Literature DB >> 23574801

Use of electronic health record data to identify skin and soft tissue infections in primary care settings: a validation study.

Pamela J Levine1, Miriam R Elman, Ravina Kullar, John M Townes, David T Bearden, Rowena Vilches-Tran, Ian McClellan, Jessina C McGregor.   

Abstract

BACKGROUND: Epidemiologic studies of skin and soft tissue infections (SSTIs) depend upon accurate case identification. Our objective was to evaluate the positive predictive value (PPV) of electronic medical record data for identification of SSTIs in a primary care setting.
METHODS: A validation study was conducted among primary care outpatients in an academic healthcare system. Encounters during four non-consecutive months in 2010 were included if any of the following were present in the electronic health record: International Classification of Diseases, Ninth Revision (ICD-9) code for an SSTI, Current Procedural Terminology (CPT) code for incision and drainage, or a positive wound culture. Detailed chart review was performed to establish presence and type of SSTI. PPVs and 95% confidence intervals (CI) were calculated among all encounters, initial encounters, and cellulitis/abscess cases.
RESULTS: Of the 731 encounters included, 514 (70.3%) were initial encounters and 448 (61.3%) were cellulitis/abscess cases. When the presence of an ICD-9 code, CPT code, or positive culture was used to identify SSTIs, 617 encounters were true positives, yielding a PPV of 84.4% [95% CI: 81.8-87.0%]. The PPV for using ICD-9 codes alone to identify SSTIs was 90.7% [95 % CI: 88.5-92.9%]. For encounters with cellulitis/abscess codes, the PPV was 91.5% [95% CI: 88.9-94.1%].
CONCLUSIONS: ICD-9 codes may be used to retrospectively identify SSTIs with a high PPV. Broadening SSTI case identification with microbiology data and CPT codes attenuates the PPV. Further work is needed to estimate the sensitivity of this method.

Entities:  

Mesh:

Year:  2013        PMID: 23574801      PMCID: PMC3637223          DOI: 10.1186/1471-2334-13-171

Source DB:  PubMed          Journal:  BMC Infect Dis        ISSN: 1471-2334            Impact factor:   3.090


Background

In recent years, ICD-9 diagnosis codes have been more commonly used for retrospective identification and classification of SSTIs from administrative and electronic health records (EHR).[1-6] Although this is a simple and straightforward method for case identification, these data are not collected for research purposes and may be subject to misclassification. While ICD-9 code validity has been assessed for other infections and diseases, there have been no reported evaluations of their use in the retrospective identification of SSTIs. The inherently subjective nature of various medical diagnoses combined with extrinsic factors such as human error or delays in data entry may affect the validity of these codes. The variability in ICD-9 code validity for identifying specific diagnoses depends upon the disease studied and clinical setting, as well as the specific algorithm used for case identification (i.e., which specific ICD-9 codes were used and if other clinical data were included).[7-10] Further, in scenarios where there is no definitive gold standard, the definition of ‘true’ disease may impact positive predictive value (PPV).[10] Consequently, it is crucial to assess the validity of using diagnosis codes to detect specific cases of interest, such as SSTI infections. Since valid methods of case ascertainment are critical to minimize the effects of misclassification in epidemiologic and outcomes studies of SSTIs, our primary objectives in this study were to (1) estimate the PPV of ICD-9 diagnosis codes for the retrospective identification of SSTIs in an outpatient primary care setting and (2) determine whether modifying the SSTI identification algorithm to include additional diagnostic indicators (i.e., wound culture and incision and drainage) would improve the precision of prediction results.

Methods

A validation study was conducted among ambulatory primary care patients at Oregon Health & Science University (OHSU). OHSU is a large academic healthcare system that includes two hospitals and numerous outpatient clinics throughout the greater Portland, Oregon metropolitan area; the OHSU healthcare system has over 750,000 patient encounters annually. The EpicCare EHR system (Epic Systems) is used for both inpatient and outpatient encounters throughout this system. For this study, encounters occurring in January, April, July or October 2010 in outpatient, non-specialty clinics of the Family Medicine, Internal Medicine and Pediatrics departments were eligible for inclusion; these months were selected to be representative of the calendar year and minimize seasonal or secular variations in the data. Patient encounters were included if any of the following criteria were present in the EHR: an SSTI ICD-9 diagnosis code [erysipelas: 035; carbuncle and furuncle: 680.x; cellulitis and abscess: 681.0, 681.00, 681.01, 681.10, 681.9, 682.x; acute lymphadenitis: 683.x; impetigo: 684.x; other local infections of skin and subcutaneous tissue: 686.x; other specified diseases of hair and hair follicles: 704.8], Current Procedural Terminology (CPT) code for incision and drainage (IND) [10060/1, 10080/1, 10120/1, 10140, 10160, 10180], or a positive wound or tissue microbiology culture. Encounters with missing electronic data were excluded. This study was approved by the Oregon Health & Science University institutional review board.

