[Management of purpura fulminans apropos of 21 cases: diagnostic delay and therapeutic problems]
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Khaled Menif1, Asma Hamdi, Ammar Khaldi
1Service de Réanimation Pédiatrique Polyvalente, Hôpital d'enfants de Tunis.
Insights
Delays in recognizing purpura fulminans (PF) by parents and healthcare providers led to insufficient treatment. Improved public education and clinician training are crucial for better outcomes in critically ill children with PF.
Area of Science:
- Pediatrics
- Intensive Care Medicine
- Infectious Diseases
Background:
- Purpura fulminans (PF) is a severe condition requiring prompt diagnosis and management.
- Diagnostic and therapeutic delays contribute to poor outcomes in children with PF.
Purpose of the Study:
- To evaluate diagnostic and therapeutic delays in children with purpura fulminans admitted to the pediatric intensive care unit (PICU).
- To identify factors contributing to delayed care and suboptimal treatment in PF cases.
Main Methods:
- Retrospective descriptive study of children with PF admitted to the Children's Hospital of Tunis PICU (January 2000 - January 2006).
- Data collected on symptom duration, treatments, and healthcare provider interactions.
- Optimal care defined by parental, first-line, and hospital doctor actions.
Main Results:
- Twenty-one PF cases were analyzed.
- Delayed parental recognition occurred in 11 children; first-line doctors missed the diagnosis in 62%.
- 52.2% of patients died, with longer hospitalization in general pediatrics for deceased patients.
Conclusions:
- Suboptimal treatment of PF stems from failures in recognition by parents, general practitioners, and hospital doctors.
- Public education and enhanced clinician training in recognition, resuscitation, and stabilization are vital for improving PF outcomes.
Aim:
To evaluate the diagnostic delay and therapeutic insufficiencies delay before the transfer in ICU of the children admitted in the ICU of the children's hospital of Tunis with a purpura fulminans (PF).
Methods:
A retrospective, descriptive study, of children with PF referred between January 2000 and January 2006 to a the paediatric intensive care unit (PICU) of the children's hospital of Tunis. The PF diagnosis was retained in any child presenting a feverish purpura and circulatory insufficiency signs. The optimal diagnostic and therapeutic charge taking was defined in three levels: parental, the first line doctors, and the hospital doctors. The symptoms' duration and the various treatments which were lavished to the patients were taken from the medical observations of the patients transferred in our PICU.
Results:
Twenty one observations were collected. Twelve patients (57.1%) were addressed by a doctor exerting in a dispensary or by a free practicing doctor, 5 patients (23.8%) were transferred from a regional hospital and 4 children (19.1%) directly consulted the children hospital of Tunis urgencies delayed parental recognition occured in 11 children. The PF diagnosis was not evoked by the first line doctor in 62%. Eleven (52.4%) of the children with meningococcal disease were seen but not admitted by a doctor in the 48 hours before admission. Apart from 2 patients (9.5%) who were hospitalized in reanimation directly of the urgencies, all the other patients forwarded by a general pediatry service. In general pediatry, the PF diagnosis was not evoked in 3 cases (15.8%), 31.6% of patients had unnecessary a lumbar punctures and shock was not recognised or treated in 26.3%. Twelve patients (52.2%) died. The duration of hospitalization in general pediatry is significantly higher among deceased patients (5.5 +/- 6.6 hours) than among the surviving patients (2.6 +/- 1.5 hours); p < 0.05.
Conclusion:
Suboptimal treatement in PF is due to failure of parents, general practioners and hospital doctors to recognise specific features of the illness. Improvement in outcome could be achieved by public education and better training of clinicians in recognition, resuscitation, and stabilisation of seriously ill children.
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