Literature DB >> 35120064

International Classification of Diseases (ICD) Codes Fail to Accurately Identify Injection Drug Use Associated Endocarditis Cases.

Erin Barnes1, James Peacock, Laura Bachmann.   

Abstract

OBJECTIVES: Infective endocarditis (IE) secondary to injection drug use (IDU-IE) is a disease with high morbidity, cost, and rapid demographic evolution. Studies frequently utilize combinations of International Statistical Classification of Diseases (ICD) codes to identify IDU-IE cases in electronic medical records. This is a validation of this identification strategy in a US cohort.
METHODS: Records from January 1, 2004 to September 31, 2015 for those aged ≥18yo with any ICD-coded IE encounter (inpatient or outpatient) were retrieved from the electronic medical record and then manually reviewed and classified as IDU-IE by strict and inclusive criteria. This registry was then used to assess the diagnostic accuracy of 10 identification algorithms that combined substance use, hepatitis C, and IE ICD codes.
RESULTS: IE was present in 629 of the 2055 manually reviewed records; 109 reported IDU within 3 months of IE diagnosis and an additional 32 during their lifetime (141 cases). In contrast, no algorithm identified more than 46 (33%) of these cases. Algorithms assessing encounters with both an IE and substance use code had specificities >99% but sensitivities ≤11% with negative predictive values of 83% to 84% and positive predictive values ranging from 75% to 91%. Use of a hepatitis C OR substance use code with an IE-coded encounter resulted in higher sensitivities of 22% to 32% but more false positives and overall positive predictive value of <70%. This algorithm limited to age ≤45yo had the best, but still low, discrimination ability with an area under the receiver operating characteristic curve of 0.62.
CONCLUSION: Substance use and hepatitis C codes have poor ability to accurately classify an IE-coded encounter as IDU-IE or routine IE.
Copyright © 2021 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Society of Addiction Medicine.

Entities:  

Mesh:

Year:  2022        PMID: 35120064      PMCID: PMC8815841          DOI: 10.1097/ADM.0000000000000814

Source DB:  PubMed          Journal:  J Addict Med        ISSN: 1932-0620            Impact factor:   3.702


The US opioid epidemic began in the late 1980s and early 1990s with changes to regulatory structures, reimbursement incentives, patient advocacy action, and aggressive drug marketing[1] resulting in US use of 99% and 83% of the world's hydrocodone and oxycodone supplies by 2010.[2] Increases in overdose deaths, hepatitis A, B, C, and HIV followed.[3-7] Overdose data followed by viral infectious disease reports were key in alerting the nation to the opioid crisis and then informing public health policy due to the clear definitions and regular mandated reporting of these events. Lagging behind these reports are studies on the rising trends of IDU-IE. Multiple papers have now been published establishing a steep rise in IEs associated with substance use in a variety of locations and settings.[8-13] These descriptive studies have been vital in highlighting the lack of addiction medicine infrastructure and sharp divide between care for substance use disorders versus that for routine internal medicine care, particularly in rural areas.[8,10,11] The high monetary costs and morbidity from IDU-IE have also been highlighted by these studies with hospitals struggling to absorb costs of this underinsured population.[9,14] The growing body of literature on the barriers and effects of IDU-IE on patients, communities, and providers highlight the need for ongoing high quality, timely epidemiologic studies of this patient group and the outcomes of research focused on their care. The opioid epidemic led to a shift in the epidemiology of IDU-IE in addition to changing health costs, impacted locations, and recognition of need for more evidence-based guidelines for clinical decision making.[15] Wurcel et al have provided one of the most comprehensive assessments of the epidemiology and morbidity of this disease through query of the National Inpatient Sample database.[13] The search strategy used was an adapted strategy from Cooper et al[16] and together these search strategies have formed the basis for many other studies by researchers assessing IDU-IE within their own institutions.[8,14] However, the accuracy of ICD coding for IE in general and IDU-IE in particular is suspect. A recent British study found that fewer than 50% of cases with an IE code were true IE cases and that the incidence and characteristics of the disease varied depending on the quality of the coding algorithms used.[17] A large US study similarly found that combinations of primary and secondary codes for IE were required to achieve a sensitivity above 25%.[18] The largest IDU-IE code validation study is a recent Canadian study, which found that combining IE and substance use disorder codes achieve ∼87% sensitivity and 64% specificity with more code combinations required to increase sensitivity above 90%. However, this conclusion was based on an ICD-10 system in use since 2000 in another country.[19] How accurate these methods are in the United States for IDU-IE is unknown. We describe here the results and accuracy of ICD-9 code-based algorithms to identify IDU-IE cases as compared to a database created through manual review of every individual who had an endocarditis code associated with their chart in any context or setting.

