Literature DB >> 23067108

The epidemiology, diagnosis, and cost of dyspepsia and Helicobacter pylori gastritis: a case-control analysis in the Southwestern United States.

Douglas Mapel1, Melissa Roberts, Andrew Overhiser, Andrew Mason.   

Abstract

BACKGROUND: Dyspepsia is among the most common complaints evaluated by gastroenterologists, but there are few studies examining its current epidemiology, evaluation, and costs. We examined these issues in a large managed care system in the Southwestern United States.
METHODS: We conducted a retrospective case-control analysis of adults with incident dyspepsia or a Helicobacter pylori-related condition in years 2006 through 2010 using utilization data. Medical record abstraction of 400 cases was conducted to obtain additional clinical information.
RESULTS: A total of 6989 cases met all inclusion and exclusion criteria. Women had a substantially higher risk of dyspepsia than men (14 per 1000 per year vs 10 per 1000; p < .001), and the incidence of dyspepsia increased with age such that persons in their seventh decade had almost twice the risk of those aged 18-29. Hispanic persons had a significantly higher risk of dyspepsia and positive H. pylori testing. Dyspepsia cases had a higher prevalence of other chronic comorbidities than their matched controls. Dyspepsia patients had healthcare costs 54% higher than controls even before the diagnosis was made, and costs in the initial diagnostic period were $483 greater per person, but subsequent costs were not greatly affected. Among those aged 55 and younger, the "test and treat" approach was used in 53% and another 18% had an initial esophagogastroduodenoscopy, as compared to 47 and 27%, respectively, among those over the age of 55.
CONCLUSIONS: Women and older adults have a higher incidence of dyspepsia than previously appreciated, and Hispanics in this region also have a higher risk. Current guidelines for dyspepsia evaluation are only loosely followed.
© 2012 Blackwell Publishing Ltd.

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Year:  2012        PMID: 23067108      PMCID: PMC3607406          DOI: 10.1111/j.1523-5378.2012.00988.x

Source DB:  PubMed          Journal:  Helicobacter        ISSN: 1083-4389            Impact factor:   5.753


Dyspepsia is defined as “chronic or recurrent pain or discomfort centered in the upper abdomen” and is among the most common reasons for visits to primary care providers or referrals to gastroenterology specialists [1-7]. Dyspepsia may be a sign of acute or chronic Helicobacter pylori infection, which was shown to be an etiology for dyspepsia after its first identification from stomach biopsy cultures in the early 1980s [8]. Dyspepsia is also a cause of concern for patients over the age of 50 because of the increased incidence of gastric malignancy [9]. Current guidelines for the evaluation and management of dyspepsia emphasize testing for the presence of H. pylori infection among persons less than the age of 55 (known as the “test and treat” approach) who do not also have “alarm symptoms” (e.g., weight loss, progressive dysphagia, recurrent vomiting, gastrointestinal bleeding, or a family history of gastrointestinal cancer) and live in a region where the prevalence of H. pylori is 10% or greater [10,11]. H. pylori eradication therapy is effective in many cases of peptic ulcer disease and resolves symptoms in a substantial proportion with nonulcer dyspepsia [12,13]. It is also presumed that this strategy will reduce the risk of MALT lymphoma and gastric carcinoma, both of which are known to be associated with H. pylori infection [14-16]. Guidelines recommend esophagogastroduodenoscopy (EGD) for those presenting with dyspepsia plus alarm symptoms, or who have dyspepsia and are over the age of 55 [10,11]. Even though dyspepsia is a very common clinical complaint and the guidelines for its evaluation and management are well established, there are remarkably few current data on the epidemiology and management of dyspepsia and even fewer data on dyspepsia-related healthcare utilization and costs [17]. Current epidemiologic data could be useful to clinicians to help identify persons at risk of dyspepsia and other H. pylori-related complications. Dyspepsia-related utilization data are also needed to compare current clinical practice against the accepted guidelines to identify specific opportunities to improve care. Utilization and cost data could be useful to those who make decisions about allocation of healthcare resources. The purpose of this study is to describe the current epidemiology, diagnostic evaluation, treatment, healthcare utilization for, and direct medical costs of dyspepsia and H. pylori gastritis in one large integrated healthcare system based in the Southwestern United States.

Methods

This study is a retrospective observational case–control study of adult patients enrolled in the Lovelace Health Plan (LHP), an insurance program operated by Ardent Health Systems who also owns Lovelace Health Systems, a network of hospitals and clinics in New Mexico. The LHP offers a range of employer and self-pay traditional private insurance, health maintenance and preferred provider plans, and Medicaid and Medicare managed care programs. Lovelace Health Systems is based in Albuquerque and is closely affiliated to a multispecialty physician group. Data for this project consisted of LHP administrative and billing data that are routinely abstracted for health services research purposes and were supplemented by data from an electronic medical record (EMR) chart review for 400 randomly selected case patients. Data abstracted from the chart review were used to validate study assumptions about clinical diagnoses and outcomes.

