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Published on: September 18, 2011
Lessons learned from administration of high-dose methylprednisolone sodium succinate for acute pediatric spinal cord
Michelle C Caruso1, Margot C Daugherty2, Suzanne M Moody2
1Divisions of1Pharmacy.
Insights
Methylprednisolone sodium succinate (MPSS) for acute spinal cord injury (ASCI) in children was rarely administered correctly. Steroid use in pediatric ASCI patients led to significantly more complications, questioning its clinical benefit.
Area of Science:
- Pediatric Traumatology
- Neurological Surgery
- Pharmacology
Background:
- Methylprednisolone sodium succinate (MPSS) was previously a standard treatment for acute spinal cord injury (ASCI) in adults, but recent guidelines suggest discontinuing its use due to uncertain benefits and known risks.
- Evidence regarding the efficacy and safety of MPSS in pediatric patients with ASCI is limited, despite its historical use.
- This study aims to evaluate MPSS administration and associated complications in a pediatric trauma center.
Purpose of the Study:
- To assess the adherence to institutional guidelines for ordering and administering high-dose MPSS in pediatric patients with ASCI.
- To determine the frequency and types of complications associated with MPSS use in pediatric ASCI cases.
- To provide data to inform clinical practice regarding MPSS therapy in pediatric ASCI.
Main Methods:
- A retrospective chart review of 602 patients under 17 years old admitted for blunt trauma with concern for ASCI was conducted.
- Inclusion criteria specified age, trauma type, physician concern, and admission duration or MPSS treatment; exclusion criteria removed penetrating trauma, lack of ASCI documentation, and incomplete records.
- Data collected included MPSS order accuracy, administration timeline adherence, and a predefined list of complications.
Main Results:
- Of 354 included patients, 59 received MPSS. Only 22% of these received the therapy according to the recommended protocol for both ordering and administration.
- Patients receiving steroids for ASCI experienced complications in 55.6% of cases, significantly higher than the 24.2% rate in those not receiving steroids (p = 0.008).
- Even in patients without ASCI, steroid administration was associated with a significantly higher complication rate (43.5%) compared to non-steroid users (19.1%, p = 0.006).
Conclusions:
- High-dose MPSS for pediatric ASCI is not reliably administered according to established protocols.
- Pediatric patients receiving MPSS for ASCI demonstrate a significantly increased likelihood of experiencing adverse complications.
- The findings support the removal of high-dose MPSS as a treatment option for pediatric ASCI due to increased complications and questionable efficacy.
Abstract:
OBJECTIVE Methylprednisolone sodium succinate (MPSS) has been studied as a pharmacological adjunct that may be given to patients with acute spinal cord injury (ASCI) to improve neurological recovery. MPSS treatment became the standard of care in adults despite a lack of evidence supporting clinical benefit. More recently, new guidelines from neurological surgeon groups recommended no longer using MPSS for ASCI, due to questionable clinical benefit and known complications. However, little information exists in the pediatric population regarding MPSS use in the setting of ASCI. The aim of this paper was to describe steroid use and side effects in patients with ASCI at the authors' Level 1 pediatric trauma center in order to inform other hospitals that may still use this therapy. METHODS A retrospective chart review was conducted to determine adherence in ordering and delivery according to the guideline of the authors' institution and to determine types and frequency of complications. Inclusion criteria included age < 17 years, blunt trauma, physician concern for ASCI, and admission for ≥ 24 hours or treatment with high-dose intravenous MPSS. Exclusion criteria included penetrating trauma, no documentation of ASCI, and incomplete medical records. Charts were reviewed for a predetermined list of complications. RESULTS A total of 602 patient charts were reviewed; 354 patients were included in the study. MPSS was administered in 59 cases. In 34 (57.5%) the order was placed correctly. In 13 (38.2%) of these 34 cases, MPSS was administered according to the recommended timeline protocol. Overall, only 13 (22%) of 59 patients received the therapy according to protocol with regard to accurate ordering and administration. Among the patients with ASCI, 20 (55.6%) of the 36 who received steroids had complications, which was a significantly higher rate than in those who did not receive steroids (8 [24.2%] of 33, p = 0.008). Among the patients without ASCI, 10 (43.5%) of the 23 who received steroids also experienced significantly more complications than patients who did not receive steroids (50 [19.1%] of 262, p = 0.006). CONCLUSIONS High-dose MPSS for ASCI was not delivered to pediatric patients according to protocol with a high degree of reliability. Patients receiving steroids for pediatric ASCI were significantly more likely to experience complications than patients not receiving steroids. The findings presented, including complications of steroid use, support removal of high-dose MPSS as a treatment option for pediatric ASCI.
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