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Antibiotic Prescriptions and Prophylaxis in Italian Children. Is It Time to Change? Data from the ARPEC Project

  • Maia De Luca ,

    Contributed equally to this work with: Maia De Luca, Daniele Donà

    maiadeluca@gmail.com

    Affiliation Immunology and Infectious Diseases Unit, University Hospital Pediatric Department, Bambino Gesù Children's Hospital, Rome, Italy

  • Daniele Donà ,

    Contributed equally to this work with: Maia De Luca, Daniele Donà

    Affiliation Division of Pediatric Infectious Diseases, Department for Woman and Child Health, University of Padua, Padua, Italy

  • Carlotta Montagnani,

    Affiliation Paediatric Infectious Diseases Unit, Department of Paediatric Medicine, Anna Meyer Children's University Hospital, Florence, Italy

  • Andrea Lo Vecchio,

    Affiliation Department of Translational Medical Sciences—Section of Pediatrics, University of Naples Federico II, Naples, Italy

  • Marta Romanengo,

    Affiliation Acute Care and Emergency Department, G. Gaslini Children's Hospital, Genoa, Italy

  • Claudia Tagliabue,

    Affiliation Pediatric Highly Intensive Care Unit, Department of Pathophysiology and Transplantation, Università degli Studi di Milano, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milano, Italy

  • Chiara Centenari,

    Affiliation Paediatric Unit, Versilia Hospital, Lido di Camaiore, Italy

  • Patrizia D’Argenio,

    Affiliation Immunology and Infectious Diseases Unit, University Hospital Pediatric Department, Bambino Gesù Children's Hospital, Rome, Italy

  • Rebecca Lundin,

    Affiliation Division of Pediatric Infectious Diseases, Department for Woman and Child Health, University of Padua, Padua, Italy

  • Carlo Giaquinto,

    Affiliation Division of Pediatric Infectious Diseases, Department for Woman and Child Health, University of Padua, Padua, Italy

  • Luisa Galli,

    Affiliation Paediatric Infectious Diseases Unit, Department of Paediatric Medicine, Anna Meyer Children's University Hospital, Florence, Italy

  • Alfredo Guarino,

    Affiliation Department of Translational Medical Sciences—Section of Pediatrics, University of Naples Federico II, Naples, Italy

  • Susanna Esposito,

    Affiliation Pediatric Highly Intensive Care Unit, Department of Pathophysiology and Transplantation, Università degli Studi di Milano, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milano, Italy

  • Mike Sharland,

    Affiliation Infection and Immunity, Division of Clinical Sciences, St. Georges University of London, London, United Kingdom

  • Ann Versporten,

    Affiliation Laboratory of Medical Microbiology, Vaccine & Infectious Disease Institute, University of Antwerp, Antwerp, Belgium

  • Herman Goossens,

    Affiliation Laboratory of Medical Microbiology, Vaccine & Infectious Disease Institute, University of Antwerp, Antwerp, Belgium

  •  [ ... ],
  • Giangiacomo Nicolini

    Affiliation Pediatric Unit, San Martino Hospital, Belluno, Italy

  • [ view all ]
  • [ view less ]

Abstract

Background

Antimicrobials are the most commonly prescribed drugs. Many studies have evaluated antibiotic prescriptions in the paediatric outpatient but few studies describing the real antibiotic consumption in Italian children’s hospitals have been published. Point-prevalence survey (PPS) has been shown to be a simple, feasible and reliable standardized method for antimicrobials surveillance in children and neonates admitted to the hospital. In this paper, we presented data from a PPS on antimicrobial prescriptions carried out in 7 large Italian paediatric institutions.

Methods

A 1-day PPS on antibiotic use in hospitalized neonates and children was performed in Italy between October and December 2012 as part of the Antibiotic Resistance and Prescribing in European Children project (ARPEC). Seven institutions in seven Italian cities were involved. The survey included all admitted patients less than 18 years of age present in the ward at 8:00 am on the day of the survey, who had at least one on-going antibiotic prescription. For all patients data about age, weight, underlying disease, antimicrobial agent, dose and indication for treatment were collected.

Results

The PPS was performed in 61 wards within 7 Italian institutions. A total of 899 patients were eligible and 349 (38.9%) had an on-going prescription for one or more antibiotics, with variable rates among the hospitals (25.7% - 53.8%). We describe antibiotic prescriptions separately in neonates (<30 days old) and children (> = 30 days to <18 years old). In the neonatal cohort, 62.8% received antibiotics for prophylaxis and only 37.2% on those on antibiotics were treated for infection. Penicillins and aminoglycosides were the most prescribed antibiotic classes. In the paediatric cohort, 64.4% of patients were receiving antibiotics for treatment of infections and 35.5% for prophylaxis. Third generation cephalosporins and penicillin plus inhibitors were the top two antibiotic classes. The main reason for prescribing antibiotic therapy in children was lower respiratory tract infections (LRTI), followed by febrile neutropenia/fever in oncologic patients, while, in neonates, sepsis was the most common indication for treatment. Focusing on prescriptions for LRTI, 43.3% of patients were treated with 3rd generation cephalosporins, followed by macrolides (26.9%), quinolones (16.4%) and carbapenems (14.9%) and 50.1% of LRTI cases were receiving more than one antibiotic. For neutropenic fever/fever in oncologic patients, the preferred antibiotics were penicillins with inhibitors (47.8%), followed by carbapenems (34.8%), aminoglycosides (26.1%) and glycopeptides (26.1%). Overall, the 60.9% of patients were treated with a combination therapy.

