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. 2012 Dec 12;2(4):145–147. doi: 10.5588/pha.12.0058

Screening tuberculosis patients for diabetes mellitus in Fiji: notes from the field

S Gounder 1,, A D Harries 2,3
PMCID: PMC4463061  PMID: 26392974

Abstract

Diabetes (DM) is a problem in Fiji and threatens tuberculosis (TB) control efforts. A review was conducted of all TB patients registered in Fiji in 2011 to assess routine practices of screening for DM. Of 221 TB patients, 138 (62%) had their DM status recorded in their case folders; 18 (13%) had a known history of DM. Random blood glucose (RBG) was performed in 91 (76%) of the remaining 120 patients: 47(52%) had RBG ≥ 6.1 mmol/l, but only three were further investigated, of whom one was diagnosed with DM. There are deficiencies in screening TB patients for DM in Fiji, and improvements are needed.

Keywords: operational research, tuberculosis, diabetes mellitus, Fiji


There is good evidence to suggest that diabetes mellitus (DM) increases the risk of tuberculosis (TB).1,2 DM patients with TB also experience worse treatment outcomes than patients without DM, with an increased risk of death and recurrent disease.3 DM is a growing problem in Fiji; about 16% of the population have DM, but many cases are not diagnosed and treated.4 Although Fiji is classified as a low TB burden country, this has become a matter of concern for the National Tuberculosis Programme (NTP), as DM may lead to an increase in TB case burden and hamper current TB control efforts.

When TB patients are registered in Fiji, they should be asked whether they have DM. For those with no known history of DM, random blood glucose (RBG) measurements should be performed, followed by confirmatory fasting blood glucose (FBG) measurements in patients whose RBG is above a certain threshold. It has been recommended that patients whose RBG is ≥6.1 mmol/l be investigated further, as they are at high risk of having DM.5 There has been no formal assessment in Fiji about whether these recommendations are adhered to. We therefore conducted a retrospective study to determine 1) what proportion of TB patients were recorded as having DM, and 2) whether RBG measurements had been performed and recorded along with the results.

METHODS

This was a cross-sectional study involving a review of patients’ medical folders. Fiji (population approximately 837 000) is an island nation in the South Pacific with 322 islands, of which 106 are permanently inhabited.6

The Fiji NTP was established in 1951 and adopted the DOTS strategy in 1997. There are three DOTS Centres, each in the three administrative divisions of the country, where TB patients are registered and receive the intensive phase of treatment for 2–3 months. According to international recommendations, DM status is supposed to be assessed and recorded in patient case folders during registration.7 First, patients are asked if they are known to have DM. In those with no known history of DM, an RBG is conducted; if the RBG is ≥6.1 mmol/l, an FBG is carried out. Patients who have FBG ≥ 7.0 mmol/l are diagnosed as DM, and are referred for DM care.

All TB patients recorded in the TB patient registers in the three DOTS Centres from January to December 2011 were included in the study. The following data were collected from the patient folders into a structured questionnaire: age; sex; ethnicity; type of TB; DM status, if known; in those with no known DM, whether an RBG had been performed; the number with RBG ≥ 6.1 mmol/l; and in these, whether an FBG had been performed and the result.

The data were collected from January to March 2012 and double-entered into EpiData, version 3.1 (EpiData Association, Odense, Denmark). The χ2 test was used to assess differences in proportions between groups, with odds ratios (ORs) and 95% confidence intervals (CIs). Differences at the 5% level were regarded as significant.

Ethics approval was obtained from the Ethics Advisory Group of the International Union Against Tuberculosis and Lung Disease, the National Health Research Committee and the Fiji National Research Ethics Review Committee.

RESULTS

There were 221 TB patients, of whom 138 (62%) had their DM status recorded. Of these, 18 (13%) had a known history of DM (Table 1). The main observation was a significantly higher rate of DM in Indo-Fijians compared with indigenous Fijians (OR 7.0, 95%CI 2–24, P < 0.001), and the fact that the DM rate approached 50% in adults aged ≥55 years.

TABLE 1.

