• Tidak ada hasil yang ditemukan

EDITORIAL Multi-drug-resistant tuberculosis (MDR-TB)

N/A
N/A
Protected

Academic year: 2024

Membagikan "EDITORIAL Multi-drug-resistant tuberculosis (MDR-TB)"

Copied!
1
0
0

Teks penuh

(1)

The page number in the footer is not for bibliographic referencing www.tandfonline.com/ojfp 5

EDITORIAL

Multi-drug-resistant tuberculosis (MDR-TB): Current situation in South Africa

Multi-drug-resistant tuberculosis (MDR-TB) is a form of tuberculosis (TB) infection which is resistant to treatment with at least two of the most powerful first-line anti-TB drugs, namely isoniazid and rifampicin.

Globally, MDR-TB caused an estimated 480 000 new TB cases and 250 000 deaths in 2015 and accounted for 3.3% of all new TB cases worldwide.1 MDR-TB, or rifampicin-resistant TB, causes 3.9% of new TB cases and 21%

of previously treated TB cases, and most MDR-TB cases occur in South America, southern Africa, India, China, and the former Soviet Union.1

A South African Health Systems Trust report indicated that despite a global slowing down in new TB cases since 2003, South Africa recorded the world’s second-highest rate of new cases in 2006 after Swaziland. More people died of TB in South Africa that year than in any other country in the world. Zimbabwe and Mozambique had the next highest TB death rates. The global TB cure rate for 2005 was 78%, but South Africa’s cure rate was only 58%, which was the third worst in the world.2

The WHO 2016 global report on country profiles for the 30 high-burden countries for tuberculosis paints a very sobering picture for South Africa. In 2015, with the estimated population of 54 million, the incidence rate for TB (including HIV+TB) was 834 cases per 100 000. Furthermore, the incidence rate for MDR- TB was 37 cases per 100  000 and the TB treatment coverage (notified/estimated incidence) was 63%. In 2015, the South African national TB budget was US$425 million.3 The latter should have produced better TB control outcomes as countries with less financial resources performed better. For example, in 2015, Kenya, with a population of 46 million, recorded the TB incidence rate (including HIV+TB) of 233 cases per 100  000 population, MDR-TB incidence rate of 4.3 cases per 100 000 population, and TB treatment coverage (notified/estimated incidence) of 76%

with a national TB budget of US$59 million.3

We are aware that MDR-TB is man-made due to the following factors:

a. Poor patient adherence to complete the full course of TB treatment

b. Healthcare providers prescribing the wrong treatment, wrong dose, or length of time for TB drugs

c. Inadequate monitoring of patients while on their anti-TB drugs (DOTS)

d. Irregular anti-TB drug supply at health facilities

Obviously to reduce the incidence of MDR-TB, it is imperative that TB is treated correctly the first time. It is these man-made factors that result in the emergence of MDR-TB. Healthcare providers need to be better trained at our various nursing colleges and medical schools on how to manage TB, with regular and intense follow-up in-service training sessions. In addition, patients need more motivation and education to appreciate the importance of adherence to the six-month TB treatment programme. Issues of patient monitoring, while taking their drugs, can be addressed by employing more community health workers to supervise and motivate patients. The problem with irregular drug supplies can be addressed by proper drug stock planning and regular payment of drug suppliers by provincial health departments.

In South Africa, the human and financial resources are available for the successful implementation of the national TB control programme to ultimately reduce the incidence of MDR-TB.

However, a well-coordinated implementation strategy between the national and provincial health departments is lacking. That is the crux of the matter that is causing the country’s lower than expected TB control outcomes.

Prof. Gboyega A Ogunbanjo Editor-in-chief: SAFPJ References

1. World Health Organization. “Diagnosis and notification of multidrug-resistant TB”

(PDF). WHO MDR TB Factsheet (2016 Update). http://www.who.int/tb/challenges/

mdr/mdr_tb_factsheet.pdf [accessed 29 April 2017]

2. Kerry Cullinan. South Africa has worst TB prevalence in the world – report. Health Systems Trust 2017 report. http://www.hst.org.za/news/south-africa-has-worst- tb-prevalence-world-report [accessed 29 April 2017]

3. World Health Organization. WHO 2016 global report on country profiles for the 30-high burden countries for tuberculosis http://www.who.int/tb/publications/

global_report/gtbr2016_annex2.pdf?ua=1 [accessed 29 April 2017]

Referensi

Dokumen terkait

Berdasarkan hasil penelitian dan pembahasan dapat disimpulkan bahwa karakteristik penderita Tuberculosis Multidrug Resistant (TB MDR) di Sulawesi Tenggara tahun

Hasil analisis menunjukkan bahwa ada hubungan tidak langsung antara persepsi kerentanan dengan kejadian MDR TB melalui variabel kepatuhan pasien dalam minum

penelitian yang berjudul : “ Perbandingan Nilai Neutrofil Limfosit Rasio (NLR) Pada Pasien TB Paru dan MDR TB ” dan setelah mengetahui dan menyadari sepenuhnya resiko

Kesimpulan penelitian ini adalah karakteristik penderita tuberkulosis paru dengan multidrug-resistant Tuberculosis (MDR-TB) di RSUD Ulin Banjarmasin periode Desember

Penggunaan paduan obat yang tidak adekuat, yaitu jenis obatnya yang kurang atau di lingkungan tersebut telah terdapat resistensi terhadap obat yang digunakan, misalnya memberikan

Inadequate treatment of MDR-TB may worsen patients’ outcome, consequently increasing the risk of extensive drug resistance.3 Without proper treatment, multidrug resistant strains can

In 2014, there were 9.6 million new cases of active TB and 1.5 million deaths worldwide.[1] The standard treatment for TB comprises an intensive phase with isoniazid, rifampicin,

Beberapa penelitian lain juga hasil yang sama yaitu terdapatnya hubungan yang signifikan terhadap kejadian MDR-TB pada pasien yang memiliki riwayat pengobatan TB sebelumnya [14],[28],