Conclusions

Our study provides insight on the Italian situation in terms of antibiotic prescriptions in hospitalized neonates and children. An over-use of third generation cephalosporins both for prophylaxis and treatment was the most worrisome finding. A misuse and abuse of carbapenems and quinolones was also noted. Antibiotic stewardship programs should immediately identify feasible targets to monitor and modify the prescription patterns in children’s hospital, also considering the continuous and alarming emergence of MDR bacteria.

Background

Antimicrobials are the most commonly prescribed drugs in the community and hospital setting, especially among paediatric patients [1]. However, antibiotics are often unnecessarily used both in the community, where too many children receive broad-spectrum antibiotics for viral infections, and in the hospital, where long courses of broad-spectrum antibiotics are frequently prescribed [2]. Recent studies have found that up to 50% of antimicrobial prescriptions are inappropriate [3,4].

The emergence of multi-drug resistant (MDR) pathogens and their rapid global spread, strictly associated with an inappropriate use of antimicrobials, are important global public health threats with a substantial impact on patient outcomes such as hospital length of stay and mortality, as well as on healthcare costs [58]. The European Antimicrobial Resistance Surveillance Network (EARS-Net) system has reported a dangerous rise in MDR bacteria in the last years showing that some countries such as Italy are strongly contributing to this worrying increase [9].

Many studies have evaluated antibiotic prescriptions in the paediatric outpatient population highlighting the problem that Italian prescribing habits that differ from those of other European countries. An Italian child is more likely to be exposed to antibiotics than children are in North Europe [10] and, in particular, the prevalence of antibiotic prescriptions in childhood have been reported to be 4 times higher than in the UK and 6 times higher than in the Netherlands [11,12]. Moreover, Italy reported the highest prescription rate (1.3 per infants per year) in a study comparing antibiotic use in the first year of life in five European countries [13]. In fact, data from the Gagliotti et al study in 2006 show that the 55% of Italian infants in the community have already received at least one course of antibiotics at 1 year of age and 84% at 2 years of age [14].

Although a positive correlation between outpatient and inpatient antibiotic use has been noted [15], few studies describing the real antibiotic consumption in Italian children’s hospitals have been published. A single centre study was carried out in Rome in 2008 [16] confirming the abuse of antibiotics observed in the outpatient population. A more recent paper evaluating the trend of antibiotic use in all the paediatric wards of Emilia-Romagna Region over an 8-year-period [17] indicated a slight increase of antibiotic consumption over time, an inadequate tendency to prefer penicillin plus inhibitors to plain penicillins, an over-use of third generation cephalosporins and a worrisome increase in linezolid prescriptions.

In this paper, we present the results of a point-prevalence survey (PPS) on antibiotic prescriptions carried out in seven large Italian paediatric institutions in 2012. The aims of our study were: i) to describe prevalence rates of antibiotic prescriptions for prophylaxis and treatment of infections for neonatal (<30 days) and paediatric (age ≥30 days) patients in seven Italian centers; ii) to evaluate antibiotic prescriptions, indications, number and type of antibiotic agents and administration route in the same age sub-groups both for prophylaxis and treatment of infections; iii) to describe over-all consumption and off-label use of particular classes of antibiotics, such as carbapenems and quinolones, in our cohort; and iiii) to identify targets for improving the quality of antimicrobial prescribing in these centers.

Methods

This research has been conducted according to the principles expressed in the Declaration of Helsinki. Ethical approval has been obtained for the coordinating centre. No consent was given, because data were collected by reviewing medical charts and were analyzed anonymously. Every patient record was given a unique non-identifiable survey number, which was automatically generated by a computer program specifically designed for anonymous data entry.

A 1-day PPS on antibiotic use in hospitalized children was performed in Italy between October and December 2012 as part of the Antibiotic Resistance and Prescribing in European Children project (ARPEC). Seven paediatric or mixed adult-paediatric hospitals in seven Italian cities were involved (Genoa, Milan, Padua, Florence, Viareggio, Rome and Naples). The survey included all admitted patients less than 18 years of age present in the ward at 8:00 am on the day of the survey who had at least one on-going antibiotic prescription. The wards of admission were: medical (general neonatal and maternal wards, and general paediatric wards), special medical (cardiology, nephrology, onco-hematology, neuromuscolary, neurology, bronchopneumology, infectious diseases unit), neonatal and paediatric intensive care (NICUs and PICUs), surgical (neonatal surgery, paediatric surgery, orthopedics, neurosurgery). For feasibility reasons, one hospital provided data from randomly selected wards, maintaining the patient distribution among medical, special medical, surgical and intensive care units, in agreement with the coordinating centre. Full details of the ARPEC methodology are described elsewhere [18].

Results

The PPS was performed in 61 wards within seven Italian institutions. Characteristics of the centres involved are shown in Table 1. A total of 899 patients was present in the hospitals at 8:00 am on the day of the survey and 349 (38.9%) of these had an on-going prescription for one or more antibiotics. However, this rate was variable among the hospitals ranging from 25.7% to 53.8% (Table 1). Combination therapies were variably used among the institutions (21.7–60.3%) with a ratio between number of prescribed antibiotics and treated patients ranging from 1.25 to 1.76 (Table 1).

