Should patients with abnormal liver function tests in primary care be tested for chronic viral hepatitis: cost minimisation analysis based on a comprehensively tested cohort
© Arnold et al; licensee BioMed Central Ltd. 2011
Received: 11 August 2010
Accepted: 3 March 2011
Published: 3 March 2011
Liver function tests (LFTs) are ordered in large numbers in primary care, and the Birmingham and Lambeth Liver Evaluation Testing Strategies (BALLETS) study was set up to assess their usefulness in patients with no pre-existing or self-evident liver disease. All patients were tested for chronic viral hepatitis thereby providing an opportunity to compare various strategies for detection of this serious treatable disease.
This study uses data from the BALLETS cohort to compare various testing strategies for viral hepatitis in patients who had received an abnormal LFT result. The aim was to inform a strategy for identification of patients with chronic viral hepatitis. We used a cost-minimisation analysis to define a base case and then calculated the incremental cost per case detected to inform a strategy that could guide testing for chronic viral hepatitis.
Of the 1,236 study patients with an abnormal LFT, 13 had chronic viral hepatitis (nine hepatitis B and four hepatitis C). The strategy advocated by the current guidelines (repeating the LFT with a view to testing for specific disease if it remained abnormal) was less efficient (more expensive per case detected) than a simple policy of testing all patients for viral hepatitis without repeating LFTs. A more selective strategy of viral testing all patients for viral hepatitis if they were born in countries where viral hepatitis was prevalent provided high efficiency with little loss of sensitivity. A notably high alanine aminotransferase (ALT) level (greater than twice the upper limit of normal) on the initial ALT test had high predictive value, but was insensitive, missing half the cases of viral infection.
Based on this analysis and on widely accepted clinical principles, a "fast and frugal" heuristic was produced to guide general practitioners with respect to diagnosing cases of viral hepatitis in asymptomatic patients with abnormal LFTs. It recommends testing all patients where a clear clinical indication of infection is present (e.g. evidence of intravenous drug use), followed by testing all patients who originated from countries where viral hepatitis is prevalent, and finally testing those who have a notably raised ALT level (more than twice the upper limit of normal). Patients not picked up by this efficient algorithm had a risk of chronic viral hepatitis that is lower than the general population.
Liver Function Tests are ordered in large numbers in primary care
Liver function tests (LFTs) are comprised of a panel of five to eight analytes that are processed inexpensively in large batches. LFTs are one of the most commonly performed "blood tests" in primary care, such that in 2003 the laboratory at University Hospital Birmingham received 67,182 requests for LFTs from 83 General Practitioner (GP) practices, serving a population of 300,000 (Cramb R; Chemical Pathology Specialist).
Enigmatic responses to abnormal LFTs in primary care settings
An abnormal LFT may signify a serious disease that can be identified only through further testing. These conditions include liver diseases, such as primary biliary cirrhosis (PBC), diseases of other organs such as Paget's disease of bone, and multi-organ diseases such as haemochromatosis. However, the majority of people with an abnormal LFT in primary care settings will not have any such previously undetected disease. They will have either no disease at all, or will be manifesting the effects of alcohol abuse or obesity. The doctor is likely to be aware, or at least suspicious, of these behaviours when ordering LFTs, but this does not exclude the presence of other diseases that may aggravate liver damage. There is thus a real question about which specific further tests, if any, a GP should order when an abnormal LFT result is obtained in a patient with non-specific symptoms, or as a result of routine testing. In some cases there may be a clear indication for further tests. For example, if the patient has a family history of haemochromatosis then their iron saturation should be measured. In some cases the pattern of LFT abnormality may suggest a diagnosis - for example, an isolated raised unconjugated bilirubin suggests Gilbert's disease, while a high blood level of alkaline phosphatase (ALP) is indicative of PBC. In most cases however, no unambiguous clinical indication for follow-on testing exists. The literature deals mostly with the pattern of abnormality given a diagnosis, rather than the probability of the various diagnoses given a pattern of abnormal LFTs. It is therefore not surprising that guidelines for GPs [1–5] confronted by an abnormal LFT in patients with non-specific symptoms or detected fortuitously are inconsistent, or that the way GPs respond has been found to be eclectic . A point on which guidelines do agree is that the LFT panel should be repeated following an abnormal result.
Criteria for selection of a topic for decision analysis
it is a serious disease;
it is treatable in the prodromal phase;
failure to identify the condition can lead to permanent damage;
it can be diagnosed with a high specificity by a familiar and inexpensive test;
it is among the more prevalent of the serious diseases;
it is not a condition such as alcohol misuse or obesity, which can be diagnosed from history and examination.
Viral, genetic, and autoimmune diseases of the liver (tested for by a "liver panel"), their prevalence in the British population and diagnostic algorithms.*
Prevalence amongst adult population (%)
Blood tests done on all members of the cohort (to diagnose or screen for the disease)
Chronic viral hepatitis C
Hepatitis C virus antibody (HCV Ab)
Viral marker positive.
Chronic viral hepatitis B
Hepatitis B viral markers (HBV Surface Ag)
Viral marker positive.
