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Volume Five,  Number 3     December 1999

CONTENTS

13PATH-RESULTS LINE

MEASURING LIPIDS AFTER A MYOCARDIAL INFARCTION, MAJOR ILLNESS, SURGERY OR TRAUMA

MENINGOCOCCAL DISEASE UPDATE

MULTIDISCIPLINARY THYROID CLINIC AT THE SIR CHARLES GARDINER HOSPITAL/PATHCENTRE

PREMIER'S AWARD FOR PATHCENTRE

PATHCENTRE VISITING LECTURER 1999

HOW SAFE IS BLOOD?

 

13PATH-RESULTS LINE

PathCentre has recently introduced a direct result enquiry line - 13PATH (137284). This is a dedicated number which will bypass switchboards and remains available 24 hours, 7 days a week. PathCentre reception is available for general enquiries on 1800 675 274.

To compliment the 13PATH number, we have introduced a system called TELE-Q. If all our operators are busy TELE-Q will divert your call so you can leave your enquiry as a message. We will return your call at the very first opportunity with the information you require.


MEASURING LIPIDS AFTER A MYOCARDIAL INFARCTION, MAJOR ILLNESS, SURGERY OR TRAUMA

Following a myocardial infarction, major illness, surgery or trauma the concentration of serum cholesterol, triglycerides and HDL-cholesterol change significantly and cannot be used for diagnosis of lipid disorders. Serum cholesterol and HDL will drop significantly, whereas levels of serum triglycerides increase and will remain elevated for several weeks.

The concentrations of cholesterol, triglycerides and HDL do not change significantly within the first 24 hours after a major event and can be measured during this time. If this is not done lipids can be measured 3 months after a major event when they have returned to equilibrium.


MENINGOCOCCAL DISEASE UPDATE

Of the 13 capsular types of Neisseria meningitidis only two (serogroups B and C) cause the majority of disease in Australia, with serogroup B predominating in most states, including Western Australia. There is a spectrum of acute clinical presentation between the extremes of pure meningitis and meningococcaemia. In Australia in 1997, two of 86 meningitis patients (2%) and 13 of 146 meningococcaemia patients (9%) died. This increased mortality of septicaemia compared to meningitis is well recognised. Meningococcal disease occurs sporadically throughout the year, however, the majority of cases occur during late winter, which may be related to the circulation of respiratory viruses and/or an increase in indoor activities allowing more respiratory secretion contact. Almost half of cases occur in children less than 5 years old and a further 25% occur in the 15 to 24 years age group.

Antibiotic susceptibility

A steady decrease in the susceptibility of N. meningitidis to penicillin has been seen over the last five years, both in Australia and overseas. As yet, true resistance has not been a problem, however, approximately 75% of invasive isolates are considered "less sensitive" (MIC 0.06 – 0.5 mg/L) to penicillin. Penicillin, in appropriate doses, remains effective for the treatment of disease due to these "less sensitive" strains.

Clinical Diagnosis

The hallmarks of meningococcal disease are fever and a petechial rash. The development of vomiting and drowsiness is suggestive of meningitis. Early in the disease, a less distinctive maculopapular rash may develop that appears more typical of a viral infection. The major problems with early diagnosis of the disease are the nonspecific symptoms and signs and, in sporadic cases, the lack of community and medical awareness. The glass test, used to demonstrate non-blanching petechia, is promoted for parents in England but not in Australia.

Laboratory Diagnosis

Depending on the clinical circumstance, the specimens suitable for microbiological confirmation of meningococcal disease include blood, cerebrospinal fluid (CSF), synovial fluid, skin lesion aspirate, and throat swab. Blood cultures are positive in about 50% of cases overall but are more likely to be positive in meningococcaemia compared to meningitis. In about half of patients with systemic disease, meningococci can be isolated from a throat swab with a 97% phenotypic correlation to the invasive isolate. In up to two thirds of cases with a petechial rash, either the microscopy or culture of a skin lesion aspirate will be positive. Some laboratories also offer latex particle agglutination (LPA) testing for blood and CSF, however, this is not performed at PathCentre due to problems of sensitivity and specificity. Gram stain microscopy of CSF and other sterile sites demonstrating Gram negative diplococci can give a presumptive diagnosis.