Case Identification and Control Matching

All adults aged 18 or older who were continuously enrolled in the LHP for at least 12 months during the study period (July 1, 2004 to June 30, 2010) were eligible. The case cohort comprises patients with an outpatient diagnosis of dyspepsia or potentially suffering gastrointestinal distress because of the presence of H. pylori. Each case was matched to three control patients who had no utilization for gastrointestinal illnesses. Cases were identified based on the earliest occurrence of a clinical diagnosis related to dyspepsia or a potentially H. pylori-caused condition, utilization of a specific test or procedure for H. pylori, or a prescription claim for an indicated H. pylori treatment therapy (see Appendix I for specific inclusion criteria). For diagnosis, procedure, or pharmacy events occurring on the same day, patients are classified first according to the diagnosis, and in the absence of a diagnosis code, according to procedure, and in the absence of a procedure, type of pharmacotherapy. The date of the earliest occurrence is the index date for the case. Patients who had a history of upper gastrointestinal cancers or other gastrointestinal disorders that would make management by the usual guidelines inappropriate were excluded (see Appendix I for specific exclusion criteria). The exclusion criteria were revised by the two authors who are experienced gastroenterology physicians to help ensure that the dyspepsia cases and non-dyspepsia controls reflect current clinical practice in this region. Each case was matched to three non-dyspepsia control patients for the purpose of comparing their utilization and identifying other comorbidities that may be risk factors for H. pylori. Controls had at least one episode of similar utilization (outpatient or emergency department (ED) visit) for a non-gastrointestinal complaint. Matching was performed based on the following parameters: sex (exact match), utilization date (within ±6 months of the index date for the case), type utilization (outpatient or ED visit), age at utilization (±2 years as of the index date for the case). Patients with gastroesophageal reflux disease (GERD) or alarm symptoms were identified using closely related International Classification of Disease, 9th Revision, Clinical Modification (ICD-9-CM) codes, including those that matched the alarm symptoms listed in guidelines for use of endoscopy for dyspepsia [18] (Appendix II).

Study Variables and Analysis

Patient sex, age, and type of health insurance at the time of the index event were derived from administrative records. Hispanic ethnicity was derived using a locally developed and validated software program that assigns ethnicity based on surname. Comorbidities were determined using two methods – the Klabunde/Deyo adaptation of the Charlson index [19] and the Elixhauser method [20]. The Elixhauser method is based on inpatient diagnoses and diagnosis related group (DRG) and was adapted in this study so that outpatient information could be incorporated. Comorbidities were assessed based on ICD-9 diagnosis codes and counted if subjects had an ICD-9 code of interest for a hospitalization, an ED visit or ≥2 outpatient visits. Healthcare utilization (hospitalizations, ED visits, outpatient visits, laboratory visits, and outpatient prescription fills) was derived from the administrative claims. Ambulatory events included laboratory events. Costs assessed for the study were direct medical costs from the perspective of a health system. All costs are stated as 2009 US dollars. Medical services costs were determined by first applying 2009 Medicare rates for specific CPT/HCPCS codes, and then in the absence of Medicare rates, average actual paid rates (cost for the health plan) adjusted to 2009 costs using the Medical Care Services consumer price index for procedures performed in non-Lovelace facilities. Pharmacy costs were assessed using 80% of published average wholesale price (AWP) for specific medications by National Drug Code (NDC) identifier, multiplied by the prescription quantity dispensed. Pharmacy costs were adjusted to December 2009 prices using the Medical Care Commodities consumer price index. Total direct healthcare costs were the sum of medical services and pharmacy costs. Medical service costs are divided by hospitalization, ED visit, and outpatient visits. For group comparisons, differences were assessed using Pearson's chi-squared test for categorical variables and Student's t-test for continuous variables. All statistical tests were two-sided with a level of significance of 0.05 and were conducted with SAS v 9.2 for Windows (SAS Institute, Cary, NC, USA).

Results

A total of 6989 patients met all inclusion and exclusion criteria (Fig. 1). Most cases (86%) met the inclusion criteria by a scheduled outpatient office visit associated with a dyspepsia-related diagnosis, 12% were diagnosed at the time of an urgent care or ED visit, and the remaining 2% were identified only by a prescription fill for an antibiotic combination indicated for H. pylori (Table 1). Patients selected for the EMR review were randomly selected from each of the specific categories shown in Table 1. On the basis of EMR information, the index date was confirmed as a new episode for 89% of the diagnosis identified cases; for 5%, there were notes documenting complaints of dyspepsia or gastritis in the 6 months prior to the index date but no associated utilization, and for 6%, there was documentation of dyspepsia or gastritis occurring prior to the index date, but the exact time of the previous occurrence was not provided. Among procedure identified cases, the EMR review found the index date to be the first incidence of dyspepsia for 92%, with 6% having EMR evidence in the baseline period of dyspepsia or gastritis that were not in the claims data, and 3%, EMR notes relating to dyspepsia or gastritis earlier than the index date, but with no specific dates.
Figure 1

Patients meeting inclusion and exclusion criteria.

Table 1

Final case cohort inclusion groups by service location

Ambulatory visitED or urgent care visitRx onlyTotal
Basis for inclusionSpecific categoryN = 5994N = 865N = 130N = 6989
Diagnosis aHelicobacter pylori diagnosis929
Gastric or duodenal ulcer30260
Dyspepsia59271
Other GI diagnosis1427244
GI signs or symptoms2666465
Diagnosis identified cases5928
ProcedureEGD260
H. pylori-related test83910
Procedure identified cases885
Prescription≥2 H. pylori antibiotics406130
Prescription identified cases176

ED, emergency department; EGD, esophago-gastro-duodenoscopy, GI, gastrointestinal.

Subjects categorized in the order shown; thus, the 302 subjects with an ulcer diagnosis did not have an H. pylori diagnosis, the 592 with dyspepsia did not have an ulcer diagnosis or H. pylori diagnosis, etc.

