CC BY-NC-ND 4.0 · Journal of Digestive Endoscopy 2021; 12(01): 031-035
DOI: 10.1055/s-0041-1728232
Original Article

Current Trends in Etiological Profile of Acute Upper Gastrointestinal Bleeding in Northern India: A Retrospective Analysis of 5-Year Endoscopic Data

Vishal Bodh
1   Department of Gastroenterology, IGMC, Shimla, Himachal Pradesh, India
,
Brij Sharma
1   Department of Gastroenterology, IGMC, Shimla, Himachal Pradesh, India
,
Rajesh Kumar
1   Department of Gastroenterology, IGMC, Shimla, Himachal Pradesh, India
,
Rajesh Sharma
1   Department of Gastroenterology, IGMC, Shimla, Himachal Pradesh, India
› Author Affiliations
Source(s) of Support None.
 

Abstract

Introduction The etiological spectrum of acute upper gastrointestinal bleeding (AUGIB) varies from region to region. This study was performed to find out the latest etiological spectrum of the AUGIB in a tertiary care hospital in North India and to compare it with etiological spectra from a previous study from the same center and from the other regions of India.

Methods Clinical notes and endoscopic data of all consecutive patients who had presented with AUGIB in Indira Gandhi Medical College Shimla, Himachal Pradesh, from May 2015 to December 2019, were analyzed retrospectively with the objective of finding out the various endoscopic etiologies that lead to AUGIB. The findings were compared with the previous study from the same center and with the data from the other regions of the country.

Results A total of 1,513 patients were enrolled and majority were males (74.6%) with male:female ratio of 2.9:1. Majority were 41 to 60 years (46.46%) of age. Melena was the presenting complaint in 93.98% and hematemesis in 46.06%. Peptic ulcer disease (PUD; 46.19%) was the commonest cause of AUGIB followed by portal hypertension (26.23%). Other less common causes were erosive mucosal disease, erosive esophagitis, neoplasm, Mallory–Weiss tear, gastric angiodysplasia, anastomotic site ulcers, and Dieulafoy’s lesion.

Conclusion PUD was still the commonest cause of AUGIB followed by portal hypertension. This is in agreement with the previous report from the same center and in contrast to the reports from other studies from Northern and Western India that create the impression that portal hypertension related bleeding is the most common cause of AUGIB in India.


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Introduction

Acute upper gastrointestinal bleeding (AUGIB), presenting with symptoms of hematemesis, melena, and/or hematochezia, is an important medical emergency. AUGIB is defined as bleeding derived from a source proximal to the ligament of Treitz and is associated with significant morbidity and mortality.[1] AUGIB presents with a wide range of clinical severity, ranging from insignificant bleeds to catastrophic hemorrhage.[2] The incidence of upper gastrointestinal bleeding (UGIB) ranges from 50 to 150/100,000 population annually, and time trend analyses suggest that it is more common in elderly people.[3] Patients can be divided as having either variceal or nonvariceal sources of UGIB as the two have different management protocols and prognoses.[4] The variceal source includes lesions that arise by virtue of portal hypertension, namely, gastroesophageal varices and portal hypertensive gastropathy; and the nonvariceal includes lesions seen in the general population (peptic ulcer, erosive gastritis, reflux esophagitis, Mallory–Weiss syndrome, tumors, etc.).

The etiological spectrum of UGIB varies from region to region.[5] Population-based epidemiological data revealing the current trends in India are sparse. Globally, the prevalence of Helicobacter pylori infection has decreased due to better hygiene, early diagnosis, and eradication.[6] These factors have contributed to the changing trends in UGIB. Once frequent, UGIB due to peptic ulcer has now declined all over the globe as demonstrated by various researchers.[7] [8]

The primary diagnostic test for evaluation of UGIB is endoscopy. Endoscopy for UGIB has a sensitivity of 92 to 98% and specificity of 30 to 100%.[9]

At present, there are limited data on endoscopic etiological profile of patients of UGIB from India and particularly from this region. Therefore, this study was performed to find out the current etiological spectrum of the UGIB in the state of Himachal Pradesh in North India and to compare it with previous study from the same center to know the change in etiological profile. This etiological spectrum was also compared with the reported etiological spectrum from the other regions of India to know the current status in the country.


