Print ISSN:-2249-8176

Online ISSN:-2348-7682

CODEN : PJMSD7

Current Issue

Year 2024

Volume: 14 , Issue: 3

  • Article highlights
  • Article tables
  • Article images

Article Access statistics

Viewed: 157

Emailed: 0

PDF Downloaded: 365


Latha V, Tanveer Ahmed T M, and Shyamala G: Clinical profile of multi-drug reisitance tuberculosis in adults


Introduction

Tuberculosis is age old disease which is known to cause suffering and death. Among the many disease known to mankind, tuberculosis is thought to be one of the oldest human diseases of all. Mankind has known TB as far the literature goes back. As per ancient sources it was called as “rajayakshma” (meaning “wasting disease”). In 460-377 B C in the era of Hippocrates a greek doctor, the tuberculosis disease is mentioned as “pthisis”, which means “to consume”.1 The “tuberculosis” is derived from latin word “tubercula” meaning “a small lump”1, 2, 3 The discovery of tubercular bacillus was by Dr. Robert Koch in 1884. 4, 5, 6

The introduction of streptomycin in year 1994 made a bench mark of start of antibiotic era in TB treatment. The joyous dream of curing tb became a reality in mid 1940s with the availability of isoniazide, paraaminosalicylic acid (PAS).

Perhaps the lengthy drug duration course treatment of TB became a short course treatment with rifampicin, pyrazinamide and ethambutol came to exhistence in subsequent years. However the mere availability of anti-tubercular drugs became a tedious cause in the emergence of drug resistance TB due to the indiscriminate use of antituberculosis drugs and laxity in monitoring of tedious drug regimens, which broke the euphoria which we had initially, the ability to cure TB, which led to emergence of multidrug resistance strain of Mycobacterium tuberculosis. And this worrisome disease MDR-TB is prevalent worldwide.7, 8, 9

Drug resistance tuberculosis affected 8000 patients in 2017 in a worldwide reocrd. Of these 82% had multidrug resistance TB. Drug resistance tuberculosis occurred more common in 3 main countries worldwide, i.e. India (24%), China (13%) and Russian Federation (10%). Globally 3.5% of new TB cases and 18% of previously treated cases had MDR/RR-TB.10, 11

Definition of multi drug résistance- a TB patient, whose biological specimen is resistance to both rifampicin and isoniazide with or without resistance to other first line drugs.12 Definition of XDR- extensive drug resistance – a MDR TB patient, whose biological specimen is additionally resistant to a fluroquinolone and second line injectable anti- drug.12 The present study aimed to asses distribution of drug resistance and assessing their clinical profile.

Materials and Methods

The prospective study was conducted in patients admitted in medical college hospitals affiliated to Vijayanagar Institute of Medical Sciences, Ballari, period of two years from November 2016 to October 2018. All patients admitted during the study period with history of fever with cough for more than 2 weeks, loss of appetite, weight loss, hemoptysis, breathlessness were taken for study. All patients’ demographic data, age, sex, occupation, place of stay, comorbidities like diabetes, hypertension, COPD, smoking and alcohol consumption history, history of diagnosed with HIV and on ART, previous history of tuberculosis and ATT collected. All patients were subjected to routine investigation and sputum AFB, drug resistance tuberculosis was diagnosed by CBNAAT.

Statistical analysis

Information gathered for this study encrypted and recorded in a spreadsheet. Statistical analysis was performed using MS excel. Variables were calculated by mean, standard deviation for quantitative variables, frequency and proportions for qualitative variables.

Results

This study included 150 patients diagnosed with pulmonary tuberculosis, 28(18.7%) of them fount to have drug resistance tuberculosis. All 28 patients had rifampicin and isoniazid resistance. Out of 28 patients with multi- drug resistance TB, majority are males (n=24, 85.7%) than females (n=4, 14.2%). In our study, drug resistance tuberculosis, showed that maximum MDR-TB patients were in the age group of 30-40 years. (mean age = 36.28 years, standard deviation (SD) 13.97 years; range 18 – 70 years). Majority of them were in rural areas (n=20, 71.5%) and were of upper lower and lower socio class (64.2%). 64.2% had history of alcohol consumption and 71.4% had history of smoking and 16.7% were tobacco chewers. HIV (39.3%) was the commonest co-morbidity among the study group followed by diabetes (35.7%), hypertension (35.7%) and COPD (28.6%).