Patients meeting inclusion and exclusion criteria. Final case cohort inclusion groups by service location ED, emergency department; EGD, esophago-gastro-duodenoscopy, GI, gastrointestinal. Subjects categorized in the order shown; thus, the 302 subjects with an ulcer diagnosis did not have an H. pylori diagnosis, the 592 with dyspepsia did not have an ulcer diagnosis or H. pylori diagnosis, etc. In this cohort, women were substantially more likely to have dyspepsia than men (Table 2 and Fig. 2). Across the 5-year study period, women averaged 14 incident cases per 1000 per year, while men averaged 10 per 1000 per year (p < .001). The mean age for the cohort was 52, but the age-adjusted incidence of dyspepsia was lowest among younger adults and increased with age until a peak in the seventh decade (Fig. 2). Dyspepsia cases were slightly more likely to be Hispanic (43.6%) than their age- and gender-matched controls (39.9%), and cases were also slightly more likely to be enrolled in Medicare or Medicaid than their matched controls (Table 2). In the EMR review, we found that of the 81 men who had some form of H. pylori testing, 36% were positive, as compared to 24% of the 157 women tested (p = .06). Of the 49 Hispanic persons who had a H. pylori test, 41% tested positive, as compared to 17% of 103 non-Hispanic white people (p < .01).
Table 2

Baseline demographic characteristics for dyspepsia case and control cohorts

CaseControlap Valueb
No. of patients698920967
Age, mean (SD)52.5 (18.4)52.4 (18.6)0.71
Age categories, N (column %)
 Age 18–391811 (26)5510 (26)0.55
 Age 40–552011 (29)6112 (29)0.55
 Age 56–701774 (25)5180 (25)0.26
 Age > 701393 (20)4165 (20)0.90
Gender, N (column %)
 Women4476 (64)13428 (64)1.00
 Men2513 (36)7539 (36)
Hispanic3049 (44)8369 (40)<0.0001
Insurancec, N (column %)
 Commercial4619 (66)15371 (73)<0.0001
 Medicare1403 (20)3894 (19)0.0055
 Medicaid1025 (15)1757 (8)<0.0001

Cases matched to controls based on gender, age (±2 years), type of index event, index month/year (within ±6 months).

Chi-square test for frequencies; Student's t-test for means.

Individuals may have >1 type of insurance.

Figure 2

Annual incidence of dyspepsia (cases per 1000) by age and gender. *p Value for difference between women and men in this age group <.05.

Annual incidence of dyspepsia (cases per 1000) by age and gender. *p Value for difference between women and men in this age group <.05. Baseline demographic characteristics for dyspepsia case and control cohorts Cases matched to controls based on gender, age (±2 years), type of index event, index month/year (within ±6 months). Chi-square test for frequencies; Student's t-test for means. Individuals may have >1 type of insurance. Other non-gastrointestinal illnesses (comorbidities) were much more common among persons with dyspepsia than among their matched controls (Table 3). Among dyspepsia cases, 29.8% had one or more other significant comorbidities as compared to 18.1% of controls (p < .001). The Charlson index, which is a prognostic score based on serious comorbidities that affect short-term survival, was increased in 10.7% of cases as compared to 6.2% of controls (Table 3). Hypertension, diabetes, and chronic obstructive pulmonary disease (COPD) were the most common chronic conditions among both cases and controls and increased by more than 50% among cases. However, the highest odds (greater than 2.0) were seen for COPD, drug abuse, fluid and electrolyte disorders, obesity, and rheumatoid arthritis/collagen vascular diseases. Deficiency anemias, such as iron and vitamin B12 deficiency, were three times more common among cases (Table 3).
Table 3

Baseline comorbidities among dyspepsia case and control cohorts

Comorbidity assessmentaCaseControlbp Valuec
No. of patients698920967
Charlson Comorbidity Indexd, N (%)
 Charlson = 06239 (89.3)19676 (93.8)<0.001
 Charlson = 1587 (8.4)1026 (4.9)<0.001
 Charlson ≥ 2163 (2.3)265 (1.3)<0.001
Elixhauser comorbidities (adapted)e, N (%)
 Alcohol abuse46 (0.7)62 (0.3)<0.001
 Chronic blood loss anemia7 (0.1)32 (0.2)0.31
 Chronic obstructive pulmonary. disease328 (4.7)415 (2.0)<0.001
 Coagulopathy13 (0.2)34 (0.2)0.67
 Congestive heart failure59 (0.8)103 (0.5)<0.001
 Deficiency anemias169 (2.4)170 (0.8)<0.001
 Depression174 (2.5)279 (1.3)<0.001
 Diabetes (with chronic complications)87 (1.2)145 (0.7)<0.001
 Diabetes (without chronic complications)508 (7.3)992 (4.7)<0.001
 Drug abuse42 (0.6)46 (0.2)<0.001
 Fluid and electrolyte disorders62 (0.9)65 (0.3)<0.001
 Hypertension851 (12.2)1555 (7.4)<0.001
 Hypothyroidism223 (3.2)361 (1.7)<0.001
 Liver disease9 (0.1)13 (0.1)0.08
 Lymphoma10 (0.1)22 (0.1)0.41
 Metastatic cancer7 (0.1)35 (0.2)0.21
 Obesity119 (1.7)163 (0.8)<0.001
 Other neurological disorders102 (1.5)179 (0.9)<0.001
 Paralysis17 (0.2)17 (0.1)<0.001
 Peripheral vascular disease56 (0.8)86 (0.4)<0.001
 Psychoses199 (2.8)229 (1.1)<0.001
 Pulmonary circulation disease22 (0.3)63 (0.3)0.85
 Renal failure34 (0.5)70 (0.3)0.07
 Rheumatoid arth/collagen vasc dz127 (1.8)162 (0.8)<0.001
 Solid tumor withoutmetastasis91 (1.3)296 (1.4)0.50
 Valvular disease54 (0.8)121 (0.6)0.07
 Weight loss32 (0.5)21 (0.1)<0.001
 Any Elixhauser comorbidity2084 (29.8)3787 (18.1)<0.001

Only comorbidities with >10 patients are shown.