The current NH&MRC guidelines for the control of meningococcal disease recommend that either parenteral penicillin or a third generation cephalosporin be administered prior to referral to hospital for suspected cases. Although this has been reported to improve the clinical outcome, it will reduce the frequency of positive cultures, particularly from blood. One study demonstrated a reduction in isolation rate from 50% to 5%. Cerebrospinal fluid and skin aspirates are likely to remain culture positive for longer, and a throat swab culture will be unaffected by penicillin therapy. The NH&MRC guidelines state that throat swabs should be reserved for outbreak situations in patients with suspected meningococcal disease, especially if they have received prior antibiotics. The role of lumbar puncture in meningococcal disease has been debated for some time. Although sensitive (89-94%) in meningitis cases, the main concern is the rare occurrence of brainstem herniation due to raised intracranial pressure. In addition, there is a high frequency of negative CSF findings (8%) early in meningococcal meningitis which may mislead clinicians into withholding antibiotics prior to culture results.

Meningococcal PCR

The trend to preadmission administration of antibiotics, together with an increasing reluctance to perform lumbar punctures, will reduce the number of culture proven cases and increase the proportion of presumptive cases. Polymerase chain reaction (PCR) of meningococcal DNA is a sensitive and specific method for diagnosis that can be performed on EDTA blood, CSF, and specimens from other sterile sites. PathCentre has introduced a diagnostic PCR for meningococcal disease. PCR screening in England and Wales has shown this technique to be very sensitive and specific. Recommendations for the use of PCR are shown in the Table. Complementary to the diagnostic PCR, PathCentre is also developing a PCR system for serogroup confirmation from meningococcal cases without a positive culture. This distinction is important due to the availability of a polysaccharide vaccine against serogroup C, but not serogroup B. This vaccine can be used in the control of serogroup C meningococcal outbreaks. A more efficacious conjugate serogroup C vaccine able may be available in Australia soon. This will make case ascertainment and serogroup information of greater importance in the future.

 

TABLE. Recommendations for the use of diagnostic PCR for meningococcal disease.

For further information contact Dr David Speers, Clinical Microbiologist, PathCentre on (08) 9346 3122.


MULTI-DISCIPLINARY THYROID CLINIC AT THE SIR CHARLES GAIRDNER HOSPITAL/PATHCENTRE

A Multi-Disciplinary Thyroid Clinic has been established at the Sir Charles Gairdner Hospital. This clinic will expedite the investigation and management of patients with thyroid disease, with a special emphasis on thyroid nodules and cancers. The clinic has the services of SCGH surgeons, endocrinologists, nuclear medicine physicians, radiologists and PathCentre pathologists who are available for consultation on the day of the clinic.

Patients may be booked into the clinic by telephoning 9346 3632 at SCGH or by sending a SCGH referral form for an outpatients appointment and specifying the ‘Multi-Disciplinary Thyroid Clinic’. Patients will be seen by an endocrine surgeon or endocrinologist, who will decide on the need for further testing, which will generally be done the same day. Test results will be included in the letter of reply to referring practitioners.

Services provided by PathCentre pathologists will include immediate reporting of direct or image-guided fine needle aspiration (FNA) of thyroid lesions, and rapid routine thyroid function testing.

FNA of palpable thyroid lesions and thyroid function testing will remain available to individual practitioners through the usual direct referral to PathCentre.


PREMIER'S AWARD FOR PATHCENTRE

As this issue of PathCentre News goes to press our PathCentre laboratory system is approaching the 5th anniversary of its formation. In that time we have striven hard to meet the requirements of all doctors and patients who use PathCentre for their pathology testing. We have worked to maintain our acknowledged leadership at the scientific cutting edge of pathology – we are the main referral centre for the most difficult and complex tests, and our pathologists are generally those to whom our colleagues in other laboratories turn when they require that extra level of specialist expertise. At the same time we have maintained our level of teaching and research in clinically oriented pathology and continue to be the main public health and forensic laboratory in WA.

Our efforts in changing PathCentre into a modern laboratory system in place of our three separate predecessors has been recognised in the Premier’s Awards for excellence in management. We gained the distinction of being "Highly Commended", ahead of the many other entrants and finalists in the category of "Change Management". Everyone at PathCentre is proud of this achievement which acknowledges the endeavours of our entire staff.

