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2.
J Hosp Med ; 14(8): 474-481, 2019 08.
Article in English | MEDLINE | ID: mdl-31386613

ABSTRACT

BACKGROUND: While medical complexity is associated with pediatric readmission risk, less is known about how increases in medical complexity during hospitalization affect readmission risk. METHODS: We conducted a five-year retrospective, case-control study of pediatric hospitalizations at a tertiary care children's hospital. Cases with a 30-day unplanned readmission were matched to controls based on admission seasonality and distance from the hospital. Complexity variables included the number of medications prescribed at discharge, medical technology, and the need for home healthcare services. Change in medical complexity variables included new complex chronic conditions and new medical technology. We estimated odds of 30-day unplanned readmission using adjusted conditional logistic regression. RESULTS: Of 41,422 eligible index hospitalizations, we included 595 case and 595 control hospitalizations. Complexity: Polypharmacy after discharge was common. In adjusted analyses, being discharged with ≥2 medications was associated with higher odds of readmission compared with being discharged without medication; children with ≥5 discharge medications had a greater than four-fold higher odds of readmission. Children assisted by technology had higher odds of readmission compared with children without technology assistance. Change in complexity: New diagnosis of a complex chronic condition (Adjusted Odds Ratio (AOR) = 1.75; 1.11-2.75) and new technology (AOR = 1.84; 1.09-3.10) were associated with higher risk of readmission when adjusting for patient characteristics. However, these associations were not statistically significant when adjusting for length of stay. CONCLUSION: Polypharmacy and use of technology at discharge pose a substantial readmission risk for children. However, added technology and new complex chronic conditions do not increase risk when accounting for length of stay.


Subject(s)
Chronic Disease/therapy , Comorbidity , Hospitals, Pediatric , Patient Readmission/statistics & numerical data , Polypharmacy , Adolescent , Child , Child, Preschool , Female , Hospitalization , Humans , Infant , Infant, Newborn , Length of Stay/statistics & numerical data , Longitudinal Studies , Male , Retrospective Studies , Self-Help Devices
3.
Health Serv Res ; 53(3): 1992-2004, 2018 06.
Article in English | MEDLINE | ID: mdl-28670682

ABSTRACT

OBJECTIVE: To design and test the validity of a method to identify homelessness among Medicaid enrollees using mailing address data. DATA SOURCES/STUDY SETTING: Enrollment and claims data on Medicaid expansion enrollees in Hennepin and Ramsey counties who also provided self-reported information on their current housing situation in a psychosocial needs assessment. STUDY DESIGN: Construction of address-based indicators and comparison with self-report data. PRINCIPAL FINDINGS: Among 1,677 enrollees, 427 (25 percent) self-reported homelessness, of whom 328 (77 percent) had at least one positive address indicator. Depending on the type of addresses included in the indicator, sensitivity to detect self-reported homelessness ranged from 30 to 76 percent and specificity from 79 to 97 percent. CONCLUSIONS: An address-based indicator can identify a large proportion of Medicaid enrollees who are experiencing homelessness. This approach may be of interest to researchers, states, and health systems attempting to identify homeless populations.


Subject(s)
Ill-Housed Persons/statistics & numerical data , Medicaid/organization & administration , Medicaid/statistics & numerical data , Postal Service/statistics & numerical data , Humans , Insurance Claim Review , Minnesota , United States , Urban Population
4.
Biomed Res Int ; 2017: 1467056, 2017.
Article in English | MEDLINE | ID: mdl-28785574

ABSTRACT

BACKGROUND: Optimal treatment for localized prostate cancer (LPC) is controversial. We assessed the effects of personality, specialists seen, and involvement of spouse, family, or friends on treatment decision/decision-making qualities. METHODS: We surveyed a population-based sample of men ≤ 75 years with newly diagnosed LPC about treatment choice, reasons for the choice, decision-making difficulty, satisfaction, and regret. RESULTS: Of 160 men (71 black, 89 white), with a mean age of 61 (±7.3) years, 59% chose surgery, 31% chose radiation, and 10% chose active surveillance (AS)/watchful waiting (WW). Adjusting for age, race, comorbidity, tumor risk level, and treatment status, men who consulted friends during decision-making were more likely to choose curative treatment (radiation or surgery) than WW/AS (OR = 11.1, p < 0.01; 8.7, p < 0.01). Men who saw a radiation oncologist in addition to a urologist were more likely to choose radiation than surgery (OR = 6.0, p = 0.04). Men who consulted family or friends (OR = 2.6, p < 0.01; 3.7, p < 0.01) experienced greater decision-making difficulty. No personality traits (pessimism, optimism, or faith) were associated with treatment choice/decision-making quality measures. CONCLUSIONS: In addition to specialist seen, consulting friends increased men's likelihood of choosing curative treatment. Consulting family or friends increased decision-making difficulty.


