Sie sind auf Seite 1von 6

See discussions, stats, and author profiles for this publication at: https://www.researchgate.

net/publication/290993233

Etiology of Hemoptysis in India Revisited

Article · January 2016

CITATIONS READS

2 327

7 authors, including:

Naveed Shah Manzoor Wani


Government Medical College Srinagar Sher-i-Kashmir Institute of Medical Sciences
32 PUBLICATIONS   178 CITATIONS    29 PUBLICATIONS   35 CITATIONS   

SEE PROFILE SEE PROFILE

Rakesh Bhargava Zuber Ahmad


Aligarh Muslim University Aligarh Muslim University
71 PUBLICATIONS   214 CITATIONS    63 PUBLICATIONS   264 CITATIONS   

SEE PROFILE SEE PROFILE

Some of the authors of this publication are also working on these related projects:

Government medical college, Srinagar View project

654321 View project

All content following this page was uploaded by Manzoor Wani on 18 January 2016.

The user has requested enhancement of the downloaded file.


International Journal of Medical and Health Sciences
Journal Home Page: http://www.ijmhs.net ISSN:2277-4505

Original article

Etiology of Hemoptysis in India Revisited

Naveed Nazir Shah1, Manzoor Ahmad Wani2*, Syed Quibtiya Khursheed3, Rakesh Bhargava4, Zuber Ahmad5,
Khurshid Ahmad Dar6, Altaf Ahmad Bachh7

1
Assistant professor, Chest Diseases Hospital, Government Medical College, Srinagar,
2
Registrar, Department of General Medicine, SKIMS Medical College, Bemina,
3
Registrar, Department of General Surgery, Government Medical College, Srinagar,
4&5
Professors, Department of TB and Chest, J.N Medical College, AMU, Aligarh,
6
Lecturer, Chest diseases hospital, Government Medical College, Srinagar,
7
Lecturer, Department of Chest Medicine, SKIMS Medical College, Bemina.

ABSTRACT

Aims and Objectives: To study the changing trend in the causes of hemoptysis in India. Materials and Methods: Total of 246
patients complaining of hemoptysis were taken up for this prospective study. The study was approved by the local ethics
committee and informed consent from all patients were obtained prior to commencement of the study. All the patients were fully
investigated to find out the etiology of hemoptysis. Besides routine investigations, bronchoscopy was also done in patients, where
non bronchoscopic methods failed to reveal the cause. Other investigations like CT scan, FNAC/Biopsy was done in selective
patients. Results: The most common etiologies of hemoptysis in our study were tuberculosis[27.9%] followed by
malignancy[18.6%] and bronchiectasis[16.5%].Out of 246 patients,145 patients had mild hemoptysis [58.9%], 57 had moderate
[23.1%], 44 had severe hemoptysis [17.8%]. 32.2% patients of mild hemoptysis were diagnosed as bronchogenic carcinoma, 97%
of the patients with idiopathic hemoptysis were having mild hemoptysis. Of the 57 patients with moderate hemoptysis, 25% were
diagnosed as having bronchogenic carcinoma, 41.6% were having tuberculosis as the etiology for hemoptysis. Tuberculosis
(46.4%) and bronchiectasis (42.8%) were the most common etiologies in patients with severe hemoptysis. Conclusion: In India,
the most common cause of hemoptysis still remains tuberculosis, although the incidence has significantly decreased.

KEYWORDS: Hemoptysis, Tuberculosis, brochiectasis

INTRODUCTION

Hemoptysis is defined as expectoration of blood originating arteries(5%)[2]. The etiology for hemoptysis varies among
from lungs or bronchotracheal tree[1]. The material that is different series according to time of publication, the
produced varies from blood tinged sputum to virtually pure geographic location, and the diagnostic tests employed. In
blood. Hemoptysis is a frightening symptom for the patients India, first thing which comes to mind in a patient with
and can be a manifestation of serious underlying disease. hemoptysis is tuberculosis and patients are often treated for
The vast majority of hemoptysis events originate from the pulmonary kochs without proper evaluation.
bronchial arteries (90%) as compared with the pulmonary

