstract:
Postoperative fever and pericardial-pleural reaction, designated postpericardiotomy syndrome (PPS), is a common complication of cardiac surgery involving entry into the pericardium. To determine whether the etiology of PPS is viral or immunologic, we undertook a prospective, triple-blind study of consecutive long-term survivors of intrapericardial surgery in the pediatric age group. We evaluated clinical evidence of syndrome and concurrent appearance of antiheart antibody (AHA) by indirect immunofluorescence and antiviral antibody (AVA) by complement fixation in sera preoperatively and serially postoperatively. Incidence of PPS was 27% overall in 400 subjects, but only 3.5% in infants younger than 2 years of age. AHA in high titer appeared in all patients with PPS. A fourfold or greater rise in titer to AVA was found in 70% of these but in only 5% of those with negative AHA and no PPS. AVA rise, tested in 280 consecutive patients, was to no single one of the eight viruses studied (adenovirus, cytomegalovirus, and coxsackievirus B 1-6). Instead, the rise and fall, consistent with antiviral response to a recent infection, was exhibited usually to one but occasionally to two or more viruses, and the viral prevalence changed from year to year, as did that in the community. The study suggests that concurrent fresh or reactivated viral illness plays a role in triggering the immunologic response that characterizes the PPS.
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