Antibiotics on the postnatal ward A n audit and cost-analysis of current practices Dr Rachel Hayward & Dr Sybil Barr UHW Neonatal Unit.

Slides:



Advertisements
Similar presentations
Implementing NICE guidance
Advertisements

PreTerm PreLabour Rupture of Membranes Max Brinsmead PhD FRANZCOG February 2013.
Journal Club October 2012 Supervised by Prof.Abdulrahim Rouzi Presented by Dr.Ayman Bukhari.
The ACOG Task force on hypertension in pregnancy
Infection & Preterm Birth. Objectives Understand magnitude of problem of PTB. Gain understanding of role of infection in spontaneous PTB. Overview of.
Quality Education for a Healthier Scotland Multidisciplinary The Unwell Infant? Promoting multiprofessional education and development in Scottish maternity.
Primary Care Management of Urinary Tract Infection in Pregnant Women Dr. Charlotte Cooke Northumbria Healthcare NHS Foundation.
Danger Signs in Newborn
Doug Simkiss Associate Professor of Child Health Warwick Medical School Management of sick neonates.
Pretem Labor Ramzy Nakad, MD.
Severe Sepsis Initial recognition and resuscitation
By Dr. Gacheri Mutua.  Is a blood infection that occurs in an infant younger than 90 days old.  Occurs in 1 to 8 per 1000 live births highest incidence.
Neonatal Sepsis NICU Night Team Curriculum. Sepsis: Objectives Define Sepsis Review common pathogens causing sepsis in a neonate Review clinical findings.
Neonatal Sepsis Kirsten E. Crowley, MD June, 2005.
STREPTOCOCCUS GROUP A and B. Group B Streptococcus ● Group B Streptococcus is a bacterial infection of Streptococcus agalactiae. It is a facultative anaerobic.
1 Neonatal Sepsis By Dr. Nahed Said Al- Nagger. 2 Objectives: Define neonatal sepsis. 1. List the causes make neonates susceptible to infection. 2. State.
NICU Case Presentation Jon Palma, MD Neonatology Fellow March 2010.
Elective Cesarean Delivery, Neonatal Intensive Care Unit Admission, and Neonatal Respiratory Distress 楊明智.
To treat or not to treat? Infants born with maternal chorioamnionitis Mary Angela Woodward,MD April 29,2015.
Neonatal Group B Streptococcal Infections
Nov 2007 ACoRN © Infection Sequence. Nov 2007ACoRN ©
 By:Sh.Nariman MD,Neonatologist  Tehran University of medical Sciences  Arash Women Hospital.
Perinatal CDC Prevention Guidelines Priscilla Joe, MD.
Induction of Labour Audit
Special care of preterm babies
Neonatal Sepsis Islamic University Nursing College.
Paediatric Microbiology Dr Amy Chue ID/Microbiology Registrar Dr Peter Munthali Consultant Microbiologist.
Preterm labor.
Max Brinsmead MB BS PhD May 2015 T ERM P RE L ABOUR R UPTURE OF M EMBRANES (T ERM PROM)
Hannah Spiers Samuel Agaba Bwindi Community Hospital Neonatal Audit.
Neonatal Sepsis Maria Angelica M. Geronimo. Epidemiology Newborn Health in the Philippines: A Situation Analysis June 2004.