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Methods

In this study we did a retrospective review of the clinical and endoscopic notes of the patients above 1 year of age who presented with AUGIB and underwent diagnostic and therapeutic esophagogastroduodenoscopy (EGD) in the Department of Gastroenterology, Indira Gandhi Medical College (IGMC) and Hospital, Shimla. All patients who had presented with AUGIB in the form of hematemesis, melena, and hematochezia with hemodynamic instability from May 2015 to December 2019 and underwent EGD in the Department of Gastroenterology, IGMC, Shimla, were enrolled in the study. EGD was done by senior gastroenterologist using Olympus EXERA II GIF-H180 Gastroscope after initial hemodynamic stabilization within 72 hours (preferably within the first 24 hours) of bleed to determine the etiology and perform the endoscopic therapy. During endoscopy, band ligation was done for bleeding large esophageal varices, and N-butyl cyanoacrylate glue was injected in bleeding gastric varices. For bleeding peptic ulcer, diluted adrenaline was injected around the ulcer base and argon plasma coagulation of the bleeding lesion was performed.

The data analyzed included age, gender, presenting complaint (hematemesis, melena, hematochezia), and endoscopic findings. The objective of the study was to find out the various endoscopic etiologies that lead to AUGIB. Results are displayed in tables and figures, with the categorical variables presented as numbers and percentages. The results of the present study were compared with the previous study by Kashyap et al from the same center to find out any change in the endoscopic etiological profile of the UGIB.[10] Also, an extensive search from different journals and publications was done to analyze the causes of UGIB in different regions of India. Comparison was made between the present study and other studies on UGIB, to evaluate the current etiological and clinical spectrum of bleeding in different regions of India.


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Results

A total of 1,513 patients had presented with AUGIB and had underwent EGD from May 2015 to December 2019, in Department of Gastroenterology, IGMC, Shimla. The majority of the patients were male (74.6%), and the male:female ratio was 2.9:1 ([Table 1]). Most of the patients were in age group of 41 to 60 years (46.5%) followed by 61 to 80 years (25.8%), 21 to 40 years (22.3%), more than 80 years (2.8%), and 1 to 20 years (2.6%; [Table 1]).

Table 1

Epidemiological features, clinical presentation, and endoscopic diagnosis of the patients presenting with acute upper gastrointestinal bleeding

Number of patients (n = 1,513)

Percentage (%)

Males

1,129

74.6

Females

384

25.4

1–20 y

40

2.6

21–40 y

337

22.3

41–60 y

703

46.5

61–80 y

391

25.8

>80 y

42

2.8

Melena

1,422

94.0

Hematemesis

697

46.1

Hematemesis and melena

651

43.0

Melena was the presenting complaint in 94.0% (1,422/1,513) and hematemesis was present in 46.1% (697/1,513). Both hematemesis and melena were seen in 43.0% (651/1,513; [Table 1]).

The commonest cause of UGIB was peptic ulcer disease (PUD), accounting for 46.2% cases. Among the 699 PUD patients, majority had duodenal ulcer (n = 532/699, 76.1%) followed by gastric ulcer (n = 105/699, 15%) and simultaneous duodenal and gastric ulcer (n = 62/699, 8.9%). Among the 699 patients presented with peptic ulcer bleed, majority had Forrest Class III ulcer (n = 582/699, 83.3%) followed by Forrest IIc (n = 46/699, 6.6%), Forrest IIb (n = 31/699, 4.4%), Forrest Ib (n = 18/699, 2.6%), and Forrest IIa (n = 15/699, 2.1%). Seven patients (1%) had Forrest Ia ulcers with active spurting bleed ([Table 2]).