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Table 1. Characteristics of the 7 Italian institutions involved in the ARPEC project.

https://doi.org/10.1371/journal.pone.0154662.t001

A wide variability also existed in the proportions of patients treated with at least one antibiotic stratified by ward type. In particular, special medical wards and intensive care units accounted for higher proportions of patients receiving antibiotics compared to surgical and medical wards (“Fig 1”).

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Fig 1. Proportion of paediatric patients treated with at least one antibiotic by ward type.

https://doi.org/10.1371/journal.pone.0154662.g001

Characteristics of all patients enrolled are summarized in Table 2. Median patient age was 24 months and 12.3% were less than 30 days old. Overall, 24.6% of patients were affected by a medical/surgical underlying condition and the most frequent was an oncologic/hematologic disease. Noteworthy is that the rate of oncologic/hematologic patients admitted to the hospital at the time of the survey was 5% (45/899), but this rate increased to 22.3% (78/349) looking at the group of patients receiving antibiotics. These data reflect the fact that oncologic and hematologic patients were responsible for a large proportion of antibiotic consumption in our survey.

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Table 2. Characteristics of the 349 Italian patients enrolled in the 24-hour ARPEC PPS.

https://doi.org/10.1371/journal.pone.0154662.t002

We analyzed antibiotic prescriptions separately in neonates and children (Table 3).

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Table 3. Demographic characteristics and antibiotic prescription patterns of the neonates and children enrolled in the study.

https://doi.org/10.1371/journal.pone.0154662.t003

Neonates

At the time of the survey, 248 neonates were admitted in participating hospitals and 43 were receiving antibiotics (17.3%). As shown in Table 3, neonates treated with antibiotics were mostly admitted in the NICUs (83.7%, 36/43). Moreover, 62.8% (27/43) of newborns were receiving antibiotics for prophylaxis and only 37.2% (16/43) were being treated for infection. The top two active antibiotic prescriptions were penicillins (69.8%, 30/43) and aminoglycosides (58.1%, 25/43). Details about indications to receive antibiotics are summarized in Table 3. All antibiotic classes prescribed are listed in “Fig 2”.

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Fig 2. Antibiotic prescriptions among the neonates and children.

https://doi.org/10.1371/journal.pone.0154662.g002

Antibiotic prophylaxis in neonates

The main indication to prescribe antibiotic prophylaxis was medical risk factors (e.g. prematurity, maternal fever during labor, prolonged rupture of the membranes), accounting for 55.8% of all indications for antibiotic therapy in the neonatal subset. The other neonatal patients were receiving prophylaxis for surgical reasons. Monotherapy was prescribed in 10 of the 27 patients on prophylaxis (37%), and penicillin was the most prescribed antibiotic (7/10). Combination therapies in the other 17/27 patients (63%) were variable: penicillins were combined with aminoglycosides in 7/17 cases, while glycopeptides were used with third generation cephalosporins in 3 cases and with aminoglycosides in 3 cases. The last 4 patients received 3 drug combination therapy, including glycopeptides plus aminoglycosides combined with metronidazole (2/4) or penicillin (2/4).

Antibiotic treatment in neonates

Among all the indications for antibiotic treatment of infection in neonates, the most common was sepsis (30.2%, 13/43). Monotherapy was used just in two cases (one case treated with ampicillin and the other treated with meropenem). Penicillins plus aminoglycosides was by far the preferred combination therapy (8/11), while in the other patients (3/11) glycopeptides were used widely in combination with other classes of antibiotics.

Children

The paediatric group was composed of 651 patients, 47% (306/651) of whom had an active antibiotic prescription at the time of the PPS. In the group of patients with active antibiotic prescriptions, 64.4% (197/306) were being treated for infections and 35.5% (109/306) for prophylaxis (Table 3). Third generation cephalosporins and penicillin plus enzyme inhibitors were the most commonly used antibiotic classes. More details about indications to therapy are reported in Table 3. All antibiotic classes prescribed are listed in “Fig 2”.

Antibiotic prophylaxis in children

Approximately half of the children on antibiotics for prophylaxis received antibiotics for surgical reasons (52.3%, 57/109), the others for medical problems (47.7%, 52/109). The most prescribed antibiotics were third generation cephalosporins for surgery (35.9%, 20/57), used as monotherapy in 14/20 cases and combined most often with metronidazole in the other cases (3/20). Cotrimoxazole was the most commonly prescribed agent for the medical problems (67.3%, 35/52), mainly used as monotherapy (30/35).

Antibiotic treatment in children

The main reason for prescribing antibiotics for infection among children was lower respiratory tract infections (LRTI) (34%, 67/197), followed by febrile neutropenia/fever in oncologic patients (11.7%, 23/197). Focusing on prescriptions for LRTI, 43.3% (29/67) of patients were treated with third generation cephalosporins, followed by macrolides (26.9%, 18/67), quinolones (16.4%, 11/67) and carbapenems (14.9%, 10/67). Cephalosporins were used as monotherapy in 13/29 cases and combined in the other 16 cases, mostly with macrolides (6/16). For 73.1% (49/67) of children with LRTI, the route of antibiotic administration was parenteral.

