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Aminosyn PF or trophamine: which provides more protection from cholestasis associated with total parenteral

M L Forchielli1, K M Gura, R Sandler

  • 1Combined Program in Gastroenterology and Nutrition, Children's Hospital, Boston, Massachusetts, USA.

Insights

This study reviewed 70 infants receiving total parenteral nutrition (TPN) to assess amino acid formulations for preventing cholestasis associated with TPN (CATPN). Results indicate TPN duration, not specific formulas like Aminosyn PF or Trophamine, significantly impacts CATPN development.

Area of Science:

  • Neonatal Medicine
  • Pediatric Gastroenterology
  • Clinical Nutrition

Background:

  • Cholestasis is a common complication in infants requiring long-term total parenteral nutrition (TPN).
  • Specific infant amino acid formulations, Aminosyn PF and Trophamine, are hypothesized to prevent cholestasis associated with TPN (CATPN).
  • Other factors like prematurity, sepsis, surgery, and ECMO can also contribute to cholestasis in infants.

Purpose of the Study:

  • To compare the effectiveness of Aminosyn PF and Trophamine in preventing CATPN in infants.
  • To identify risk factors associated with the development of CATPN.

Main Methods:

  • Retrospective review of 70 infants under one year old receiving TPN for at least 14 days.
  • Cholestasis defined as conjugated serum bilirubin ≥ 2 mg/dl; CATPN diagnosed after excluding other causes.
  • Liver function tests monitored at baseline and on days 7, 15, and 21 of TPN; regression analysis used for risk factor evaluation.

Main Results:

  • 30 infants (42.8%) developed cholestasis; 15 (21.4%) had CATPN, and 15 (21.4%) had cholestasis from other causes.
  • Among 15 CATPN cases, 7 received Trophamine, 6 received Aminosyn PF, and 2 received both.
  • Only the duration of TPN was a statistically significant factor (p=0.0063) in developing CATPN.

Conclusions:

  • The study could not confirm that Trophamine is more effective than Aminosyn PF in preventing CATPN.
  • TPN duration emerged as a significant risk factor for developing CATPN in infants.
  • Further research may be needed to fully elucidate preventative strategies for CATPN.

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