Table 2

Endoscopic finding/diagnosis of the patients presenting with acute upper gastrointestinal bleeding

Number of patients (n = 1,513)

Percentage (%)

Peptic ulcer disease

699

46.2

A—duodenal ulcer

532

35.2

B—gastric ulcer

105

6.9

C—both gastric and duodenal ulcer

62

4.1

Forrest I A

7

0.5

Forrest I B

18

1.2

Forrest II A

15

1.0

Forrest II B

31

2.0

Forrest II C

46

3.0

Forrest III

582

38.5

Portal hypertension

397

26.2

Esophageal variceal bleed

356

23.5

Gastric variceal bleed

37

2.4

Portal hypertensive gastropathy

4

0.3

Erosive mucosal disease

91

6.0

Reflux erosive esophagitis

63

4.2

Gastric malignancy

45

3.0

Mallory–Weiss tear

42

2.8

Gastric angiodysplasia

3

0.2

Anastomotic ulcers in previous gastric surgery patients

3

0.2

Esophageal malignancy

3

0.2

Periampullary malignancy

2

0.1

Dieulafoy’s lesion

1

0.1

Obscure

164

10.8

Portal hypertension related bleeding, including esophageal varices, gastric varices, and portal hypertensive gastropathy, was responsible for bleed in 26.2%. Among the 397 patients with portal hypertension related bleed, majority had esophageal variceal bleed (n = 356/397, 89.7%) followed by gastric variceal bleed (n = 37/397, 9.3%) and portal hypertensive related bleed (n = 4/389, 1.0%; [Table 2]). Neoplasms comprised 3.3% of the total cases, of which carcinoma stomach was most common (3%) followed by esophageal (0.2%) and periampullary (0.1%) malignancy. Other less common causes were erosive mucosal disease (6.0%), gastroesophageal reflux disease with erosive esophagitis (4.2%), Mallory–Weiss tear (2.8%), gastric angiodysplasia (0.2%), anastomotic site ulcers in previous gastric surgery patients (0.2%), and Dieulafoy’s lesion (0.1%). In 10.8% of the patients, no obvious cause could be found on EGD ([Table 2]). These were labeled as having obscure bleed and were subjected to further investigations.


#

Discussion

UGIB is a common medical emergency seen in tertiary care centers. The etiology of UGIB may vary in different geographical regions. In this study, we retrospectively analyzed the endoscopic data of 1,513 patients from Northern India who presented with acute UGIB.

The present study shows that the PUD is the commonest cause of UGIB in the state of Himachal Pradesh in Northern India followed by portal hypertension related bleed. This is in agreement with the previous study by Kashyap et al from the same center.[10] Though the percentage of the patients with PUD has decreased (from 61% in previous study to 46.2% in present study) and percentage of the patients with portal hypertension related bleed has increased (from 10.8% in previous study to 26.2% in the present study) compared with the previous study, still the PUD is the leading cause followed by portal hypertension related bleed ([Table 3]).

Table 3

Comparison of the endoscopic etiological spectrum of the present study with the previous study from the same center

Endoscopic diagnoses

Percentage of patients: present study (2020) from Shimla

Percentage of patients: previous study (2005) from Shimla 19

Peptic ulcer disease (duodenal ulcer + gastric ulcer)

46.2

61.0

Portal hypertension

26.2

10.8

Erosive mucosal disease

6.0

11.7

Mallory–Weiss tear

2.8

10.8

Reflux esophagitis

4.2

2.7

Tumors

3.3

3.6

[Table 3] shows comparison of the patient profile and endoscopic etiologic spectrum of the UGIB from different parts of India.[11] [12] [13] [14] [15] [16] [17] Though to a variable degree, but male preponderance was seen in all the studies on UGIB from different regions of India (Table 3).[11] [12] [13] [14] [15] [18] [19] Most of the patients presenting with UGIB in present study were in age group of 41 to 60 years (46.5%). Similar findings have been reported by Parvez et al from Eastern India where majority (54%) of the patients were in the age group of 20 to 60 years. Prasad et al from South India reported that majority of patients (52.3%) presenting with acute UGIB were also in the age group of 41 to 60 years.[16] But western studies report a higher age at presentation, which is due to elderly population in their community.[17] [20]