Metal storage disease: Iron
0.25 (prevalence of phenotype; homozygous plus complex heterozygous) 
Genotype if iron saturation >50%.
Primary biliary cirrhosis (PBC)
Raised antibodies and raised ALP level.
Smooth Muscle Ab
Raised antibodies and raised ALT, AST or globulin exceeding twice the upper limit of normal. Confirmed by hepatologist.
Metal storage disease: Copper
Low levels of caeruloplasmin.
Alpha-1 antitrypsin deficiency
Low Alpha-1antitrypsin levels followed by phenotype testing.
The purpose of the decision analysis described here is to inform the selection of an efficient strategy for the diagnosis of chronic viral hepatitis. Such a strategy should optimise the trade-off between detection rate and cost.
The BALLETS study
The objective of the BALLETS study was to correlate the pattern of abnormal LFTs in primary care with the 'final' diagnosis. This was accomplished by fully investigating a cohort of patients with abnormal LFTs and no known liver disease by means of a panel of tests for the specific viral, auto-immune and genetic diseases shown in Table 1. This comprehensive investigation by means of the standard "liver panel" acts like a concertina, bringing forward the diagnosis of conditions, such as viral hepatitis and PBC, that would take years or decades to manifest if followed-up in the usual way. The BALLETS study was funded by the UK National Institute for Health Research through its Health Technology Assessment (HTA) programme. The full protocol is available online .
· Clinical data, including: country of birth, alcohol history, Body Mass Index (BMI), drug and medicine use, and reason for LFT testing.
· A repeat LFT.
· Ultrasound of upper abdomen.
· Ultrasound of upper abdomen.
Patients were followed up for two years, at which point LFTs were repeated along with a further ultrasound of the upper abdomen (results of the follow-on study will be reported at a later date).
A simple decision tree was constructed in Microsoft Excel (Microsoft Corp., Redmond Washington) to enable costs per case detected to be calculated for seven strategies . The strategies were developed in consultation with a GP and hepatologist (P. Gill and J. Neuberger respectively) who were aware of the relevant literature and guidelines.
■ Strategy A: repeat the LFT panel and then perform a specific test for viral hepatitis if an abnormality is still present on re-testing. This could be considered the intuitive response by a GP on receiving an abnormal LFT in a patient without the indictors of a specific disease, and is the strategy recommended in the literature [1–5].
■ Strategy B: perform a viral test in all patients with an abnormal ALT. The rationale for this strategy is that ALT is the most specific indicator of viral hepatitis , and has been recommended as the testing criterion by other authors [16–18].
■ Strategy C: select ALT as the trigger for viral testing, but nominate a higher threshold at twice the upper limit of normal, as recommended by Jamali . This is also the threshold for instigating viral therapy for HBV in certain treatment guidelines [20–22].
■ Strategy D: perform a test for viral infection in all patients who originate from a country with an intermediate or high prevalence of viral hepatitis according to World Health Organisation (WHO) criteria [23–25]. Screening has been shown to be cost-effective for people who were born in prevalent countries and it is likely that testing would be more cost-effective still in a population with abnormal LFTs [21, 26].
■ Strategy E: combine the two previous strategies by testing those who have an ALT exceeding twice the upper limit of normal and who also originate from a prevalent country.
■ Strategy F: test all patients from prevalent countries as well as those with an ALT exceeding twice the upper-limit of normal.
■ Strategy G: test all patients for viral hepatitis irrespective of the type or extent of abnormal LFT results.
There is also an option to take no action with respect to viral hepatitis, and while this may be a sound decision in some cases, for example when a LFT is ordered in the hope that a positive result will prompt a reduction in alcohol intake, this was not considered here.
In this study the hepatitis status for all patients was known. Moreover most had an ALT test result and the results of a repeat LFT panel. Thus it was possible to evaluate the performance of each of the above strategies.
Populating the decision tree with probabilities/statistical model
All 1,236 patients were used in the evaluation of strategy G, but for all other strategies the effective sample size was reduced because of missing data in some of the patient records. Estimates of the proportion of patients undergoing viral tests, and the proportion of actual cases detected (sensitivity) were obtained using the sample of patients available for evaluating each strategy. The positive predictive value of a strategy was defined as the proportion of hepatitis cases among those selected for viral testing. Confidence limits for this quantity were calculated using Wilson's method for Binomial data .
Estimation of costs
The direct costs incurred at the time of the test were the laboratory costs of the liver function and viral hepatitis tests (personal correspondence with Pathology Lab Manager); the GP costs for scheduling each test; and following up on results. Administrative costs were estimated by estimating the time implications for a secretary to add patients to appointment slots and a receptionist to check the patient in for an appointment (personal correspondence with MidReC: West Midlands Research Consortium. Figures correct as of February 2009). The costs are presented in pounds sterling (£) (and were correct for the year 2009). Non-health service costs (patient travel cost and lost earnings) were not measured, but are considered in the discussion.