Subject(s)
Clinical Decision-Making , Personality , Prostatic Neoplasms/psychology , Social Support , Demography , Humans , Male , Men , Middle Aged
5.
J Am Board Fam Med ; 30(3): 288-297, 2017.
Article in English | MEDLINE | ID: mdl-28484061

ABSTRACT

BACKGROUND: Controversy surrounds treatment for localized prostate cancer (LPC). OBJECTIVES: To assess men's localized prostate cancer (LPC) knowledge and its association with decision-making difficulty, satisfaction and regret. METHODS: Population-based sample of 201 men (104 white, 97 black), ≤ 75 years with newly diagnosed LPC completed a self-administered survey. RESULTS: Mean age was 61(±7.6) years; two-thirds had less than a Bachelor's degree. Mean LPC knowledge was low, 5.87 (±2.53, maximum score 11). More than a third of men who received surgery or radiation did not know about serious long-term treatment side effects. Fewer than half of the men correctly answered comparative side effect and survival benefit questions between surgery and radiation. Knowledge gaps were greatest among black men, men with lower education, single men. Tumor aggressiveness (i.e. PSA level, Gleason score) and treatment choice were not associated with knowledge. Knowledge was not associated with decisional satisfaction or regret. However, greater knowledge was associated with greater decision-making difficulty (P = .018). CONCLUSIONS: Significant LPC knowledge gaps existed across groups, with greater knowledge gaps among black men. The association of decision-making difficulty with knowledge was independent of race. Better patient education is needed, but may not alleviate men's decision-making difficulty due to inherent scientific uncertainty.


Subject(s)
Decision Making , Health Knowledge, Attitudes, Practice , Patient Participation/psychology , Patient Preference/psychology , Prostatic Neoplasms/therapy , Adult , Black or African American/psychology , Aged , Clinical Decision-Making , Cross-Sectional Studies , Emotions , Health Care Surveys , Humans , Logistic Models , Male , Michigan , Middle Aged , Patient Satisfaction , Prostatic Neoplasms/ethnology , Prostatic Neoplasms/psychology , Uncertainty , White People/psychology
6.
Fam Pract ; 34(1): 90-97, 2017 02.
Article in English | MEDLINE | ID: mdl-28034917

ABSTRACT

BACKGROUND: Active surveillance (AS) is recognized as a reasonable treatment option for low-risk localized prostate cancer (LPC) but continues to be chosen by a minority of men. To date, limited data are available regarding reasons why men with low-risk LPC adopt AS. PURPOSE: The aim of this study is to better understand conceptualizations, experiences and reasons why men with low-risk LPC and their partners adopt AS. METHODS: We conducted five focus groups (FGs), three among men with low-risk LPC who had chosen AS and two with their partners. FGs were video/audio recorded, transcribed and analysed using qualitative thematic analysis. RESULTS: A total of 12 men and 6 partners (all women) participated in FG discussions. The most common reasons for choosing AS were seeing the LPC as 'small' or 'low grade' without need for immediate treatment and trusting their physician's AS recommendation. The most common concerns about AS were perceived unreliability of prostate specific antigen, pain associated with prostate biopsies and potential cancer progression. Partners saw themselves as very involved in their husbands' treatment decision-making process, more than men acknowledged them to be. Multiple terms including 'watchful waiting' were used interchangeably with AS. There appeared to be a lack of understanding that AS is not simply 'doing nothing' but is actually a recognized management option for low-risk LPC. CONCLUSIONS: Emphasizing the low risk of a man's LPC and enhancing physician trust may increase acceptability of AS. Standardizing terminology and presenting AS as a reasonable and recognized management option may also help increase its adoption.