Melena was the most common presentation in our study (95.1%) followed by hematemesis (46.1%) and combined hematemesis and melena (43.0%). Similar findings are seen in a study by Singh and Panigrahi where melena was the presenting complaint in 95.1%, hematemesis was present in 43.1%, and both hematemesis and melena were seen in 41.8% ([Table 4]).[14] In contrast, the study by Parvez et al from eastern India revealed that hematemesis was the more common presentation (60.8%).[12] In an another study by Mahajan and Chandail from Jammu among patients aged 40 years or more, presentation with combined hematemesis and melena (68.1%) was more common.[15]

Table 4

Comparison of clinical and etiological spectrum of upper gastrointestinal bleeding in different regions of India

Present Study

Delhi18

Mumbai19

Chennai11

Kolkata12

Kerala13

Odisha14

Jammu15

Year of study

2020

1983

2001

2015

2016

2009

2012

2015–2017

Study population

1,513

408

398

408

337

1,582

608

1,270

Male:female ratio

2.9:1

3:1

3.5:1

2.2:1

4:1

NA

3.6:1

1.6:1

Melena (%)

94.0

NA

NA

NA

50.7

NA

95.1

10.9

Hematemesis (%)

46.1

NA

NA

NA

60.8

NA

43.1

20.9

Hematemesis + melena (%)

43.0

NA

NA

NA

NA

NA

41.8

67.8

Peptic ulcer disease (duodenal + gastric ulcer) (%)

46.2

30

15.3

17.8

40.2

35

58.7

18.3

Portal hypertension bleed (%)

26.2

45.5

56

33.3

33.8

30.9

12.8

43.5

Erosive mucosal disease (%)

6.0

8.5

4.5

43.6

10.6

13

1.2

16.2

Malignancy (%)

3.3

NA

0.75

2.4

2.9

2

7.9

2.4

When nonvariceal bleeding versus variceal is considered as the etiology of UGIB, there are variable results in India. In the present study, PUD (46.2%) was the predominant etiology followed by the portal hypertensive bleed (26.2%; [Table 3]). Similar findings reporting duodenal ulcer being the most common cause of UGIB followed by variceal bleed have been reported by Parvez et al[12] from Kolkata and Singh and Panigrahi[14] from Odisha ([Table 4]). This is in contrast to the spectra reported by Anand et al[18] from Delhi, Rathi et al[19] from Mumbai, and Mahajan and Chandail[15] from Jammu, of Northern and Western India, that create the impression that variceal bleeding is the most common cause of UGIB in India ([Table 4]).

In developing countries, like India, there is gross disparity in health care access, with advanced health care technologies and well-trained health care specialists being concentrated among the urban minority.[21] Endoscopy services are unavailable in almost all public primary and secondary care centers in India.[21] Peptic ulcer related bleeds are likely to more often cease spontaneously and rebleed less frequently vis-a-vis variceal bleeds.[22] The distance to the nearest available endoscopy service might be a confounding factor when looking for epidemiological differences in the etiology of UGIB in India. This difference has been reported by Das[23] in his retrospective audit of etiology of UGIB in a district center (DC), providing diagnostic UGIB services every weekend, vis-a-vis a tertiary care academic center (TC), in West Bengal, eastern India. There were significant differences between the etiologies of UGIB in the two centers. PUD was more frequent in the DC, while varices were more frequent in the TC as the cause of AUGIB. Similarly, another recent study from a tertiary care center of same region in eastern India by Banerjee et al[24] also reported portal hypertension (62.30%) as the most common etiology of UGIB followed by PUD (16.70%). So, the studies done from the tertiary care centers of eastern India revealed the portal hypertension related bleed to be the most common of AUGIB, while the study performed in the DC of the same region showed the PUD-related bleed as the most common etiology of AUGIB. This clearly reflects the disparity in the access to health care. PUD as the most common etiology of AUGIB is seen in the present study, similar to the findings seen by Das[23] in DC, as our center is also a peripheral tertiary health care center, situated in the hilly state of Himachal Pradesh.