Patient identification and data collection

Data were electronically abstracted from the institution’s research data warehouse (RDW), a data repository that stores clinical, laboratory, and administrative data from the electronic medical record data systems. Study subjects were identified for inclusion through the RDW. For eligible patients, the following data were collected: demographics, SSTI ICD-9 codes, CPT codes for IND, wound/tissue culture results, temperature, encounter dates, and clinic location.

Data validation and supplemental data collection

A chart review-based validation was performed to confirm SSTI diagnoses (the classification of SSTIs based on detailed chart review is hereafter referred to as the “gold standard”). During their assessment, reviewers determined the appropriate diagnosis and associated ICD-9 diagnosis code for each encounter using physician notes to ascertain the existence of an SSTI and specific type of infection by reviewing clinician notes pertaining to the body site(s) of infection, presence of erythema, purulence, spontaneous drainage, crusting, discoloration, identification and number of nodules/papules, and follicular involvement. Patient characteristics and past medical history were also considered. In cases where incision and drainage was performed or spontaneous drainage was noted, the infection was considered to be purulent. Reviewers also used provider notes and other encounter data to determine whether the encounter was an initial or follow-up visit for the SSTI. If minimal documentation was present, the provider’s diagnosis (i.e., SSTI based on ICD-9 code) was considered valid. To reduce inter-rater variability, all reviewers received study-specific training and standardized documentation for assessing SSTI diagnoses were developed based upon clinical infectious disease texts.[11-14] Reviewers extracted data into a Microsoft Access form (2007, Microsoft Corporation) to standardize the collection of data and the information used to confirm the diagnosis. Medical records were reviewed independently by at least two members of the study team to further improve reliability. If reviewers disagreed, a third reviewer served as the tie-breaker. Data extracted during the detailed chart review were stored in a Microsoft Access database.

Data analysis

We created two algorithms for the identification of any SSTI and one algorithm for the identification of only cellulitis/abscess using EHR data. For each algorithm, the PPV was calculated using the chart review-based SSTI diagnosis as the gold standard. The three different algorithms were as follows: (1) presence of any SSTI ICD-9 [035, 680–684, 686.x, 704.8] or IND CPT code [10060/1, 10080/1, 10120/1, 10140, 10160, 10180], or a positive wound culture; (2) presence of any SSTI ICD-9 code; (3) presence of SSTI ICD-9 codes for cellulitis/abscess [681.00, 681.0, 681.1, 681.10, 681.9, 682.x]. For cellulitis/abscess diagnoses, an additional PPV was calculated where true positives were both correctly coded and body-site specific (e.g., a leg abscess confirmed by chart review was correctly identified with the ICD-9 code specifying cellulitis and abscess of leg – 682.6). Table 1 describes the different SSTI identification algorithms for which PPVs were calculated and the criteria used to identify true positives. All PPVs were calculated using both the total study sample and initial (i.e., not follow-up) encounters only. Descriptive statistics were calculated to describe demographic information such as age and gender, initial visit status, and encounter department. All data were analyzed with SAS (version 9.2, SAS Corporation, Cary NC).
Table 1

Description of skin and soft tissue infection identification algorithms evaluated

Test criteriaDefinition of true positive
Any of the following criteria:
Any SSTI present
 SSTI ICD-9 code
 Incision and drainage CPT code
 Positive wound culture
SSTI ICD-9 code
Any SSTI present
Cellulitis/Abscess ICD-9 code
Cellulitis and/or abscess present
Cellulitis/Abscess ICD-9 code, body site specificCellulitis and/or abscess present at body site indicated by ICD-9 code

Note: SSTI, skin and soft tissue infection; ICD-9, International Classification of Diseases, Ninth Revision; CPT, current procedural terminology.

Description of skin and soft tissue infection identification algorithms evaluated Note: SSTI, skin and soft tissue infection; ICD-9, International Classification of Diseases, Ninth Revision; CPT, current procedural terminology.