The number of cases detected per 100 patients was estimated as the sensitivity of the strategy (cases detected divided by cases present) multiplied by the prevalence (per 100 patients) of viral hepatitis in the whole sample of 1,236 patients. For each strategy the cost per case detected was then computed as the ratio of the cost per patient to the number of cases detected per patient. The strategy which minimised this quantity was taken as the base case. For each alternative strategy the incremental cost-effectiveness ratio (ICER) was computed, defined as the incremental cost per additional case detected compared to the base case. The analysis is deterministic and does not consider the impact of sampling variability. The results of these analyses were compared with published results of cost-effectiveness analysis of screening for chronic viral hepatitis, bearing in mind likely differences between a screening and a diagnostic population. We used this analysis to develop a "fast and frugal" heuristic  which we offer to readers for their consideration.
Chronic viral hepatitis cases
Demographic features of patients with and without viral hepatitis
Not Viral Hepatitis
Diagnosis - Alcohol abuse
Review - CVD
Review - Cholesterol
Review - Hypertension
Review - Diabetes
Review - Medication
Medical - Review other
Results of initial LFT for viral hepatitis cases using laboratory-specific criteria for abnormality
Country of Origin (prevalence of viral hepatitis)
Hong Kong (High)
The country of origin was recorded in 1,208 of the 1,236 study cases, and of these, 170 people were born in a country with an intermediate or high prevalence of viral hepatitis (based on WHO definitions of prevalence [23–25]) and 1,038 were from low-risk countries. The high-risk group contained 11 of the 13 cases (85%) of viral hepatitis. None of the 13 cases admitted to use of intravenous drugs at any time.
Comparison of ALT and AST results in HBV or HCV cases versus non-hepatitis cases
HBV or HCV
Yield, sensitivity and Positive Predictive Values (PPV) of different detection strategies
Strategy for viral testing
No. of patients*
PPV (%) 95% Confidence Limits
A. If repeat LFT panel is abnormal
B. If ALT abnormal on primary test
C. If ALT > 2 upper limit of normal on primary test
D. If patient born in a country of intermediate to high viral hepatitis prevalence.
E. If patient born in a country of intermediate to high viral hepatitis prevalence and ALT > 2 upper limit of normal on primary test.
F. If patient born in a country of intermediate to high viral hepatitis prevalence, or ALT > 2 upper limit of normal on primary test.
G. Test all cases
Costs and Cost Minimisation Analysis
Cost estimates for resources used
GP consultation cost to check LFT results
Receptionist to check patient in for appointment (2 mins)
Secretary time (1 min)
Phlebotomist time (5 mins)
Sample analysis: LFT
Sample analysis: Hepatitis B surface Ag and Hepatitis C
Cost per 100 patients (£)*
Cases detected per 100 patients
Cost per case detected (£)
Incremental cost per 100 patients (with base = E)
Incremental cases detected per 100 patients (base = E)
Summary of main findings
The BALLETS study is the first GP based study where the entire cohort was comprehensively tested for additional diseases (such as viral hepatitis) after an abnormal LFT, using the full analyte panel and normal reference ranges. We have shown that an abnormal LFT alone does not select out a population where the prevalence rate approaches a threshold which would justify viral screening. We have assessed the validity of the various strategies a GP could adopt, at least as far as viral hepatitis is concerned, when faced with an abnormal LFT of uncertain provenance. The intuitive response for a GP in such a situation would be to repeat the LFT, an approach advocated by current literature. This study shows that this may not be the optimal policy. This strategy is the most expensive, even more so than viral testing all patients, as the costs incurred include repeating the LFT as well as viral testing the majority. The study also shows that if ALT is notably raised (greater than twice the upper limit of normal), then the probability of chronic viral hepatitis is high (nearly 8%), but sensitivity is low. The strategy of testing all people from prevalent countries is the second most efficient, in terms of cost per case detected, and detects almost twice as many cases as the most efficient strategy - testing for viral infection when two conditions (birth in a prevalent country and an ALT greater than twice the upper limit of normal) are satisfied. The relative financial disadvantages of the strategy of repeating the LFT would be even greater if patient costs were included, as the extra visit would have to be factored in.
Previous literature on LFTs and liver diseases
Search strategy for studies looking prospectively at patients who have received an abnormal LFT*
Liver Function Test Search Strings (limited using the subheadings; blood, analysis and metabolism)
Hepatitis Search Strings
Liver Function Test
Liver Diseases (diagnosis)
Liver Diseases (epidemiology)
Liver Diseases (enzymology)
Liver Diseases (virology)
With Limits added (Humans and Pub date post 1980)
With Limits added (Humans and Pub date post 1980)
Papers returned = 35070
Papers returned = 8526
When strategies combined using term AND = 1448 papers whose abstracts were read
Studies that have followed up patients from the general population after abnormal LFT
Author and Country
Type of Study and population studied
Patients with abnormal LFTs (%)
Prevalence of viral hepatitis in patients with abnormal LFTs
McLernon DJ et al.  Scotland
Record Linkage; laboratory database of GP tests, hospital admissions and death certificates.
Bilirubin, Albumin, ALP, GGT, ALT, AST (transaminases sometimes combined). GP selected
Median follow up of 3.7 years. Risk of under ascertainment.
