Skip to main content
Gastroenterology Research and Practice logoLink to Gastroenterology Research and Practice
. 2015 Apr 1;2015:948574. doi: 10.1155/2015/948574

The Utility of Capsule Endoscopy in Patients under 50 Years of Age with Recurrent Iron Deficiency Anaemia: Is the Juice Worth the Squeeze?

Prabhjot Singh Sidhu 1, Mark E McAlindon 1, Kaye Drew 1, Reena Sidhu 1,*
PMCID: PMC4397481  PMID: 25922603

Abstract

Background and Aims. The role of capsule endoscopy (CE) in the <50 years of age patients with iron deficiency anaemia (IDA) remains unclear. We aim to assess its utility in this cohort. Methods. All patients referred for CE for recurrent IDA were included retrospectively. Patients were divided into Group 1 (<50 years) and Group 2 (≥50 years). Results. There were 971 patients with recurrent IDA and 28% belonged to Group 1. The mean age was 40 years in this group with a DY of 28% (n = 76). Significant diagnoses included erosions and ulcers (26%; n = 71), small bowel (SB) angioectasia (AE) (10%; n = 27), SB tumours (3%; n = 7), Crohn's disease (3%; n = 7), SB bowel strictures (1%; n = 3), and SB varices (1%; n = 2). On logistic regression, the presence of diabetes (P = 0.02) and the use of warfarin (P = 0.049) was associated with increased DY. The DY in Group 2 was 38% which was significantly higher than in Group 1 (P = 0.02). While SB tumours were equally common in both groups, AE was commoner in Group 2 (P < 0.001). Conclusion. A significant proportion of patients <50 years are referred for CE. Although the DY is lower compared to those ≥50 years, significant pathology is found in this age group. CE is advisable in patients <50 years old with recurrent IDA and negative bidirectional endoscopies.

1. Introduction

Iron deficiency anaemia (IDA) still remains a common cause for referral to a gastroenterologist (up to 13%) and is often caused by chronic occult gastrointestinal bleeding [1, 2]. In patients where bidirectional endoscopy has been normal and the IDA persists, investigating the small bowel (SB) is warranted. It has been shown that, in patients with IDA, 30% of patients will have normal bidirectional endoscopies [3]. In view of this, both the American Gastroenterological Association (AGA) and the British Society of Gastroenterology (BSG) have recommended SB investigation in particular to detect lesions such as SB angioectasia (AE), Crohn's disease, and neoplasia [2, 4].

In 2001, the introduction of small bowel capsule endoscopy (SBCE) into clinical practice opened new doors in the investigation of obscure gastrointestinal bleeding (OGIB) where the cause had not yet been identified by esophagogastroduodenoscopy (OGD) and colonoscopy [5]. Today, it is the first line investigative tool for suspected SB bleeding. The DY for SBCE ranges from 34% to 92% for OGIB [6]. In anaemia exclusively, the DY is between 57% and 78% [7, 8] and, in those over 70 years of age, AE is the commonest cause of OGIB (30–40%) [9, 10]. Whilst there are many studies investigating the use of CE in OGIB, there is a paucity of studies looking specifically at the use of CE for the sole indication of IDA. The literature on the use of CE in patients < 50 years is also very limited [11].

The purpose of our study was to evaluate the utility of CE in patients under the age of 50 years presenting with recurrent IDA to a single tertiary institution in the United Kingdom. We study clinical parameters that may predict a higher DY and factors that had a subsequent impact on patient management.

2. Methods and Materials

2.1. Patients

All patients routinely referred for SBCE from June 2002 to November 2012 for investigation of recurrent IDA were included in this study. In the Sheffield Teaching Hospitals NHS Trust and its referring hospitals, haemoglobin concentrations below 13 g/dL in men and below 11 g/dL in women are references used to define anaemia. Prior to referral for CE, all patients had undergone upper and lower gastrointestinal investigation with a negative DY either locally (Sheffield Teaching Hospitals NHS Trust) or at the primary referring hospital. This study was part of the small bowel endoscopy study approved by the North Sheffield Ethics Committee (07/2308/13). Data was collected retrospectively on age, sex, indication, comorbidity, SBCE findings, DY, management change, and subsequent procedures undertaken. Significant findings on SBCE, which were deemed to be the cause of the patients clinical presentation only, were included in the diagnostic yield. Data was also collected specifically on the use of nonsteroidal anti-inflammatory (NSAIDS), warfarin, and blood transfusions.