Results

Through the electronic data warehouse, 737 of 46,045 encounters were identified that met all inclusion criteria. After chart review, 6 were excluded due to missing data in the EHR. Thus 731 encounters were included in the final analysis dataset. Of these, 54.4% were for female patients and the mean patient age was 39.1 years (standard deviation, ±23.7 years); 70.3% of the encounters were the initial visit for diagnosis and treatment of the SSTI (Table 2). Family medicine had the largest proportion of visits (61.4%) of the three outpatient departments and 13.2% of those visits were in patients under age 18. Cellulitis/abscess was the most common SSTI (68.3%) identified through chart review, followed by folliculitis (8.9%) and impetigo (8.9%), carbuncle/furuncle (6.0%), and other SSTIs (7.8%). Of the 100 wound cultures performed among the 617 SSTIs confirmed through chart review, 66 (66.0%) were positive cultures. S. aureus was the most frequently isolated pathogen. Among initial encounters for SSTIs, antibiotic treatment alone was prescribed in 68.4% of visits, IND alone was performed in 3.9%, IND and antibiotics were given in 11.9%, and neither IND nor antibiotic treatment was given in 15.8% of encounters. Trimethoprim/sulfamethoxazole (28.0%), cephalexin (19.2%) and mupirocin (16.2) were the most commonly prescribed antibiotics.
Table 2

Patient demographics and encounter characteristics

 Family medicine
Internal medicine
Pediatrics
Overall
(n=449)(n=163)(n=119)(n=731)
Age, mean years ± SD
42.9 ± 21.0
53.1 ± 15.0
5.5 ± 5.4
39.1 ± 23.7
Female sex
257 (57.2)
88 (54.0)
53 (44.5)
398 (54.4)
Race
 
 
 
 
 White
413 (92.0)
145 (89.0)
93 (78.2)
651 (89.1)
 Black
11 (2.4)
11 (6.7)
7 (5.9)
29 (4.0)
 Asian/Pacific Islander
13 (2.9)
2 (1.2)
11 (9.2)
26 (3.6)
 Other
5 (1.1)
4 (2.5)
6 (5.0)
15 (2.1)
 Unknown/not reported
7 (1.6)
1 (0.6)
2 (1.7)
10 (1.4)
Hispanic ethnicity
8 (1.8)
1 (0.6)
26 (21.8)
35 (4.8)
Initial encounter for SSTI
290 (64.6)
115 (70.6)
109 (91.6)
514 (70.3)
Encounter month
 
 
 
 
 January
116 (25.8)
27 (16.6)
27 (22.7)
170 (23.3)
 April
98 (21.8)
40 (24.5)
42 (35.3)
180 (24.6)
 July
116 (25.8)
48 (29.4)
30 (25.2)
194 (26.5)
 October
119 (26.5)
48 (29.4)
20 (16.8)
187 (25.6)
ICD-9 code for SSTI
449 (100.0)
163 (100.0)
119 (100.0)
731 (100.0)
CPT code for IND
61 (13.6)
11 (6.7)
4 (3.4)
76 (10.4)
Positive wound culture
62 (13.8)
16 (9.8)
25 (21.0)
103 (14.1)
SSTI Identification Criteria
 
 
 
 
 ICD-9 or CPT code or positive culture
449 (100.0)
163 (100.0)
119 (100.0)
731 (100.0)
 ICD-9 SSTI code only
412 (91.8)
147 (90.2)
110 (92.4)
669 (91.5)
 Cellulitis/Abscess ICD-9 code
305 (67.9)
101 (62.0)
42 (35.3)
448 (61.3)
 Cellulitis/Abscess ICD-9 code, body site specific267 (59.5)86 (52.8)35 (29.4)388 (53.1)

Note: Data are no. (%), unless otherwise indicated. The “Other” race category includes Native Americans, Alaskan Natives, and individuals reporting multiple races.

SD, standard deviation, SSTI, Skin and soft tissue infection,ICD-9, International Classification of Diseases, 9th Revision, CPT, Current Procedure Terminology, IND, Incision and drainage.