The point of this, as with everything we do is, to provide the best possible service to satisfy our referring doctors and their patients. The Premier’s Award notwithstanding, the true test of our work is what the medical community and the general community think of us. We are most gratified that as a result of our efforts to enhance the value of our services in pathology our referring doctors continue to seek PathCentre as their pathology provider. We intend to keep it this way and to do our very best to respond to your needs.


PATHCENTRE VISITING LECTURER 1999

The Division of Tissue Pathology was honoured to host Professor Bernd Scheithauer, Consultant and Professor of Pathology, Mayo Medical School of Medicine, Rochester, Minnesota, U.S.A. for two weeks in August as the second annual PathCentre Visiting Lecturer.

Professor Scheithauer is internationally recognised as one of the pre-eminent surgical pathologists of his generation. His areas of interest and expertise include the surgical pathology of the central and peripheral nervous systems and the pituitary gland. Professor Scheithauer is author or co-author of several texts which are regarded as classics in their fields. He has published over 360 scientific papers.

During his extremely successful visit, Professor Scheithauer conducted a series of outstanding lectures, seminars and teaching sessions, which were attended by specialists, trainees and staff from all pathology and neuroscience disciplines in Perth's medical and scientific community. Professor Scheithauer worked tirelessly with the staff of Anatomical Pathology, conducting educational and teaching sessions with consultants and registrars. He also attended and conducted a number of PathCentre's clinicopathological meetings. The great success of his visit has further strengthened the already close ties and links that exist between Professor Scheithauer and his department at the Mayo Clinic with PathCentre's Division of Tissue Pathology, a collaborative relationship that hopefully will continue to flourish.

Professor Bernd Scheithauer.


HOW SAFE IS BLOOD?

The recent media publicity of the case of HIV being transmitted by transfusion has again raised the awareness of the risks of blood transfusion. Although the general public is mainly concerned about the risks associated with infectious agents, the major complications associated with transfusion of blood components are due to the effects of blood storage, leucocytes and allo-immunisation. The risk of developing a transfusion-related complication is related to the number of transfusions (donor exposures) and the blood products transfused. No blood product, including autologous and directed blood donations, can be guaranteed to be 100% safe even with the most sophisticated testing available.

In Western Australia, the Australian Red Cross Blood Service (ARCBS) North-West region provides one of the safest blood transfusion services in the world. This is based on voluntary unpaid donors, a high proportion of whom are regular and long-term donors. All blood donors, at the time of collection of blood, complete a legally binding blood donor declaration and a detailed medical questionnaire. This is to exclude those donors who may be at risk of transmitting a disease by transfusion.

Currently the ARCBS tests for hepatitis B surface antigen and antibodies to hepatitis C, HIV-1, HIV-2, HTLV-1 and syphilis. The blood will only be released from the ARCBS when all these tests have been satisfactorily completed. If any of the tests are positive the blood will not be released.

As the majority of tests for infectious agents are based on the detection of an antibody in the donor, there is a "window period" in which an antibody will not be detectable despite the donor having been exposed to the infectious agent. As a result of this, the ARCBS will soon be introducing new tests to directly detect viral sequences in the donor blood (antigen tests). This nucleic acid testing (NAT) will reduce the window period for HIV from 22 to 11 days and for hepatitis C from 70 - 80 days down to 10 - 30 days. These tests will be introduced in the first half of 2000.

From the Table (below) you can see that even with current testing methods the risk of transfusion transmitted infections is very low. The introduction of NAT will further reduce the incidence of transfusion transmitted infections and increase the safety of transfused blood.

In addition to risks of infection as a result of transfusions, there are other risks which must be considered prior to a transfusion being given. These risks include:

Despite these risks of transfusion, Australia has one of the world’s safest blood supplies. All patients should, however, be informed of the risks of blood prior to the commencement of a transfusion.

For further information please contact Dr Wendy Erber, Clinical Director of Haematology at PathCentre (08) 9346 2702 or the Australian Red Cross Blood Service (08) 9325 3333.

Infectious Agent

Window Period

Transfusion Risk

Hepatitis B

  1:100,000

Hepatitis C

70-80 days (10-30) days

1:100,000 (1:500,000)

HIV-1,2

22 days (11days)

1:2,000,000 (1:5,000,000)

HTLV-l/ll   1:1,000,000
Syphilis   1:2,000,000

Current risks of transfusion transmitted infections. (Risks with Nucleic Acid Testing).

 

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Last Updated: Monday, 14 February 2000 09:00