Int J Med Health Sci. Jan 2016,Vol-5;Issue-1 9


The main aim of present study was to revisit the various An endoscopic diagnosis of bronchitis was made on account
etiologies of hemoptysis using bronchoscopic and non of presence of generalized inflammation of the airways
bronchoscopic methods, and to define the characteristics (redness and swelling of mucosa), indistinct cartilage rings,
associated with different etiologies. presence of small diverticula in the bronchial mucosa and
dilatation of the mucous gland ducts in the bronchial wall. A
non-bleeding abnormality was not considered a definitive
MATERIALS AND METHODS lesion but was consistently recorded. The influence of FOB
The present study was conducted on patients, attending the was determined by noting whether or not changes in the
Outpatient Department (OPD) and those who were admitted clinical diagnosis and management of the hemoptysis
in the wards (IPD) of Department of Tuberculosis and Chest occurred, based on results of each FOB. A final diagnosis
Diseases, Jawaharlal Nehru Medical College Hospital, for the hemoptysis was based on the definitive diagnosis
Aligarh Muslim University, Aligarh, India for 3 year and/or review of subsequent historical, radiological,
duration. Total of 246 patients complaining of hemoptysis surgical, or autopsy information, if sufficient to establish a
were taken up for this prospective study. The study was probable cause of bleeding. CT scan/ CT guided FNAC or
approved by the local ethics committee and informed biopsy, percutaneus FNAC or biopsy was done in selected
consent from all patients were obtained prior to patients.
commencement of the study.
Detailed clinical history was recorded and the patients were
thoroughly examined with a detailed reference to the general RESULTS
physical examination pertaining to the respiratory diseases.
The complaints which were evaluated in detail included Out of the total of 246 patients with hemoptysis, chest
hemoptysis (amount, time of onset in relation to duration of roentgenogram was interpreted as normal or with non-
other symptoms), cough, sputum production, chest pain, localizing abnormalities in 48. Four of them did not give
dyspnoea, fever, weight loss, anorexia, hoarseness of voice, consent for bronchoscopy. Of the remaining 198 patients
dysphagia, and symptoms suggestive of malignancy. History with localizing findings on the chest roentgenogram,
of cigarette smoking, cardiopulmonary disease, hematuria diagnosis was made in 141 by non-bronchoscopic measures.
and symptoms of nasal, oropharyngeal, laryngeal disease, or Sixty of these patients were having persistent hemoptysis
gastrointestinal disease were noted, if any. The presenting and were planned for therapeutic bronchoscopy. Fifty seven
quantity of hemoptysis was estimated as best as possible patients with abnormal roentgenogram not diagnosed by
from the patient’s history, and was classified arbitrarily non-bronchoscopic techniques were planned up for
according to the severity into mild(<30ml/day), bronchoscopy. Hence, a total 157 patients underwent
moderate(30-200ml/day), or severe(>200ml/day) depending fibreoptic bronchoscopy. In none of the patients was there
upon the amount of bleeding. an abnormality of clotting, or a bleeding source found on
otolaryngologic examination. Out of 246 patients with
Baseline routine laboratory investigations including hemoptysis, 157 patients underwent bronchoscopy.
hemogram, ESR, KFT,ABG was done in all patients.
Patients were asked to collect sputum in sterile wide The age of the patients ranged between 23 to 85 years. The
mouthed vials after rinsing the mouth with plain water in the mean age of the patients was 58.76 years. Out of 246
morning to bring out first cough sample, which was then patients , 178 were males [72.3%], 68 [27.7%] females. 150
sent to the laboratory on at least 3 consecutive days for (a) were smokers[60.9%], 96 were nonsmokers. Among
Cytopathological examination to look for malignant cells (b) smokers, 90% were males. The most common etiologies of
Sputum for acid fast bacilli by Ziehl Nelson technique and hemoptysis in our study[Table 1] were tuberculosis[27.9%]
(c) Sputum smear and culture for bacteria, and fungus. Chest followed by malignancy[18.6%] and bronchiectasis[16.5%].
Roentgenography (Posteroanterior view and Right or left Other less common causes were bronchitis, pneumonia, lung
lateral view) was done in all patients. abscess and congestive heart failure [table 1].
Fibreoptic bronchoscopy(FOB) was done in 157 patients.
FOB was done using Olympus (BF Te2e) model in an 145 patients had mild hemoptysis[58.9%], 57 had moderate
endoscopy room or bedside. Medical records were analyzed [23.1%], 44 had severe hemoptysis [17.8%]. 32.2% patients
for the quantity and duration of hemoptysis, prior diagnostic of mild hemoptysis were diagnosed as bronchogenic
procedures, timing of FOB (in relation to hemoptysis), carcinoma, 97% of the patients with idiopathic hemoptysis
endoscopic findings and results of any accessory were having mild hemoptysis. Of the 57 patients with
procedures. Although attempt was made to perform the moderate hemoptysis, 25% were diagnosed as having
procedure as soon as possible, FOB was performed up to 10 bronchogenic carcinoma, 41.6% were having tuberculosis as
days following the initial event because of technical the etiology for hemoptysis. Tuberculosis (46.4%) and
problems. For the purpose of this study, a definitive (or bronchiectasis (42.8%) were the most common etiologies in
endoscopic) diagnosis for hemoptysis was made if FOB patients with severe hemoptysis. FOB was done in 157
revealed a specific bleeding lesion, endobronchial mass, or patients and bleeding site was localized in 76 patients.
positive and specific microbiology, cytology or histology.

