• Due for Review
  • Alert Indication
  • Drug Type Probiotic bacteria Trade Name
  • Maximum daily dose 2 capsules (500 mg) daily Route
  • Administration Oral: Administer with feeds if possible. Monitoring
  • Contraindications No known contraindications. Precautions
  • Drug Interactions None reported. Adverse Reactions
  • Storage Store at 2−8°C. Special Comments
  • Probiotics for prevention of NEC in preterm infants
  • Probiotics for prevention of late onset sepsis (LOS) in preterm infants
  • Neonatal Intensive Care Drug Manual




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    Original version Date: 15/11/2016

    Author: Neonatal Medicines Formulary Consensus Group

    Current Version number: 2

    Current Version Date: 23/12/2020

    Risk Rating: Low

    Due for Review: 23/12/2025

    Approval by: DTC

    Approval Date:TBA


    Infloran®


    Revision Date : 16-5-2019

    Approved: TC/KOH




    Alert




    Indication


    1) Preterm neonates < 34 weeks gestation or < 1800 g birth weight: For prevention of necrotising enterocolitis (NEC), late-onset sepsis, mortality and reduction in time to reach full feeds.[1-3]

    2) Small for gestational age, preterm neonates with abnormal umbilical artery Doppler for prevention of NEC and reduction in time to reach full feeds. [1, 4]



    3) The safety and efficacy for other populations of infants at risk of NEC, sepsis or feed intolerance including infants with asphyxia, undergoing exchange transfusion, abdominal surgical conditions and congenital heart disease has not been assessed in clinical studies.

    Action

    Probiotics promote colonisation of the gut with beneficial organisms, preventing colonisation by pathogens, improving the maturity and function of gut mucosal barrier, and modulating the immune system (e.g. TLR4 receptor, nuclear factor-kB and inflammatory cytokines) to the advantage of the host. [5]

    Drug Type

    Probiotic bacteria

    Trade Name

    Infloran

    Presentation

    250 mg capsule containing Lactobacillus acidophilus [109 colony-forming units, NCDO 1748; National Collection of Dairy Organisms] and Bifidobacterium bifidum [109 colony-forming units, NCDO 1453; National Collection of Dairy Organisms, Reading, United Kingdom]; Laboratorio Farmaceutico, Italy. [6, 7]

    Dosage/Interval


    Commence the dose soon after birth irrespective of the feeds.
    Birthweight < 1 kg: Commence with ½ capsule (125 mg) daily until neonate is on 40 mL/kg/day of oral feeds and then change to 1 capsule daily until 34–36 weeks or considered no longer at risk of NEC.
    Birthweight ≥ 1 kg: Commence 1 capsule (250 mg) daily and continue until 34–36 weeks or considered no longer at risk of NEC.

    Maximum daily dose

    2 capsules (500 mg) daily

    Route

    Oral/Orogastric

    Preparation/Dilution



    The contents of ONE capsule should be dissolved in 2 mL of mother’s EBM/donor human milk/water for injection/formula. Draw up required volume (1 mL for 125 mg and 2 mL for 250 mg)

    Administration

    Oral: Administer with feeds if possible.

    Monitoring




    Contraindications

    No known contraindications.

    Precautions

    Administration of the probiotics may be discontinued during periods when the integrity of the gut mucosa is considered compromised. The common scenarios include intestinal perforation, severe sepsis, critical illness, bile aspirates, NEC and surgical gut anomalies.[8] No efficacy or safety data available on use of probiotics in infants after definite NEC.

    Drug Interactions

    None reported.

    Adverse Reactions


    Rare.

    Probiotic sepsis has been reported in preterm neonates with surgical conditions, immune suppression and when gut barrier is compromised. [8]



    Stability

    Bifidobacterium bifidum is particularly heat sensitive, so once the capsule is open it should be used immediately.

    Storage

    Store at 2−8°C.

    Special Comments


    Please note: There are 2 Infloran preparations. (1) Infloran and (2) Infloran infantis.

    Infloran infantis is not available in Australia.

    Infloran contains Bifidobacterium bifidum and Lactobacillus acidophilus.

    Infloran infantis contains Bifidobacterium infantis and Lactobacillus acidophilus.


    Median 2 to 3 x 109 CFU dose has been shown to prevent NEC.[7] There is no known benefit in terms of prevention of NEC with doses higher than 3 x 109 CFU. One capsule of Infloran should provide minimum of 2 x 109 CFU. Studies have shown that up to 2 capsules/day dose is well tolerated by older premature neonates (> 1500 g).[8]
    All probiotic preparations given to newborn infants should have undergone quality testing in an Australian TGA equivalent regulated system including batch to batch testing for colony count to rule out contamination.[8]
    The intestinal barrier could be compromised during severe sepsis and critical illness. Probiotics may be discontinued in the initial stages of severe late onset sepsis, suspected NEC, or critical illness.[8]

    Evidence summary

    Several systematic reviews and randomised controlled trials have shown that enteral probiotics significantly reduce the risk of NEC (≥ stage II), late onset sepsis, all-cause mortality and time to full enteral feeds. [1-3] (LOE 1, GOR A) Multiple strains of probiotics may be more effective in preventing NEC and mortality than single strains. [9] (LOE I, GOR B)