Cases matched to controls based on gender, age (±2 years), index month/year (within ±6 months).

Chi-square test for frequencies; Student's t-test for means.

Based on 6 months prior to index date; Note that neither case nor control patients had ulcer diagnoses (one of the Charlson comorbidities) as patients with pre-index ulcers were excluded.

Based on ICD-9-CM diagnoses associated with any emergency department visit or hospitalization, or ≥2 outpatient visits.

Baseline comorbidities among dyspepsia case and control cohorts Only comorbidities with >10 patients are shown. Cases matched to controls based on gender, age (±2 years), index month/year (within ±6 months). Chi-square test for frequencies; Student's t-test for means. Based on 6 months prior to index date; Note that neither case nor control patients had ulcer diagnoses (one of the Charlson comorbidities) as patients with pre-index ulcers were excluded. Based on ICD-9-CM diagnoses associated with any emergency department visit or hospitalization, or ≥2 outpatient visits. Correspondingly, dyspepsia patients had higher utilization of medical services in every category in the 6 months before they were diagnosed or treated for dyspepsia or H. pylori (Table 4). Not surprisingly, dyspepsia cases had more prescription fills for a non-steroidal anti-inflammatory drug (NSAID) at baseline than controls (17.9 vs 10.5%), although NSAID use is undoubtedly understated for both groups because of undocumented over the counter utilization. Among cases included in the EMR review, 19% had claims evidence of NSAID use, and another 10% had evidence of NSAID or COX-2 inhibitor use based on EMR records. From the index date through the first 7 days of the follow-up periods, dyspepsia cases averaged $1091 for visits and procedures and $54 for treatment, while matched controls averaged $625 and $36, respectively. Healthcare costs in the remainder of the follow-up period were substantially increased from those in the 6 months before diagnosis, although the ratio of total direct costs for cases to controls was approximately the same, 1.5:1, in the baseline period and from 7 days through 6 months post-index.
Table 4

Healthcare utilization for dyspepsia case and control cohorts during the 6-month baseline and follow-up periods and the 8-day index period

BaselineaIndex + 7 daysaFollow-up (after 7 days)a



CaseControlbCaseControlbCaseControlb
Healthcare utilization patients with ≥1 visit (% of cohort)
 Ambulatory visits84.465.191.293.293.183.2
 ED visits11.24.013.811.216.18.6
 Hospitalizations4.53.02.01.310.77.8
 Hospitalizations >1 day3.52.41.60.87.96.1
Patients with ≥1 prescription claim (% of cohort)
 NSAID17.910.51.51.816.112.6
 Cox-2 inhibitors1.20.90.20.11.10.7
Healthcare utilization rate (visits per 100 persons)
 Ambulatory visits517327140125767557
 ED visits17516122612
 Hospitalizations (any)75221914
 Hospitalizations >1 day4321107
Costs (US$ per person, mean)
 Outpatient services$1625$1106$635$373$3025$1912
 ED services$251$83$358$196$483$196
 Hospitalizations$272$178$97$57$728$548
 Subtotal – medical services$2148$1367$1091$625$4235$2656
 Pharmacy$837$576$54$36$1166$751
 Total direct cost$2985$1943$1144$661$5401$3407
 Ratio total direct cost (case/control)1.541.731.59

AWP, average wholesale price; ED, emergency department; NSAID, non-steroidal anti-inflammatory drug; SD, standard deviation.

All differences between cases and controls were significant (p < .001), based on chi-square test for frequencies and proportions, and Student's t-test for means except for NSAID and Cox-2 inhibitor use for index + 7 days (p > .05), and any hospitalization for index + 7 days (p = .002).

Cases matched to controls based on gender, age (±2 years), index month/year (within ±6 months); cases = 6989, controls = 20,967.

Healthcare utilization for dyspepsia case and control cohorts during the 6-month baseline and follow-up periods and the 8-day index period AWP, average wholesale price; ED, emergency department; NSAID, non-steroidal anti-inflammatory drug; SD, standard deviation. All differences between cases and controls were significant (p < .001), based on chi-square test for frequencies and proportions, and Student's t-test for means except for NSAID and Cox-2 inhibitor use for index + 7 days (p > .05), and any hospitalization for index + 7 days (p = .002). Cases matched to controls based on gender, age (±2 years), index month/year (within ±6 months); cases = 6989, controls = 20,967. The diagnostic testing at the time of initial diagnosis was stratified by those aged 55 and younger versus those over the age of 55 to assess overall compliance with guidelines. Among patients aged 55 and younger, 53% had some form of H. pylori diagnostic testing, and another 18% had an EGD at the time of initial diagnosis (Table 5). The presence of alarm or GERD symptoms had only a modest effect on the likelihood of obtaining an EGD: 32% of patients with alarm symptoms and 24% of those with GERD had an EGD, as compared to 14% with no additional documented symptoms.
Table 5

Occurrence of EGD, Helicobacter pylori testing, or H. pylori treatment by age category and evidence of alarm symptoms or GERD at the time of initial diagnosis