2.2. Capsule Endoscopy

With patient consent, SBCE (Pillcam, Given Imaging, Yokneam Illit, Israel) was performed in patients with recurrent IDA. The procedure involved an overnight fast for 12 h after ingestion of two sachets of polyethylene glycol solution (Kleen-Prep; Norgine, Middlesex, UK). The capsule was ingested with water and 80 mg simethicone (Infacol, Forest Laboratories, Kent, UK) and data subsequently downloaded onto the computer workstation as per standard protocol [5]. All videos were analysed by either experienced consultant gastroenterologist (RS and MEM) or experienced advanced nurse practitioner (KD).

2.3. Statistical Analysis

The data were analysed using SPSS version 18 (SPSS Inc., Chicago, IL, USA). Regression analysis was carried out to determine which clinical factors predicted diagnosis and management change. A P value of less than 0.05 was considered statistically significant.

3. Results

3.1. Study Population

A total of 1324 patients were referred for SBCE for investigation of obscure gastrointestinal bleeding (OGIB). All patients had undergone both upper and lower gastrointestinal investigations (at times, multiple) without a DY. Of the 1324 patients, 73% (n = 971) were referred solely with recurrent IDA while the remaining were referred with overt bleeding (OB) (n = 353). Those with recurrent IDA were then segregated into 2 groups based on age. Group 1 was populated with patients <50 years of age while Group 2 was populated with those ≥50 years of age. The cumulative DY for patients with recurrent IDA in our study was 66%.

3.2. Group 1

Group 1 comprised 28% (n = 275) of the aforementioned 971 patients. The mean age in Group 1 was 40 years, with the age ranging from 17 to 49 years with 61% (n = 168) of patients being female. The DY in Group 1 was 28% (n = 76) with no difference between the sexes. All significant diagnoses found in this age group are tabulated in Table 1. Interestingly, 6 out of 7 SB tumours were found in females. On logistic regression, the presence of diabetes mellitus (P = 0.02) and the use of warfarin (P = 0.049) were associated with increased DY. Management was altered in 75% (n = 57) of patients with a DY on CE. Further procedures undertaken locally in patients with a management change included double balloon enteroscopy (DBE) (n = 11), push enteroscopy (PE) (n = 2), repeat OGD (n = 2), and surgery (n = 2). On logistic regression, the only clinical factors that influenced a management change were SBAE (P = 0.02).

Table 1.

Distribution of all the findings on capsule endoscopy in patients <50 and ≥50 years of age with recurrent iron deficiency anaemia.

All CE findings Group  1 (n = 275) (%) Group  2 (n = 696) (%) P value (95% CI; odds ratio)
SB ulcers and erosions 71 (26) 174 (25) 0.815 (0.8 to 1.4; 1.0)
SBAE 27 (10) 198 (28) <0.0001 (0.2 to 0.4; 0.3)
SB tumour 7 (3) 9 (1) 0.177 (0.3 to 5.4; 2.0)
SB Crohn's disease 7 (3) 10 (1) 0.245 (0.7 to 4.7; 1.8)
Unspecified blood in the SB 6 (2) 37 (5) 0.038 (0.2 to 1.0; 0.4)
SB strictures 3 (1) 8 (1) 0.934 (0.3 to 3.6; 1.0)
SB varices 2 (1) 3 (0.4) 0.568 (0.3 to 10.2; 1.7)
Others SB findings (polyps, diverticulum, dieulafoy, endometriosis, and celiac) 6 (2) 23 (3) 0.353 (0.3 to 1.6; 0.7)
UGIT erosions and ulcers 6 (2) 46 (7) 0.008 (0.1 to 0.7; 0.3)
Unspecified blood in the UGIT 3 (1) 23 (3) 0.066 (0.1 to 1.1; 0.3)
GAVE 2 (1) 21 (3) 0.051 (0.1 to 1.0; 0.2)
Other UGIT findings (portal hypertensive gastropathy, varices, AE, tumour, and UGIT polyps) 8 (3) 31 (5) 0.273 (0.3 to 1.4; 0.6)
Colorectal lesions 4 (2) 16 (2) 0.404 (0.2 to 1.9; 0.6)

CE: capsule endoscopy; IDA: iron deficiency anaemia; 95% CI: 95% confidence interval; SB: small bowel; AE: angioectasia; UGIT: upper gastrointestinal tract; GAVE: gastric antral vascular ectasia.