So, the variable spectrum of the etiology of the AUGIB seen in our country could represent either a true epidemiological difference or reflect skewed access to health care. It seems likely that the studies conducted in the major referral centers of India may represent the referral bias in the etiological spectrum of AUGIB, as critical patients with variceal bleed requiring endoscopic and surgical intervention from all over the region were referred to these hospitals, which may have added on to the percentage of patients with variceal bleed. These figures are thus not representative of the actual etiological spectrum of AUGIB in this country.


#

Conclusion

PUD-related bleed is still the commonest cause of UGIB in the state of Himachal Pradesh in North India followed by portal hypertension related bleed. This is in agreement with the previous report from the same center suggesting a similar trend for the etiological spectrum of the UGIB in this region and in contrast to other studies from North and West India that create the impression that portal hypertension related variceal bleeding is the most common cause of UGIB in India.


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Conflict of Interest

None.

  • References

  • 1 Ghosh S, Watts D, Kinnear M. Management of gastrointestinal haemorrhage. Postgrad Med J 2002; 78 (915) 4-14
  • 2 Rockall TA, Logan RF, Devlin HB., Northfield TC. National Audit of Acute Upper Gastrointestinal Haemorrhage. Selection of patients for early discharge or outpatient care after acute upper gastrointestinal haemorrhage. Lancet 1996; 347 (9009) 1138-1140
  • 3 Thomopoulos KC, Vagenas KA, Vagianos CE. et al. Changes in aetiology and clinical outcome of acute upper gastrointestinal bleeding during the last 15 years. Eur J Gastroenterol Hepatol 2004; 16 (02) 177-182
  • 4 Ginn JL, Ducharme J. Recurrent bleeding in acute upper gastrointestinal hemorrhage: transfusion confusion. CJEM 2001; 3 (03) 193-198
  • 5 van Leerdam ME. Epidemiology of acute upper gastrointestinal bleeding. Best Pract Res Clin Gastroenterol 2008; 22 (02) 209-224
  • 6 Frugis S, Czeczko NG, Malafaia O. et al. Prevalence of Helico-bacter pylori ten years ago compared to the current prevalence in patients undergoing upper endoscopy. Arq Bras Cir Dig 2016; 29 (03) 151-154
  • 7 Jiang M, Chen P, Gao Q. Systematic review and net-work meta-analysis of upper gastrointestinal hemorrhage interventions. Cell Physiol Biochem 2016; 39 (06) 2477-2491
  • 8 Roberts-Thomson IC. Rise and fall of peptic ulceration: a disease of civilization?. J Gastroenterol Hepatol 2018; 33 (07) 1321-1326
  • 9 Jaskolka JD, Binkhamis S, Prabhudesai V, Chawla TP. Acute gastrointestinal hemorrhage: radiologic diagnosis and management. Can Assoc Radiol J 2013; 64 (02) 90-100