TotalAlarm SxGERD, no Alarm SxNo Alarm Sx or GERD




N%N%N%N%
Age ≤55 years
 Total cases38226003312891
 EGD
 EGD with biopsy57815a16928a692134012a
 Other diagnostic EGD1293a254a134913b
 Any EGD68218a18932a802441314a
H. pylori test/treatment
H. pylori test202553a28247a21264153153a
H. pylori treatment61316b9316631945716b
H. pylori test AND treatment36610a591050152579a
H. pylori test OR treatment227259a31653a22568173160a
Age > 55 years
  Total cases31675942482325
EGD
 EGD with biopsy71623a28348a652636816a
 Other diagnostic EGD2036a8114a1771055b
 Any EGD86527a33957a783244819a
H. pylori test/treatment
H. pylori test147947a19934a15462112648a
H. pylori treatment57018b9616471942718b
H. pylori test AND treatment38212a559401628712a
H. pylori test OR treatment166753a24040a16165126655a

EGD, esophago-gastro-duodenoscopy; GERD, gastroesophageal reflux disease; Alarm Sx, alarm symptoms.

Significant difference between age categories for measure, p < .01.

Significant difference between age categories for measure, p < .05.

Occurrence of EGD, Helicobacter pylori testing, or H. pylori treatment by age category and evidence of alarm symptoms or GERD at the time of initial diagnosis EGD, esophago-gastro-duodenoscopy; GERD, gastroesophageal reflux disease; Alarm Sx, alarm symptoms. Significant difference between age categories for measure, p < .01. Significant difference between age categories for measure, p < .05. More patients over the age of 55 had an EGD than those under 55 (27 vs 18%; p < .01), but the proportion was still low given the guideline recommendation that all over the age of 55 with dyspepsia have an EGD (Table 5). Patients over the age of 55 were only slightly less likely to have a H. pylori test (47 vs 53%; P < 0.1), and the “test and treat” approach was about the same (16 vs 18%; P < 0.5). However, the majority of those who had documented alarm symptoms (57%) did have an EGD, and those who had GERD were more likely to have an EGD than those without alarm symptoms or GERD (32 vs 19%; p < .01). In the EMR review, we found that of the 143 persons aged 55 and under who had a H. pylori test, 17% had a positive result, and that of the 171 persons over the age of 55 who had a H. pylori test, 27% had a positive result (p < .05).