METHODS

Before study initiation the research protocol was approved by the Wake Forest Baptist Health IRB. The medical records of all patients ≥18 years of with an ICD-9 IE code (appendix 1) for any encounter type (inpatient or outpatient) during January, 1 2004 to September 30, 2015, as the US changed to ICD-10 on October 1, 2015, were identified resulting in a study cohort of 2055 unique individuals. ICD codes used are those cited in previous literature.[12,13] Each record was individually reviewed (EWB) and the diagnosis of IE was either accepted or rejected utilizing “strict” or “inclusive” case definitions. Patients who had an implantable cardiac device were removed from the cohort and not considered further. Strict cases included those with possible or definite IE by the modified Duke Criteria.[20] Inclusive cases encompassed those patients who did not meet Duke Criteria but who were diagnosed and treated as IE by their physicians and who would therefore be reasonable cases for an ICD-based algorithm to identify. Rarely, cases of IE were acquired in the hospital more than 72 hours after admission for a noninfectious indication. Given that the sole goal of this investigation was to identify IE associated with the injection of substances, these cases were only included in the inclusive case definition regardless of how many Duke criteria they fulfilled. Strict and inclusive criteria were also developed for determining if a case was associated with IDU. Those who reported injection in the 3 months before admission met strict criteria whereas those with ANY history of IDU met inclusive criteria. We included coding which included amphetamines/stimulants as at our institution many patients report frequent injection of opioids mixed with methamphetamine or cocaine or alternative between periods of isolated stimulant and then isolated opioid use. Only self-reported IDU was relied upon to determine criteria fulfillment. Urine drug screens were not considered due to their variable drug detection profiles,[21] provider bias in determining who receives these tests, and the inability to cross check positive results with prescribed medications or medications received in the ED before the screen was drawn. Those cases where physicians were merely suspicious of IDU but no confirmation ever was obtained from the patient were not counted as IDU-IE to avoid introducing provider bias. All cases which were identified and classified through comprehensive review of the 2055 patients were then compared to the patients identified by 10 different ICD-based algorithm searches (Table 1, Appendix 2). Each individual was counted only once even if they had multiple IE admissions so that the algorithms were measured against their ability to identify an individual rather than specific encounters. The age cutoff of ≤45 years old is significantly younger than the cutoff of age 64 used by Cooper[16] and Wurcel.[13] This limitation is hoped to increase specificity and is 1.5 standard deviations above the mean age of 92 persons in the IDU-IE population examined previously. The total number of individuals identified and the number of IDU-IE cases identified by strict and inclusive criteria were assessed and compared to the findings from the comprehensive search. Sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV), and area under the receiver operating characteristic curve (AUC-ROC) for both strict and inclusive case definitions of IDU-IE were assessed for each algorithm. Individuals which were identified by the algorithms but did not have IE at all, much less IDU-IE, are reported but were not considered “true negatives” for the calculations of specificity, NPV, and AUC-ROC for the purpose of these calculations (the diseased state was classified as IDU-IE for “disease present” and IE without IDU for “disease absent”). However, leaving these cases out altogether in calculations artificially deflates the false positive rate while artificially inflating specificity, PPV, and AUC-ROC. A true calculation using these cases would require analogous true negatives to be all cases in the hospital that did not have IE during this time which is a calculation of dubious use and relevance to this study. For the purposes of transparency, additional calculations where the false positives include cases returned by the algorithm without IE were included in the appendix (Appendix 3) for readers to reference as they see fit.
TABLE 1

Variations of Combined Endocarditis and Drug Use Codes Used for Case Identification