NEONATAL SEPSIS. Neonatal sepsis can be either: Early neonatal sepsis: -Acquired transplacentally -Ascending from the the vagina, -During birth (intrapartum.
TEMPLATE DESIGN © BackgroundResultsDiscussions and Conclusions Key and References REFERENCES RCOG Green Top Guideline.
Risk factors for severe disease from pandemic (H1N1) 2009 virus infection reported to date are considered similar to those risk factors identified for.
NEONATAL SEPSIS Ekawaty Lutfia Haksari Perinatology, Department of Child Health Gadjah Mada University.
Outcome of CSF Analysis in Babies with Elevated CRPs but Clinically Well Dr Charlotte Davidson, Dr David Deekollu Prince Charles Hospital, Cwm Taf University.
Jessica Gosney 25 th February * Background * Aims * Methods * Standards * Results * Discussion * Recommendations.
Fetal Distress in labor Dr.Maysara Mohamed. What is fetal distress? Fetal distress is the term commonly used to describe fetal hypoxia. Hypoxia may result.
Jeanine Spielberger MD 9/23/2013 INTRAPARTUM ANTIBIOTIC PROPHYLAXIS FOR GROUP B STREPTOCOCCAL INFECTION.
Newborns At Risk for Sepsis Algorithm
Antibiotic Use on the Postnatal Ward Inching towards NICE Dr R Morris Dr M Pickup Dr S Banerjee Department of Neonatal Medicine, Singleton Hospital, Swansea.
PNEUMONIA BY: NICOLE STEVENS.
AUDIT ON THE USE OF OXYTOCIN IN THE MANAGEMENT OF DELAY IN THE FIRST STAGE OF LABOUR Dr. MK Liew, T Oliver, Dr. D Basu University Hospital of North Tees,
All Wales Audit into the Management of Respiratory Distress Syndrome in Preterm Infants Dr Chris Course (ST2) Dr Ian Morris (Neonatal GRID Trainee) Dr.
Audit of babies treated with therapeutic hypothermia in Wales in 2014 Dr.Rajarajan Kannapiran RGH, ABUHB.
 Prolonged pregnancy  Decreased fetal movements  Hypertension in pregnancy  Diabetes in pregnancy  Fetal growth restriction  Multiple gestation.
Dr S Knowles National Maternity Hospital Holles Street Dublin
GBS Prophylaxis indicated for mother? Adequate treatment?
Infection & Preterm Birth
Vital statistics in obstetrics.
Prevention, Diagnosis and Treatment of protracted Labor
Intrapartum CTG.
Pre-labor Rupture of Membranes (PROM)
Dr S Knowles National Maternity Hospital, Dublin
Dr U S SABITHA Assistant professor Dept of OBGyn PESIMSR, KUPPAM
Evidence based management of preterm labour
Maternal and child mortality
CASE 4 Dr Sani Aliyu Consultant in Microbiology & Infectious Diseases Cambridge University Hospitals.
WHO recommendations on interventions to improve preterm birth outcomes
Neonatal Sepsis.
Dr S Knowles National Maternity Hospital, Dublin
Generic Sepsis Screening & Action Tool
Early Onset Sepsis: GBS
Sun Mon Tue Wed Thu Fri Sat
Sun Mon Tue Wed Thu Fri Sat
Premature rupture of membranes (PROM)
Preterm prelabour rupture of the membranes (PPROM)
Sun Mon Tue Wed Thu Fri Sat
Fetal Distress Dr. Mahboubeh Valiani Academic Member of IUMS
Presentation transcript:

