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This Consultation Toolkit to accompany the process of updating the Global Strategy ... experiences and best-practice inn
Acute aortic syndrome (see chapter 6) ... syndrome. Exacerbated COPD or other chronic lung disease. Other causes, including ...... Post MI: Dressler syndrome.
Oct 10, 2016 - Recent Haptic feedback Technologies. 14 ... Ualizing hap c illusion between two and more units ..... Steering wheel with a potentiometer.
Aug 11, 2009 - institutions small and large, from art museums and science centers and historical sites, ...... In order
Aug 11, 2009 - If our museums are only held back because we lack the tools ... That, like fractals, if we all individual
http://allafrica.com/stories/200810090254.html ... world/2008/0929/1222420015020.html. 2 .... Melting ice caps cause ris
Finally we would like to thank Mariana Buican (Romania, chemistry and physics ..... Finally we offer some recommendation
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Across the world people are grappling with the problem of child sexual abuse and what to do about it. Some countries hav
ambiguous "keywords" and crawling rules. Arts & Culture. Cyber. Finance. Food & Recipes. Health & Medicine.
Learning Resource Exchange8 or the eTwinning platform9 (project galleries and resources project kits) are seen as great
Welcome to the Self-Organised Learning Environment (SOLE) Toolkit, a School in the Cloud ... Enhance computer literacy.
Ensure infants receive systematic bilirubin monitoring as per the treatment graph and risk nomograms recommended by evid
Quality-Based Procedure Hyperbilirubinemia in Term and Late Pre-Term Infants (≥ 35 weeks)
TOOLKIT
April 2014
Introduction Quality-Based Procedures (QBP) are an integral part of Ontario’s Health System Funding Reform (HSFR) and a key component of the Patient-Based Funding. This reform plays a key role in advancing the government’s quality agenda and its Action Plan for Health Care. HSFR has been identified as an important mechanism to strengthen the link between the delivery of high quality care and fiscal sustainability. QBPs involve clusters of patients with clinically related diagnoses or treatments. The Ministry of Health and LongTerm Care recognizes that paediatric procedures require a different set of considerations that take into account the relatively small critical mass of patients (when compared to the adult population), as well the increased complexity of certain procedures when being performed on, or delivered to, a paediatric patient. The key objectives of the QBP for Hyperbilirubinemia in Term and Late Pre-Term Infants (≥ 35 weeks) are to: •
Ensure all newborns receive bilirubin screening between 24-72 hours of life (if not clinically indicated and performed earlier)
•
Ensure infants receive systematic bilirubin monitoring as per the treatment graph and risk nomograms recommended by evidence-based guidelines
•
Utilize health care resources responsibly through avoidance of unnecessary/excessive testing, timely discharge, appropriate outpatient follow-up and minimization of preventable readmission
•
Reduce the incidence of severe hyperbilirubinemia and acute bilirubin encephalopathy
This toolkit serves as a complement to the QBP Clinical Handbook for Hyperbilirubinemia in Term and Late Pre-Term Infants (≥ 35 weeks). The toolkit details the clinical pathway and the tools clinicians can use to implement the QBP. Additional Resources: For more detailed information about the QBP, its development and recommendations, a copy of the Clinical Handbook can be downloaded from the Ministry of Health and Long-Term Care website. For information regarding the implementation of QBPs, the Ontario Hospital Association has created a toolkit to support the implementation of QBPs. It can be downloaded at: http://www.oha.com/KnowledgeCentre/Library/Toolkits/Pages/Default.aspx
1
Clinical Pathway for the Management of Hyperbilirubinemia in Term and Late Pre-Term Infants (≥35 weeks)
2
Clinical Pathway Instructions Legend: AAP = American Academy of Pediatrics Guidelines
CPS = Canadian Paediatric Society Guidelines
NICE = National Institute for Clinical Evidence Guidelines
For a description of the levels of evidence used in each guideline, please refer to Appendix A.
Instructions
Recommendations
Support For Recommendations
UNIVERSAL SCREENING 1
Identify newborns of mothers with red cell antibodies (isoimmunization)
-‐ All mothers should be tested for blood type (ABO and Rh(D)) and screened for red cell antibodies during pregnancy
-‐ If mother not tested during pregnancy, cord blood should be sent for blood group and direct anti-globulin test (DAT) -‐ Significance of various antibodies differs
2
Newborns of mothers with red cell antibodies should have blood group evaluation and direct anti-globulin test (DAT)
-‐ Consultation with a neonatologist or paediatrician suggested due to risk of bilirubin encephalopathy
CPS
-‐ Significance of various antibodies differs
CPS
-‐ Further evaluation, closer follow-up and earlier therapy may be required -‐ Consultation with a paediatric haematologist or neonatologist suggested
3
Measure cord blood for haemoglobin and Total Serum Bilirubin (TSB)
-‐ Measurement of haemoglobin and bilirubin from cord blood suggested as part of initial evaluation for DAT positive infants of mothers with red cell antibodies
CEAG Consensus
4
If cord TSB level ≥ 100µmol/L
-‐ Critical value, suggestive of need for exchange transfusion
NICE
-‐ Multiple intensive phototherapy should be initiated without delay, while continuing pathway (Step # 17) and initiating consult (Step #18)