3.3. Group 2

Group 2 was made up of 72% (n = 696) of the aforementioned 971 patients. The mean age was 68 years with the age ranging from 50 to 92 years with 58% (n = 407) of patients being female. The DY was 38% (n = 267) with no difference between the sexes. Significant diagnoses found in this age group are tabulated in Table 1. On logistic regression, the presence of haematological disease (P = 0.02), chronic renal disease (P = 0.03), and chronic liver disease (P = 0.04) and being transfusion dependent (P = 0.049) were associated with increased DY. Management was altered in 72% (n = 191) of patients with a DY on CE. Further procedures undertaken locally in patients with a management change included DBE (n = 28), PE (n = 20), repeat OGD (n = 16), colonoscopy (n = 8), and surgery (n = 7) with 17% (n = 32) of patients receiving APC therapy. On logistic regression, clinical factors that were associated with a management change included the presence of a comorbidity (P = 0.001) and SBAE (P < 0.001) and being transfusion dependent (P = 0.04).

3.4. Comparisons between the Two Groups

On group comparison, DY was significantly higher in Group 2 (age ≥ 50 years) (P = 0.002) (95% CI = 1.2 to 2.2; odds ratio = 1.6) than in Group 1. There was no significant difference in management change in patients with a DY (P = 0.55) or total number of procedures undertaken locally, although significantly more patients required APC therapy in Group 2 (P = 0.025) (95% CI = 1.3 to 75.5; odds ratio = 10.1). SB erosions and ulcers (26%; n = 71) were the commonest finding in Group 1 while SBAE (28%; n = 198) was in Group 2. In addition, Group 2 had significantly more comorbidities. There was also significantly more patients on NSAIDS (P = 0.041) and warfarin (P = 0.001) as well as being transfusion dependent (P = 0.01) and having had a previous transfusion (P = 0.001) in Group 2 as tabulated in Table 2.

Table 2.

Distribution of anticoagulation and transfusions in the <50 and ≥50 years of age patients.

Medication Group  1 (n = 275) (%) Group  2 (n = 696) (%) P value (95% CI; odds ratio)
Warfarin 5 (2) 74 (11) <0.001 (0.1 to 0.4; 0.2)
Nonsteroidal anti-inflammatories 14 (5) 63 (9) 0.042 (0.3 to 1.0; 0.5)
Transfusion dependent 8 (3) 52 (8) 0.010 (0.2 to 0.8; 0.4)
Previous transfusion 6 (2) 57 (8) 0.002 (0.1 to 0.6; 0.3)

4. Discussion

The purpose of this study was to establish the importance of CE in the investigation of younger patients with recurrent IDA of which there is limited data. Recent work by Koulaouzidis et al. has been encouraging in trying to address this shortcoming. With a DY of 25% for sinister/significant lesions in the ≤40 years of age patients, they highlight the importance of prioritising the young patient when investigating IDA with CE [11]. Their study however still had a relatively small sample size (n = 221). Our study builds on their findings with a much larger sample size (n = 971), is of an unselective nature, and is representative of CE findings in routine practice. In our study, we have demonstrated that the DY in patients <50 years was 28%. Significant pathology identified in this group included SB tumours, ulcers, and AE.

In the <50 years of age patients, SBAE is the second commonest finding after erosions and ulcers. It is found in 10% of the <50 years of age cohort and in 28% of the ≥50 year of age cohort. Although SBAE is a disease primarily inflicting the elderly, we found that SBAE also impacts as a factor in management change in both the <50 years of age patients and the ≥50 years of age patients.

SB tumours were found in 1.7% of our cohort with recurrent IDA. This is slightly lower than that of previously published work of 3.9% to 8.8% [8, 12, 13]. This result may be a reflection of CE being routinely performed in patients with recurrent IDA as compared to the stringent criteria set in other studies. In our <50 years of age patients cohort, SB tumours were found in 3% of patients which is similar to findings by Koulaouzidis et al. [11]. In addition, SB tumours were more common in females in the <50 years of age patients cohort.

In this study, we found that the DY of 66% in all patients with recurrent IDA is in keeping with DY of recent published work [8, 11, 12, 1417]. We also found that diabetes mellitus and warfarin influenced the DY in the <50 years of age patients, whilst it was haematological disease, chronic renal failure, and chronic liver disease and being transfusion dependent that influenced DY in the ≥50 years of age patients. This is as predicted and partly explained by commonality of pathology found in these age groups. In addition, other investigators [11] including our previous work [18] have also shown that transfusions, warfarin usage, and chronic liver disease influenced DY.