Pendino GM et al.  Italy
Prospective Cohort Study; general population.
AST, ALT, GGT.
High baseline rate of viral hepatitis; 5.6%.
Kim HC et al.  Korea
Record Linkage: insurance data and death certificates.
Outcome was liver disease mortality.
Yano E et al.  Japan
Prospective Cohort Study; "healthy" office workers.
AST, ALT, GGT.
Assumed that all liver cancer and cirrhosis was a result of viral hepatitis.
Daniel S et al.  USA
Prospective Cohort Study; primary care population.
ALT, AST raised 50% above normal on at least two occasions across a six month period.
Marker was negative patients only, so infected patients excluded from analysis.
Mathiesen UL et al.  Sweden
Prospective Cohort Study; primary care population.
AST, ALT raised for at least 6 months. (ALP had to be normal).
Whitehead MW et al.  UK
Prospective Cohort Study; primary care population.
AST markedly raised (10 times (>400 U/l) above the upper limit of normal.)
Bellentani S et al.  Italy
Prospective Cohort; general population.
AST, ALT, GGT.
Hultcrantz R et al.  Scandinavia
Prospective Cohort Study; primary care population.
AST, ALT moderately raised for at least 6 months.(ALP had to be below twice the upper limit of normal).
Two of the remaining nine English language papers described record linkage studies. One such study was based on the Korean insurance database that was linked with death certificates . This study reported that increased ALT, even within the upper end of the normal range, was associated with eventual death from liver disease. A study carried out in Scotland linked general practice and hospital databases [31, 32]. However, this was a retrospective study so a full liver screen was not conducted and follow-up was for a median of four years only, whereas many diseases, including chronic viral hepatitis, have much longer prodromal periods .
The other seven studies were prospective cohort studies, based on testing asymptomatic members of the general population. The famous Dionysos study based on three analytes from the LFT analyte panel  is included among these. In this study an impressive 6,917 citizens from two communities in northern Italy were screened. Although they tested all those who had an abnormal LFT (n = 1473) for viral hepatitis, for which they found a prevalence rate of 2.4%, they did not describe the pattern of LFT results in infected patients. Another Italian study by Pendino and colleagues (2005) screened 1,645 inhabitants from a town in southern Italy, with both a LFT (ALT, AST and GGT) and viral screen . The prevalence of viral hepatitis is much higher in this region because of a significant immigrant population, and they performed a more extensive analysis on the impact of viral hepatitis on LFTs. Of the 319 (19.4%) individuals who received an abnormal LFT, nearly 18% were infected with viral hepatitis. However, the LFT missed 34 (40%) of the 92 cases of viral hepatitis present in the community. Perhaps the most comprehensive prospective analysis looking at the effect of viral hepatitis on the individual analytes was carried out on a population of Japanese office workers . The study used data from compulsory health checks, which included an ALT, AST and GGT panel along with certain additional tests, such as a viral screen, that were added for study purposes. They found that ALT was the most sensitive of the three analytes used, detecting nearly half the cases of viral hepatitis, whilst being abnormal in 14% of the cohort (278 abnormal results in 1,973 participants). The remaining four prospectively designed studies were carried out in general practices and were therefore closer in population terms to the BALLETS cohort. However, three of these were restricted to patients with persistently abnormal LFTs over a six month period [36–38] and one of these did not include a test for viral hepatitis. The final prospective study by Whitehead (1999) was small and based on only one analyte .
After this review of the literature we concluded that there has been no published study that fully investigated a cohort of patients in primary care with an abnormal LFT result (from the full LFT analyte panel).
Strengths and limitations of the study
The main strength lies in the unique nature of the BALLETS cohort, being the only prospective study that has looked at the consequences of an abnormal LFT from a full analyte panel in primary care. The main limitation of our study relates to the rather small number of cases of chronic viral hepatitis (n = 13) and hence wide confidence limits on the results. That said the results are plausible, in the sense that they are consistent with the pathophysiology of hepatitis and in line with what was found in non-practice settings (see literature review above). They are available for meta-analysis with potential future studies.
We deliberately selected multi-cultural inner city populations in order to provide a sizable sub-group of people from countries where chronic viral hepatitis is common, as a result of infection during infancy (hepatitis B), and iatrogenic infection (hepatitis C).
Our study considers only one disease type, chronic viral hepatitis, while GP decision making must take into account other diseases, such as haemochromatosis, as well as other behavioural and social motivations for testing [41, 42]. That said, our conclusion that repeating the LFT "offers more than it delivers," may well apply to diseases such as PBC and haemochromatosis.
Lastly we have presented an analysis for cost minimisation and incremental cost per case detected. This is not a full cost-effectiveness or decision analysis. Donnan et al. did attempt a decision analysis . However this decision analysis was intended to find the most cost-effective strategy in the short term and used a limited time horizon of one year. LFTs are often ordered to prevent poor outcome in the long term, with many serious liver diseases, viral hepatitis included, manifesting over decades. Anxiety resulting from a false positive result was included in the model while long term health gains as a result of successful case finding and treatment were not captured.
