Clinical Advice
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        Haematinic GuidelinesHEFT Pathology Guideline Investigation and Referral Pathways for Anaemia in Primary CareProduced by: Dr Sukhbir Kaur (Senior Clinical Biochemist) Approved by: Dr Kartsios Charalampos (Consultant Haematologist) Dr Marcus Mottershead (Consultant Gastroenterology) This guidence covers the following areas2. Iron Deficiency Anaemia Testing in Adults 3. Iron Deficiency Anaemia Treatment and Monitoring Advice 4. Vitamin B12 Deficiency Testing, Treatment and Monitoring 5. Folate Deficiency Testing, Treatment and Monitoring Advice 
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        Clinical Decision LimitsPhoning limits for biochemistry tests are as follows:Decision limits for phoning Analyte Phone results below or equal to: Phone results above or equal to: Units Notes Sodium 120 150 mmol/L Potassium 2.5 6.5 mmol/L Urea - Adults: 30 Paediatrics: 10 mmol/L Except those on renal wards or under renal consultants. Creatinine - Paediatrics: 200 umol/L eGFR Adults: 15 - ml/min AKI - 2 Not CKD patients (AKI 2 discretionary) Glucose 2.5 25 mmol/L Calcium adjusted 1.8 3.5 mmol/L Magnesium 0.4 - mmol/L Phosphate 0.3 - mmol/L AST - 600 U/L ALT - 600 U/L Total CK - 5000 U/L Amylase - 500 U/L Digoxin - 2.5 ng/mL Theophylline - 25 mg/L Phenytoin - 25 mg/L Lithium - 1.5 mmol/L Troponin T - GP only: >14 ng/L GP only Ammonia - 100 umol/L Ethanol - Paediatrics only: any detectable mg/L Paediatrics only Paracetamol - 10 mg/L Not ED patients Salicylate - 300 mg/L Not ED patients Conj bilirubin (DBIL) - Paediatrics only: 25 umol/L Paediatrics only Total bilirubin - Paediatrics only: 225 umol/L Paediatrics only Carbamazepine - 25 ug /mL Iron - ED only: 70 umol/L ED only Phenobarbitone - 70 mg/L CSF Gluc 3.3 - mmol/L CSF Prot - 0.45 g/L Lactate - 2.3 CRP - 300 Total bile acids - 20 Methotrexate Phone all umol/L Immunology results to be telephoned:- CD4 count <200 cells/cumm or <10% on new patients (paediatric levels are different, but agreed with Paed consultants)
- Lymphocyte subsets in infants <2yo: Any T cell subset below age-related normal range, any other abnormality suggesting SCID (e.g. MHC class II deficiency). (Note this is not exclusive: any abnormality may be discussed with requesting clinician)
- New positive GBM antibodiest
- New positive MPO antibodies
- New positive PR3 antibodies
- New paraprotein IgG , A or M  > 20g/L
- IgD or IgE (any size)
- serum monoclonal free light chains (any size, whether or not with intact paraprotein)
 
 Abnormal Laboratory Test Results – Triggers for Telephoning Results HaematologyHaemoglobin White Blood Cell Count <8.0 g/dl normochromic and normocytic Low result – neutropenia <0.5 x 10 9/L <7.0 g/dl microcytic and hypochromic High result – White cell count >40 x 10 9/L <7.0 g/dl macrocytic or Lymph count > 20 x 10 9/L <5.0 g/dl renal patients Any presence of blast cells Platelets Clotting Studies Lower limit - <70 x 10 9/L INR - >5.0 Upper limit - >1000 x 10 9/L PTT - >180 seconds Fibrinogen < 1.0g/l - All Positive Malaria Screens
- All Anti FXa results >1.20 iu/ml
- If the patient is known to the department and has had a similar result within the previous 7 days then the urgent contact is not necessary.