Discussion

Our analysis found that dyspepsia and H. pylori-related gastrointestinal diagnoses were remarkably common among adults in this health system, with an annual incidence of 13 per 1000. A unique finding was that women were substantially more likely to have dyspepsia than men, especially in the fifth decade. The incidence among adults increased with age until the fifth decade in women and the seventh decade in men. Dyspepsia patients had a substantially higher prevalence of chronic comorbidities as compared to their age- and gender-matched controls, especially in conditions such as COPD and alcohol abuse that are associated with cigarette smoking or other exposures that also can cause gastritis. Some conditions such as deficiency anemias were substantially increased even prior to the diagnosis of dyspepsia. However, over two-thirds of dyspepsia patients had no other active chronic illness at the time of initial diagnosis. Healthcare utilization and direct medical cost are higher among dyspepsia patients, but after accounting for the costs directly related to dyspepsia evaluation and management, the proportional difference in direct healthcare costs between cases and controls was not subsequently affected. The test and treat approach was found in slightly more than half of the patients under the age of 55. However, contrary to current guidelines, only 27% of persons aged 55 and over had an EGD. Although the value of alarm symptoms as an indication for testing is a controversial issue [21], the presence of alarm symptoms did appear to modestly affect EGD utilization. This population-based assessment suggests that the increased risk of dyspepsia among women and older adults merits additional investigation. Although review articles and guidelines often note that dyspepsia is a common complaint, there are few studies that have examined the epidemiology of dyspepsia. El-Serag et al. [22] conducted a systematic review of international studies published between 1976 and 2002 that reported population-based surveys of the prevalence of dyspepsia. The survey methods were highly variable and confounded by GERD symptoms, but when the definition of dyspepsia is restricted to upper abdominal pain, lifetime estimates ranged from 5 to 12% worldwide. There is a great degree of overlap between dyspepsia and GERD, making examination of the epidemiology of either complaint somewhat confounded. A review of studies that examined the overlap between dyspepsia and GERD by Gerson et al. [23] found that 38% (range, 21–63%) of patients with GERD also report dyspepsia symptoms. They also found that patients with dyspepsia were at risk of subsequent development of GERD, and that those with both dyspepsia and GERD had substantially worse health-related quality of life scores as compared to just GERD alone. The American Gastroenterological Association guidelines for the evaluation and management of dyspepsia suggest that those initially presenting with both dyspepsia and GERD complaints be managed as GERD [10,11], but we found that those with both diagnoses were evaluated more aggressively than those with dyspepsia alone. We were surprised to find that approximately two-thirds of dyspepsia patients were women, with much of the difference between men and women occurring at middle age. The American Gastroenterological Association guidelines do not discuss sex as a risk factor for dyspepsia. In their review of 22 dyspepsia studies, El-Serag et al. found that six reported a slightly higher incidence of dyspepsia among women (range, 10–30% greater), three found a higher incidence among men (range, 5–10% greater), and the rest did not report any differences [22]. Data from other surveys suggest that there may be differences by sex in presenting gastrointestinal symptoms or gastritis complications. In a comparison of the first diagnosis of gastrointestinal complaints among adults aged 18–65 enrolled in US managed care plans, women comprised 61% of 14,593 patients with nonulcer dyspepsia, as compared to 53% of 3456 patients with peptic ulcer disease, 54% of 36,233 with gastroesophageal reflux, and 66% of 44,129 patients with abdominal signs and symptoms of undetermined cause [24]. In their analysis of the Healthcare Cost and Utilization Project Nationwide Inpatient Sample, which captures a 20% stratified sample of all hospitalizations in the United States, Wang et al. reported that 46.5% in 1993 and 49.1% in 2006 admitted with a primary diagnosis of peptic ulcer (ICD-9-CM 531–533) were women, suggesting that there is no gender difference in the complication of ulceration with bleeding and perforation [25]. Gastric cancer continues to have a male-to-female ratio of 2:1, although the incidence of gastric cancer continues to decline especially among men [9]. The prevalence of sero-positive H. pylori infection among adults participating in the Third National Health and Nutrition Survey in the United States was slightly higher among men (34%) than women (31%) [26]. In our EMR review, we found that men were more likely to have a positive H. pylori test, although we are reluctant to draw conclusions from this observation because of the limitations of the study design. It is possible that gender-based differences in healthcare seeking behavior within this system could also explain our observed differences, but we do not have evidence from this or other studies in this system to support that theory. Age was also an important risk factor for dyspepsia in our cohort, with persons in the seventh decade having twice the risk of young adults. Remarkably few epidemiologic studies have examined age as a risk factor for dyspepsia [22], and guidelines do not identify age as a dyspepsia risk factor [10,11]. The prevalence of H. pylori infection is known to increase with age, and surveys have found that a majority over the age of 60 in the United States are colonized, but the recommendation that all persons aged 55 and older have EGD is based on concern for malignancies, not the higher risk of H. pylori [27,28]. A higher proportion of persons over the age of 55 in our EMR review who were tested for H. pylori had a positive result (27 vs 17%) but additional studies are needed to see whether this accurately reflects the true H. pylori infection rate in our population. The revised National Institute for Clinical Excellence dyspepsia guidelines from the UK do not support routine EGD for dyspepsia at any age, but they do encourage urgent referral for endoscopy for patients over the age of 55 who have unexplained and persistent recent onset dyspepsia [29]. Our analysis found that persons over the age of 55 were only slightly less likely to have some form of H. pylori testing than those aged 55 and younger (47 vs 53%), but more likely to have an EGD (27 vs 18%). Perhaps this result should not be too surprising: in a recent survey of gastroenterologists and primary care providers, only 27% of general internal medicine doctors and 36% of nurse practitioners agreed with this guideline [30]. Randomized clinical trials for dyspepsia treatment have usually excluded persons aged 65 and older [31], and cost-effectiveness studies on dyspepsia management ignore age as a factor even though elderly patients have much higher average total medical costs and non-gastrointestinal comorbidities [32]. In our review of the literature, we could not find any articles presenting actual direct medical cost data for dyspepsia patients who were treated within the last decade. In a study of 1987 US National Medical Expenditure Survey, dyspepsia patients were shown to be heavy users of healthcare resources, averaging 14 visits and US$3850 in overall healthcare charges per patient per year [33]. Actual cost data for dyspepsia evaluation and management are needed for more accurate assessments of the cost-benefits of various approaches. While H. pylori eradication therapy is highly cost effective for peptic ulcer disease, the cost effectiveness of H. pylori eradication therapy in nonulcer dyspepsia is less certain [34]. Cost-effectiveness studies to date tend to be based on estimated costs for various services, and their results are heavily dependent on the actual costs for the more expensive diagnostic procedures [35]. Current cost-effectiveness studies also tend to ignore the impact of age and comorbidities in their calculations, but our analysis reveals that these factors are not inconsequential. There are limitations to our study that should be considered. Our case identification methods are based on a system using billing and procedure codes that may have missed or misclassified some dyspepsia patients. Our EMR review was able to validate that over 90% of the cases were incident cases of dyspepsia, and the rest were re-exacerbations of chronic symptoms, but it is still possible that some patients were misclassified by our case identification system. In a study that examined the validity of a similar system used to identify H. pylori patients, Thirumurthi et al. [36] found that the positive predictive value (PPV) for the ICD-9-CM diagnostic code 041.86 was 97.4% in the outpatient setting, but that triple eradication drug therapy had a PPV of only 73.7%. Another limitation is that our results represent the practice patterns of physicians included in one managed care system, and their choices are undoubtedly affected by the availability of specific services such as the urea breath test, which might be more accessible in other systems. The majority of dyspepsia patients in our cohort are managed by primary care providers, and a recent survey has demonstrated that they may be less specific than gastroenterologist in distinguishing dyspepsia from GERD or irritable bowel syndrome [30]. Our analysis is based on provider data, and given that patients have access to over-the-counter proton-pump inhibitors and other home treatments for GERD and dyspepsia, one can assume that those who seek medical attention for these symptoms are a selected population. However, even with the growth of over-the-counter treatments and reduction in the population prevalence of H. pylori infection, our analysis confirms that dyspepsia continues to be a very common clinical complaint and has a costly impact on the healthcare system.
CodeDescription
041.86Helicobacter pylori (H. pylori)
531.xGastric ulcer
532.xDuodenal ulcer
533.xPeptic ulcer
534.xGastrojejunal ulcer
535.00–535.61Other gastrointestinal codes related to H. pylori
536.8Dyspepsia and other specific disorders of function of the stomach
536.9Unspecified functional dyspepsia
789.xAbdominal signs and symptoms of undetermined cause
CodeDescription
43239Upper gastrointestinal endoscopy (EGD) with biopsy
78267Urea breath test, C-14 (isotopic); acquisition for analysis
78268Urea breath test, C-14 (isotopic); analysis
83009H. pylori, blood test analysis for urease activity, non-radioactive isotope (e.g., C-13)
83013H. pylori; breath test analysis for urease activity, non-radioactive isotope (e.g., C-13)
83014H. pylori; drug administration
86677Antibody; H. pylori
87338Infectious agent antigen detection by enzyme immunoassay technique, qualitative or semiquantitative, multiple-step method; H. pylori, stool
87339Infectious agent antigen detection by enzyme immunoassay technique, qualitative or semiquantitative, multiple-step method; H. pylori
CodeDescription
001–009Intestinal infectious diseases [only applies to 1 month prior to index date]
150–159Malignant neoplasm of digestive organs and peritoneum
195.2Malignant neoplasm abdomen
197.4Secondary malignant neoplasm of small intestine including duodenum
230.xCarcinoma in situ of digestive organs
235.5Neoplasm of uncertain behavior of other and unspecified digestive organs
307.5xOther and unspecified disorders of eating
452Portal vein thrombosis
456.0–456.21Esophageal varices
520–579Diseases of the digestive system
643Excessive vomiting in pregnancy
747.61Gastrointestinal vessel anomaly [bleeding]
750.3Tracheoesophageal fistula esophageal atresia and stenosis
750.4Other specified anomalies of esophagus
750.7Other specified anomalies of stomach
935.1–935.2Foreign body in esophagus, stomach
938Foreign body in digestive system unspecified
983.0–983.9Toxic effect of corrosive aromatics, acids, and caustic alkalis
V10.03–V10.04Personal history of malignant neoplasm of esophagus or stomach
V44, V55Artificial opening status, openings requiring attention/ management
CodeDescription
43200Esophagus endoscopy
43202Esophagus endoscopy, biopsy
43234Upper gastrointestinal endoscopy, examination
43235Upper gastrointestinal endoscopy, diagnosis
43237Endoscopic ultrasound examination, esophagus
43238Upper gastrointestinal endoscopy w/ultrasound fine needle biopsy
43242Upper gastrointestinal endoscopy w/ultrasound fine needle biopsy
43259Endoscopic ultrasound examination
GERD
CodeDescription
530.11Reflux esophagitisa
530.81Esophageal refluxa
787.1Heartburn