Neither our decision analysis, nor that in Donnan's HTA report , considered cost-effectiveness. We tackle this limitation by considering our results in the context of published cost-effectiveness analyses for screening for viral hepatitis (i.e. studies that found screening was cost-effective in populations with high prevalence rates e.g. migrants) and attempt to produce a "fast and frugal heuristic"  to guide practice.
Implications for practice: a fast & frugal heuristic
The intuitively appealing practice of repeating abnormal LFTs (strategy A) gets little support from our analysis. It is the most expensive option, both in absolute terms and in terms of cost per case detected, compared to all five alternative strategies (Table 7) - including that of simply testing everyone for viral infection.
The most important question a doctor can ask a patient with abnormal LFTs is their country of origin. This holds good whether the person settles in an area of high or low ethnic mix, since infections are acquired in infancy (hepatitis B), or as a result of sub-standard medical practices, such as needle sharing (hepatitis C). Once infected, people "take their risk with them" - less people will need to be tested in a low ethnic mix area, but those from prevalent countries still need testing. The strategy of testing people from prevalent countries promises good value for money. In this study, 11 of the 13 cases originated in medium or high risk countries. Thus the prevalence of chronic hepatitis viral infection (positive predictive value) among people with an abnormal LFT who were born in a prevalent country was 6.5% (11/170, 95% CI: 3.7%-11.2%, see table 5), while the prevalence among the home born population (of all ethnic groups) was less than 0.2% (2/1038, CI: 0.05%-0.7%). Our findings support viral testing only in the former group, consistent with the threshold prevalence for both HBV and HCV, of approximately 3% at which population screening becomes cost-effective [21, 43, 44].
Four of the strategies, C, D, E and F, entail viral testing in a population where the rate of hepatitis exceeds the 3% threshold for which testing has proven cost-effective in screening programs (Table 5). The cost-effective threshold is probably a little lower in a diagnostic population than in a screening population (costs of inviting people to attend are lower and cases detected might be a slightly higher risk) but no other strategy yields a population with a hepatitis rate exceeding even 2%.
It is hard to ignore a level this high, and the wide confidence levels from our data suggest the need for flexibility .
The progression for undetected chronic viral hepatitis is worse for patients with ALT greater than twice the upper limit of normal, and this level has been used as a threshold for treatment in guidelines.
If chronic viral hepatitis is not present at this level a more in-depth search for other causes of hepato-cellular damage is indicated.
We draw the line on further viral testing after this algorithm has been followed, unless of course further clinical indicators emerge. The likelihood of a case of viral hepatitis being present following the exclusions in this algorithm is approximately 0.1% in our study. This is considerably below the UK population prevalence.
This analysis indicates that the strategy of repeating LFTs in asymptomatic patients, advocated by current guidelines, is less sensitive and far more expensive than viral testing those patients born in countries where viral hepatitis is prevalent. Despite few cases of viral hepatitis the data on costs of the various strategies is strong and the results of prevalence rates within the cohort are consistent with other literature. The finding that a notably raised ALT level was also effective at identifying infected patients inspired the construction of a "fast and frugal" heuristic that might aid GPs who are faced with abnormal LFTs in asymptomatic patients, with regards to viral hepatitis. Our proposal addresses the diagnostic problem by identifying a clear high-risk population originating in prevalent countries. The residual population who are not immigrants from such countries are at low risk. However, this should not override clinical judgement. Its overall cost in other settings will depend on the relative proportions of patients in these risk-strata, but our results suggest that the cost of automatic testing of high-risk individuals will be repaid in terms of additional cases detected.
it is more efficient to determine country of origin with a view to viral testing, than to simply repeat the LFT;
it is more cost-effective to test the whole LFT positive population for viral hepatitis, than to repeat the LFT with a view to viral testing if it remains positive.
DTA - Medical student, Cardiff University
LMB - BALLETS study coordinator, University of Birmingham
RPJ - Formerly researcher for BALLETS; currently Health Economist, University of Nottingham
RJL - Professor of Clinical Epidemiology, University of Birmingham
AJG - Research fellow, University of Birmingham
The authors would like to thank Dr P. Gill (University of Birmingham) and Prof J. Neuberger (University Hospital Birmingham) for their help in constructing the various strategies for detecting viral hepatitis; Dr R. Cramb (University Hospital Birmingham) for sharing his expertise on current Liver Function Test practice; Dr D. McLernon (University of Aberdeen) and Dr M. Lazo (Johns Hopkins Bloomberg School of Public Health) for their helpful comments on the manuscript; Mr P. Chilton (University of Birmingham) for his assistance in the preparation of this manuscript; and the BALLETS study group, consisting of Prof D. Altman, Prof D. Armstrong, Dr R. Cramb, Dr P. Gill, Prof R. Jones, Dr K. Khan, Prof T. Marteau, Prof K. Moons, Prof J. Neuberger, Dr S. Olliff, Prof J Raftery, Prof R. Raine, Prof G. Rottenberg, Prof R. Swaminathan, and Dr M. Wilkinson.
The BALLETS study was funded by the National Institute for Health Research through its Health Technology Assessment (HTA) Programme. This grant provided the funding for the data collection as well as funding the authors. The full protocol is available online at http://www.hta.ac.uk/protocols/200300380001.pdf.