Subject(s)
Patient Acceptance of Health Care/psychology , Patient Preference/psychology , Prostatic Neoplasms/psychology , Prostatic Neoplasms/therapy , Spouses/psychology , Watchful Waiting , Aged , Biopsy/adverse effects , Decision Making , Disease Progression , Female , Focus Groups , Humans , Male , Middle Aged , Pain/etiology , Prostate-Specific Antigen/blood , Prostatic Neoplasms/blood , Prostatic Neoplasms/pathology , Qualitative Research , Reproducibility of Results , Risk Factors , Trust
7.
Am J Manag Care ; 22(6): 427-31, 2016 06.
Article in English | MEDLINE | ID: mdl-27355810

ABSTRACT

OBJECTIVES: With insurance enrollment greater than expected under the Affordable Care Act, uncertainty about the availability and timeliness of healthcare services for newly insured individuals has increased. We examined primary care appointment availability and wait times for new Medicaid and privately insured patients before and after Medicaid expansion in Michigan. STUDY DESIGN: Simulated patient ("secret shopper") study. METHODS: Extended follow-up of a previously reported simulated patient ("secret shopper") study assessing accessibility of routine new patient appointments in a stratified proportionate random sample of Michigan primary care practices before versus 4, 8, and 12 months after Medicaid expansion. RESULTS: During the study period, approximately 600,000 adults enrolled in Michigan's Medicaid expansion program, representing 57% of the previously uninsured nonelderly adult population. One year after expansion, we found that appointment availability remained increased by 6 percentage points for new Medicaid patients (95% CI, 1.6-11.1) and decreased by 2 percentage points for new privately insured patients (95% CI, -0.5 to -3.8). Over the same period, the proportion of appointments scheduled with nonphysician providers (nurse practitioners or physician assistants) increased from 8% to 21% of Medicaid appointments (95% CI, 5.6-20.2) and from 11% to 19% of private-insurance appointments (95% CI, 1.3-14.1). Median wait times remained stable for new Medicaid patients and increased slightly for new privately insured patients, both remaining within 2 weeks. CONCLUSIONS: During the first year following Medicaid expansion in Michigan, appointment availability for new Medicaid patients increased, a greater proportion of appointments could be obtained with nonphysician providers, and wait times remained within 2 weeks.


Subject(s)
Appointments and Schedules , Health Services Accessibility/statistics & numerical data , Medicaid/organization & administration , Nurse Practitioners/supply & distribution , Outcome Assessment, Health Care , Primary Health Care/organization & administration , Female , Health Care Reform , Health Services Accessibility/economics , Humans , Insurance Coverage/economics , Insurance Coverage/statistics & numerical data , Male , Michigan , Nurse Practitioners/economics , Patient Protection and Affordable Care Act , Patient Simulation , Risk Assessment , United States , Waiting Lists
8.
J Natl Cancer Inst ; 108(6): djv436, 2016 Jun.
Article in English | MEDLINE | ID: mdl-26917630

ABSTRACT

BACKGROUND: Cancer prevention and screening guidelines are ideally suited to the task of providing high-quality benefit-harm information that informs clinical practice. We systematically examined how US guidelines present benefits and harms for recommended cancer prevention and screening interventions. METHODS: We included cancer screening and prevention recommendations from: 1) the United States Preventive Services Task Force, 2) the American Cancer Society, 3) the American College of Physicians, 4) the National Comprehensive Cancer Network, and 5) other US guidelines within the National Guidelines Clearinghouse. Searches took place November 20, 2013, and January 1, 2014, and updates were reviewed through July 1, 2015. Two coders used an abstraction form to code information about benefits and harms presented anywhere within a guideline document, including appendices. The primary outcome was each recommendation's benefit-harm "comparability" rating, based on how benefits and harms were presented. Recommendations presenting absolute effects for both benefits and harms received a "comparable" rating. Other recommendations received an incomplete rating or an asymmetric rating based on prespecified criteria. RESULTS: Fifty-five recommendations for using interventions to prevent or detect breast, prostate, colon, cervical, and lung cancer were identified among 32 guidelines. Thirty point nine percent (n = 17) received a comparable rating, 14.5% (n = 8) received an incomplete rating, and 54.5% (n = 30) received an asymmetric rating. CONCLUSIONS: Sixty-nine percent of cancer prevention and screening recommendation statements either did not quantify benefits and harms or presented them in an asymmetric manner. Improved presentation of benefits and harms in guidelines would better ensure that clinicians and patients have access to the information required for making informed decisions.


