JAMA Internal Medicine

JAMA Internal Medicine(英文缩写 JAMA INTERN MED),ISSN 2168-6106,eISSN 2168-6114 是一本学术期刊。本页汇总该期刊的最新影响因子、分区信息以及最新收录于 PubMed 的文献,帮助您快速了解期刊全貌。

2026 年数据 · 影响因子
26.300
JCR 分区
Q1
CAS 分区
B1
近一年发文量
448
本站 PubMed 收录统计

发文量统计区间:2025-09-01 至 2026-08-31,按本站收录文献的发表日期统计。

ISSN: 2168-6106 · eISSN: 2168-6114 · 缩写: JAMA INTERN MED

期刊介绍

选择期刊介绍栏目

期刊简介

JAMA Internal Medicine 是国际内科学领域的高影响力同行评审期刊,主要发表成人内科临床研究、循证医学证据与临床实践改进相关论文。内容覆盖心血管、内分泌、感染、肿瘤筛查、老年医学及卫生政策等方向,读者群为内科医师、临床研究者、医学教育者与卫生决策人员。

研究方向

聚焦成人内科疾病的诊断、治疗与预防,常刊载随机临床试验、队列与病例对照研究、系统综述与荟萃分析、诊断准确性研究,以及临床实践、医疗质量和卫生政策分析。亦设有评论、观点与临床挑战类栏目,强调研究对日常诊疗决策的直接参考价值。

期刊特色

研究取向偏重方法学严谨、样本量充分且具有临床可操作性的证据,论文通常要求明确的研究问题、规范统计分析与利益冲突披露。适合从事临床研究、循证医学、医疗质量改进及卫生政策研究的作者与读者,对写作清晰度和结果解读的审慎性要求较高。

投稿难度

投稿难度整体较高,竞争激烈,但并非仅由分区决定。选题需具备明确的临床意义与新颖性,研究设计、统计方法和伦理规范须经得起严格审查。建议提前完善方案与数据管理,重视阴性或非显著结果的合理解读,并预留充分时间应对多轮修改。

历年影响因子趋势

JCR 数据年份影响因子JCR 分区
202144.424Q1
202239.000Q1
202322.500Q1
202423.300Q1
202526.300Q1

JAMA Internal Medicine 最新收录文献

  1. JCR分区: Q1 CAS分区: B1 影响因子: 26.3
  2. JCR分区: Q1 CAS分区: B1 影响因子: 26.3

    2. Antidiscrimination Laws and Kidney Transplant for Patients With Developmental Disabilities.

    作者:
    Brittany N Hand, J Madison Hyer, Melica Nikahd, Andrew Gothard, Guy Brock, John Gardner, Lauren Bishop, Lindsay Shea, Lauren Wang, Austin D Schenk
    日期:
    2026-09-21

    该文献暂无摘要。

  3. JCR分区: Q1 CAS分区: B1 影响因子: 26.3

    3. Buprenorphine via Telehealth-Closing the Gap for Pregnant and Postpartum Women With Opioid Use Disorder.

    作者:
    Rachel K Landis, Mishka Terplan, Barbara Andraka-Christou, Jonathan Cantor
    日期:
    2026-09-21

    该文献暂无摘要。

  4. JCR分区: Q1 CAS分区: B1 影响因子: 26.3

    4. Steatotic Liver Disease Risk Scores to Predict Cirrhosis and Hepatocellular Carcinoma.

    作者:
    Catherine Mezzacappa, Janet P Tate, Jessie Torgersen, Melissa Skanderson, Tamar H Taddei, Amy C Justice
    日期:
    2026-09-21

    Most individuals with steatotic liver disease (SLD) do not develop advanced liver disease. Multiple risk scores for SLD-associated cirrhosis and hepatocellular carcinoma (HCC) have been proposed, but their utility to inform decisions about surveillance for advanced liver disease is unknown. To compare the clinical utility of SLD risk scores for predicting cirrhosis and hepatocellular carcinoma in patients with noncirrhotic steatotic liver disease. This cohort study used data from the national US Veterans Affairs health system of adults with imaging-confirmed SLD without viral hepatitis or primary liver disease from 2008 and 2020. Nine clinical risk scores were calculated at the time of the first imaging results that demonstrated hepatic steatosis. Individuals were followed up until cirrhosis, HCC, death, or 6 months after last follow-up visit. Data were analyzed between November 1, 2025, and May 11, 2026. Nine risk scores evaluated for prediction of cirrhosis or HCC within 10 years were: (1) ALBI, albumin-bilirubin; (2) aMAP, age-male-albumin-bilirubin-platelet; (3) APRI, the aspartate aminotransferase-to-platelet ratio; (4) BARD, body mass index, age, alanine aminotransferase-to-aspartate aminotransferase ratio, and diabetes; (5) FIB-4, fibrosis-4 index; (6) NFS, nonalcoholic fatty liver disease fibrosis; (7) SAFE, steatosis-associated fibrosis estimator; and 2 additional scores. First diagnosis of cirrhosis and first diagnosis of HCC identified using VA and Medicare diagnosis codes and data from the VA Cancer Registry. Cox proportional hazards models were used to calculate time-dependent 10-year probabilities of each outcome predicted by 9 risk scores. Decision curves were generated for each outcome by calculating the net benefit, a weighted measure of true and false positives over a prespecified range of risk thresholds at which a clinician may reasonably recommend intervention. Nine risk scales were used to quantify the risk of cirrhosis or HCC within 10 years. The analysis included 853 131 patients (median [IQR] age, 61 [51-68] years; 62 168 females [7.3%] and 790 965 males [92.7%]) whose median (IQR) BMI was 31.3 (27.6-35.5) and 275 898 (32.3%) had diabetes; of these, 33 794 (3.96%) developed cirrhosis and 2978 (0.35%) developed HCC within 10 years. The FIB-4, APRI, and SAFE scores demonstrated the greatest discrimination of cirrhosis risk, while the SAFE, Tate, and FIB-4 scores demonstrated the greatest discrimination of HCC risk. The SAFE score demonstrated the greatest net benefit predicting cirrhosis. A score of 29.5 corresponded to a 10-year cirrhosis risk of 2.5% and yielded a net benefit of 0.019, or 1.9 additional individuals who develop cirrhosis per 100 individuals classified as at-risk patients. At a 0.25% 10-year risk of HCC, the SAFE score had a net benefit of 0.0016 (1.6 additional true positives per 1000 individuals). The findings of this cohort study show that the SAFE score may inform decisions to repeat screening for cirrhosis in patients with SLD. Clinical risk scores for HCC demonstrated minimal utility to inform HCC screening decisions for patients with noncirrhotic SLD.