Antibiotics on the postnatal ward A n audit and cost-analysis of current practices Dr Rachel Hayward & Dr Sybil Barr UHW Neonatal Unit

Background Antibiotics for early-onset neonatal infection NICE clinical guideline 149 Risk factor Invasive GBS infection in a previous baby Maternal GBS colonisation, bacteriuria or infection in the current pregnancy Prelabour rupture of membranes Preterm birth following spontaneous labour (before 37 weeks' gestation) Suspected or confirmed rupture of membranes for more than 18 hours in a preterm birth Intrapartum fever higher than 38°C, or confirmed or suspected chorioamnionitis Parenteral antibiotic treatment given to the woman for confirmed or suspected invasive bacterial infection (such as septicaemia) at any time during labour, or in the 24-hour periods before and after the birth** Suspected or confirmed infection in another baby in the case of a multiple pregnancy ** Table 1 Risk factors for early-onset neonatal infection, including 'red flags'**

Clinical indicator Altered behaviour or responsiveness Altered muscle tone (for example, floppiness) Feeding difficulties (for example, feed refusal) Feed intolerance, including vomiting, excessive gastric aspirates and abdominal distension Abnormal heart rate (bradycardia or tachycardia) Signs of respiratory distress Respiratory distress starting more than 4 hours after birth *** Hypoxia (for example, central cyanosis or reduced oxygen saturation level) Jaundice within 24 hours of birth Apnoea Signs of neonatal encephalopathy Seizures *** Need for cardio–pulmonary resuscitation Need for mechanical ventilation in a preterm baby Need for mechanical ventilation in a term baby *** Persistent fetal circulation (persistent pulmonary hypertension) Temperature abnormality (lower than 36°C or higher than 38°C) unexplained by environmental factors Signs of shock *** Unexplained excessive bleeding, thrombocytopenia, or abnormal coagulation (International Normalised Ratio greater than 2.0) Oliguria persisting beyond 24 hours after birth Table 2 Clinical indicators of possible early-onset neonatal infection (observations and events in the baby), including 'red flags'***

NICE CG149 Recommendations ‘If a baby needs antibiotic treatment it should be given as soon as possible and always within 1 hour of the decision to treat’ Measure the C-reactive protein concentration 18–24 hours after presentation. Consider stopping the antibiotics at 36 hours if: 1.blood culture is negative, & 2.initial clinical suspicion of infection was not strong, & 3.baby's clinical condition is reassuring, no clinical indicators of infection, & 4.levels and trends of C-reactive protein concentration are reassuring. Consider establishing hospital systems to provide blood culture results 36 hours after starting antibiotics to facilitate timely discontinuation of treatment and discharge from hospital.

Current Audit AIMS: 1.To determine inefficiencies in current practices regarding antibiotics and neonates managed on the postnatal ward 2.To compare current practices with those recommended in the NICE clinical guideline: CG149 Antibiotics for early-onset neonatal infection 3.To conduct a cost-analysis of current practices

Audit Sample size 34 Average gestation Time to cannulation Time to processing cultures Time to authorised blood culture result Number of additional antibiotic doses Number of additional days in hospital Risk Factor% Maternal sepsis35 Prom23 Prem12 Grunting10 Pathological CTG6 GBS6 Neonatal temperature4 Offensive liquor2 Rash2

Results Criteria: antibiotic treatment should always be given within 1 hour of the decision to treat None within 1 hour Average time: 4 hours 48 minutes Mon4h 15min Tues2h 15min Wed6h Thu5h Fri4 h 21min Sat3h 53min Sun7h 30min

Results Criteria: consider stopping antibiotics at 36 hours if blood culture is negative Average time: 12 hours 48 minutes Mon9h 50min Tue14h 13min Wed13h 24min Thu14h Fri6h 58min Sat15h 53min Sun7h 22min

Microbiology Service Working hoursTime Mon h 50min Tue h 13min Wed h 24min Thu h Fri h 58min Sat h 53min Sun h 22min Average time to take cultures: 4 hours 48 minutes Average time to reach lab: 12 hours 48 minutes 48 hours of incubation plus 1 hour for authorisation 66 hours 36 minutes

Cost analysis

Each additional 24 hours of antibiotics on the postnatal ward costs £511 Current study: £12,343 71% of 34 neonates required only 36 hours of antibiotics 34 x £511 x 0.71 = £12,343

CG149 Implementation of CG149 is expected to have the following benefits and savings: 1.Reduced length of hospital stay : earlier diagnostic testing (< 1hour after decision to treat) : cessation of treatment after 36 hours of starting antibiotic treatment 2. Reducing the current length of treatment from 3 days to 2 would result in potential annual savings of : Based on predicted number of neonates per year on PNW antibiotics in 2014: 12/7 x 380 = 651 (380 babies recorded from 1 st January to 31 st July) Predicted 71% of these will only require 36 hours of antibiotics (not 5, 7 or 10 days of treatment) 0.71 x 615 = x £511 = £223,000

Recommendations 1. Cannulation and commencement of antibiotics at delivery 2. Repeat CRP within 24 hours of initial CRP 3. Optimise the collection and processing of blood cultures hour microbiology reporting system