Subject(s)
Early Detection of Cancer , Mass Screening , Neoplasms/prevention & control , Practice Guidelines as Topic/standards , Primary Prevention/methods , Decision Making , Early Detection of Cancer/adverse effects , Early Detection of Cancer/statistics & numerical data , Humans , Mass Screening/adverse effects , Mass Screening/statistics & numerical data , Neoplasms/diagnosis , Primary Prevention/trends , United States/epidemiology
9.
Health Aff (Millwood) ; 34(8): 1399-406, 2015 Aug.
Article in English | MEDLINE | ID: mdl-26202057

ABSTRACT

The Affordable Care Act expands health insurance coverage to millions of Americans, but the availability of health care services for the newly insured population remains uncertain. We conducted a simulated patient (or "secret shopper") study to assess primary care appointment availability and wait times for new patients with Medicaid or private insurance before and after implementation of Michigan's Medicaid expansion in 2014. The expansion, which was made possible through a section 1115 waiver, has a unique requirement that new beneficiaries must be seen by a primary care provider within 60-90 days of enrollment. During a period of rapid coverage expansion in Michigan, we found that appointment availability increased 6 percentage points for new Medicaid patients and decreased 2 percentage points for new privately insured patients, compared to availability before the expansion. Wait times remained stable, at 1-2 weeks for both groups. Further research is needed to determine whether access to primary care for newly insured patients will endure over time.


Subject(s)
Medicaid/statistics & numerical data , Primary Health Care/statistics & numerical data , Appointments and Schedules , Health Care Reform , Health Services Accessibility/statistics & numerical data , Humans , Insurance Coverage , Medicaid/economics , Michigan , Patient Protection and Affordable Care Act/economics , Patient Protection and Affordable Care Act/statistics & numerical data , Primary Health Care/economics , United States
10.
Clin Orthop Relat Res ; 473(8): 2479-86, 2015 Aug.
Article in English | MEDLINE | ID: mdl-25518806

ABSTRACT

BACKGROUND: Available studies disagree regarding the influence of patient sex on mortality and complications after spine surgery. We sought to conduct a systematic review and pool the results of existing research to better understand this issue. QUESTIONS/PURPOSES: We performed a systematic review to address two questions: (1) Does sex (male versus female) influence mortality after spine surgery? (2) Does sex impact the development of postoperative complications after spine surgery? METHODS: This systematic review was performed through a query of PubMed using a structured search algorithm. Additional queries of Embase, SCOPUS, Web of Science, and the tables of contents of orthopaedic and neurosurgical journals were also conducted using search terms such as "sex factors", "male or female", "risk factors", and "spine surgery". Selected papers were independently abstracted by three of the authors (AJS, ENR, EIW) and pooling was performed. Our literature search returned 720 studies, of which 99 underwent full review. Of these, 50 were selected for final abstraction. The Cochrane Q test was used to assess study heterogeneity; significant study heterogeneity was present and so a random-effects model was used. A Harbord test was used to evaluate for the presence of publication bias; this analysis found no statistically significant evidence of publication bias. RESULTS: Males were at increased odds of mortality after spine surgery (odds ratio [OR], 1.63; 95% confidence interval [CI], 1.35-1.97; p<0.001). No differences between the sexes were identified for the odds of complications (OR, 1.04; 95% CI, 0.95-1.13; p=0.42). CONCLUSIONS: Our results determined that males were at elevated odds of mortality but not of complications after spine surgery. These results should be used to inform preoperative discussion and decision-making at the time of surgical consent. Future work should be directed at determining the underlying factors responsible for increased mortality among males and prospective studies specifically designed to evaluate sex-based differences in outcomes after spine surgery. LEVEL OF EVIDENCE: Level III, therapeutic study.


Subject(s)
Health Status Disparities , Orthopedic Procedures/adverse effects , Orthopedic Procedures/mortality , Postoperative Complications/mortality , Spine/surgery , Female , Humans , Male , Odds Ratio , Risk Assessment , Risk Factors , Sex Factors , Treatment Outcome
11.
J Am Acad Child Adolesc Psychiatry ; 53(11): 1225-33, 1233.e1-9, 2014 Nov.
Article in English | MEDLINE | ID: mdl-25440312