Algorithm 1Time range January 1, 2004 to September 31, 2015 with ANY encounter associated with both an ICD for endocarditis and a substance use code in the same encounter
Algorithm 2Time range January 1, 2004 to September 31, 2015with ANY encounter associated with both an ICD for endocarditis and an OPIOID use code in the same encounter
Algorithm 3Algorithm 1 limited to inpatient encounters
Algorithm 4Algorithm 2 limited to inpatient encounters
Algorithm 5Algorithm 1 if you limit the group to those age 45 or younger at time of the coded encounter
Algorithm 6Algorithm 2 if you limit the group to those age 45 or younger at the time of the coded encounter
Algorithm 7Time range January 1, 2004 to September 31, 2015 with ANY encounter associated with both an ICD for endocarditis and a substance use code in the same encounter OR rather than the substance use code being in the same encounter as the endocarditis code, they have a hepatitis C code in the same encounter as the endocarditis code
Algorithm 8Algorithm 7 limited to those aged 45 or younger at the time of encounter
Algorithm 9Time range January 1, 2004 to September 31, 2015 who EVER had an endocarditis code and substance use code appear on their chart. The codes no longer need to coincide in the same encounter but merely any type of encounter with an endocarditis code and any type of encounter when a substance use code was utilized
Algorithm 10Time range January 1, 2004 to September 31, 2015 who EVER had both an endocarditis code and OPIOID use code appear on their chart where the codes no longer need to coincide in the same encounter but merely have one encounter of any kind where there was an endocarditis code and another encounter of any kind where there was a substance use code
Variations of Combined Endocarditis and Drug Use Codes Used for Case Identification

RESULTS

Comprehensive case review identified 629 total IE cases with 1426 individuals failing to have IE by strict or inclusive definitions. Frequently, IE seems to have been erroneously associated with a patient who had valve surgery for chronic degenerative valve disease, a history of rheumatic carditis, or a case where endocarditis was considered in the differential diagnosis but ultimately ruled out consistent with the findings from Fawcett et al.[17] One hundred nine patients met strict criteria for both IDU and IE and with that number increasing to 141 IDU-IE cases when inclusive definitions were used (Table 2). In contrast, the highest number of IDU-IE cases identified by any algorithm was 46 cases identified by algorithm 7.
TABLE 2

Number of Individuals and Cases Identified by Each Search Algorithm

CohortTotal NIDU-IE by StrictIDU-IE by InclusiveStrict IE CasesInclusive IE CasesNo IE by Strict or InclusiveFalse Positives StrictFalse Positives InclusiveFalse Negatives StrictFalse Negatives Inclusive
Comprehensive1091411426
Algorithm 1191414141635595127
Algorithm 2141111121313398130
Algorithm 3181414141534395127
Algorithm 4121010111112299131
Algorithm 5151313131322296128
Algorithm 611991010122100132
Algorithm 794324671771761477795
Algorithm 853253241458282184109
Algorithm 9501520313613353094121
Algorithm 1037171927307201892124

Two patients were identified in each of these cohorts with cardiac implantable devices. They were excluded from total counts and calculations.

Strict criteria: include those who report injection in the last 3 months before presentation and endocarditis fulfil at least possible Modified Duke criteria. Inclusive: includes those who report a lifetime history of injection drug use and additionally includes endocarditis cases that did not meet Modified Duke Criteria but were treated as endocarditis as well as hospital acquired cases.

IDU-IE indicates Injection drug use associated infective endocarditis;

Number of Individuals and Cases Identified by Each Search Algorithm Two patients were identified in each of these cohorts with cardiac implantable devices. They were excluded from total counts and calculations. Strict criteria: include those who report injection in the last 3 months before presentation and endocarditis fulfil at least possible Modified Duke criteria. Inclusive: includes those who report a lifetime history of injection drug use and additionally includes endocarditis cases that did not meet Modified Duke Criteria but were treated as endocarditis as well as hospital acquired cases. IDU-IE indicates Injection drug use associated infective endocarditis; Those algorithms which relied solely on both IE and substance use ICD codes occurring during an encounter (algorithms 1–6) had very high specificity ≥99.2% (Table 3). However, this group also had the highest number of true false negatives leading to sensitivities of only 9.3% to 11.0% for strictly-defined cases and 6.4% to 9.2% for inclusively-defined cases. Sensitivity improved when the codes for endocarditis and substance use were not required to coincide in the same encounter (algorithms 9 and 10) but remained <15% while specificity remained >95%. In this group of codes (1–6, 9–10), PPV was highest in algorithms 5 and 6 which restricted to ages ≤45 at 85% to 92% and comparable NPVs of 79% to 84%. These algorithms resulted in an AUC-ROC no greater than 0.55, however, suggesting that when faced with an individual coded as IE, relying on a substance use code to determine if the case is IDU-IE fares no better than a coin-flip.
TABLE 3