For diagnosis/procedure/prescription identified cases, ICD-9-CM could not appear 6 months before index; for procedure/prescription identified cases, ICD-9-CM also not on index date.

ALARM
CodeDescription
280.0Iron deficiency anemia secondary to chronic blood loss
280.1Iron deficiency anemia secondary to inadequate dietary iron intake
280.8Other specified iron deficiency anemias
280.9Unspecified iron deficiency anemia
281.0Pernicious anemia
281.1Other vitamin B12 deficiency anemia
281.2Folate-deficiency anemia
281.9Unspecified deficiency anemia
285.9Unspecified anemia
438.82Dysphagia due to cerebrovascular disease
531.0Acute gastric ulcer w/hemorrhagea
531.4Chronic or unspecified gastric ulcer w/hemorrhagea
531.6Chronic or unspecified gastric ulcer w/hemorrhage and perforationa
532.0Acute duodenal ulcer with hemorrhagea
532.2Acute duodenal ulcer with hemorrhage & perforationa
532.4Chronic or unspecified duodenal ulcer with hemorrhagea
533.0Acute peptic ulcer with hemorrhagea
533.2Acute peptic ulcer with hemorrhage & perforationa
533.4Chronic or unspecified peptic ulcer with hemorrhagea
534.0Acute gastrojejunal ulcer with hemorrhagea
534.4Chronic or unspecified gastrojejunal ulcer with hemorrhagea
535.01Acute gastritis with hemorrhagea
535.11Atrophic gastritis with hemorrhagea
535.21Gastric mucosal hypertrophy with hemorrhagea
535.31Alcoholic gastritis with hemorrhagea
535.41Other specified gastritis with hemorrhagea
535.51Unspecified gastritis & gastroduodenitis with hemorrhagea
535.61Duodenitis with hemorrhagea
536.2Persistent vomitingb
578.0Hematemesisb
578.1Blood in stoolb
578.9Unspecified hemorrhage of gastrointestinal tractb
783.21Loss of weight
787.01Nausea with vomiting
787.03Vomiting alone
787.20Dysphagia, unspecified
787.22Dysphagia, oropharyngeal phase
787.23Dysphagia, pharyngeal phase
787.24Dysphagia, pharyngoesophageal
787.29Other dysphagia
789.3xAbdominal or pelvic swelling, mass, or lumpa
793.4Nonspecific abnormal findings on radiological & other examination of the gastrointestinal tract
V16.0Familial history of malignant neoplasm of gastrointestinal tract

ICD-9-CM part of inclusionary diagnosis criteria.

For diagnosis/procedure/prescription identified cases, ICD-9-CM could not appear 6 months before index; for procedure/prescription identified cases, ICD-9-CM also not on index date.

  35 in total

Review 1.  American gastroenterological association technical review on the evaluation of dyspepsia.

Authors:  Nicholas J Talley; Nimish B Vakil; Paul Moayyedi
Journal:  Gastroenterology       Date:  2005-11       Impact factor: 22.682

2.  American Gastroenterological Association medical position statement: evaluation of dyspepsia.

Authors:  Nicholas J Talley
Journal:  Gastroenterology       Date:  2005-11       Impact factor: 22.682

3.  Practice patterns for managing Helicobacter pylori infection and upper gastrointestinal symptoms.

Authors:  Colin W Howden; Steven W Blume; Gregory de Lissovoy
Journal:  Am J Manag Care       Date:  2007-01       Impact factor: 2.229

4.  Comorbidity measures for use with administrative data.

Authors:  A Elixhauser; C Steiner; D R Harris; R M Coffey
Journal:  Med Care       Date:  1998-01       Impact factor: 2.983

Review 5.  Clinical economics review: gastroenterology.