This study also highlights a significant number of UGIT findings in patients undergoing CE for recurrent IDA. There has been similar reports in the literature, highlighting the importance of meticulous upper and lower gastrointestinal endoscopic examination [19, 20].

Limitations of this study included its retrospective nature, all referrals made were taken at face value, and we did not revisit the history to scrutinise any previous investigation undertaken. In addition, we did not have the menopausal status for all the females <50 years of age and our study lacked the long term follow-up data on patients which would have helped to strengthen this study. A further limitation was that there were also three reporters for all the SBCE included in this study (RS, MEM, and KD). However, we have previously demonstrated that our experienced nurse reader is equally competent as a consultant gastroenterologist in the detection of small bowel pathology and in providing a final SBCE report [21].

5. Conclusion

A significant proportion of patients <50 years of age with recurrent IDA were referred for CE. Although the DY is lower compared to those over 50 years, significant pathology is found in this age group. CE is advisable in patients <50 years of age with recurrent IDA and negative bidirectional endoscopies.

Abbreviations

CE:

Capsule endoscopy

SBCE:

Small bowel capsule endoscopy

OGIB:

Obscure gastrointestinal bleeding

DBE:

Double balloon enteroscopy

APC:

Argon plasma coagulation

GI:

Gastrointestinal

OR:

Odds ratio

CI:

Confidence interval.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

Authors' Contribution

Reena Sidhu designed the study. Prabhjot Singh Sidhu and Reena Sidhu collected and analysed the data. Prabhjot Singh Sidhu wrote the initial draft, Reena Sidhu critically appraised the paper, and all authors approved the final version of the paper.