Accuracy and Discriminatory Capability of ICD-9 Algorithm-based Searches

AUC-ROC StrictSensitivity Strict % (95% CI)Specificity Strict % (95% CI)PPV Strict % (95% CI)NPV Strict % (95% CI)AUC-ROC InclusiveSensitivity Inclusive % (95% CI)Specificity Inclusive % (95% CI)PPV Inclusive % (95% CI)NPV Inclusive % (95% CI)
Algorithm 155.111.0 (6.4–18.3)99.2 (98.0–99.7)75.0 (50.5–89.8)84.2 (81.1–86.9)54.39.2 (5.5–15.1)99.4 (98.2–99.8)81.3 (57.0–93.4)79.1 (75.7–82.2)
Algorithm 254.910.1 (5.7–17.2)99.6 (98.6–99.9)84.6 (57.8–95.7)84.1 (81.0–86.8)53.77.8 (4.4–13.3)99.6 (98.5–99.9)84.6 (57.8–95.7)78.9 (75.5–81.9)
Algorithm 355.211.0 (6.4–18.3)99.4 (98.3–99.8)80.0 (54.8–93.0)84.2 (81.1–86.9)54.49.2 (5.5–15.1)99.6 (98.5–99.9)86.7 (62.1–96.3)79.2 (75.8–82.2)
Algorithm 454.59.2 (5.1–16.1)99.8 (98.9–100)90.9 (62.3–98.4)84.0 (80.9–86.7)53.47.1 (3.9–12.6)99.8 (98.8–100)90.9 (62.3–98.4)78.8 (75.4–81.8)
Algorithm 554.910.1 (5.7–17.2)99.6 (98.6–99.9)84.6 (57.8–95.7)84.1 (81.0–86.8)54.28.5 (4.9–13.3)99.8 (98.8–100)92.3 (66.7–98.6)79.1 (75.7–82.1)
Algorithm 654.08.3 (4.4–15.0)99.8 (98.9–100)90.0 (59.6–98.2)83.8 (80.7–86.5)53.16.4 (3.4–11.7)99.8 (98.8–100)90.0 (59.6–98.2)78.7 (75.3–81.7)
Algorithm 759.828.4 (20.8–37.5)91.2 (88.4–93.3)40.3 (30.0–51.4)85.9 (82.7–88.5)62.231.2 (24.1–39.3)93.2 (90.7–95.1)57.1 (46.0–67.6)82.4 (79.0–85.4)
Algorithm 859.022.0 (15.3–30.7)96.0 (93.9–97.3)53.3 (39.1–67.1)85.4 (82.4–88.1)59.622.0 (15.9–29.5)97.1 (95.2–98.3)68.9 (54.3–80.5)81.2 (77.8–84.1)
Algorithm 954.713.8 (8.5–21.5)95.8 (93.7–97.2)40.5 (26.3–56.5)84.1 (81.0–86.8)55.414.2 (9.4–20.9)96.5 (94.5–97.8)54.1 (38.4–69.0)79.6 (76.1–82.6)
Algorithm 1056.512.8 (8.2–19.3)97.5 (95.8–98.6)60.0 (42.3–75.4)79.5 (76.0–82.5)55.212.8 (8.2–19.3)97.5 (95.8–98.6)60.0 (42.3–75.4)79.5 (76.0–82.5)

Strict criteria: include those who report injection in the last 3 months before presentation and endocarditis fulfills at least possible Modified Duke criteria. Inclusive Criteria: includes those who report a lifetime history of injection drug use and additionally includes endocarditis cases that did not meet Modified Duke Criteria but were treated as endocarditis as well as hospital acquired cases.

AUC-ROC indicates area under the receiver operating characteristic curve; CI, confidence interval; NPV, Negative Predictive Value; PPV, Positive Predictive Value.

