Key result
Pretransplant Glenn or Fontan physiology was a significant risk factor for developing posterior reversible encephalopathy syndrome after pediatric heart transplantation (RR 4.99; 95% CI 1.19-21.0; p=0.036).
Why the study?
Does preexisting Glenn/Fontan physiology increase the risk of posterior reversible encephalopathy syndrome (PRES) in pediatric heart transplant recipients?
Cohort (n=128)
Does preexisting Glenn/Fontan physiology increase the risk of posterior reversible encephalopathy syndrome (PRES) in pediatric heart transplant recipients?
Preexisting Glenn or Fontan physiology is a newly identified, significant risk factor for posterior reversible encephalopathy syndrome (PRES) in pediatric heart transplant recipients.
Answers are grounded in this paper and cite their sources.
May support targeted PRES monitoring in Glenn/Fontan recipients; leaves open need for prospective validation.
Identification of risk factors for PRES after organ transplant can improve early detection and avoid permanent neurological injury. High calcineurin-inhibitor levels and hypertension are recognized risk factors for PRES in adult transplant recipients. Limited data exist regarding PRES after pediatric HTx, with studies limited to case reports. We performed a retrospective review of 128 pediatric HTx recipients to identify risk factors for PRES. Seven of 128 (5.5%) recipients developed PRES at a median of 10 days (5-57) after HTx. The median age of recipients with PRES was 10.0 yr (5.7-19.0), compared to 1.4 yr (0.0-19.8) for recipients without PRES (p = 0.010). Fewer than half of recipients with PRES had elevated post-transplant calcineurin-inhibitor levels (n = 3) and/or preceding severe hypertension (n = 3). Four of seven who developed PRES (57%) had pretransplant Glenn or Fontan physiology (G/F). G/F was a significant risk factor for PRES (RR 4.99, 95% CI: 1.19-21.0, p = 0.036). Two recipients (29%), both with severe PRES, had residual neurological symptoms. In summary, PRES occurred in 5.5% of pediatric HTx recipients and presented early after HTx. All recipients with PRES were > 5 yr. Patients with pretransplant G/F were at increased risk, a risks factor not previously described.
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Eilers et al. (2016) conducted a cohort in Pediatric heart transplantation (n=128). Preexisting Glenn or Fontan physiology vs. Without preexisting Glenn or Fontan physiology was evaluated on Posterior reversible encephalopathy syndrome (PRES) (RR 4.99, 95% CI 1.19-21.0, p=0.036). Pretransplant Glenn or Fontan physiology was a significant risk factor for developing posterior reversible encephalopathy syndrome after pediatric heart transplantation (RR 4.99; 95% CI 1.19-21.0; p=0.036).
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