AJG received financial support from the EPSRC Multidisciplinary Assessment of Technology Centre for Healthcare (MATCH) programme (EPSRC Grant GR/S29874/01).
- Limdi JK, Hyde GM: Evaluation of abnormal liver function tests. Postgrad Med J. 2003, 79 (932): 307-312. 10.1136/pmj.79.932.307.View ArticlePubMedPubMed CentralGoogle Scholar
- Theal RM, Scott K: Evaluating asymptomatic patients with abnormal liver function test results. Am Fam Physician. 1996, 53 (6): 2111-2119.PubMedGoogle Scholar
- Giannini EG, Testa R, Savarino V: Liver enzyme alteration: a guide for clinicians. CMAJ. 2005, 172 (3): 367-379.View ArticlePubMedPubMed CentralGoogle Scholar
- Pratt DS, Kaplan MM: Evaluation of abnormal liver-enzyme results in asymptomatic patients. N Engl J Med. 2000, 342 (17): 1266-1271. 10.1056/NEJM200004273421707.View ArticlePubMedGoogle Scholar
- Cobbold JF, Anstee QM, Thomas HC: Investigating mildly abnormal serum aminotransferase values. BMJ. 341: c4039-10.1136/bmj.c4039.Google Scholar
- Sherwood P, Lyburn I, Brown S, Ryder S: How are abnormal results for liver function tests dealt with in primary care? Audit of yield and impact. BMJ. 2001, 322: 276-278. 10.1136/bmj.322.7281.276.View ArticlePubMedPubMed CentralGoogle Scholar
- Butt AA: Hepatitis C virus infection: the new global epidemic. Expert Rev Anti Infect Ther. 2005, 3 (2): 241-249. 10.1586/14787184.108.40.206.View ArticlePubMedGoogle Scholar
- Lavanchy D: Hepatitis B virus epidemiology, disease burden, treatment, and current and emerging prevention and control measures. J Viral Hepat. 2004, 11 (2): 97-107. 10.1046/j.1365-2893.2003.00487.x.View ArticlePubMedGoogle Scholar
- Trepo C, Pradat P: Hepatitis C virus infection in Western Europe. J Hepatol. 1999, 31 (Suppl 1): 80-83. 10.1016/S0168-8278(99)80379-1.View ArticlePubMedGoogle Scholar
- Weber B, Van der Taelem-Brule N, Berger A, Simon F, Geudin M, Ritter J: Evaluation of a new automated assay for hepatitis B surface antigen (HBsAg) detection VIDAS HBsAg Ultra. J Virol Methods. 2006, 135 (1): 109-117. 10.1016/j.jviromet.2006.02.009.View ArticlePubMedGoogle Scholar
- Tanaka E, Ohue C, Aoyagi K, Yamaguchi K, Yagi S, Kiyosawa K, Alter HJ: Evaluation of a new enzyme immunoassay for hepatitis C virus (HCV) core antigen with clinical sensitivity approximating that of genomic amplification of HCV RNA. Hepatology. 2000, 32 (2): 388-3893. 10.1053/jhep.2000.9112.View ArticlePubMedGoogle Scholar
- Kanwal F, Farid M, Martin P, Chen G, Gralnek IM, Dulai GS, Spiegel BM: Treatment alternatives for hepatitis B cirrhosis: a cost-effectiveness analysis. Am J Gastroenterol. 2006, 101 (9): 2076-2089. 10.1111/j.1572-0241.2006.00769.x.View ArticlePubMedGoogle Scholar
- Thompson Coon J, Rogers G, Hewson P, Wright D, Anderson R, Cramp M, Jackson S, Ryder S, Price A, Stein K: Surveillance of cirrhosis for hepatocellular carcinoma: systematic review and economic analysis. Health Technol Assess. 2007, 11 (34): 1-206.View ArticlePubMedGoogle Scholar
- BALLETS Study. [http://www.hta.ac.uk/protocols/200300380001.pdf]
- Weinstein M, Fineberg H: Clinical Decision Analysis. 1980, Philadelphia: W. B. Saunders CoGoogle Scholar
- Yano E, Tagawa K, Yamaoka K, Mori M: Test validity of periodic liver function tests in a population of Japanese male bank employees. J Clin Epidemiol. 2001, 54 (9): 945-951. 10.1016/S0895-4356(01)00355-9.View ArticlePubMedGoogle Scholar
- Lu SN, Wang JH, Kuo YK, Kuo HL, Chen TM, Tung HD, Lee CM, Chen SC: Predicting the prevalence of antibody to hepatitis C virus (HCV) in a community by the prevalence of elevated levels of alanine aminotransferase: a method to identify areas endemic for HCV. Am J Trop Med Hyg. 2002, 67 (2): 145-150.PubMedGoogle Scholar
- Wang CS, Wang ST, Chou P: Using the prevalence of an elevated serum alanine aminotransferase level for identifying communities with a high prevalence of hepatitis C virus infection. Arch Intern Med. 2001, 161 (3): 392-394. 10.1001/archinte.161.3.392.View ArticlePubMedGoogle Scholar