Accuracy and Discriminatory Capability of ICD-9 Algorithm-based Searches Strict criteria: include those who report injection in the last 3 months before presentation and endocarditis fulfills at least possible Modified Duke criteria. Inclusive Criteria: includes those who report a lifetime history of injection drug use and additionally includes endocarditis cases that did not meet Modified Duke Criteria but were treated as endocarditis as well as hospital acquired cases. AUC-ROC indicates area under the receiver operating characteristic curve; CI, confidence interval; NPV, Negative Predictive Value; PPV, Positive Predictive Value. Including hepatitis C as an alternative to substance use codes at the time of an IE-coded encounter (algorithms 7 and 8) allowed the highest number of cases to be identified. This strategy produced the highest respective sensitivities of 28.4 and 22.0% for strictly defined cases. These algorithms identified more false positive cases as well, however, so their specificities are lower than for groups 1 to 6. Specificity was lowest for algorithm 7 at 91.2% but when limited to those under 45 years of age in algorithm 8, the specificity rose to 96.0%. PPV for these algorithms was <53% for strictly defined cases and <69% for inclusively defined cases which is significantly worse than for algorithms 1 to 6; the trade-off gains in NPV were mild in comparison, remaining no better than 85.9%. The AUC-ROC of algorithm 7 was the highest for all algorithms for both strict (0.60) and inclusive (0.62) criteria.