For oncology patients affected by neutropenic fever/fever, the preferred antibiotics were penicillins with enzyme inhibitors (47.8%, 11/23), followed by carbapenems (34.8%, 8/23), aminoglycosides (26.1%, 6/23) and glycopeptides (26.1%, 6/23). Penicillins with enzyme inhibitors were used in monotherapy in 5/11 cases and combined mostly with aminoglycosides in the other 6 cases. Carbapenem monotherapy was prescribed in 4/8 cases, while combination therapy with anti-Gram positive agents (glycopeptides or oxazolidinones) was preferred in the other cases. The route of antibiotic administration was parenteral in the 95.7% of cases (22/23).

Use of Carbapenems

Among the 899 patients admitted to the hospital at the time of the survey, 32 (3.6%) were being treated with carbapenems. Focusing on the group of 349 patients with active antibiotic prescriptions at the time of the PPS, 8.9% (32/349) were receiving carbapenems (in particular 4.6% [2/43] in the neonatal group and 9.8% [30/306] in the paediatric group). Considering the overall rates of therapy by department, those with the highest rates of carbapenem prescription were the special medical wards (14.2%, 19/134) and the intensive care units (11.2%, 9/80), compared to 2.6% (2/76) in medical wards and 1.7% (1/59) in surgical wards. Indications for prescription of carbapenems were community-acquired infections in 53.1% of cases, hospital-acquired infections in 37.5% and prophylaxis in 9.3%. Febrile neutropenia was the most common reason for carbapenem prescription (34.8%, 8/23). Therapy was empirically prescribed in 62.5% (20/32) of patients. Carbapenems were mostly prescribed in combination with one or more other antibiotics (65.6%, 21/32), most commonly with glycopeptides (10/21), followed by quinolones (4/21), cotrimoxazole (4/21) and aminoglycosides (3/21). Meropenem was the most prescribed carbapenem, with great heterogeneity in doses and number of administrations recorded. Daily doses of meropenem ranged from 19 mg/kg/day to 129 mg/kg/day, while the mean dose was 70 mg/kg/day. Off-label prescription of carbapenems (i.e. below 3 months of age) was recorded in 18.7% (6/32) of patients and the indications were LRTI, sepsis and surgical prophylaxis.

Use of Quinolones

In the entire cohort of patients admitted to the hospital, 3% (27/899) were prescribed quinolones. Among the patients with active antibiotic prescriptions, this rate was 7.7% (27/349). None of them were neonates, but 37% (10/27) were below 2 years of age. Considering the overall rates of prescriptions into the departments, the special medical wards (10.4%, 14/134) and intensive care units (7.5%, 6/80) reported the highest rates of quinolone prescription, compared to 6.6% (5/76) in medical wards and 3.4% (2/59) in surgical wards. Indications for prescription of quinolones were community-acquired infections in 44.4% of cases, hospital-acquired infections in 40.7%and prophylaxis in 14.8%. Considering the rates of antibiotic prescription by indication, the most common indication was LRTI (17.6%, 12/67). Among the group affected by LRTI, 41.6% (5/12) had an underlying chronic lung disease including cystic fibrosis and 25% (3/12) congenital immunodeficiency. In general, quinolone therapy was empirically prescribed in 63% of patients. Quinolones were prescribed as monotherapy just in 29.6% (8/27) of patients. In the other cases, they were widely combined with other antibiotics (70.4%, 19/27), especially with third generation cephalosporins (5/19). The mostly prescribed quinolone was ciprofloxacin. Focusing on ciprofloxacin, the prescribed daily dose ranged from 6 mg/kg/day to 30 mg/kg/day, while the mean dose was 18 mg/kg/day.

Discussion

The 1-day ARPEC PPS provided very useful data on hospital antibiotic prescriptions for paediatric and neonatal patients in Italy. According to data collected in seven large Italian institutions, 38.9% of inpatients received at least one antibiotic prescription during hospitalization. This rate is similar to the mean rate reported from the worldwide ARPEC PPS (36.7%) [18].

To better analyze antibiotic prescription patterns and their appropriateness, we assessed antibiotic prescriptions for prophylaxis and treatment of infection separately.

Our results show that overall 39% of patients were prescribed antibiotics for prophylaxis with the highest rate observed in the neonatal population (63% of neonatal prescriptions were for this indication). The main indication for neonatal prophylaxis was the presence of perinatal conditions (e.g. prematurity, maternal fever during labor, prolonged rupture of the membranes). Prophylactic monotherapy was prescribed just in 37% of neonates and penicillin was the preferred agent, while combination prophylactic therapies including penicillin plus aminoglycosides or glycopeptides plus cephalosporins/aminoglycosides were widely used in neonatal patients. This approach is not in-line with the international literature. Although neonates represent a high risk population due to their immature immune system and the invasive procedure they are likely to undergo in NICU (e.g. indwelling catheters, invasive mechanical ventilation), recent reviews reject the routine use of antibiotic prophylaxis due to lack of efficacy in many conditions [1922]. Moreover, in 2010 the Center for Disease Control and Prevention revised their guidelines regarding the prevention of perinatal Group B streptococcal disease in healthy neonates, restricting the need for prophylaxis only to well-defined subgroups of patients [23]. Prolonged courses of antibiotics have also been associated with increased risk of necrotizing enterocolitis or death in low birth weight infants [24].