Patient demographics and encounter characteristics Note: Data are no. (%), unless otherwise indicated. The “Other” race category includes Native Americans, Alaskan Natives, and individuals reporting multiple races. SD, standard deviation, SSTI, Skin and soft tissue infection,ICD-9, International Classification of Diseases, 9th Revision, CPT, Current Procedure Terminology, IND, Incision and drainage. “True” SSTIs were confirmed in 617 of the encounters, a prevalence of 1.3%. Table 3 presents the positive predictive value for each of the SSTI identification algorithms calculated among all encounters and among only initial encounters for the SSTI. The highest PPV was for detecting cellulitis/abscess based on ICD-9 codes at (PPV = 91.5%; 95% CI: 88.9-94.1%), and the lowest was for the identification cellulitis/abscess specific to body site (PPV = 52.6%; 95% CI: 47.6-57.6%). PPVs were lower overall when the SSTI identification algorithm was restricted to initial visits.
Table 3

Positive predictive values for each skin and soft tissue infection identification algorithm

 
Initial visits
All visits
SSTI identification criteriaTrue positives/encountersPPV (95% CI)True positives/encountersPPV (95% CI)
ICD-9 or CPT code or positive culture
413/514
80.4 (76.9-83.8)
617/731
84.4 (81.8-87.0)
ICD-9 SSTI code only
404/455
88.8 (85.9-91.7)
607/669
90.7 (88.5-92.9)
Cellulitis/Abscess ICD-9 code
228/254
89.8 (086.0-93.5)
410/448
91.5 (88.9-94.1)
Cellulitis/Abscess ICD-9 code, body site specific116/21454.2 (47.5-60.9)204/38852.6 (47.6-57.6)

Note: SSTI, skin and soft tissue infection; ICD-9, International Classification of Diseases, Ninth Revision; CPT, current procedural terminology; CI, confidence interval.

Positive predictive values for each skin and soft tissue infection identification algorithm Note: SSTI, skin and soft tissue infection; ICD-9, International Classification of Diseases, Ninth Revision; CPT, current procedural terminology; CI, confidence interval.

Discussion

This study demonstrated that ICD-9 codes may be used to identify SSTIs in primary care outpatient settings with a high PPV. While we had hypothesized that broadening our SSTI identification algorithm to utilize additional clinical data (i.e., wound cultures and procedure codes) would improve the performance of our algorithm, of the 61 additional encounters included with these expanded criteria, only 10 were true SSTIs. Consequently, inclusion of these data resulted in a reduction in PPV compared to an algorithm based only on ICD-9 codes. Our study is the first to assess the PPV for EHR-based algorithms for the identification of SSTIs in a primary care outpatient setting. An earlier study by Tracy et al. evaluated the PPV of clinical cultures positive for S. aureus for the identification of non-invasive S. aureus infections in a Veterans Affairs patient population. While this study noted a high PPV for SSTIs (PPV = 95%; 95% CI: 86-98%), it is important to note this approach does not detect uncultured infections [15]. In our primary care patient sample, only 36 (5%) of patients had a positive culture for S. aureus. Thus, depending on the research question, an ICD-9 based method of case identification may more appropriately capture cases of SSTIs for study. The range of PPVs observed across the different algorithms illustrates the importance of validation. In this study, we measured high PPVs using ICD-9 codes to detect SSTIs which means in turn that few patients are likely to be misclassified as an SSTI case. Still, because our study did not include patients without SSTI ICD-9 codes, we were unable to measure sensitivity. As a result, the false negative rate (i.e., misclassifying true SSTIs as non-cases) by applying an algorithm based on ICD-9 codes remains unknown. It should also be noted that, as PPV varies with prevalence, this validation study may not be generalizable to other patient populations. Also, in this patient population, providers coded infections themselves within the EpicCare EHR system and thus PPV may vary in settings where providers do not perform the coding or in which the method of coding (e.g., the EHR system) varies. Our study also did not address more complicated/severe infections such as diabetic foot infections, infected pressure ulcers, or surgical site infections. Finally, given that this was a retrospective study, the gold standard was based upon chart review and thus limited by the level of detail in the provider’s notes. Of note, our study revealed that after evaluation of treatment patterns for true SSTIs, 33.0% of encounters (15.8% of initial encounters) received no antibiotic treatment or IND. While smaller, less severe SSTIs may not require medical intervention, the relatively large proportion of untreated patients may reflect the inclusion of follow-up visits in this study.

Conclusion

This study demonstrates that algorithms which use ICD-9 codes to detect SSTIs can achieve a high PPV in ambulatory primary care settings. While the number of SSTI cases that would not be detected by this approach was unmeasured, the ICD-9 based SSTI identification method would likely capture those patients with a single diagnosis for their visit. Thus, these diagnosis codes may be useful in facilitating internal process improvement and quality initiatives as well as future studies exploring both the epidemiology and outcomes associated with SSTIs.