DISCUSSION

In this study we found that in this ICD-9 based cohort relying on simultaneous encoding of endocarditis and substance use was a highly specific but very insensitive measure of case identification with many IDU-IE cases missed. Hepatitis C codes used for identification in place of substance use codes identified more cases but did so at the expense of specificity with more false positives occurring. In all cases, using more inclusive definitions served to marginally improve specificity with greater gains achieved for algorithms 7 to 10 than 1 to 6. Sensitivity was slightly worsened for algorithms 1 to 6, improved for 7 and 9, and worsened for algorithms 8 and 10. Regardless, no algorithm using any set of criteria achieved an AUC-ROC of 0.7 with the best AUC-ROC of 0.62 achieved by algorithm 7 when inclusively defined criteria were used. Our study does come to different conclusions than the Canadian study by Ball et al.[19] In their algorithm assessing coding for IE with hepatitis C or drug use, they had a much better sensitivity and PPV of 87% and 83% respectively. Meanwhile, our algorithms had much higher specificity and NPV compared to their 64% and 70% respectively. The reasons for this likely lie in the fact that the Canadian centers involved in the study had both infectious diseases and addiction medicine physicians. Having addiction medicine physicians seeing patients may improve coding for both addiction and psychiatric diagnoses. In contrast, WFBMC does not have inpatient addiction medicine physicians and the capacity for our psychiatry consult colleagues to consult inpatient on these patients is limited. The Canadian authors also had a prospective list of IE patients maintained by both groups which may have in part overlapped the 2014 to 2016 time period they examined, though this is not clear in the manuscript. It is possible that knowing a prospective database focusing on these patients was occurring could have altered and improved coding by their peers. Unfortunately, this study raises questions about what we truly do and do not know about the epidemiology and costs of IDU-IE in the current setting of the United States opioid epidemic. Our findings suggest that national assessments of IDU-IE may be underestimated on a significant scale. It may be that the underestimation wrought by the substance use coding found in this study was balanced out in past studies by what is likely an overestimate of IE in general such as has been found to occur when certain ICD-based IE strategies are used.[17] Even if our reports of underestimation were to hold true on a national scale, whether or not the inclusion of these potentially missing cases would affect descriptions of the characteristics and outcomes of the IDU-IE cohort is unknown. Groups across the country are finding similar demographic changes in their IDU-IE cohorts including a proportion of females ranging from about 1/3 to 1/2 of cases, a rise in White and rural cases, significantly younger age, and similar inpatient mortality and relapse rates.[8-12,15,16,22-27] These observations are consistent with demographic changes seen in other IDU-associated conditions such as overdose deaths and infections such as Hepatitis C.[4,5,28,29] This consistency across location and method (many studies,[9,16,17] but not all,[10,18-21] used combined IE and substance use ICD based pulls for case identification) would seem to suggest that the general demographic trends may well be correct in overall direction and err only in a matter of scale. In addition to the likely underestimation of morbidity, the monetary costs of SUD and associated complications are also likely much higher than previously reported. Each case of IDU-IE costs an estimated $47,8998 to $180,31414. As our study suggests that up to 3-fold as many cases exist as have been identified, a conservative correction would increase reports by a factor of 1.5-fold and would result in an additional 4265 patients in the 2000 to 2013 cohort reported by Wurcel et al with a corresponding additional $204,289,235 to $769,039,210 in unreported health care charges. An extra 250 people with IDU-related IE would also be included in the NC study from 2010 to 2015 with additional costs of 11 million dollars for the year of 2015 alone.[12] Those diseases which are more common or costly receive more national attention, interagency collaboration, external grant funding, and internal resources so that our national underestimation of both cases and cost may have far reaching effects on our ability to effectively and comprehensively treat this population. The larger and more concerning issue raised here is our possible inability to accurately identify all IDU-IE cases in real-time. At present, ICD-based coding methods are the standard for case identification. Yet the data presented here suggest these codes are a woefully inadequate tool to capture trends and changes in IDU-IE epidemiology. This observation has many implications. First, at least 1 study has identified IDU-IE case rise as a marker of increased IDU in a region.[30] Real-time and accurate identification of an IDU-IE spike could then conceivably allow earlier and more targeted resource intensification to areas in need. Second, the opioid epidemic has continued to evolve with heroin and fentanyl analogs now playing a larger role than prescription opioids[31,32] and methamphetamine injection steadily increasing.[33-35] How these changing dynamics will affect the epidemiology and pathophysiology of IDU-IE or interact with the other overlapping infectious syndemics of hepatitis and sexually transmitted diseases is unclear. Timely and accurate IDU-IE case identification could alert agencies and community stakeholders to evolving infectious trends associated with changing substance use patterns which would further enhance stakeholder decision-making and resource development and deployment. Requiring IE or at least IDU-IE to be a reportable disease for health departments may be one way to better capture the epidemiology of this condition. Finally, accurate identification strategies are needed for researchers to extract sufficient cases from the electronic medical record to compare and identify effective infection and addiction treatment strategies in this group which is otherwise very difficult to study in adequate numbers in a prospective manner. It may be that the heterogeneity of coding behaviors amongst providers and the inherent data limitations within administrative coding will never allow coded data to fully meet these needs. Machine learning technologies such as natural language processing, which can process text and context within physician notes themselves, are advancing in the medical field and may provide a novel path forward to bridge these gaps.[36,37] There are many potential limitations to this study. First, it was a single center and retrospective review. The lack of precision in the coding which we identified may be limited to our institution alone and may not translate to external sites or national databases. However, as our medical center employs physicians who have trained and worked at institutions from all over the world, there would be no a priori reason to believe they would be a unique and isolated group in their coding practices. As noted in our comparisons to Ball et al's study above, it is possible that a medical center with a dedicated addiction medicine consult group or robust inpatient psychiatric consult service for IDU-IE patients may have better coding for substance use related conditions than we had at our institution. Secondly, even though a very wide net was cast by seeking documentation of IE in any context in any encounter type to minimize the chances of missing a case, it is still possible that some cases of IE were missed, particularly if they were not coded for IE at all and given that we did not use “E” Codes to supplement the CM codes. Based on the hundreds of records reviewed that had no endocarditis but were associated with an IE ICD-9 code, we believe it is unlikely that any significant number of cases were missed. Third, this study was conducted on an Epic-based EMR system. How each electronic medical record stores and retrieves data is unique and results with different EMRs may differ. Fourth, the US transitioned to ICD-10 coding on October 1, 2015 and there are many additional codes available in that system which may increase the ability to identify these cases using ICD-coded strategies. However, there remains no dedicated code to signify substance use through an injected route in ICD-10 with some systems creating proxy codes, for example, F19.10 appears as a suggested code if “injection drug use” is typed into our EMR though that code is technically the code for “other psychoactive substance abuse, uncomplicated.” Regardless, it will be some time before the accuracy of the ICD-10 codes can be compared to ICD-9 for identifying cases of IDU-related IE in the US. Fifth, the scale of the data extraction from the comprehensive data set precluded having 2 individuals each rank the cases and compare results. Cases that did not clearly meet case definitions were adjudicated by a panel of 3 infectious diseases physicians but bias may still remain from having a single individual data extractor. Sixth, many more combinations of ICD codes than were tested here exist and could potentially prove useful; full assessment of larger numbers of codes and information from a wider range of fields is ongoing. Finally, some may disagree with the strictness of the case definitions used here including the decision to exclude those where the physicians strongly suspected IDU but it was never self-reported. The decision to use such strict criteria was made to prevent bias. It was also based on the belief that future studies may attempt to pull detailed and complex data from cases to test hypotheses and assess treatment responses where rigorous case definitions will be paramount. There is great need for a unified definition of IDU-IE to insure further internally consistent and comparable research in this field.