  • 10 Kashyap R, Mahajan S, Sharma B. et al. A clinical profile of acute upper gastrointestinal bleeding at moderate altitude. JIACM 2005; 6: 224-228
  • 11 Krishnakumar R, Padmanabhan P, kumar Prem, Selvi C, kumar Ram, Joe A. Upper GI bleed- a study of 408 cases. Indian J Gastroenterol 2007; 26 (suppl 2) A133
  • 12 Parvez M, Goenka MK, Tiwari IK, Goenka U. Spectrum of upper gastrointestinal bleed: an experience from eastern India. J Dig Endosc 2016; 7: 55-61
  • 13 Gajendra O, Ponsek T, Varghese J, Sadasivan S, Nair P, Narayanan VA. Single center study of upper GI endoscopic findings in patients with overt and occult upper GI bleed. Indian J Gastroenterol 2009; 28: A111
  • 14 Singh SP, Panigrahi MK. Spectrum of upper gastrointestinal hemorrhage in coastal Odisha. Trop Gastroenterol 2013; 34 (01) 14-17
  • 15 Mahajan P, Chandail VS. Etiological and endoscopic profile of middle aged and elderly patients with upper gastrointestinal bleeding in a tertiary care hospital in North India: a retrospective analysis. J Midlife Health 2017; 8 (03) 137-141
  • 16 Prasad NRV, Ali SM, Ganapathy V, Sreenath GS, Kumar SS. Acute upper gastrointestinal bleeding in a tertiary care hospital in South India - have we improved the outcomes?. Trop Gastroenterol 2016; 37 (03) 168-176
  • 17 Marmo R, Koch M, Cipolletta L. et al. Italian registry on upper gastrointestinal bleeding (Progetto Nazionale Emorragie Digestive–PNED 2). Predicting mortality in non-variceal upper gastrointestinal bleeders: validation of the Italian PNED Score and prospective comparison with the Rockall Score. Am J Gastroenterol 2010; 105 (06) 1284-1291
  • 18 Anand CS, Tandon BN, Nundy S. The causes, management and outcome of upper gastrointestinal haemorrhage in an Indian hospital. Br J Surg 1983; 70 (04) 209-211
  • 19 Rathi P, Abraham P, Jakareddy R, Pai N. Spectrum of upper gastrointestinal bleeding in western India. Indian J Gastroenterol 2001; 20 (suppl 2) A37
  • 20 Romagnuolo J, Barkun AN, Enns R, Armstrong D, Gregor J. Simple clinical predictors may obviate urgent endoscopy in selected patients with nonvariceal upper gastrointestinal tract bleeding. Arch Intern Med 2007; 167 (03) 265-270
  • 21 Report of the National Commission on Macroeconomics and Health. Ministry of Health and Family Welfare. Government of India, New Delhi, 2005
  • 22 Wara P. Incidence, diagnosis, and natural course of upper gastrointestinal hemorrhage. Prognostic value of clinical factors and endoscopy. Scand J Gastroenterol Suppl 1987; 137: 26-27
  • 23 Das K. Endoscopy outreach and upper gastrointestinal bleed: an audit. Indian J Gastroenterol 2014; 33 (05) 478-479
  • 24 Banerjee A, Bishnu S, Dhali GK. Acute upper gastrointestinal bleed: an audit of the causes and outcomes from a tertiary care center in eastern India. Indian J Gastroenterol 2019; 38 (03) 190-202