All patients included were of Pulmonary TB, out of which 10(35.7%) patients had bilateral lung involvement on chest X-ray and cavity was seen in all 28 patients.

Fever was the most common symptom occurring in 92.9% patients followed by cough with expectoration (89.2%), loss of appetite and weight (89.8%) and shortness of breath (39.2%).

Majority (78.6%) of patients had previously taken treatment for TB and 35.7% did not complete their treatment.

Outcome-wise 78.6% patients were under treatment and 21.4% patients had been expired.

Table 1

Demographic parameters

Number(n)

Percentage (%)

Sex

Male

24

85.7%

Female

4

14.3%

Age

18-29

6

21.4%

30-39

11

39.3%

40-49

5

17.9%

50-59

3

10.7%

>60

3

10.7%

Residence

Urban

8

28.5%

Rural

20

71.5%

Previous history of ATT and not completed treatment

Yes

16

57.1%

No

12

42.9%

Relapse

yes

4

14.3%

no

24

85.7%

H/o Smoking

Yes

20

71.5%

no

8

28.5%

H/o Alcohol consumption

Yes

18

64.3%

No

10

35.7%

HIV positive status

Yes

11

39.2%

No

17

60.8%

Diabetes

Yes

10

35.7%

No

18

64.3%

Hypertension

Yes

10

35.7%

No

18

64.3%

COPD

Yes

8

28.5%

No

20

71.5%

Table 2

Symptomatology

Symptoms

No. of patients

Percentage (%)

Fever

26

92.9%

Cough with / without expectoration

25

89.2%

Loss of apatite

25

89.2%

Hemoptysis

10

35.7%

Breathlessness

11

39.2%

Loss of weight

25

89.2%

Chest pain(pleuritic type)

6

21.4%

Discussion

In this study, the mean age group of our study population was 30-39yrs,in study conducted by Sharma et al (2011) 13 35.5yrs was mean age, which indicates that in MDR-TB group of individual that are affected are relatively younger age, who belongs to productive age group both socially and economically.

The M:F ratio (male to Female) was 6:1 i.e more in favor of males (M= 85.7% [n=24] F=14.3% [n=4] which when compared to study by Joseph et al conducted in 2011 shows 66% of males had MDR-TB.

In our study the resident of 71.5% of the patients was rural areas when compared to study by Joseph et al (2011) 14 69% patients had residence to urban areas.

Primary resistance was found in 10.7% whereas 89.3% had secondary resistance, however 10.7% of patients and 63.4% patients had Primary resistance and secondary resistance respectively in study by Datta et al (2009).15

In our study, 64.2% of cases had bilateral fibrocavitatory changes on Chest X-ray as compared to study of Singla et al(2009) 16 84% had bilateral involvement. Whereas cavity in lung tissue was seen in 82.1% of cases, in study conducted by Singla et al the prevalence of cavity was 43%. 89.2% patients had cough as predominant symptom

When comes to associated co-morbidities diabetes mellitus and HIV were commonest. In a study, Kim et al had 18.7% and 17.1% had diabetes mellitus as most common co-morbidity in extensively drug resistant tuberculosis and multi drug resistant tuberculosis patients respectively. 17

About n=20 (71.5%) patients had history of smoking and 64.3% (n=18) gave history of consumption of alcohol. history of tobacco chewing was elicited in 16.7% of patients.

In study by Marahatta had observed that smoking is associated with the Isoniazid resistance. 18

In a study in Delhi, smoking was associated factor with 40.8%, 37.7% & 50% of the multi-drug resistant tuberculosis, prextensively drug resistant tuberculosis & extensively drug resistant tuberculosis respectively. 19

As part of all prospective study, our study had few drawbacks i.e study duration was short.

