# Use of RESERVE-Antibiotics in Newborns: Clinical Experience of Two NICUs in the Metropolitan Area of Palermo

**Authors:** Veronica Notarbartolo, Deborah Bacile, Bintu Ayla Badiane, Agnese Lo Leggio, Vita Maria Angileri, Vincenzo Duca, Mario Giuffré

PMC · DOI: 10.3390/antibiotics15020231 · Antibiotics · 2026-02-21

## TL;DR

This paper discusses the use of last-resort antibiotics in newborns in two NICUs in Palermo, highlighting the challenges of treating antibiotic-resistant infections.

## Contribution

The study presents clinical experiences with RESERVE antibiotics in neonatal care, contributing to limited evidence on their use in newborns.

## Key findings

- Four newborn patients were treated with last-generation antibiotics over three years.
- The use of these antibiotics is increasing due to multidrug-resistant organisms causing sepsis.
- Standardized treatment approaches are needed for neonatal antibiotic-resistant infections.

## Abstract

Background: The increasingly indiscriminate use of antibiotic therapy in the neonatal period has led to the emergence of multidrug-resistant organisms (MDROs), which are responsible for sepsis that is increasingly difficult to treat and associated with high morbidity and mortality. Increasingly frequently, in neonatal intensive care units (NICUs), it is necessary to use last-generation antibiotics belonging to the RESERVE group according to the current classification of the World Health Organization (WHO). Methods: Among these drugs, ceftazidime-avibactam, ceftolozane-tazobactam and meropenem-vaborbactam are increasingly used in infections caused by Enterobacterales (i.e., E. cloacae complex, Klebsiella spp.), which are often responsible for late-onset sepsis (LOS) in newborns, especially in preterms. Results: Here, we present the experience of four newborn patients in the city of Palermo, treated over a period of 3 years. Conclusions: The comparison between different diagnostic–therapeutic management approaches and a review of the most recent literature can contribute to identifying more standardized pharmacological schemes, especially in the neonatal period, where scientific evidence about this topic is still very limited.

## Linked entities

- **Chemicals:** ceftazidime-avibactam (PubChem CID 90643431), ceftolozane-tazobactam (PubChem CID 86291594), meropenem-vaborbactam (PubChem CID 86298703)
- **Species:** Enterobacterales (taxon 91347)

## Full-text entities

- **Genes:** CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}
- **Diseases:** congenital malformations (OMIM:163000), hemothorax (MESH:D006491), MDR (MESH:D018088), ectasia (MESH:D004108), meningoencephalitis (MESH:D008590), fibrosis (MESH:D005355), hyperglycemia (MESH:D006943), critically ill (MESH:D016638), IUGR (MESH:D005317), esophageal atresia (MESH:D004933), atrial septal defect (MESH:D006344), injury to (MESH:D014947), oligohydramnios (MESH:D016104), inflammation (MESH:D007249), edema (MESH:D004487), meningitis (MESH:D008580), congenital intestinal malformation (MESH:D007409), dysmorphic (MESH:D057215), diabetic (MESH:D003920), intra-abdominal infections (MESH:D059413), neurological involvement (MESH:C538190), irritability (MESH:D001523), hepatosplenomegaly (MESH:C535727), K. Pneumoniae (MESH:D011014), obstruction at the sigmoid colon (MESH:D012811), multiorgan dysfunction (MESH:D009102), aganglionosis (MESH:D006627), hematemesis (MESH:D006396), pleural effusion (MESH:D010996), leukopenia (MESH:D007970), tracheoesophageal fistula (MESH:D014138), LOS (MESH:D000071074), bilious vomiting (MESH:D014839), colonic atresia (MESH:C562562), respiratory distress (MESH:D012128), fever (MESH:D005334), acute (MESH:D000208), proteinuria (MESH:D011507), duodenal dysmotility (MESH:D004382), ventricular septal defect (MESH:D006345), seizures (MESH:D012640), apnea (MESH:D001049), cytopenia (MESH:D006402), KPC (MESH:C565455), hypertension (MESH:D006973), hypothyroidism (MESH:D007037), death (MESH:D003643), polyhydramnios (MESH:D006831), epileptic (MESH:D004827), opisthotonic posturing (MESH:D054972), Nosocomial infections (MESH:D003428), ascites (MESH:D001201), anemia (MESH:D000740), atelectasis (MESH:D001261), hypertonia (MESH:D009122), premature rupture of membranes (MESH:D005322), urinary tract infections (MESH:D014552), toxicity (MESH:D064420), genetic anomalies (MESH:D020022), thrombocytopenia (MESH:D013921)
- **Chemicals:** paracetamol (MESH:D000082), oxygen (MESH:D010100), ceftolozane-tazobactam (MESH:C000594038), Ceftolozane (MESH:C519491), aminoglycoside (MESH:D000617), ibuprofen (MESH:D007052), teicoplanin (MESH:D017334), metronidazole (MESH:D008795), Meropenem (MESH:D000077731), Carbapenem (MESH:D015780), vancomycin (MESH:D014640), CAZ (MESH:D002442), insulin (MESH:D007328), methicillin (MESH:D008712), Tazobactam (MESH:D000078142), gentamicin (MESH:D005839), fosfomycin (MESH:D005578), CAZ-AVI (MESH:C000595613), Vaborbactam (MESH:C000626994), AVI (-), amikacin (MESH:D000583), piperacillin-tazobactam (MESH:D000077725), CVC (MESH:C506967), vitamin K (MESH:D014812), cephalosporin (MESH:D002511), ursodeoxycholic acid (MESH:D014580), ampicillin (MESH:D000667), MER-VAB (MESH:C000654127)
- **Species:** Escherichia coli (E. coli, species) [taxon 562], Klebsiella pneumoniae (species) [taxon 573], Acinetobacter (genus) [taxon 469], Enterobacter cloacae complex (species group) [taxon 354276], Pseudomonas aeruginosa (species) [taxon 287], Enterobacterales (order) [taxon 91347], Enterobacter hormaechei (CDC Enteric Group 75, species) [taxon 158836], Enterobacter cloacae (species) [taxon 550], Staphylococcus epidermidis (species) [taxon 1282], Homo sapiens (human, species) [taxon 9606], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Staphylococcus aureus (species) [taxon 1280], Serratia marcescens (species) [taxon 615]

## Full text

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## References

29 references — full list in the complete paper: https://tomesphere.com/paper/PMC12937599/full.md

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Source: https://tomesphere.com/paper/PMC12937599