Int J Med Health Sci. Jan 2016,Vol-5;Issue-1 10


Table 1: Final diagnosis in patients who presented with hemoptysis.
Causes Number(%) Patients in which FOB was done
Bronchitis 19(7.8%) 15(78.9%)
Malignancy 45(18.6%) 39(86.7%)
Tuberculosis (active) 45(18.6%) 24(53.3%)
Tuberculosis (inactive) 22(9%) 9(40.9%)
Bronchiectasis 40(16.5%) 25(62.5%)
Pneumonia 12(4.9%) 4(13.3%)
Congestive Heart Failure 8(3.3%) -
Lung abscess 8(3.3%) 3(37.5%)
Aspergilloma 5(2%) 2(40%)
Pseudohemoptysis (Bleeding from upper respiratory 2(0.8%) 2(100%)
tract)
Idiopathic 32(13.3%) 32(100%)
TOTAL 242(100%) 157(64.8%)

DISCUSSION
Different parts of the world have reported different malignancy were the most common causes of hemoptysis[3-
etiological patterns of hemoptysis. In developed countries, 10]. Recent studies showed a change in the trend in causes
tuberculosis is becoming less important cause of bleeding of hemoptysis[11-18]. Tuberculosis decreased to 7% in
from the lungs, but in our country tuberculosis still remains contrast to 13-61% in previous studies[6-8].
the most common cause. The rate of occurrence of bronchogenic carcinoma remained
Of all the patients in our study, tuberculosis was the most similar. However the incidence of infective pathologies like
common etiology of hemoptysis in 27.6% cases followed by tuberculosis and bronchiectasis remains high in developing
malignancy in 18.6% and bronchiectasis in 16.5%. countries like ours accounting for the difference in the
Bronchitis was the etiological factor in only 7.8% cases. In etiologies of hemoptysis in our studies compared with other
previous studies conducted between 1930-1960, recent studies. Causes of hemoptysis in various studies is
bronchiectasis, tuberculosis and shown in Table 2.

Table 2: Causes of hemoptysis by percentage in various studies

Cause
Study
Carcinoma Bronchiectasis Bronchitis Tuberculosis Abscess Pneumonia Infarction Cardiac Unknown
Jackson and
Diamond[3] 20 32 17 * 12 6 - - 8
(n=436)
Heller[4]
2 7 15 39 1 3 1 2 16
(n=413)
Abbott[5]
21 21 2 22 6 2 2 1 4
(n=497)
Levitt[6]
(n=717) 12 15 - 47 5 1 - 7 5
Moersch[7]
(n=200) 24 27 9 6† 5 3† 1 1† 8

Saunders &
Smith[8] 3† 37 12 2§ 2 - - 9 18
(n=100)
Pursel &
Lindskog[9] 19 23 5 13 3 5 3 - 15
(n=105)

Int J Med Health Sci. Jan 2016,Vol-5;Issue-1 11


Lyons[10]
(n=200) 12 21 - 61 4 - - - 2

Gong Jr. &


Salvatierra[11] 24 40 - 3 - 3 2 4 11
(n=129)
Johnston &
Reisz[21] 19 1 37 7 2 5 1 1 3
(n=148)
Santiago[22]
(n=264) 29 0.5 23 6 - 11 - - 22
Alaou[23]
(n=291) 34 15 3.5 19 - 7 - - 3
Knott-
Craig[24] 51
5 - 73 - 4 - - 8
(all had TB)
(n=120)
McGuinness
[25] (n=57) 12 25 5 16 - 12 - - 19
Domoua[26]
(n=142) 4.2 11.2 - 49.3 - 13.3 - - -
Hirshberg[27]
(n=208) 19 20 18 1 - 16 - - 8
Abal[28]
(n=52) - 21.2 5.8 15.4 - - - - 25
Fidan[29]
(n=108) 34.3 25 - 17.6 - 10.2 - - -
Unsal[30]
(n=143) 18.9 22.4 5.6 11.2 - 4.9 - - 13.2
Present study
18.6 16.5 7.8 27.6 3.3 4.9 - 3.3 13.2

*Excluded from study, Selection criteria biased against inclusion of patients with this diagnosis.