 HPA Microbiology – List of abnormal results telephoned to clinical staffBacteriology- Gram stain results of positive blood culture on Day 1
- Positive CSF results
- Positive sterile site results
- Significant in-patient results from enteric bench
- Multi resistant gram negative and gram positive isolates including mupirocin resistant MRSA
- Group B streptococcal isolates from neonates
- Group A in patient isolates
- Positive Legionella urinary antigen and Pneumococcal urine antigen results
- Smear and culture positive Mycobacteria
- Antibiotic assay results outside normal ranges
- Any other significant results at the discretion of Medical Microbiologists
 Virology- Serological evidence of acute infection with Hep A, Hep B and in pregnant patients CMV, Parvovirus and Rubella
- New diagnoses of HIV
- VZV IgG negative from exposed patients at risk of severe VZV infection
- New diagnosis of Hep B, Hep C and HIV in haemodialysis patients
- Evidence of Hep B/Hep C and HIV in needle stick injury source patients
- Clinically important positive respiratory PCR results i.e.: influenza, RSV in immunocompromised patients
- Positive PCR results in outbreaks
- Positive blood PCR for CMV and Adenovirus
- Negative blood results for CMV PCR
- Significant blood PCR results for EBV and Polyomavirus
- All positive PCR results on CSF specimens
- All positive Chlamydia PCR results on eye swabs
- All positive PCR results from neonatal unit
 
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        Tumour Marker Use in Primary CareIn the last 5 years requests for tumour marker tests from Primary Care have more than doubled. This high use in Primary Care is worrying because the majority of tumour markers (eg. CEA, CA19-9) are neither specific nor sensitive enough for use in the diagnosis of malignancy. See this link for a summary of the main tumour markers, their uses and limitations. The main use for tumour markers is in monitoring disease progression, treatment or recurrence of a histologically diagnosed cancer. A recent audit of Primary Care requests for tumour markers found that only 9% of CEA and 4% of CA19-9 were requested for these reasons; the rest being for non-specific symptoms. In contrast to the above, CA125 and PSA do have use in diagnosis of their related cancers, however it should also be noted that these are still only a diagnostic aid and should be used with caution as both can be raised in a number of other benign conditions (see table). Please click the relevant links below of links to guidelines relating to their use in Primary Care. CA125 link https://pathways.nice.org.uk/pathways/ovarian-cancer PSA link https://www.gov.uk/guidance/prostate-cancer-risk-management-programme-overview For symptoms and referral guidelines of other malignancies see the NICE Suspected Cancer Recognition and Referral guidelines. http://pathways.nice.org.uk/pathways/suspected-cancer-recognition-and-referral You can also use the search bar or test database on this website to find more specific information on the use of each tumour marker. Tumour marker Main application Other tumour elevations Other limitations CEA Monitoring colorectal adenocarcinomas Breast, lung, gastric, mesotheliomas, oesophageal and pancreatic Raised in smokers Raised in other benign renal, liver, lung or GI disease Poor sensitivity in early disease and may be absent/low in poorly differentiated tumours CA19-9 Monitoring pancreatic carcinoma Raised in obstructive jaundice, cholestasis, cirrhosis, pancreatic hepatitis and non-malignant GI disease. Not present in those negative for the Lewis blood group determinant. CA125 Monitoring ovarian carcinoma Raised in patients with ascites, pleural effusions or free fluid in the pelvis Raised in patients with congestive heart failure Raised in benign renal and liver disease and other adenocarcinomas Mildly raised in menstruation and the first two trimesters of pregnancy Can be raised in endometriosis CA15-3 Monitoring breast cancer Lung, colon, ovary Raised in benign liver, breast, ovarian disease AFP Diagnosis and monitoring of hepatocellular carcinoma and germ cell tumours Gastric and other GI (oesophageal, pancreatic) Raised in pregnancy and neonates Raised in benign liver disease PSA Diagnosis and monitoring of prostate carcinoma Also elevated in benign prostatic conditions Increases with age (as prostate size increases) Elevated in UTI, catheterisation, prostatitis or other prostate manipulation hCG Diagnosis and monitoring of germ cell tumours and gestational trophoblastic neoplasia Lung Raised in pregnancy Transiently elevated with cannabis use LDH Diagnosis and monitoring of germ cell tumours Elevated in cardiac disease and benign liver disease Elevated in some anaemias relating to non-malignant disease 
Clinical Biochemistry Advice
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                Notice of the change to the equation used to calculate estimate glomerular filtration rate (eGFR) across UHB on November 22nd 2021
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                Guidance on acute kidney injury (aki) or acute on chronic kidney disease (ackd) initial assessment & management in adults
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                Short guidance for primary care on the management of AKI
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                Fluid Analysis Guidelines
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                Interpretation of Thyroid Function Tests in Patients Not Taking Thyroxine
Haematology Clinical Advice
Clinical Protocols
Urgent GP request process for biochemistry, immunology, toxicology and haematology
Written on . Posted in Protocols