Address for correspondence

Rajesh Sharma, MD (Medicine), DNB (Gastroenterology)
Department of Gastroenterology, IGMC
Shimla, Himachal, Pradesh 171001
India   

Publication History

Article published online:
20 April 2021

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  • References

  • 1 Ghosh S, Watts D, Kinnear M. Management of gastrointestinal haemorrhage. Postgrad Med J 2002; 78 (915) 4-14
  • 2 Rockall TA, Logan RF, Devlin HB., Northfield TC. National Audit of Acute Upper Gastrointestinal Haemorrhage. Selection of patients for early discharge or outpatient care after acute upper gastrointestinal haemorrhage. Lancet 1996; 347 (9009) 1138-1140
  • 3 Thomopoulos KC, Vagenas KA, Vagianos CE. et al. Changes in aetiology and clinical outcome of acute upper gastrointestinal bleeding during the last 15 years. Eur J Gastroenterol Hepatol 2004; 16 (02) 177-182
  • 4 Ginn JL, Ducharme J. Recurrent bleeding in acute upper gastrointestinal hemorrhage: transfusion confusion. CJEM 2001; 3 (03) 193-198
  • 5 van Leerdam ME. Epidemiology of acute upper gastrointestinal bleeding. Best Pract Res Clin Gastroenterol 2008; 22 (02) 209-224
  • 6 Frugis S, Czeczko NG, Malafaia O. et al. Prevalence of Helico-bacter pylori ten years ago compared to the current prevalence in patients undergoing upper endoscopy. Arq Bras Cir Dig 2016; 29 (03) 151-154
  • 7 Jiang M, Chen P, Gao Q. Systematic review and net-work meta-analysis of upper gastrointestinal hemorrhage interventions. Cell Physiol Biochem 2016; 39 (06) 2477-2491
  • 8 Roberts-Thomson IC. Rise and fall of peptic ulceration: a disease of civilization?. J Gastroenterol Hepatol 2018; 33 (07) 1321-1326
  • 9 Jaskolka JD, Binkhamis S, Prabhudesai V, Chawla TP. Acute gastrointestinal hemorrhage: radiologic diagnosis and management. Can Assoc Radiol J 2013; 64 (02) 90-100
  • 10 Kashyap R, Mahajan S, Sharma B. et al. A clinical profile of acute upper gastrointestinal bleeding at moderate altitude. JIACM 2005; 6: 224-228
  • 11 Krishnakumar R, Padmanabhan P, kumar Prem, Selvi C, kumar Ram, Joe A. Upper GI bleed- a study of 408 cases. Indian J Gastroenterol 2007; 26 (suppl 2) A133
  • 12 Parvez M, Goenka MK, Tiwari IK, Goenka U. Spectrum of upper gastrointestinal bleed: an experience from eastern India. J Dig Endosc 2016; 7: 55-61
  • 13 Gajendra O, Ponsek T, Varghese J, Sadasivan S, Nair P, Narayanan VA. Single center study of upper GI endoscopic findings in patients with overt and occult upper GI bleed. Indian J Gastroenterol 2009; 28: A111
  • 14 Singh SP, Panigrahi MK. Spectrum of upper gastrointestinal hemorrhage in coastal Odisha. Trop Gastroenterol 2013; 34 (01) 14-17
  • 15 Mahajan P, Chandail VS. Etiological and endoscopic profile of middle aged and elderly patients with upper gastrointestinal bleeding in a tertiary care hospital in North India: a retrospective analysis. J Midlife Health 2017; 8 (03) 137-141
  • 16 Prasad NRV, Ali SM, Ganapathy V, Sreenath GS, Kumar SS. Acute upper gastrointestinal bleeding in a tertiary care hospital in South India - have we improved the outcomes?. Trop Gastroenterol 2016; 37 (03) 168-176
  • 17 Marmo R, Koch M, Cipolletta L. et al. Italian registry on upper gastrointestinal bleeding (Progetto Nazionale Emorragie Digestive–PNED 2). Predicting mortality in non-variceal upper gastrointestinal bleeders: validation of the Italian PNED Score and prospective comparison with the Rockall Score. Am J Gastroenterol 2010; 105 (06) 1284-1291
  • 18 Anand CS, Tandon BN, Nundy S. The causes, management and outcome of upper gastrointestinal haemorrhage in an Indian hospital. Br J Surg 1983; 70 (04) 209-211
  • 19 Rathi P, Abraham P, Jakareddy R, Pai N. Spectrum of upper gastrointestinal bleeding in western India. Indian J Gastroenterol 2001; 20 (suppl 2) A37
  • 20 Romagnuolo J, Barkun AN, Enns R, Armstrong D, Gregor J. Simple clinical predictors may obviate urgent endoscopy in selected patients with nonvariceal upper gastrointestinal tract bleeding. Arch Intern Med 2007; 167 (03) 265-270
  • 21 Report of the National Commission on Macroeconomics and Health. Ministry of Health and Family Welfare. Government of India, New Delhi, 2005
  • 22 Wara P. Incidence, diagnosis, and natural course of upper gastrointestinal hemorrhage. Prognostic value of clinical factors and endoscopy. Scand J Gastroenterol Suppl 1987; 137: 26-27
  • 23 Das K. Endoscopy outreach and upper gastrointestinal bleed: an audit. Indian J Gastroenterol 2014; 33 (05) 478-479
  • 24 Banerjee A, Bishnu S, Dhali GK. Acute upper gastrointestinal bleed: an audit of the causes and outcomes from a tertiary care center in eastern India. Indian J Gastroenterol 2019; 38 (03) 190-202