Although tuberculosis is still the most common cause in our with hemoptysis had inactive tuberculosis.This suggests
study, the incidence has markedly decreased in comparison that even if the patient of pulmonary tuberculosis who is on
with other studies from India in the past[19]. This decrease treatment or who has completed ATT presents with
in the incidence of tuberculosis can be attributed to better hemoptysis again, we should not think that patient is not
and newer tuberculosis control programme, in which both responding or the infection is drug resistant.
the diagnosis and the treatment is free and directly observed,
what is called as Directly Observed Treatment, Short-course
(DOTS)[20]. The incidence of bronchiectasis in our study CONCLUSION
was 16.5% which is almost same to that of many other We conclude that pulmonary tuberculosis still remains the
studies from developing countries[19].Johnston & Reiz[21] most common cause in India, although the frequency has
found bronchitis to be the most common cause and a significantly decreased. Hemoptysis even if mild should be
dramatic decrease in bronchiectasis, 1% as compared to 7- extensively evaluated as malignancy is the second most
37% in previous studies[3-10]. common cause in our setting.
In our study malignancy was the second most common
cause (18.6%). Many other studies has also shown
REFERENCES
malignancy to be among the most common causes (Table 2).
But there are many older studies which have not shown 1. St edm a n T L, edi t or . St edm a n' s m edi ca l
malignancy to be that common[3,18,19]. The reason di ct i on a r y. 27t h edi t i on. Ph i l a del ph ia :
probably was the unavailability of better diagnostic Li pi n cot t Wi l l i am s an d Wi l kin s; 2000.
modalities like CT scan and bronchoscopy, and malignancy 2. Rem y J, Rem y- Ja r din M, Voi si n C.
probably remained in the idiopathic category. We observed
E n dova scul a r m an a gem en t of br on ch i a l
that the patients with malignancy most of the times had mild
hemoptysis which is true for other studies as well. bl e edi n g. In : But l er J, edi t or s. Th e br on ch ia l
ci r cul a t i on . Ne w Y or k: Dekker ; 1992. pp. 667 -
Hemoptysis doesn't always suggest active tuberculosis.
Hemoptysis may be present even when the disease is 723.
inactive or when the patient is on antitubercular 3. Ja cks on CL, Di a m on d S. Hem or rh a ge fr om
treatment(ATT).In our study, 22 patients who presented t h e t ra ch ea , br on ch i, an d l un gs of n on -