Known DM among TB patients in Fiji, 2011*

Characteristic Total n Known DM n (%)
All patients 138 18 (13)
Sex
 Male 74 10 (14)
 Female 64 8 (13)
Age, years
 0–14 6 0
 15–54 103 4 (4)
 ≥55 29 14 (48)
Ethnicity
 Fijian 92 8 (9)
 Indo-Fijian 25 10 (40)
 Others 21 0
TB type
 Pulmonary TB 107 14 (13)
 Extra-pulmonary TB 31 4 (13)
*

Proportion of TB patients with DM whose DM status was recorded in the patient folder.

DM = diabetes mellitus; TB = tuberculosis.

Of 120 TB patients who were recorded as not having DM, 91 (76%) had their RBG measured; 47 (52%) had an RBG ≥ 6.1 mmol/l. There were no differences in sex, age, ethnicity or type of TB (also stratified by sputum smear status) in the proportion of those with RBG performed or RBG ≥ 6.1 mmol/l (Table 2). Three (6%) patients with RBG ≥ 6.1 mmol/l had an FBG performed; one patient had FBG ≥ 7mmol/l.

TABLE 2.

Screening of TB patients in Fiji with no known DM using RBG, 2011

Characteristic Total n RBG performed n (%) RBG ≥ 6.1 mmol/l n (%)
All patients 120 91 (76) 47 (52)
Sex
 Male 64 43 (67) 25 (58)
 Female 56 48 (86) 22 (46)
Age, years
 0–14 6 3 (50) 2 (67)
 15–54 99 76 (77) 38 (50)
 ≥55 15 12 (80) 7 (58)
Ethnicity
 Fijian 84 62 (74) 34 (55)
 Indo-Fijian 15 13 (87) 4 (31)
 Others 21 16 (76) 9 (56)
TB type
 Pulmonary TB 93 73 (78) 37 (51)
 Extra-pulmonary TB 27 18 (67) 10 (56)

TB = tuberculosis; DM = diabetes mellitus; RBG = random blood glucose.

DISCUSSION

This is the first study in Fiji looking at screening practices related to DM among TB patients; the study findings show deficiencies at every level. More than one third of patients had no record of any questions or investigations in the files. While three quarters of patients with no history of DM had an RBG performed, subsequent follow-up was poor and <10% of patients who should have had FBG measurements performed actually did so. The few results that were obtained suggest that DM is a problem, particularly among Indo-Fijians and among those aged ≥55 years.

The strengths of this study are that all TB patients registered during a 1-year period were included, and the results are therefore representative of the national situation. Limitations relate to the operational nature of the study and the use of patient folders as the source of data.

International recommendations have been made about the need for bi-directional screening of DM and TB, particularly in high TB and DM burden countries.7 However, published data about how this would best be implemented in routine practice at country level are scarce.8 A recent report from China suggested that the incorporation of DM results into TB-DM registers that are linked to TB registers, combined with formal quarterly reports on numbers of patients screened for DM and numbers diagnosed with DM and referred for care, works well, and this could be a template for other countries to follow.9

In conclusion, this study shows that the routine practice of screening TB patients for DM in Fiji is suboptimal and needs to improve. A first important step will be a policy decision about incorporating screening results into TB registers and including the subsequent DM data in the quarterly reports, i.e., ‘what gets measured gets done’. Screening for DM in TB patients should lead to better and earlier detection of DM, earlier and better treatment of DM (which might otherwise have gone unrecognised) and improved clinical outcomes of DM-TB patients on anti-tuberculosis treatment.

Acknowledgments

This research was supported through an operational research course that was jointly developed and run by the Fiji National University; the Centre for Operational Research, International Union Against Tuberculosis and Lung Disease; the Operational Research Unit, Médecins Sans Frontières, Brussels; The University of Auckland, New Zealand; the Woolcock Institute of Medical Research, Sydney, Australia; and the Centre for International Child Health, The University of Melbourne, Melbourne, VIC, Australia.

Funding for this course came from the Global Fund to Fight AIDS, Tuberculosis and Malaria, the International Union Against Tuberculosis and Lung Disease and the World Health Organization.

Conflict of interest: none declared.

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