CONCLUSIONS

In the United States, using a combination of substance use, hepatitis C, and endocarditis ICD-9 coding is an insensitive strategy for identifying IDU-IE and may be no better than “flipping a coin” at distinguishing between IE cases which are associated with substance use from those which are not. To ensure that accurate and reproducible data are extracted for epidemiological and clinical studies which can be extrapolated across institutions, a standard case identification tool needs to be developed and validated.
  34 in total

1.  Drug-Associated Infective Endocarditis Trends: What's All the Buzz About?

Authors:  Alysse G Wurcel
Journal:  Ann Intern Med       Date:  2018-12-04       Impact factor: 25.391

Review 2.  Lessons learned in the abuse of pain-relief medication: a focus on healthcare costs.

Authors:  Laxmaiah Manchikanti; Mark V Boswell; Joshua A Hirsch
Journal:  Expert Rev Neurother       Date:  2013-05       Impact factor: 4.618

3.  Increases in Drug and Opioid Overdose Deaths--United States, 2000-2014.

Authors:  Rose A Rudd; Noah Aleshire; Jon E Zibbell; R Matthew Gladden
Journal:  MMWR Morb Mortal Wkly Rep       Date:  2016-01-01       Impact factor: 17.586

4.  Opiate Injection-associated Infective Endocarditis in the Southeastern United States.

Authors:  Lauren Hartman; Erin Barnes; Laura Bachmann; Katherine Schafer; James Lovato; Daniel Clark Files
Journal:  Am J Med Sci       Date:  2016-08-23       Impact factor: 2.378

5.  HIV Infection Linked to Injection Use of Oxymorphone in Indiana, 2014-2015.

Authors:  Philip J Peters; Pamela Pontones; Karen W Hoover; Monita R Patel; Romeo R Galang; Jessica Shields; Sara J Blosser; Michael W Spiller; Brittany Combs; William M Switzer; Caitlin Conrad; Jessica Gentry; Yury Khudyakov; Dorothy Waterhouse; S Michele Owen; Erika Chapman; Jeremy C Roseberry; Veronica McCants; Paul J Weidle; Dita Broz; Taraz Samandari; Jonathan Mermin; Jennifer Walthall; John T Brooks; Joan M Duwve
Journal:  N Engl J Med       Date:  2016-07-21       Impact factor: 91.245

6.  Surgical outcomes of infective endocarditis among intravenous drug users.

Authors:  Joon Bum Kim; Julius I Ejiofor; Maroun Yammine; Masahiko Ando; Janice M Camuso; Ilan Youngster; Sandra B Nelson; Arthur Y Kim; Serguei I Melnitchouk; James D Rawn; Thomas E MacGillivray; Lawrence H Cohn; John G Byrne; Thoralf M Sundt
Journal:  J Thorac Cardiovasc Surg       Date:  2016-03-12       Impact factor: 5.209

7.  Trends in Infective Endocarditis in California and New York State, 1998-2013.

Authors:  Nana Toyoda; Joanna Chikwe; Shinobu Itagaki; Annetine C Gelijns; David H Adams; Natalia N Egorova
Journal:  JAMA       Date:  2017-04-25       Impact factor: 56.272

8.  A Cost Analysis of Hospitalizations for Infections Related to Injection Drug Use at a County Safety-Net Hospital in Miami, Florida.

Authors:  Hansel Tookes; Chanelle Diaz; Hua Li; Rafi Khalid; Susanne Doblecki-Lewis
Journal:  PLoS One       Date:  2015-06-15       Impact factor: 3.240

9.  Trends in Black and White Opioid Mortality in the United States, 1979-2015.

Authors:  Monica J Alexander; Mathew V Kiang; Magali Barbieri
Journal:  Epidemiology       Date:  2018-09       Impact factor: 4.822

10.  Repeat Infective Endocarditis in Persons Who Inject Drugs: "Take Another Little Piece of my Heart".

Authors:  Glen Huang; Erin W Barnes; James E Peacock
Journal:  Open Forum Infect Dis       Date:  2018-11-16       Impact factor: 3.835

View more
  1 in total

1.  Natural Language Processing and Machine Learning to Identify People Who Inject Drugs in Electronic Health Records.

Authors:  David Goodman-Meza; Amber Tang; Babak Aryanfar; Sergio Vazquez; Adam J Gordon; Michihiko Goto; Matthew Bidwell Goetz; Steven Shoptaw; Alex A T Bui
Journal:  Open Forum Infect Dis       Date:  2022-09-12       Impact factor: 4.423

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.