  5. JCR分区: Q1 CAS分区: B1 影响因子: 26.3

    5. Lessons From a Hepatitis C Program in California Prisons.

    作者:
    Tyler N A Winkelman, Elise Woodward
    日期:
    2026-09-14

    该文献暂无摘要。

  6. JCR分区: Q1 CAS分区: B1 影响因子: 26.3

    6. Effective Palliative Care for Hospice Transitions.

    作者:
    May Hua, Miguel Cid, Claire Barshied, Rachel C Shelton, Grace Hu, Natasha Stekl, Carrie Brill, Elise C Carey, R Sean Morrison
    日期:
    2026-09-14

    Variation in hospice use for patients with cancer exists between palliative care programs, but factors underlying this heterogeneity are unknown. To identify hospital and palliative care program factors that may impact the ability of palliative care teams to affect hospice use in cancer. This multicenter qualitative study included 6 palliative care programs in the United States. Using a cohort of patients with metastatic cancer who received specialist palliative care, a positive-negative deviance approach was used to select 3 programs with high and 3 programs with low performance on hospice use. In-depth site visits were conducted and included semistructured interviews with palliative care and oncology clinicians and patients as well as in-person observation. Interviews were conducted from February 2025 to January 2026. Site visits were conducted from May 2025 to January 2026. Program-specific practices and their potential effect on hospice use for patients with cancer. A total of 93 interviews and 424 hours of in-person observation were conducted across 6 palliative care programs in the Midwest, Upper South, and Deep South regions of the United States. Interview participants had a median (IQR) age of 43 (37-47) years; 68 (73.1%) were female; clinicians had a median (IQR) of 11 (5-16) years of experience. There were notable differences in the relationships between palliative care and oncology teams between high- and low-performing programs. At high-performing programs, the relationship was characterized by mutual trust and respect, warmth and familiarity, and empathy for each other, whereas at low-performing programs, the relationship was characterized by a lack of trust and familiarity and negative regard for each other. Factors observed in programs with positive relationships included intentionality in relationship building, physical presence and proximity between teams, use of real-time communication, and the palliative care team having a service-oriented mentality and a reputation for reliable service. At high-performing programs, observable differences in care included collaborative care delivery, increased access and timeliness of palliative care, and earlier introduction of hospice by oncology clinicians. In this multicenter qualitative study, differences in the relationship between palliative care and oncology teams were identified that may mechanistically affect end-of-life patient outcomes. These findings are important to ensure the delivery of high-quality care for all patients with cancer.

  7. JCR分区: Q1 CAS分区: B1 影响因子: 26.3

    7. On the Road, Again.

    作者:
    Eleanor R Menzin
    日期:
    2026-09-14

    该文献暂无摘要。

  8. JCR分区: Q1 CAS分区: B1 影响因子: 26.3

    8. Universal Opt-Out Hepatitis C Virus Testing and Treatment on Entry in California State Prisons.

    作者:
    Ziping Ye, Kimberley D Lucas, Nathan W Furukawa, Amanda A Honeycutt, Donna Kalauokalani, Amy T Krawiec, Teresa Puente, Joshua A Salomon, Marissa B Reitsma
    日期:
    2026-09-14

    该文献暂无摘要。

  9. JCR分区: Q1 CAS分区: B1 影响因子: 26.3

    9. Institutional Fear of Falling-Causes, Consequences, and Cures.

    作者:
    Hanne R Dolan, Terry P Haines, Ronald I Shorr
    日期:
    2026-09-14

    该文献暂无摘要。

  10. JCR分区: Q1 CAS分区: B1 影响因子: 26.3

    10. Caring Collectively Through Palliative Care Partnerships.

    作者:
    Sandra Shi, Lona Mody, Cary P Gross
    日期:
    2026-09-14

    该文献暂无摘要。

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指标接近的期刊