- Jamali R, Khonsari M, Merat S, Khoshnia M, Jafari E, Bahram Kalhori A, Abolghasemi H, Amini S, Maghsoudlu M, Deyhim MR, Rezvan H, Pourshams A: Persistent alanine aminotransferase elevation among the general Iranian population: prevalence and causes. World J Gastroenterol. 2008, 14 (18): 2867-2871. 10.3748/wjg.14.2867.View ArticlePubMedPubMed CentralGoogle Scholar
- D'Souza R, Foster GR: Diagnosis and treatment of chronic hepatitis B. J R Soc Med. 2004, 97 (7): 318-321.View ArticlePubMedPubMed CentralGoogle Scholar
- Veldhuijzen IK, Toy M, Hahné SJ, De Wit GA, Schalm SW, De Man RA, Richardus JH: Screening and Early Treatment of Migrants for Chronic Hepatitis B Virus Infection Is Cost-Effective. Gastroenterology. 2009, 138 (2): 522-530. 10.1053/j.gastro.2009.10.039.View ArticlePubMedGoogle Scholar
- Persico M, Persico E, Suozzo R, Conte S, De Seta M, Coppola L, Palmentieri B, Sasso FC, Torella R: Natural history of hepatitis C virus carriers with persistently normal aminotransferase levels. Gastroenterology. 2000, 118 (4): 760-764. 10.1016/S0016-5085(00)70145-4.View ArticlePubMedGoogle Scholar
- World Health Organization, Geneva: Introduction of hepatitis B vaccine into childhood immunization services. 2001, Geneva: Department of Vaccines and BiologicalsGoogle Scholar
- World Health Organization: Internation Travel and Health. Situation as on 1 January 2005. 2005, Geneva: Marketing and Dissemination, World Health OrganizationGoogle Scholar
- World Health Organization: International Travel and Health. Situation as on 1 January 2010. 2010, Geneva: WHO PressGoogle Scholar
- Hutton DW, Tan D, So SK, Brandeau ML: Cost-effectiveness of screening and vaccinating Asian and Pacific Islander adults for hepatitis B. Ann Intern Med. 2007, 147 (7): 460-469.View ArticlePubMedGoogle Scholar
- Newcombe RG: Two-sided confidence intervals for the single proportion: comparison of seven methods. Stat Med. 1998, 17 (8): 857-872. 10.1002/(SICI)1097-0258(19980430)17:8<857::AID-SIM777>3.0.CO;2-E.View ArticlePubMedGoogle Scholar
- Todd PM, Gigerenzer G: Precis of Simple heuristics that make us smart. Behav Brain Sci. 2000, 23 (5): 727-741. 10.1017/S0140525X00003447. discussion 742-780View ArticlePubMedGoogle Scholar
- Dufour DR, Lott JA, Nolte FS, Gretch DR, Koff RS, Seeff LB: Diagnosis and monitoring of hepatic injury. II. Recommendations for use of laboratory tests in screening, diagnosis, and monitoring. Clin Chem. 2000, 46 (12): 2050-2068.PubMedGoogle Scholar
- Kim HC, Nam CM, Jee SH, Han KH, Oh DK, Suh I: Normal serum aminotransferase concentration and risk of mortality from liver diseases: prospective cohort study. BMJ. 2004, 328 (7446): 983-10.1136/bmj.38050.593634.63.View ArticlePubMedPubMed CentralGoogle Scholar
- McLernon DJ, Donnan PT, Ryder S, Roderick P, Sullivan FM, Rosenberg W, Dillon JF: Health outcomes following liver function testing in primary care: a retrospective cohort study. Fam Pract. 2009, 26 (4): 251-259. 10.1093/fampra/cmp025.View ArticlePubMedGoogle Scholar
- Donnan PT, McLernon D, Dillon JF, Ryder S, Roderick P, Sullivan F, Rosenberg W: Development of a decision support tool for primary care management of patients with abnormal liver function tests without clinically apparent liver disease: a record-linkage population cohort study and decision analysis (ALFIE). Health Technol Assess. 2009, 13 (25): iii-iv. ix-xi,1-134View ArticleGoogle Scholar
- Dore GJ, Freeman AJ, Law M, Kaldor JM: Is severe liver disease a common outcome for people with chronic hepatitis C?. J Gastroenterol Hepatol. 2002, 17 (4): 423-430. 10.1046/j.1440-1746.2002.02730.x.View ArticlePubMedGoogle Scholar
- Bellentani S, Tiribelli C, Saccoccio G, Sodde M, Fratti N, De Martin C, Cristianini G: Prevalence of chronic liver disease in the general population of northern Italy: the Dionysos Study. Hepatology. 1994, 20 (6): 1442-1449. 10.1002/hep.1840200611.View ArticlePubMedGoogle Scholar
- Pendino GM, Mariano A, Surace P, Caserta CA, Fiorillo MT, Amante A, Bruno S, Mangano C, Polito I, Amato F, Cotichini R, Stroffolini T, Mele A, ACE Collaborating Group: Prevalence and etiology of altered liver tests: a population-based survey in a Mediterranean town. Hepatology. 2005, 41 (5): 1151-1159. 10.1002/hep.20689.View ArticlePubMedGoogle Scholar