In the paediatric group, the rate of antibiotic prescriptions for prophylaxis was 35.5% of all the prescriptions. Approximately, half of these patients were receiving antibiotics for surgical prophylaxis in accordance with previous European reports in which the proportion of children receiving surgical prophylaxis ranged from 13 to 42% [25, 26]. Third generation cephalosporins ranked first in prescription frequency in this scenario, used often in monotherapy but combined with metronidazole in some cases, confirming their alarming overuse for this indication. This problem in fact was already raised by Ciofi et al in 2008 [16], but a recent paper published by Buccellato et al in 2015 shows that a limitation on the prescriptions of these drugs has not yet been reached [17]. However, it is worth noting that this finding was very variable among the seven centers, since some hospitals preferred the first generation cephalosporins for surgical prophylaxis, as suggested by international guidelines [27].

Cotrimoxazole was the most prescribed antibiotic for medical prophylaxis, used alone in most cases. As explanation, most of the treated children were affected by onco-hematological diseases and cotrimoxazole is the best treatment to prevent Pneumocystis jirovecii pneumonia in immunocompromised patients [28].

Regarding the prescription patterns for treatment of infection, the 37.2% of our neonatal cohort was prescribed at least one antibiotic for treating an infection, the main reason was sepsis and the most common antibiotic class was penicillins, combined with aminoglycosides in a large number of patients, in line with international literature [29, 30]. It is hard to compare prescription habits in our centres with other NICUs because of a wide variability of the rate of neonates prescribed antibiotics across hospitals, as shown by a recent multicenter study involving 127 NICUs in the US [31]. The 40-fold variations in prescription frequencies noted in this study did not appear to be related to higher infection burden, necrotizing enterocolitis incidence, surgical volume or mortality rate [31]. They have instead been attributed to frequent inappropriate courses of antibiotics in inpatient neonates, more commonly owing to an unnecessary antibiotic continuation than starting of a non-required therapy [32].

Focusing instead on the paediatric group, we noticed an excessive use of third generation cephalosporins for treatment of infection similar to that seen for surgical prophylactic use, as underlined before. In children with LRTIs, ceftriaxone was the most prescribed antibiotic, used as monotherapy or often combined with macrolides, with a wide total daily dose variability ranging from 12.1 mg/kg/day to 153.8 mg/kg/day. The frequent choice of ceftriaxone as first line therapy for treatment of uncomplicated LRTIs and, in some cases, the high dosage prescribed, are reasons of concern because they are not supported by current guidelines [33]. In fact, other European countries, as the UK and France, seem to have different prescribing patterns for LRTI, preferring amoxicillin/clavulanic acid as first line therapy [34].

An abuse of parenteral cephalosporins in Italian hospitalized children was already denounced in a study conducted by Esposito in 2001 [35] and is a well-known problem also in the adult population [36].

Noteworthy was also the widespread use of carbapenems and quinolones. Indeed, in our study population, among the 349 patients receiving antibiotics, 8.9% were being treated with carbapenems, whereas proportion of carbapenems for therapeutic use reported in the literature in European paediatric units is 4,2% [37]. Though carbapenems were prescribed in most cases for fever in cancer patients, which often requires aggressive antibiotic treatment considering the patients’ immunological status and predisposition to severe infections, we are concerned about the increasingly popular usage of these agents for community acquired-infections, empiric treatment and combination therapy. This is a very alarming finding, considering the doubling of carbapenem resistance rates in invasive isolates of Klebsiella pneumoniae reported by the European Antimicrobial Resistance Surveillance Network (EARS-Net)’s report from 2010 to 2013 [9] for Italy. We also found 18.7% off-label use in patients below 3 months of life, but this could be explained by the involvement of many of our centers in the European NEOMERO study, which aimed to evaluate pharmacokinetics, safety and efficacy of meropenem in neonatal sepsis and meningitis [38].

Similar problems were noticed also for quinolone prescription. Quinolones were widely used in our cohort, even if the license for the use of this antibiotic class below 18 years of age is restricted to few rare indications such as cystic fibrosis with pulmonary exacerbations, complicated urinary tract infections, post exposure prophylaxis against inhalational anthrax and severe infections with allergies to other antibiotics [39,40]. Among our patients, the main indication for treatment with quinolones was LRTI. In this group of patients, quinolones were often prescribed empirically and combined with other drugs, though current guidelines do not suggest quinolones as a first-line treatment considering that infections caused by pneumococci or atypical bacteria can still be successfully treated with high doses of β-lactams [41]. Furthermore, the Scottish Antimicrobial Prescribing Group (SAGP) in 2008 and the National Institute for Health and Care Excellence (NICE) in 2015 [42] recommended to avoid the use of quinolones as first line agents for empirical treatment of most commonly infections in primary care, because the overuse of these broad-spectrum antibiotics is associated with a significantly increased risk of Clostridium difficile infection [43,44]. The wide use of quinolones in our cohort could be explained by the finding that most of our patients receiving this treatment had underlying chronic pulmonary diseases, such as cystic fibrosis or secondary to immunodeficiencies, but the lack of data about their microbiological status did not allow us to evaluate the appropriateness of these prescriptions.