References

  • 1.McIntyre A. S., Long R. G. Prospective survey of investigations in outpatients referred with iron deficiency anaemia. Gut. 1993;34(8):1102–1107. doi: 10.1136/gut.34.8.1102. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.Goddard A. F., James M. W., McIntyre A. S., Scott B. B. Guidelines for the management of iron deficiency anaemia. Gut. 2011;60(10):1309–1316. doi: 10.1136/gut.2010.228874. [DOI] [PubMed] [Google Scholar]
  • 3.Rockey D. C., Cello J. P. Evaluation of the gastrointestinal tract in patients with iron-deficiency anemia. The New England Journal of Medicine. 1993;329(23):1691–1695. doi: 10.1056/nejm199312023292303. [DOI] [PubMed] [Google Scholar]
  • 4.Zuckerman G. R., Prakash C., Askin M. P., Lewis B. S. AGA technical review on the evaluation and management of occult and obscure gastrointestinal bleeding. Gastroenterology. 2000;118(1):201–221. doi: 10.1016/s0016-5085(00)70430-6. [DOI] [PubMed] [Google Scholar]
  • 5.Iddan G., Meron G., Glukhovsky A., Swain P. Wireless capsule endoscopy. Nature. 2000;405(6785):417–418. doi: 10.1038/35013140. [DOI] [PubMed] [Google Scholar]
  • 6.Bresci G., Parisi G., Bertoni M., Tumino E., Capria A. The role of video capsule endoscopy for evaluating obscure gastrointestinal bleeding: usefulness of early use. Journal of Gastroenterology. 2005;40(3):256–259. doi: 10.1007/s00535-004-1532-5. [DOI] [PubMed] [Google Scholar]
  • 7.Marmo R., Rotondano G., Rondonotti E., et al. Capsule enteroscopy vs. other diagnostic procedures in diagnosing obscure gastrointestinal bleeding: a cost-effectiveness study. European Journal of Gastroenterology and Hepatology. 2007;19(7):535–542. doi: 10.1097/meg.0b013e32812144dd. [DOI] [PubMed] [Google Scholar]
  • 8.Apostolopoulos P., Liatsos C., Gralnek I. M., et al. The role of wireless capsule endoscopy in investigating unexplained iron deficiency anemia after negative endoscopic evaluation of the upper and lower gastrointestinal tract. Endoscopy. 2006;38(11):1127–1132. doi: 10.1055/s-2006-944736. [DOI] [PubMed] [Google Scholar]
  • 9.Sidhu R., Sanders D. S., Morris A. J., McAlindon M. E. Guidelines on small bowel enteroscopy and capsule endoscopy in adults. Gut. 2008;57(1):125–136. doi: 10.1136/gut.2007.129999. [DOI] [PubMed] [Google Scholar]
  • 10.Mishkin D. S., Chuttani R., Croffie J., et al. ASGE Technology Status Evaluation Report: wireless capsule endoscopy. Gastrointestinal Endoscopy. 2006;63(4):539–545. doi: 10.1016/j.gie.2006.01.014. [DOI] [PubMed] [Google Scholar]
  • 11.Koulaouzidis A., Yung D. E., Lam J. H. P., Smirnidis A., Douglas S., Plevris J. N. The use of small-bowel capsule endoscopy in iron-deficiency anemia alone; be aware of the young anemic patient. Scandinavian Journal of Gastroenterology. 2012;47(8-9):1094–1100. doi: 10.3109/00365521.2012.704938. [DOI] [PubMed] [Google Scholar]
  • 12.Milano A., Balatsinou C., Filippone A., et al. A prospective evaluation of iron deficiency anemia in the GI endoscopy setting: role of standard endoscopy, videocapsule endoscopy, and CT-enteroclysis. Gastrointestinal Endoscopy. 2011;73(5):1002–1008. doi: 10.1016/j.gie.2011.01.006. [DOI] [PubMed] [Google Scholar]
  • 13.Koulaouzidis A., Rondonotti E., Giannakou A., Plevris J. N. Diagnostic yield of small-bowel capsule endoscopy in patients with iron-deficiency anemia: a systematic review. Gastrointestinal Endoscopy. 2012;76(5):983–992. doi: 10.1016/j.gie.2012.07.035. [DOI] [PubMed] [Google Scholar]
  • 14.Saurin J.-C., Delvaux M., Gaudin J.-L., et al. Diagnostic value of endoscopic capsule in patients with obscure digestive bleeding: blinded comparison with video push-enteroscopy. Endoscopy. 2003;35(7):576–584. doi: 10.1055/s-2003-40244. [DOI] [PubMed] [Google Scholar]
  • 15.Muhammad A., Pitchumoni C. S. Evaluation of iron deficiency anemia in older adults: the role of wireless capsule endoscopy. Journal of Clinical Gastroenterology. 2009;43(7):627–631. doi: 10.1097/mcg.0b013e318181b442. [DOI] [PubMed] [Google Scholar]
  • 16.Holleran G. E., Barry S. A., Thornton O. J., Dobson M. J., McNamara D. A. The use of small bowel capsule endoscopy in iron deficiency anaemia: low impact on outcome in the medium term despite high diagnostic yield. European Journal of Gastroenterology and Hepatology. 2013;25(3):327–332. doi: 10.1097/meg.0b013e32835b7d3a. [DOI] [PubMed] [Google Scholar]
  • 17.Sheibani S., Levesque B. G., Friedland S., Roost J., Gerson L. B. Long-term impact of capsule endoscopy in patients referred for iron-deficiency Anemia. Digestive Diseases and Sciences. 2010;55(3):703–708. doi: 10.1007/s10620-009-1046-3. [DOI] [PubMed] [Google Scholar]
  • 18.Sidhu R., Sanders D. S., Kapur K., Leeds J. S., McAlindon M. E. Factors predicting the diagnostic yield and intervention in obscure gastrointestinal bleeding investigated using capsule endoscopy. Journal of Gastrointestinal and Liver Diseases. 2009;18(3):273–278. [PubMed] [Google Scholar]
  • 19.Carey E. J., Leighton J. A., Heigh R. I., et al. A single-center experience of 260 consecutive patients undergoing capsule endoscopy for obscure gastrointestinal bleeding. The American Journal of Gastroenterology. 2007;102(1):89–95. doi: 10.1111/j.1572-0241.2006.00941.x. [DOI] [PubMed] [Google Scholar]
  • 20.Selby W. Can clinical features predict the likelihood of finding abnormalities when using capsule endoscopy in patients with GI bleeding of obscure origin? Gastrointestinal Endoscopy. 2004;59(7):782–787. doi: 10.1016/S0016-5107(04)00168-3. [DOI] [PubMed] [Google Scholar]
  • 21.Drew K., Sidhu R., Sanders D., McAlindon M. Blinded controlled trial comparing image recognition, diagnostic yield and management advice by doctor and nurse capsule endoscopists. Gut. 2011;60(supplement 1, article A195) doi: 10.1136/gut.2011.239301.412. [DOI] [Google Scholar]

Articles from Gastroenterology Research and Practice are provided here courtesy of Wiley

RESOURCES