Authors:  K Bodger; M J Daly; R V Heatley; D R Williams
Journal:  Aliment Pharmacol Ther       Date:  1996-02       Impact factor: 8.171

Review 6.  Limited value of alarm features in the diagnosis of upper gastrointestinal malignancy: systematic review and meta-analysis.

Authors:  Nimish Vakil; Paul Moayyedi; M Brian Fennerty; Nicholas J Talley
Journal:  Gastroenterology       Date:  2006-08       Impact factor: 22.682

Review 7.  Helicobacter pylori: why it still matters in 2005.

Authors:  M Brian Fennerty
Journal:  Cleve Clin J Med       Date:  2005-05       Impact factor: 2.321

Review 8.  The health economics of Helicobacter pylori infection.

Authors:  Paul Moayyedi
Journal:  Best Pract Res Clin Gastroenterol       Date:  2007       Impact factor: 3.043

9.  Who consults with dyspepsia? Results from a longitudinal 10-yr follow-up study.

Authors:  Alexander C Ford; David Forman; Alastair G Bailey; Michael B Cook; Anthony T R Axon; Paul Moayyedi
Journal:  Am J Gastroenterol       Date:  2007-02-21       Impact factor: 10.864

Review 10.  Epidemiology of gastric cancer.

Authors:  Katherine D Crew; Alfred I Neugut
Journal:  World J Gastroenterol       Date:  2006-01-21       Impact factor: 5.742

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  13 in total

1.  Ethnic, Racial, and Sex Differences in Etiology, Symptoms, Treatment, and Symptom Outcomes of Patients With Gastroparesis.

Authors:  Henry P Parkman; Goro Yamada; Mark L Van Natta; Katherine Yates; William L Hasler; Irene Sarosiek; Madhusudan Grover; Ron Schey; Thomas L Abell; Kenneth L Koch; Braden Kuo; John Clarke; Gianrico Farrugia; Linda Nguyen; William J Snape; Laura Miriel; James Tonascia; Frank Hamilton; Pankaj J Pasricha; Richard W McCallum
Journal:  Clin Gastroenterol Hepatol       Date:  2018-11-04       Impact factor: 11.382

2.  Prevalence and risk factors of Helicobacter pylori infection in Ningxia, China: comparison of two cross-sectional studies from 2017 and 2022.

Authors:  Yan Zhou; Yanhong Deng; Yanjie You; Xue Li; Di Zhang; Hailong Qi; Ruichun Shi; Li Yao; Yuanyuan Tang; Xiaofei Li; Linke Ma; Yanlin Li; Jun Liu; Yaning Feng; Xianmei Chen; Qian Hao; Xuemei Li; Yuzhen Li; Min Niu; Hengjun Gao; Feihu Bai; Shengjuan Hu
Journal:  Am J Transl Res       Date:  2022-09-15       Impact factor: 3.940

Review 3.  Autoimmune atrophic gastritis--pathogenesis, pathology and management.

Authors:  William L Neumann; Elizabeth Coss; Massimo Rugge; Robert M Genta
Journal:  Nat Rev Gastroenterol Hepatol       Date:  2013-06-18       Impact factor: 46.802

4.  Reciprocal impact of host factors and Helicobacter pylori genotypes on gastric diseases.

Authors:  Sahar Honarmand-Jahromy; Farideh Siavoshi; Reza Malekzadeh; Taher Nejad Sattari; Saeid Latifi-Navid
Journal:  World J Gastroenterol       Date:  2015-08-21       Impact factor: 5.742

Review 5.  Helicobacter pylori: evidence-based review with a focus on immigrant populations.

Authors:  Derrick Siao; Ma Somsouk
Journal:  J Gen Intern Med       Date:  2013-09-25       Impact factor: 5.128

6.  Helicobacter pylori seropositivity and cognitive performance among US adults: evidence from a large national survey.

Authors:  May A Beydoun; Hind A Beydoun; Monal R Shroff; Melissa H Kitner-Triolo; Alan B Zonderman
Journal:  Psychosom Med       Date:  2013-05-22       Impact factor: 4.312

7.  Gastric polyps: Association with Helicobacter pylori status and the pathology of the surrounding mucosa, a cross sectional study.

Authors:  Sherif Elhanafi; Mohammed Saadi; Wynee Lou; Indika Mallawaarachchi; Alok Dwivedi; Marc Zuckerman; Mohamed O Othman
Journal:  World J Gastrointest Endosc       Date:  2015-08-10

8.  Prevalence of Helicobacter pylori in Patients With Dyspepsia.

Authors:  Ramin Niknam; Mehrdad Seddigh; Mohammad Reza Fattahi; Amirreza Dehghanian; Laleh Mahmoudi
Journal:  Jundishapur J Microbiol       Date:  2014-10-01       Impact factor: 0.747

9.  Comparison of clinical symptoms after Helicobacter pylori eradication in functional dyspepsia patients based on endoscopic view of antral gastropathy.

Authors:  S Azadbakht; S Azadbakht; A Esmaili; P Rahmani
Journal:  New Microbes New Infect       Date:  2020-11-09

10.  Guideline Adherence in Dyspepsia Investigation and Treatment.

Authors:  Katelyn Dugan; Elizabeth Ablah; Hayrettin Okut; Sachin Srinivasan; William Salyers
Journal:  Kans J Med       Date:  2020-12-11
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