Int J Med Health Sci. Jan 2016,Vol-5;Issue-1 12


t uber cul osi s or i gi n . Am Re v T u ber c 1942; 19. Ra o P U. Hem opt ysi s a s a s ym pt om i n a ch est
46: 126 -138. cl i n i c. In d J Ch est Di sea se s. 1960; 2: 219.
4. Hel l er R. T h e si gn i fi ca n ce of h em opt ysi s. 20. Ch a uhan LS, T on sin g J. Revi sed n a t i on a l T B
T uber cul e. 1946; 26: 70 -74. c on tr ol pr ogr am m e in In dia .
5. Abbot OA. T h e cl i n i ca l si gn i fi ca n ce of T uber cul osi s(E di n b). 2005 Sep -N ov; 85(5 -
pul m on ar y h em or rh a ge: a st udy of 1316 6): 271 -276.
pa t i en t s wi t h ch est di sea se. Di s Ch est 21. Joh n st on H, Rei sz G. Ch an gin g spect r um of
1948: 14: 824 -842. h em opt ysi s: un der l yi n g ca uses i n 148 pa ti en t s
6. Le vi t t N. cl i n i ca l s i gni fi ca n ce of h em opt ysi s. un der goin g di a gn ost i c fl exi bl e br on ch osc op y.
J Mi ch St a t e Med Soc1951; 50: 606 -610. Ar ch Int ern M 1989; 149: 1666 -1668.
7. Moer sch HJ. Cl i n i ca l si gn i fi ca n ce of 22. Sa n ti a go S, T obi a s J, Wi l l i am AJ. A
h em opt ysi s. JAM A 1952; 148: 1461 -1465. r ea ppr a i sa l of t h e ca us es of h em opt ysi s. Ar ch
8. Sa un der s CR, Sm ith AT. Th e cl in i ca l In t ern Med 1991; 151: 2449 -2451.
si gn i fi ca n ce of h em opt ysi s. N E n gl J Med 23. Al a oui AY, Ba r t a l M, Bout a h i ri A, et al .
1952; 247: 790 -793 Cl in i ca l ch ar a ct er i sti cs a n d et i ol og y i n
9. Pur sel SE , Li n dskog GE . Hem opt ysi s: a h em opt ysi s i n a pn eum ol og y s er vi c e: 291
cl i n i ca l eva l ua t i on of 105 pa t i en t s exa min ed ca se s. Re v Ma l Respi r 1992; 9: 295 -300.
c on secut i vel y on a th or a ci c sur gi ca l ser vi ce. 24. Kn ot t -Cra i g CJ, Oost ui z en JD, Ros s ou w G, et
Am Re v Re spi r Di s 1961: 84: 329 -336. a l . Mana gem en t an d pr ogn osi s of m a ssi ve
10. L yon s HA. Di ffer en t i a l dia gn osi s of h em opt ysi s. J T h or a c Car di ova s c Sur g 1993;
h em opt ysi s a n d i t s t r ea t m en t . AT S Ne ws 105: 394 -397.
1976: 26 -30. 25. McGui n n ess G, Bea ch er J R, Ha r kin T J.
11. Gon g H Jr , Sa l va t i err a C. Clin i ca l effi ca c y of Hem opt ysi s: Pr ospe ct i ve h i gh -r esol ut i on CT /
ea r l y a n d del a yed fi ber opt i c br on ch os c op y i n br on ch os c opi c c or r el a t i on . Ch est 1994; 105:
pa t i en t s wi th h em opt ysi s. Am Re v Respi r Di s 1155-1162.
1981; 124: 221 -225. 26. Dom oua K, N’Dh a t z M, Coul i ba l y G, et a l .
12. Cor e y R, Hl a RM. Ma j or a n d m a ssi ve Hem opt ysi s: Ma i n et i ol ogi es obs er ved i n a
h em opt ysi s: r ea ss essm en t of c on ser va t i ve pn eum ol og y d epa r t m ent i n Afr i ca . Re v
m an a gem ent . Am J Med S ci 1987; 294: 301 - Pn eum ol Cl in 1994; 50: 59-62.
309. 27. Hi r sh ber g B, Bi r an I, Gl az er M, Kr a m er MR.
13. Con l on AA: Hur wi t z SS. Ma n a gem en t of Ha em opt ysi s: Aet i ol og y, e va l ua t i on a n d
m a ssi ve h em opt ysi s wi t h th e ri gi d out c om e i n a t er t i ar y r efer r a l h ospi t a l. Ch est
br on ch os c ope a n d col d sa l i n e l a va ge. T h or a x 1997; 112: 440 -444.
1980; 35: 901 -904. 28. Aba l AT , Na i r PC an d Ch eri an J.
14. Adel m a n M. Ha pon i k E F, Bl eeck er E R, Br i t t Ha em opt ysi s: Aet i ol og y, e va l ua t i on a n d
E J. Cr ypt og en i c h em opt ysi s. An n Int ern Med out c om e a pr ospe ct i ve st ud y i n a thir d wor l d
1985; 102: 829 -834. c oun tr y. Re spi r Med 2001; 95: 548 -552.
15. Sm i dd y J R, E l l i ot RC . Th e eva l ua t i on of 29. Fi da n A, Oz doga n S, Or uc O, et a l .
h em opt ysi s wi t h fi ber opt i c br on ch osc op y. Hem opt ysi s: A r et r ospe ct i ve a n a l ysi s 108
Ch est 1973; 64: 158 -162. ca se s. Re spi r Med 2002; 96: 677 -680.
16. Wea ver LJ, S ol l i da y N, Cugel l DW. Sel e ct i on 30. Un sa l E , Koksa l D, Ci m en F, Hoca NT , Si pi t
of pa t i en t s for fi ber opt i c br on ch osc op y. T . An a l ysi s of pa t i en t s wi t h h em opt ysi s i n a
Ch est 1979; 76: 7 -10. r efer en ce h ospi t a l for ch est di sea s es
17. Ja cks on CV. Sa va ge PJ, Qui n n I)L. Rol e of T uber kul oz ve T or a ks Der gi si 2006; 54: 34 -
fi ber opt i c br on ch os c op y i n pa t i en t s wi t h 42.
h em opt ysi s and a n or ma l ch est
r oen t gen ogr am . Ch est 1985; 87: 142 -144. ____________________________________________
18. Hei m er D, Ba r -Zi v J, Sch ar f SM. Fi ber opt i c
br on ch os c op y i n pa t i en t s wi t h h em opt ysi s *Corresponding author: Dr. Manzoor Ahmad Wani
a n d n on -l oca l i z in g ch est r oen t gen ogr a ph s. E-Mail: drmanzoorahmadwani@gmail.com
Ar ch Int ern Med 1985; 145: 1427 -1428.

Int J Med Health Sci. Jan 2016,Vol-5;Issue-1 13

View publication stats

Das könnte Ihnen auch gefallen