    Probiotics for prevention of NEC in preterm infants: Enteral probiotic supplementation significantly reduced the incidence of severe NEC (RR 0.43, 95% CI 0.33 to 0.56; 20 studies, 5529 infants) and mortality (typical RR 0.65, 95% CI 0.52 to 0.81; 17 studies, 5112 infants). The included trials reported no systemic infection with the supplemental probiotics organism. Probiotics preparations containing either Lactobacillus alone or in combination with Bifidobacterium were found to be effective. Conclusions: Enteral supplementation of probiotics prevents severe NEC and all-cause mortality in preterm infants. [1, 2, 9] (LOE I GOR A) Infloran containing Bifidobacterium bifidum and Lactobacillus acidophilus has been shown in a RCT to reduce the incidence of death and NEC. [7] Prospective observational studies of routine use of Infloran (B. bifidum and L. acidophilus) in preterm neonates, gestation < 32 weeks and < 1500 g, have documented its safety and potential efficacy. [10, 11]

    Probiotics for prevention of late onset sepsis (LOS) in preterm infants: Enteral probiotics supplementation significantly reduced the incidence of LOS (37 RCTs, 9416 infants; 13.9% vs 16.3%; RR 0.86; 95% CI 0.78–0.94; P = .0007; NNT 44). [2, 3] (LOE I GOR A)

    Safety: None of the included trials have reported probiotic-induced sepsis.[1-3, 9] Case reports of systemic infections caused by probiotic organisms are found in the literature. [8] Most adverse events and serious adverse events were considered unrelated to the study product and there were no major safety concerns.[8]

    Issues related to quality of probiotic products have been reported, including viability and contamination.[12, 13] Food and Drug Administration (FDA) USA issued an alert when a neonate died due to fungal sepsis from contaminated probiotic product.[13] Viability and contamination testing should be performed on every batch of probiotic product.[8]



    References

    1. Alfaleh K, Anabrees J, Bassler D, Al-Kharfi T. Probiotics for prevention of necrotizing enterocolitis in preterm infants. Cochrane Database Syst Rev. 2011:CD005496.

    2. Dermyshi E, Wang Y, Yan C, Hong W, Qiu G, Gong X, Zhang T. The "Golden Age" of Probiotics: A Systematic Review and Meta-Analysis of Randomized and Observational Studies in Preterm Infants. Neonatology. 2017;112:9-23.

    3. Rao SC, Athalye-Jape GK, Deshpande GC, Simmer KN, Patole SK. Probiotic Supplementation and Late-Onset Sepsis in Preterm Infants: A Meta-analysis. Pediatrics. 2016;137:e20153684.

    4. Deshpande G, Rao S, Patole S, Bulsara M. Updated meta-analysis of probiotics for preventing necrotizing enterocolitis in preterm neonates. Pediatrics. 2010;125:921-30.

    5. Martin CR, Walker WA. Probiotics: role in pathophysiology and prevention in necrotizing enterocolitis. Semin Perinatol. 2008;32:127-37.

    6. Infloran. Product information. Laboratorio Farmaceutico, Italy. 2002.

    7. Lin HC, Hsu CH, Chen HL, Chung MY, Hsu JF, Lien RI, Tsao LY, Chen CH, Su BH. Oral probiotics prevent necrotizing enterocolitis in very low birth weight preterm infants: a multicenter, randomized, controlled trial. Pediatrics. 2008;122:693-700.

    8. Deshpande GC, Rao SC, Keil AD, Patole SK. Evidence-based guidelines for use of probiotics in preterm neonates. BMC medicine. 2011;9:92.

    9. Chang HY, Chen JH, Chang JH, Lin HC, Lin CY, Peng CC. Multiple strains probiotics appear to be the most effective probiotics in the prevention of necrotizing enterocolitis and mortality: An updated meta-analysis. PLoS One. 2017;12:e0171579.

    10. Deshpande G, Shingde V, Downe L, Leroi M, Xiao J. Routine probiotics for preterm neonates: experience in a tertiary australian neonatal intensive care unit. J Paediatr Child Health. 2013;49:50.

    11. Samuels N, Van De Graaf R, Been JV, De Jonge RCJ, Hanff LM, Wijnen RMH, Kornelisse RF, Reiss IKM, Vermeulen MJ. Necrotising enterocolitis and mortality in preterm infants after introduction of routine probiotics in a NICU setting. Eur J Pediatr. 2016;175 (11):1733-4.

    12. Canganella F, Paganani S, Ovidi M, Vettraino AM, Bevilacqua L, Massa S, Trovatelli LD. A microbiological investigation on probiotic pharmaceutical products used for human health. Microbiological research. 1997;152:171-9.

    13. Drago L, Rodighiero V, Celeste T, Rovetto L, De Vecchi E. Microbiological evaluation of commercial probiotic products available in the USA in 2009. J Chemother. 2010;22:373-7.

    12. https://www.fda.gov/food/recallsoutbreaksemergencies/outbreaks/ucm423830.htm.





    Original version Date: 6/06/2017

    Author: Neomed Consensus Group

    Current Version number: 2

    Current Version Date: 16/5/2019

    Risk Rating: Low

    Due for Review: 16/5/2024

    Approval by: DTC

    Approval Date: TBA



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    Neonatal Intensive Care Drug Manual

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