ABSTRACT

OBJECTIVE: Atypical development of frontal-striatal-thalamic circuitry (FSTC) has been hypothesized to underlie the early course of obsessive-compulsive disorder (OCD); however, the development of FSTC white matter tracts remains to be studied in young patients. METHOD: To address this gap, we scanned 36 patients with pediatric OCD compared to 27 healthy controls, aged 8 to 19 years, with diffusion tensor imaging (DTI) to measure fractional anisotropy (FA), an index of white matter coherence. Tract-based spatial statistics (TBSS) were used to test differential effects of age on FA, across the whole brain, in those with OCD compared to healthy youth, followed by analyses in a priori regions of interest (anterior corpus callosum, anterior cingulum bundle, and anterior limb of the internal capsule [ALIC]) to further characterize developmental differences between groups. RESULTS: Patients with OCD showed more pronounced age-related increases in FA than controls in regions of interest, as well as several other white matter tracts. In patients, greater FA in anterior cingulum bundle correlated with more severe symptoms after controlling for age. CONCLUSIONS: Our findings support theories of atypical FSTC maturation in pediatric OCD by providing the first evidence for altered trajectories of white matter development in anterior corpus callosum, anterior cingulum bundle, and ALIC in young patients. Steeper age-related increases of FA in these and other select white matter tracts in OCD, compared to those in healthy controls, may derive from an early delay in white matter development and/or prolonged white matter growth; however, confirmation of these possibilities awaits longitudinal work.


Subject(s)
Corpus Striatum/pathology , Corpus Striatum/physiopathology , Diffusion Tensor Imaging , Frontal Lobe/pathology , Frontal Lobe/physiopathology , Nerve Net/pathology , Nerve Net/physiopathology , Obsessive-Compulsive Disorder/diagnosis , Obsessive-Compulsive Disorder/physiopathology , Thalamus/pathology , Thalamus/physiopathology , White Matter/pathology , White Matter/physiopathology , Adolescent , Age Factors , Anisotropy , Child , Female , Humans , Male , Obsessive-Compulsive Disorder/pathology , Obsessive-Compulsive Disorder/psychology
12.
Dev Dyn ; 243(9): 1055-66, 2014 Sep.
Article in English | MEDLINE | ID: mdl-24975120

ABSTRACT

BACKGROUND: Heterozygous mutations in the chromatin remodeling gene CHD7 cause CHARGE syndrome, a developmental disorder with variable craniofacial dysmorphisms and respiratory difficulties. The molecular etiologies of these malformations are not well understood. Homozygous Chd7 null mice die by E11, whereas Chd7(Gt/+) heterozygous null mice are a viable and excellent model of CHARGE. We explored skeletal phenotypes in Chd7(Gt/+) and Chd7 conditional knockout mice, using Foxg1-Cre to delete Chd7 (Foxg1-CKO) in the developing eye, ear, nose, pharyngeal pouch, forebrain, and gut and Wnt1-Cre (Wnt1-CKO) to delete Chd7 in migrating neural crest cells. RESULTS: Foxg1-CKO mice exhibited postnatal respiratory distress and death, dysplasia of the eye, concha, and frontal bone, hypoplastic maxillary shelves and nasal epithelia, and reduced tracheal rings. Wnt1-CKO mice exhibited frontal and occipital bone dysplasia, hypoplasia of the maxillary shelves and mandible, and cleft palate. In contrast, heterozygous Chd7(Gt/+) mice had apparently normal skeletal development. CONCLUSIONS: Conditional deletion of Chd7 in ectodermal and endodermal derivatives (Foxg1-Cre) or migrating neural crest cells (Wnt1-Cre) results in varied and more severe craniofacial defects than in Chd7(Gt/+) mice. These studies indicate that CHD7 has an important, dosage-dependent role in development of several different craniofacial tissues.


Subject(s)
Abnormalities, Multiple/genetics , CHARGE Syndrome/genetics , Craniofacial Abnormalities/genetics , DNA-Binding Proteins/genetics , Trachea/abnormalities , Abnormalities, Multiple/metabolism , Animals , CHARGE Syndrome/metabolism , Craniofacial Abnormalities/metabolism , DNA-Binding Proteins/metabolism , Gene Expression Regulation, Developmental , Mice , Mice, Knockout
13.
Mech Dev ; 129(9-12): 308-23, 2012.
Article in English | MEDLINE | ID: mdl-22705977