Abbreviations

CI: Confidence intervals; CPT: Current procedural terminology; EHR: Electronic health record; ICD-9: International classification of diseases- Ninth Revision; IND: Incision and drainage; OHSU: Oregon Health & Science University; PPV: Positive predictive value; RDW: Research data warehouse; SSTI: Skin and soft tissue infections.

Competing interests

R.K. is a member of the speakers’ bureau for Cubist Pharmaceuticals. All other authors have no other potential competing interests to report.

Authors’ contributions

PL, JMT, DTB, and JCM contributed to the study’s inception and design. PL, MRE, and JCM drafted the manuscript and shared in data collection, interpretation, and analysis. MRE provided statistical analysis. RK, RVT, and IM significantly contributed to data collection and interpretation. All authors participated in critical revisions as well as read and approved the final manuscript.

Pre-publication history

The pre-publication history for this paper can be accessed here: http://www.biomedcentral.com/1471-2334/13/171/prepub
  11 in total

1.  Changes in community-associated methicillin-resistant Staphylococcus aureus skin and soft tissue infections presenting to the pediatric emergency department: comparing 2003 to 2008.

Authors:  Mia L Karamatsu; Andrea W Thorp; Lance Brown
Journal:  Pediatr Emerg Care       Date:  2012-02       Impact factor: 1.454

2.  The validity of International Classification of Diseases, Ninth Revision, Clinical Modification diagnosis codes for identifying patients hospitalized for COPD exacerbations.

Authors:  Brian D Stein; Adriana Bautista; Glen T Schumock; Todd A Lee; Jeffery T Charbeneau; Diane S Lauderdale; Edward T Naureckas; David O Meltzer; Jerry A Krishnan
Journal:  Chest       Date:  2011-07-14       Impact factor: 9.410

3.  Predictive ability of positive clinical culture results and International Classification of Diseases, Ninth Revision, to identify and classify noninvasive Staphylococcus aureus infections: a validation study.

Authors:  LaRee A Tracy; Jon P Furuno; Anthony D Harris; Mary Singer; Patricia Langenberg; Mary-Claire Roghmann
Journal:  Infect Control Hosp Epidemiol       Date:  2010-07       Impact factor: 3.254

4.  Epidemiology and outcomes of complicated skin and soft tissue infections in hospitalized patients.

Authors:  Marcus J Zervos; Katherine Freeman; Lien Vo; Nadia Haque; Hiren Pokharna; Monika Raut; Myoung Kim
Journal:  J Clin Microbiol       Date:  2011-11-23       Impact factor: 5.948

5.  Accuracy of administrative billing codes to detect urinary tract infection hospitalizations.

Authors:  Joel S Tieder; Matthew Hall; Katherine A Auger; Paul D Hain; Karen E Jerardi; Angela L Myers; Suraiya S Rahman; Derek J Williams; Samir S Shah
Journal:  Pediatrics       Date:  2011-07-18       Impact factor: 7.124

6.  Epidemiology of dermatitis and skin infections in United States physicians' offices, 1993-2005.

Authors:  Daniel J Pallin; Janice A Espinola; Donald Y Leung; David C Hooper; Carlos A Camargo
Journal:  Clin Infect Dis       Date:  2009-09-15       Impact factor: 9.079

7.  Management of skin and soft tissue infections in community practice before and after implementing a "best practice" approach: an Iowa Research Network (IRENE) intervention study.

Authors:  Jeanette M Daly; Barcey T Levy; John W Ely; Kristi Swanson; George R Bergus; Gerald J Jogerst; Tara C Smith
Journal:  J Am Board Fam Med       Date:  2011 Sep-Oct       Impact factor: 2.657

8.  Validity of ICD-9-CM coding for identifying incident methicillin-resistant Staphylococcus aureus (MRSA) infections: is MRSA infection coded as a chronic disease?