- Daniel S, Ben-Menachem T, Vasudevan G, Ma CK, Blumenkehl M: Prospective evaluation of unexplained chronic liver transaminase abnormalities in asymptomatic and symptomatic patients. Am J Gastroenterol. 1999, 94 (10): 3010-3014. 10.1111/j.1572-0241.1999.01451.x.View ArticlePubMedGoogle Scholar
- Mathiesen UL, Franzen LE, Fryden A, Foberg U, Bodemar G: The clinical significance of slightly to moderately increased liver transaminase values in asymptomatic patients. Scand J Gastroenterol. 1999, 34 (1): 85-91. 10.1080/00365529950172880.View ArticlePubMedGoogle Scholar
- Hultcrantz R, Glaumann H, Lindberg G, Nilsson LH: Liver investigation in 149 asymptomatic patients with moderately elevated activities of serum aminotransferases. Scand J Gastroenterol. 1986, 21 (1): 109-113. 10.3109/00365528609034632.View ArticlePubMedGoogle Scholar
- Whitehead MW, Hawkes ND, Hainsworth I, Kingham JG: A prospective study of the causes of notably raised aspartate aminotransferase of liver origin. Gut. 1999, 45 (1): 129-133. 10.1136/gut.45.1.129.View ArticlePubMedPubMed CentralGoogle Scholar
- Poland GA, Jacobson RM: Prevention of Hepatitis B with the Hepatitis B vaccine. NEJM. 2004, 351: 2832-2838. 10.1056/NEJMcp041507.View ArticlePubMedGoogle Scholar
- Petrie KJ, Cameron LD, Ellis CJ, Buick D, Weinman J: Changing illness perceptions after myocardial infarction: an early intervention randomized controlled trial. Psychosom Med. 2002, 64 (4): 580-586.View ArticlePubMedGoogle Scholar
- Witte K, Allen M: A meta-analysis of fear appeals: implications for effective public health campaigns. Health Educ Behav. 2000, 27 (5): 591-615. 10.1177/109019810002700506.View ArticlePubMedGoogle Scholar
- Castelnuovo E, Thompson-Coon J, Pitt M, Cramp M, Siebert U, Price A, Stein K: The cost-effectiveness of testing for hepatitis C in former injecting drug users. Health Technol Assess. 2006, 10 (32): iii-iv. ix-xii, 1-93View ArticlePubMedGoogle Scholar
- Stein K, Dalziel K, Walker A, Jenkins B, Round A, Royle P: Screening for hepatitis C in genito-urinary medicine clinics: a cost utility analysis. J Hepatol. 2003, 39 (5): 814-825. 10.1016/S0168-8278(03)00392-1.View ArticlePubMedGoogle Scholar
- Nakamura J, Terajima K, Aoyagi Y, Akazawa K: Cost-effectiveness of the national screening program for hepatitis C virus in the general population and the high-risk groups. Tohoku J Exp Med. 2008, 215 (1): 33-42. 10.1620/tjem.215.33.View ArticlePubMedGoogle Scholar
- Health Protection Agency - Hepatitis C. [http://www.hpa.org.uk/Topics/InfectiousDiseases/InfectionsAZ/HepatitisC/]
- Health Protection Agency - Hepatitis B. [http://www.hpa.org.uk/Topics/InfectiousDiseases/InfectionsAZ/HepatitisB/]
- Worwood M: Haemochromatosis. Clin Lab Haematol. 1998, 20 (2): 65-75. 10.1046/j.1365-2257.1998.00028.x.View ArticlePubMedGoogle Scholar
- Metcalf JV, Bhopal RS, Gray J, Howel D, James OF: Incidence and prevalence of primary biliary cirrhosis in the city of Newcastle upon Tyne, England. Int J Epidemiol. 1997, 26 (4): 830-836. 10.1093/ije/26.4.830.View ArticlePubMedGoogle Scholar
- AutoImmune Hepatitis Support Group. [http://www.autoimmunehepatitis.co.uk/]
- Olivarez L, Caggana M, Pass KA, Ferguson P, Brewer GJ: Estimate of the frequency of Wilson's disease in the US Caucasian population: a mutation analysis approach. Ann Hum Genet. 2001, 65 (Pt 5): 459-463. 10.1046/j.1469-1809.2001.6550459.x.View ArticlePubMedGoogle Scholar
- de Serres FJ: Worldwide racial and ethnic distribution of alpha1-antitrypsin deficiency: summary of an analysis of published genetic epidemiologic surveys. Chest. 2002, 122 (5): 1818-1829. 10.1378/chest.122.5.1818.View ArticlePubMedGoogle Scholar
- Kim KM, Kim YJ, Lee KH, Paek D: [Clinical characteristics of factory workers with asymptomatic liver function test abnormalities found on serial health examination]. Korean J Hepatol. 2005, 11 (2): 144-156.PubMedGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2296/12/9/prepub
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