Our study highlights many feasible targets that need a prompt intervention with appropriate antimicrobial stewardship programs. International guidelines for stewardship identify a wide set of interventions including: disease-specific clinical pathways, audit with feedback and formulary restriction with preauthorization of select agents. The best type of interventions must be tailored according to local practices, resistance trends, and available resources [4]. While the most effective antimicrobial stewardship programs are built on proactive interventions, in settings where a robust antimicrobial stewardship team is hard to establish, clinical pathways tool represent a reasonable and feasible first step for implementation standardizing care without adversely affecting patient safety or outcomes [45, 46]. Moreover, annual PPS could be a useful tool to measure the impact of these interventions on antibiotic prescribing practices [18]. Thus, implementation of clinical pathways in Italian paediatric hospitals associated with annual PPSs could be a good start to reduce the abuse and misuse of antibiotics.

Our study has some limitations. First, data about microbiological isolates and antibiotic susceptibility tests, length of therapies and prophylaxis and previous antibiotic courses could have been useful to better define the appropriateness of antimicrobial prescriptions. Moreover, the characteristics of involved institutions may have affected at least in part the reliability of some results. Most institutions are in fact tertiary care hospitals that usually manage more complicated and severe cases, which might significantly impact antibiotic prescriptions. In addition, the heterogeneity among institutions, in terms of presence/absence of onco-hematology departments or intensive care units, may strongly affect antimicrobial prescription patterns. Finally, the survey was conducted in 2012 and since then a greater awareness of antibiotic stewardship programs has spread among Italian hospitals [4749].

Conclusions

Our study took a picture of the Italian situation in terms of antibiotic prescriptions in hospitalized neonates and children and identified many feasible targets that require a prompt intervention to reduce the abuse and misuse of antibiotics. Antibiotic stewardship programs should immediately introduce measures to control prescription patterns in particular for prophylaxis, both in neonatal and paediatric populations, and to limit the over-use of third generation cephalosporins, that seems to persist over-time. Surveillance and educational programs are also needed to restrict the use of carbapenems to more severe conditions. The implementation of disease-specific clinical pathways associated with annual PPSs could be a good way to monitor and ameliorate antibiotic prescription patterns in neonatal and paediatric inpatients over time, in order to reduce as much as possible the worrisome emergence of MDR bacteria in this vulnerable population.

Supporting Information

Author Contributions

Conceived and designed the experiments: MS AV HG GN. Performed the experiments: PD AG LG SE MR CT CC CG. Analyzed the data: MDL DD CM RL. Wrote the paper: MDL DD GN. Revised the manuscript: PD SE LG ALV CM MS AV.