The one more drawback is there is no follow up regards to drug side effect.

Conclusion

Our study shows prevalence of drug resistant is more common than we thought before, which is particularly affecting middle age men.

Associated co-morbidity HIV, type 2 diabetes mellitus, hypertension also common among drug resistance TB.

Among those with drug resistant TB, previous history of treatment with ATT was more common and hence early detection of drug resistance especially among relapse and failure patients, ensuring Quality DOTS Services and patient counseling and rational use of ATT and vigilance of national tuberculosis program will help to prevent the emergence of MDR TB as a major health problem.

Source of Funding

None.

Conflict of Interest

None.

References

1 

MD Rosenblatt Pulmonary tuberculosis: evolution of modern therapy.Bull NY Acad Med197349316396

2 

R Dubos J Dubos The white plaque. Tuberculosis, manand societyLittle, Brown and companyBoston1952

3 

SA Waksman The conquest of tuberculosisUniversity of California PressBerkeley and Los Angeles1964

4 

GB Webb Tuberculosis Phys Therapy193616521710.1093/ptj/16.5.217

5 

SA Rubin Tuberculosis. Captain of all these men of deathRadiol Clin North Am199533461939

6 

A Sakula Robert Koch: centenary of the discovery of the tubercle bacillus, 1882Thorax198237424651

7 

LP Ormerod Multidrug-resistant tuberculosis (MDR-TB): epidemiology, prevention and treatmentBr Med Bull200573-74172410.1093/bmb/ldh047

8 

M Zignol MS Hosseini A Wright CL Weezenbeek P Nunn CJ Watt Global incidence of multidrug-resistant tuberculosisJ Infect Dis2006194447985

9 

SK Sharma A Mohan The implications of Multidrug-resistant -TB (MDR-TB)Eur Infect Dis20071524

10 

Directorate of Health Services, Ministry of Health & Family Welfare, Government of India CTD. TB India 2017: RNTCP Status Report2017http://www.tbcindia.nic.in/ [Accessed 16 March 2021]

11 

GL Initiative Guide for providing technical support to TB laboratories in low-and middle-income countries2014http://stoptb.org/wg/gli/assets/documents/guideforprovidingtechnicalsupport_gb_web.pdf

12 

Guidelines for programmatic management of drug resistence tuberculosis in India 2016

13 

SK Sharma S Kumar PK Saha N George SK Arora D Gupta Prevalence of multidrug-resistant tuberculosis among Category II pulmonary tuberculosis patientsIndian J Med Res201113333125

14 

P Joseph VBR Desai NS Mohan JS Fredrick R Ramachandran B Raman Outcome of standardized treatment for patients with MDR-TB from Tamil NaduIndian J Med Res2011133552934

15 

BS Datta G Hassan S ManzoorKadri W Qureshi MA Kamil H Singh Multidrug-Resistant and extensively drug resistant tuberculosis in Kashmir, IndiaJ Infect Dev Ctries2010411923

16 

R Singla R Sarin UK Khalid K Mathuria N Singla A Jaiswal Seven-year DOTS-Plus pilot experience in India: results, constraints and issuesInt J Tuberc Lung Dis200913897681

17 

DH Kim HJ Kim S Park S Kong YS Kim T Kim Treatment outcomes and survival based on drug resistance patterns in multidrug-resistant tuberculosisAm J Respir Crit Care Med201018211139

18 

DK Tripathi K Srivastava Suryakant KK Srivastava Molecular profiling of drug resistant isolates of mycobacterium tuberculosis in North IndiaAdv Microbiol20122331726

19 

C Porwal A Kaushik N Makkar JN Banavaliker M Hanif R Singla Incidence and Risk Factors for Extensively Drug-Resistant Tuberculosis in Delhi RegionPLoS ONE201382e5529910.1371/journal.pone.0055299



jats-html.xsl

© 2023 Published by Innovative Publication Creative Commons Attribution 4.0 International License (creativecommons.org)