ABSTRACT

Proper morphogenesis of inner ear semicircular canals requires precise regulation of cellular proliferation, epithelial-to-mesenchymal transition, and fusion of epithelial plates. Epigenetic regulation of these processes is not well understood, but is likely to involve chromatin remodeling enzymes. CHD7 is a chromodomain-containing, ATP dependent helicase protein that is highly expressed in the developing ear and is required for semicircular canal development in both humans and mice. Here we report that mice with heterozygous loss of Chd7 function exhibit delayed semicircular canal genesis, delayed Netrin1 expression and disrupted expression of genes that are critical for semicircular canal formation (Bmp2, Bmp4, Msx1 and Fgf10). Complete loss of Chd7 results in aplasia of the semicircular canals and sensory vestibular organs, with reduced or absent expression of Otx1, Hmx3, Jagged1, Lmo4, Msx1 and Sox2. Our results suggest that Chd7 may have critical selector gene functions during inner ear morphogenesis. Detailed analysis of the epigenetic modifications underlying these gene expression changes should provide insights into semicircular canal development and help in the design of therapies for individuals with inner ear malformations.


Subject(s)
DNA-Binding Proteins/deficiency , Gene Expression Regulation, Developmental , Semicircular Canals/abnormalities , Animals , Cell Proliferation , DNA-Binding Proteins/genetics , DNA-Binding Proteins/metabolism , Epigenesis, Genetic , Epithelium/metabolism , Heterozygote , Mesoderm/growth & development , Mesoderm/metabolism , Mice , Morphogenesis/genetics , Mutation , Nerve Growth Factors/genetics , Nerve Growth Factors/metabolism , Netrin-1 , Semicircular Canals/growth & development , Semicircular Canals/metabolism , Tumor Suppressor Proteins/genetics , Tumor Suppressor Proteins/metabolism
14.
Ann Rheum Dis ; 69(12): 2204-12, 2010 Dec.
Article in English | MEDLINE | ID: mdl-20679476

ABSTRACT

BACKGROUND: Interleukin 18 (IL-18) is a novel mediator of angiogenesis in rheumatoid arthritis (RA). OBJECTIVE: To examine the role of IL-18 in RA angiogenesis and the signalling mechanisms involved. METHODS: Human dermal microvascular endothelial cell (HMVEC) chemotaxis, capillary morphogenesis assays and Matrigel plug angiogenesis assays were performed in vivo using IL-18 with or without signalling inhibitors. A novel model of angiogenesis was devised using dye-tagged HMVECs to study their homing into RA and normal (NL) synovial tissues (STs) engrafted in severe combined immunodeficient (SCID) mice. RESULTS: IL-18-mediated angiogenesis depended on Src and Jnk, as the inhibitors of Src and Jnk blocked IL-18-induced HMVEC chemotaxis, tube formation and angiogenesis in Matrigel plugs. However, inhibitors of Janus kinase 2, p38, MEK, phosphatidylinositol-3-kinase and neutralising antibodies to vascular endothelial growth factor or stromal derived factor-1α did not alter IL-18-induced HMVEC migration. These results were confirmed with Jnk or Src sense or antisense oligodeoxynucleotides. Moreover, IL-18 induced phosphorylation of Src and Jnk in HMVECs. As proof of principle, IL-18 null mice had a significantly decreased angiogenesis compared with wild-type mice in Matrigel plug angiogenesis assays in vivo. IL-18 markedly enhanced mature HMVEC homing to human RA ST compared with NL ST in SCID mice, confirming the role of IL-18-induced angiogenesis in RA ST in vivo. CONCLUSION: Targeting IL-18 or its signalling intermediates may prove to be a potentially novel therapeutic strategy for angiogenesis-dependent diseases, such as RA.


Subject(s)
Angiogenesis Inducing Agents/pharmacology , Arthritis, Rheumatoid/physiopathology , Endothelium, Vascular/drug effects , Interleukin-18/pharmacology , MAP Kinase Kinase 4/physiology , Neovascularization, Pathologic/enzymology , src-Family Kinases/physiology , Animals , Arthritis, Rheumatoid/enzymology , Arthritis, Rheumatoid/pathology , Chemotaxis/drug effects , Collagen , Disease Models, Animal , Drug Combinations , Endothelium, Vascular/cytology , Endothelium, Vascular/enzymology , Enzyme Inhibitors/pharmacology , Female , Humans , Interleukin-18/deficiency , Interleukin-18/physiology , Laminin , MAP Kinase Kinase 4/antagonists & inhibitors , Mice , Mice, SCID , Neovascularization, Pathologic/chemically induced , Neovascularization, Pathologic/pathology , Phosphorylation/drug effects , Proteoglycans , Skin/blood supply , Synovial Membrane/pathology , Synovial Membrane/transplantation , src-Family Kinases/antagonists & inhibitors
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