References

  1. 1. Van der Meer JW, Gyssens IC. Quality of antimicrobial drug prescription in hospital. Clin Microbiol Infect. 2001;7 Suppl 6:12–5. pmid:11990686
  2. 2. CDC, Antibiotic Resistance Threats in the United States, 2013 available at www.cdc.gov/drugresistance/pdf/ar-threats-2013-508.pdf
  3. 3. Hecker MT, Aron DC, Patel NP, Lehmann MK, Donskey CJ. Unnecessary use of antimicrobials in hospitalized patients: current patterns of misuse with an emphasis on the antianaerobic spectrum of activity. Arch Intern Med. 2003;163(8):972–978. pmid:12719208
  4. 4. Dellit TH, Owens RC, McGowan JE Jr, Gerding DN, Weinstein RA, Burke JP, et al. Infectious Diseases Society of America and the Society for Healthcare Epidemiology of America guidelines for developing an institutional program to enhance antimicrobial stewardship. Clin Infect Dis. 2007;44(2):159–177. pmid:17173212
  5. 5. Cosgrove SE, Carmeli Y. The impact of antimicrobial resistance on health and economic outcomes. Clin Infect Dis. 2003;36(11):1433–1437. pmid:12766839
  6. 6. Roberts RR, Hota B, Ahmad I, Scott RD 2nd, Foster SD, Abbasi F, et al. Hospital and societal costs of antimicrobial-resistant infections in a Chicago teaching hospital: implications for antibiotic stewardship. Clin Infect Dis. 2009;49(8):1175–1184. pmid:19739972
  7. 7. Evans HL, Lefrak SN, Lyman J, Smith RL, Chong TW, McElearney ST et al. Cost of Gram-negative resistance. Crit Care Med. 2007;35(1):89–95. pmid:17110877
  8. 8. Spellberg B, Guidos R, Gilbert D, Bradley J, Boucher HW, Scheld WM, et al. The Epidemic of Antibiotic-Resistant Infections: A Call to Action for the Medical Community from the Infectious Diseases Society of America. Clin Infect Dis. 2008;46(2):155–164. pmid:18171244
  9. 9. European Centre for Disease Prevention and Control. Antimicrobial resistance surveillance in Europe 2013. Annual report of the European Antimicrobial Resistance Surveillance Network (EARS-Net). Stockholm: The Centre; 2014.
  10. 10. Vaccheri A, Bjerrum L, Resi D, Bergman U, Montanaro N. Antibiotic prescribing in general practice: striking differences between Italy (Ravenna) and Denmark (Funen). J Antimicrob Chemother. 2002 Dec;50(6):989–97. pmid:12461022
  11. 11. Rossignoli A, Clavenna A, Bonati M. Antibiotic prescription and prevalence rate in the outpatient pediatric population: analysis of surveys published during 2000–2005. Eur J Clin Pharmacol. 2007;63:1099–1106. pmid:17891535
  12. 12. Nicolini G, Donà D, Mion T, Barlotta A, Girotto S, Borgia E, et al. Use of amoxicillin, amoxicillin/clavulanate and cefaclor in the Italian pediatric population. Journal of Pediatric Infectious Diseases. vol. 9, no. 1, 2014, pp. 1–9.
  13. 13. Stam J, van Stuijvenberg M, Grüber C, Mosca F, Arslanoglu S, Chirico G, et al. Antibiotic use in infants in the first year of life in five European countries. Acta Paediatr. 2012 Sep;101(9):929–34. pmid:22691104
  14. 14. Gagliotti C, Morsillo F, Resi D, Milandri M, Moro ML. Antibiotic treatments for children ages 0–23 months in a northern Italy region: a cohort study. Infection. 2006 Jun;34(3):155–7. pmid:16804659
  15. 15. Vander Stichele RH, Elseviers MM, Ferech M, Blot S, Goossens H; European Survaillance of Antibiotic Comsuption (ESAC) Project Group. Hospital consumption of antibiotics in 15 European countries: results of the ESAC Retrospective Data Collection (1997–2002). J Antimicrob Chemother. 2006 Jul;58(1):159–67. pmid:16698845
  16. 16. Ciofi Degli Atti ML, Raponi M, Tozzi AE, Ciliento G, Ceradini J, Langiano T, et al. Point prevalence study of antibiotic use in a paediatric hospital in Italy. Euro Surveill. 2008 Oct 9;13(41).
  17. 17. Buccellato E, Melis M, Biagi C, Donati M, Motola D, Vaccheri A. Use of Antibiotics in Pediatrics: 8-Years Survey in Italian Hospitals. PLoS One. 2015 Sep 25;10(9):e0139097. pmid:26405817
  18. 18. Versporten A, Bielicki J, Drapier N, Sharland M, Goossens H; ARPEC project group. The Worldwide Antibiotic Resistance and Prescribing in European Children (ARPEC) point prevalence survey: developing hospital-quality indicators of antibiotic prescribing for children. J Antimicrob Chemother. 2016 Jan 8.
  19. 19. Caffrey Osvald E, Prentice P. NICE clinical guideline: antibiotics for the prevention and treatment of early-onset neonatal infection. Arch Dis Child Educ Pract Ed. 2014 Jun;99(3):98–100. pmid:24334339
  20. 20. Inglis GD, Jardine LA, Davies MW. Prophylactic antibiotics to reduce morbidity and mortality in neonates with umbilical artery catheters. Cochrane Database Syst Rev. 2007 Oct 17;(4):CD004697. pmid:17943827
  21. 21. Inglis GD, Jardine LA, Davies MW. Prophylactic antibiotics to reduce morbidity and mortality in ventilated newborn infants. Cochrane Database Syst Rev. 2007 Jul 18;(3):CD004338. pmid:17636752
  22. 22. Jardine LA, Inglis GD, Davies MW. Prophylactic systemic antibiotics to reduce morbidity and mortality in neonates with central venous catheters. Cochrane Database Syst Rev. 2008 Jan 23;(1):CD006179. pmid:18254094
  23. 23. Verani JR, McGee L, Schrag SJ. Prevention of perinatal group B streptococcal disease—revised guidelines from CDC, 2010. MMWR Recomm Rep. 2010 Nov 19;59(RR-10):1–36. pmid:21088663
  24. 24. Cotten CM, Taylor S, Stoll B, Goldberg RN, Hansen NI, Sánchez PJ, et al. Prolonged duration of initial empirical antibiotic treatment is associated with increased rates of necrotizing enterocolitis and death for extremely low birth weight infants. Pediatrics. 2009 Jan;123(1):58–66. pmid:19117861
