Critical Care Medicine · 1997 · 216 citations · 15 references
Veterinary MedicineInfectious DiseasesSepsisBacterial InfectionsSeptic ShockPurpura Fulminans
The study aimed to assess whether recombinant tissue plasminogen activator infusion could dissolve microvascular thromboses and improve organ perfusion in a patient with fulminant meningococcemia, and to evaluate its potential for broader use. A descriptive case report of a 4‑month‑old male with fulminant meningococcemia in a pediatric ICU, who received a 1.25 mg/kg r‑tPA infusion over 4 h alongside standard care, with hemodynamic, renal, metabolic, and perfusion parameters recorded before and after treatment. The r‑tPA infusion produced dramatic improvements in hemodynamics, urine output, metabolic acidosis, and skin perfusion, indicating enhanced organ perfusion and cardiac performance. Published in Critical Care Medicine 1997; 25:1079‑1082.
Objective To investigate whether an infusion of recombinant tissue plasminogen activator would dissolve microvascular thromboses and improve organ perfusion in a patient with fulminant meningococcemia. Design Descriptive case report. Setting Fifteen-bed pediatric intensive care unit (ICU) in a university hospital. Patient A 4-month-old male with fulminant meningococcemia, refractory shock, and multiple organ failure. Interventions In addition to standard aggressive ICU care, the patient received a recombinant tissue plasminogen activator infusion at a total dose of 1.25 mg/kg over 4 hrs. Measurements and Main Results Heart rate, arterial blood pressure, urine output, and base deficit (as a reflection of severity of metabolic acidosis) were recorded immediately before the recombinant tissue plasminogen activator infusion and 4 hrs later, after completion of the recombinant tissue plasminogen activator infusion. The amount of exogenous vasopressor and inotropic support required to maintain the patient's hemodynamic status before and after recombinant tissue plasminogen activator infusion were also compared. Subjective observations regarding the patient's peripheral perfusion status were also noted. The patient showed a dramatic improvement in hemodynamics, urine output, and metabolic acidosis, as well as a perceived increase in skin perfusion after recombinant tissue plasminogen activator infusion. Conclusions In this patient, recombinant tissue plasminogen activator infusion resulted in improved organ perfusion and cardiac performance. Selective use of recombinant tissue plasminogen activator in the treatment of fulminant meningococcemia merits further investigation. (Crit Care Med 1997; 25:1079-1082)
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