Authors:  Marin L Schweizer; Michael R Eber; Ramanan Laxminarayan; Jon P Furuno; Kyle J Popovich; Bala Hota; Michael A Rubin; Eli N Perencevich
Journal:  Infect Control Hosp Epidemiol       Date:  2011-02       Impact factor: 3.254

9.  Comparative effectiveness of antibiotic treatment strategies for pediatric skin and soft-tissue infections.

Authors:  Derek J Williams; William O Cooper; Lisa A Kaltenbach; Judith A Dudley; David L Kirschke; Timothy F Jones; Patrick G Arbogast; Marie R Griffin; C Buddy Creech
Journal:  Pediatrics       Date:  2011-08-15       Impact factor: 7.124

10.  Positive predictive value of ICD-9-CM codes to detect acute exacerbation of COPD in the emergency department.

Authors:  Adit A Ginde; Chu-Lin Tsai; Phillip G Blanc; Carlos A Camargo
Journal:  Jt Comm J Qual Patient Saf       Date:  2008-11
View more
  10 in total

1.  Skin and Soft Tissue Infection in People Living With Human Immunodeficiency Virus in a Large, Urban, Public Healthcare System in Houston, Texas, 2009-2014.

Authors:  Vagish Hemmige; Cesar A Arias; Siavash Pasalar; Thomas P Giordano
Journal:  Clin Infect Dis       Date:  2020-04-15       Impact factor: 9.079

2.  Strategies for handling missing clinical data for automated surgical site infection detection from the electronic health record.

Authors:  Zhen Hu; Genevieve B Melton; Elliot G Arsoniadis; Yan Wang; Mary R Kwaan; Gyorgy J Simon
Journal:  J Biomed Inform       Date:  2017-03-16       Impact factor: 6.317

Review 3.  National Public Health Burden Estimates of Endocarditis and Skin and Soft-Tissue Infections Related to Injection Drug Use: A Review.

Authors:  Isaac See; Runa H Gokhale; Andrew Geller; Maribeth Lovegrove; Asher Schranz; Aaron Fleischauer; Natalie McCarthy; James Baggs; Anthony Fiore
Journal:  J Infect Dis       Date:  2020-09-02       Impact factor: 5.226

4.  Data-driven discovery of seasonally linked diseases from an Electronic Health Records system.

Authors:  Rachel D Melamed; Hossein Khiabanian; Raul Rabadan
Journal:  BMC Bioinformatics       Date:  2014-05-16       Impact factor: 3.169

5.  Applying Machine Learning Across Sites: External Validation of a Surgical Site Infection Detection Algorithm.

Authors:  Ying Zhu; Gyorgy J Simon; Elizabeth C Wick; Yumiko Abe-Jones; Nader Najafi; Adam Sheka; Roshan Tourani; Steven J Skube; Zhen Hu; Genevieve B Melton
Journal:  J Am Coll Surg       Date:  2021-04-05       Impact factor: 6.532

6.  Gender Differences Among Patients Hospitalized With Cirrhosis in the United States.

Authors:  Jessica B Rubin; Vinay Sundaram; Jennifer C Lai
Journal:  J Clin Gastroenterol       Date:  2020-01       Impact factor: 3.174

7.  Consensus Current Procedural Terminology Code Definition of Source Control for Sepsis.

Authors:  Shimena R Li; Robert M Handzel; Daniel Tonetti; Jason Kennedy; Katherine Shapiro; Matthew R Rosengart; Daniel E Hall; Christopher Seymour; Edith Tzeng; Katherine M Reitz
Journal:  J Surg Res       Date:  2022-03-21       Impact factor: 2.417

8.  Development and validation of a heart failure with preserved ejection fraction cohort using electronic medical records.

Authors:  Yash R Patel; Jeremy M Robbins; Katherine E Kurgansky; Tasnim Imran; Ariela R Orkaby; Robert R McLean; Yuk-Lam Ho; Kelly Cho; J Michael Gaziano; Luc Djousse; David R Gagnon; Jacob Joseph
Journal:  BMC Cardiovasc Disord       Date:  2018-06-28       Impact factor: 2.298

9.  Decreasing Incidence of Skin and Soft Tissue Infections With a Seasonal Pattern at an Academic Medical Center, 2006-2014.

Authors:  Ethan Morgan; Robert S Daum; Michael Z David
Journal:  Open Forum Infect Dis       Date:  2016-08-30       Impact factor: 3.835

10.  Automated Detection of Postoperative Surgical Site Infections Using Supervised Methods with Electronic Health Record Data.

Authors:  Zhen Hu; Gyorgy J Simon; Elliot G Arsoniadis; Yan Wang; Mary R Kwaan; Genevieve B Melton
Journal:  Stud Health Technol Inform       Date:  2015
  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.