  25. 25. Hajdu A, Samodova OV, Carlsson TR, Voinova LV, Nazarenko SJ, Tjurikov AV, et al. A point prevalence survey of hospital-acquired infections and antimicrobial use in a paediatric hospital in north-western Russia. J Hosp Infect. 2007;66(4):378–84. pmid:17573155
  26. 26. Potocki M, Goette J, Szucs TD, Nadal D. Prospective survey of antibiotic utilization in pediatric hospitalized patients to identify targets for improvement of prescription. Infection. 2003;31(6):398–403. pmid:14735382
  27. 27. Bratzler DW, Dellinger EP, Olsen KM, Perl TM, Auwaerter PG, Bolon MK, et al. Clinical practice guidelines for antimicrobial prophylaxis in surgery. Am J Health Syst Pharm. 2013 Feb 1;70(3):195–283. pmid:23327981
  28. 28. Stern A, Green H, Paul M, Vidal L, Leibovici L. Prophylaxis for Pneumocystis pneumonia (PCP) in non-HIV immunocompromised patients.Cochrane Database Syst Rev. 2014 Oct 1;10:CD005590. pmid:25269391
  29. 29. Gerdes JS. Diagnosis and management of bacterial infections in the neonate. Pediatr Clin North Am. 2004 Aug;51(4):939–59, viii-ix. pmid:15275982
  30. 30. Mtitimila EI, Cooke RW. Antibiotic regimens for suspected early neonatal sepsis. Cochrane Database Syst Rev. 2004 Oct 18;(4):CD004495. pmid:15495114
  31. 31. Schulman J, Dimand RJ, Lee HC, Duenas GV, Bennett MV, Gould JB. Neonatal intensive care unit antibiotic use. Pediatrics. 2015 May;135(5):826–33. pmid:25896845
  32. 32. Patel SJ, Oshodi A, Prasad P, Delamora P, Larson E, Zaoutis T, et al. Antibiotic use in neonatal intensive care units and adherence with Centers for Disease Control and Prevention 12 Step Campaign to Prevent Antimicrobial Resistance. Pediatr Infect Dis J. 2009; 28: 1047–51. pmid:19858773
  33. 33. Bradley JS, Byington CL, Shah SS, Alverson B, Carter ER, Harrison C, et al. The Management of Community-Acquired Pneumonia in Infants and Children Older Than 3 Months of Age: Clinical Practice Guidelines by the Pediatric Infectious Diseases Society and the Infectious Diseases Society of America. Clin Infect Dis. 2011 Oct;53(7):617–30. pmid:21890766
  34. 34. Sviestina I, Aston J, Lorrot M, Mozgis D. A comparison of antibiotic use in three specialist paediatric hospitals in France, Latvia and the UK. Eur J Hosp Pharm. 10/2014; 22(3).
  35. 35. Esposito S, Blasi F, Allegra L, Principi N; Mowgli Study Group. Use of antimicrobial agents for community-acquired lower respiratory tract infections in hospitalised children. Eur J Clin Microbiol Infect Dis. 2001 Sep;20(9):647–50. pmid:11714047
  36. 36. Vaccheri A, Silvani MC, Bersaglia L, Motola D, Strahinja P, Vargiu A, et al. A 3 year survey on the use of antibacterial agents in five Italian hospitals. J Antimicrob Chemother. 2008 Apr;61(4):953–8. pmid:18218639
  37. 37. Amadeo B, Zarb P, Muller A, Drapier N, Vankerckhoven V, Rogues AM, et al. European Surveillance of Antibiotic Consumption (ESAC) point 528 prevalence survey 2008: paediatric antimicrobial prescribing in 32 hospitals of 21 529 European countries. J Antimicrob Chemother. 2010; 65: 2247–52. pmid:20713405
  38. 38. Lutsar I, Trafojer UM, Heath PT, Metsvaht T, Standing J, Esposito S, et al. Meropenem vs standard of care for treatment of late onset sepsis in children of less than 90 days of age: study protocol for a randomised controlled trial. Trials. 2011 Sep 30;12:215. pmid:21958494
  39. 39. Lietman PS. Fluoroquinolone toxicities. An update. Drugs. 1995;49 Suppl 2:159–63. pmid:8549287
  40. 40. Andriole VT. The quinolones: past, present, and future. Clin Infect Dis. 2005;41 Suppl 2:S113–9. pmid:15942877
  41. 41. Mills GD, Oehley MR, Arrol B. Effectiveness of b lactam antibiotics compared with antibiotics active against atypical pathogens in non-severe community acquired pneumonia: meta-analysis. BMJ. 2005; 330: 456–62. pmid:15684024
  42. 42. Committee on Infectious Diseases. The use of systemic fluoroquinolones. Pediatrics. 2006 Sep;118(3):1287–92. pmid:16951028
  43. 43. Scottish Antimicrobial Prescribing Group (SAPG). Report on Antimicrobial Resistance and Use in Humans in 2008. Available: http://www.isdscotland.org/Health-Topics/Prescribing-and-Medicines/National-Medicines-UtilisationUnit/SAPG%20Report%20on%20Antimicrobial%20Resistance%20and%20Use%20in%20Humans%20in%202008.pdf
  44. 44. National Institute for Health and Care Excellence (NICE). Clostridium difficile infection: risk with broad- spectrum antibiotics. Available: https://www.nice.org.uk/advice/esmpb1/resources/clostridium-difficile-infection-risk-withbroadspectrum-antibiotics-1502609568697285
  45. 45. Jenkins TC, Knepper BC, Sabel AL, Sarcone EE, Long JA, Haukoos JS, et al. Decreased antibiotic utilization after implementation of a guideline for inpatient cellulitis and cutaneous abscess. Arch Intern Med. 2011 Jun 27;171(12):1072–1079. pmid:21357799
  46. 46. Dellit TH, Chan JD, Skerrett SJ, Nathens AB. Development of a guideline for the management of ventilator-associated pneumonia based on local microbiologic findings and impact of the guideline on antimicrobial use practices. Infect Control Hosp Epidemiol. 2008 Jun;29(6):525–533. pmid:18510462
  47. 47. Viale P, Tumietto F, Giannella M, Bartoletti M, Tedeschi S, Ambretti S, et al. Impact of a hospital-wide multifaceted programme for reducing carbapenem-resistant Enterobacteriaceae infections in a large teaching hospital in northern Italy. Clin Microbiol Infect. 2015 Mar;21(3):242–7. pmid:25658534
  48. 48. Pan A, Gagliotti C, Resi D, Moro ML. Antimicrobial stewardship programmes in Emilia-Romagna, Italy. Journal of Global Antimicrobial Resistance. 2013 Sep;1(3):175–179.
  49. 49. Buone Pratiche per il controllo dell’antibiotico resistenza. Progetto CCM 2014. Available: http://www.ccm-network.it/imgs/C_27_MAIN_progetto_452_listaFile_List11_itemName_0_file.pdf