Select Committee on Intergovernmental Organisations Written Evidence


Memorandum by the International Pharmaceutical Federation (FIP)

8Q:  Cases of TB fell progressively in the UK until the mid 1980s but started to rise again in the early 1990s. Around 6,500 cases are now reported each year, an increase of about a quarter since the early 1990s. What are the main factors of the revival of tuberculosis infections in Britain? And how could intergovernmental action help to reverse this trend?

  The vast majority of TB cases in the UK are notified as residents in London and the vast majority of these are individuals not born in the UK. However, to draw from this the conclusion that the rise of TB prevalence is due solely to immigrants from high TB prevalence countries introducing TB into an otherwise low incidence country would be inaccurate. Notification statistics demonstrate that non-UK born individuals that develop TB do so generally after they have been in the UK for some years. Although this is not always the case, it would be worth considering other factors, such as social deprivation and access to health care. Why are TB rates highest in the most deprived boroughs? What is wrong with the health and/or social systems in the UK that individuals develop TB in the UK after many years without disease in their countries of origin? Particular attention should also be paid towards "hard to reach" or high risk groups that might encourage the nosocomial spread of TB. Groups include illegal immigrants—who would not necessarily register for health care—street sex workers, intravenous and crack cocaine drug users, and homeless individuals whose lives are likely to be chaotic with TB treatment representing a low priority. Provision of directly observed treatment (DOT) in the community, such as in General Practitioners or community pharmacies, may improve access to care.

  Greater attention should also be paid towards screening systems, particularly the Port of Arrival screening offered to "high risk" immigrants for later follow-up. The various services available are largely inefficient or of unknown/unquantified efficiency. A comparison of systems may help to identify the best model (alone or integrated screening) of screening strategy. In addition, other forms of screening should be explored. For example, the ubiquity of general practitioners and community pharmacies provides a unique opportunity for identifying and treating individuals infected with TB that might not normally access healthcare.

Q9:  Tuberculosis is potentially curable by long-term antimicrobial therapies. Yet the numbers of reported cases worldwide seem to be rising. Are the necessary medicines not getting through to patients? What are the barriers to effective long-term therapy? Are we now seeing infections which stem from other conditions—eg HIV/AIDS? Or are there other reasons why a treatable disease should be spreading? How might intergovernmental action help to deal with this situation?

  TB treatment is highly efficacious and cost-effective. Taken correctly almost all TB patients would achieve a cure. There are many reasons why cure rates of 98% are not achieved and the reasons depend on the setting, for example, high versus low income countries and high versus low HIV prevalence. However, the length of treatment must play a part with the minimum duration of six-months treatment of TB and three-months treatment (recommended in the UK) for latent infection. Symptoms are likely to disappear after two weeks treatment of pulmonary TB, and extrapulmonary TB may be asymptomatic. Therefore, to continue with over five months additional treatment demands much of the patient both in terms of will power and the understanding of disease. In reducing the duration of treatment, for example, by introducing more efficacious drug treatments or including other antituberculous drugs into existing regimens to improve efficacy, may help to circumvent this problem or at least reduce the impact of non-adherence. Alternatively, greater emphasis on patient counselling and using better engagement strategies, putting patients at the centre of their care in the absence of much therapeutic choice, may help.

  Sharing of experience between different countries, including between high and low prevalence settings to identify common themes and strategies, would help in the common goal of reducing the global prevalence of TB. For example, if TB rates in the UK relate to TB rates in high TB burden countries through immigration then it makes sense to develop seamless strategies that span geographical boundaries. It should be possible for a patient to begin treatment in one country and finish treatment in another without interruption in treatment. In the absence of any new technological breakthroughs in TB it is worth also focusing on what can be best made out of existing technologies. Are pharmaceutical formulations adequate for those who struggle to adhere to treatment or children, for example? Are these accessible? Are second-line treatments readily available and/or affordable where needed? Does the ubiquity of first-line TB drugs, especially in developing countries, hampering the eradication of TB, and, if so, what measures can be put in place to prevent this from continuing?

February 2008



 
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