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Risk Factor Assessment for Acute Pulmonary Hypertension Crisis

17 juni 2026 uppdaterad av: Peking Union Medical College Hospital

Research on the Clinical Risk Factor Assessment System for Acute Pulmonary Hypertension Crisis and Its Mortality

The goal of this observational study is to learn about pulmonary hypertension crisis (PHC) - a severe, and often fatal complication - in patients with pulmonary hypertension (PH). The main questions this study aims to answer are:

What are the clinical and hemodynamic features of PHC, and what underlying pathophysiological mechanisms cause it to develop? Can these features be used to diagnostic PHC, predict who is at risk of developing it or dying from it, and develop targeted prevention and treatment of PHC?

A multi-center registry platform and biobank will be established to enroll and follow up patients with PH. Clinical data, hemodynamic measurements, and biological specimen will be collected. Risk prediction and early warning tools of PHC will be developed.

Studieöversikt

Status

Rekrytering

Detaljerad beskrivning

Pulmonary hypertension crisis (PHC) is a severe and fatal complication of pulmonary hypertension (PH), characterized by the sudden elevation of pulmonary vascular resistance, acute right hear failure and collapse of systemic circulation. However, PHC currently lacks any internationally accepted definition or diagnostic criteria, and it is still unclear which are the clinical, pathophysiological and molecular risk factors of PHC.

This study aims to establish a large clinical cohort of patients with PH, validate the definition of PHC, identify risk factors of PHC occurrence and mortality, and develop tools for the risk-prediction and early-warning of PHC.

This is a multi-center, prospective cohort study with a retrospective component for model training. Following national health-information standards, a standardized registry dataset will be established to cover demographics, clinical features, laboratory tests, imaging, and hemodynamic profile. Existing PH cohort databases will be integrated and expanded to a target of 5,000 patients. A subset of cases with right heart catheter parameters (RHC) will be extracted. A multi-center biospecimen management platform will be established.

For PHC onset, the investigators will assemble a clinical-molecular-imaging feature set and use convolutional neural networks and tree-based algorithms for feature extraction, then build a cross-modal prediction model using multi-task learning, neural networks, and a Transformer architecture. The model will be prospectively validated and tuned against real-world performance. For PHC mortality, models will be built on patients meeting the new PHC criteria, using 28-day attributable death, all-cause death, and long-term death as endpoints. Models will be trained on a retrospective cohort and then evaluated for accuracy and generalizability on both an internal validation set and an external prospective-cohort validation set.

Studietyp

Observationell

Inskrivning (Beräknad)

5000

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studiekontakt

Studieorter

      • Beijing, Kina, 100730
        • Rekrytering
        • Peking Union Medical College Hospital
        • Kontakt:
        • Huvudutredare:
          • Jinmin Peng, MD
      • Shanghai, Kina
        • Rekrytering
        • Shanghai Pulmonary Hospital
        • Kontakt:
    • Guangdong
      • Guangzhou, Guangdong, Kina
        • Rekrytering
        • Guangdong Province People's Hospital
        • Kontakt:
    • Yunnan
      • Kunming, Yunnan, Kina
        • Rekrytering
        • Yan'an Affiliated Hospital of Kunming Medical University
        • Kontakt:
          • Hailong Dai, MD
          • Telefonnummer: +86 0871 63211157
          • E-post: dhlkm@qq.com

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

  • Barn
  • Vuxen
  • Äldre vuxen

Tar emot friska volontärer

N/A

Testmetod

Icke-sannolikhetsprov

Studera befolkning

Patients with pulmonary hypertension confirmed by right heart catheterization

Beskrivning

Inclusion Criteria:

  • Pulmonary hypertension confirmed by mean pulmonary arterial pressure (mPAP) over 20 mmHg measured by right heart catheter
  • At least once per year of follow-up data collection record

Exclusion Criteria:

  • Patients with missing baseline or follow-up data
  • Complicated by other diseases with significant influence on survival, such as acute coronary syndrome, malignancy, etc.
  • Complicated by other diseases with significant influence on hemodynamics, such as sepsis, acute left heart failure, and acute pulmonary embolism, etc.
  • Receiving medications with significant influence on hemodynamics

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

Kohorter och interventioner

Grupp / Kohort
Pulmonary hypertension
Patients with right heart catheter confirmed pulmonary hypertension

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Pulmonary hypertension crisis
Tidsram: From enrollment to 3 years after enrollment
Critical increase of pulmonary vascular resistance accompanied by right heart dysfunction and systemic hypoperfusion
From enrollment to 3 years after enrollment
28 day mortality attributed to pulmonary hypertension crisis
Tidsram: From hospitalization to 28 days
Death attributed to pulmonary hypertension crisis within 28 days of hospitalization
From hospitalization to 28 days

Sekundära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
All cause mortality within hospitalization
Tidsram: From hospitalization to discharge or documented death, whichever is earlier, assessed up to 3 years
All cause death within hospitalization
From hospitalization to discharge or documented death, whichever is earlier, assessed up to 3 years
All cause mortality within 3 years
Tidsram: From the diagnosis of pulmonary hypertension crisis to documented death, assessed up to 3 years
All cause death within 3 years from the diagnosis of pulmonary hypertension crisis
From the diagnosis of pulmonary hypertension crisis to documented death, assessed up to 3 years

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Utredare

  • Huvudutredare: Jinmin Peng, MD, Peking Union Medical College Hospital

Publikationer och användbara länkar

Den som ansvarar för att lägga in information om studien tillhandahåller frivilligt dessa publikationer. Dessa kan handla om allt som har med studien att göra.

Allmänna publikationer

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart (Faktisk)

17 juni 2026

Primärt slutförande (Beräknad)

30 juni 2029

Avslutad studie (Beräknad)

31 december 2029

Studieregistreringsdatum

Först inskickad

7 juni 2026

Först inskickad som uppfyllde QC-kriterierna

15 juni 2026

Första postat (Faktisk)

17 juni 2026

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

22 juni 2026

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

17 juni 2026

Senast verifierad

1 juni 2026

Mer information

Termer relaterade till denna studie

Andra studie-ID-nummer

  • K7949
  • 2024ZD0526701 (Annat bidrag/finansieringsnummer: Ministry of Science and Technology of the People's Republic of China)

Plan för individuella deltagardata (IPD)

Planerar du att dela individuella deltagardata (IPD)?

JA

IPD-planbeskrivning

IPD that underlie the results reported in our publications will be shared after de-identification, including clinical, hemodynamic, laboratory, and imaging data (tables, figures, and appendices).

Tidsram för IPD-delning

Beginning 1 year after publication with no end date

Kriterier för IPD Sharing Access

Researchers who submit a methodologically sound proposal will be able to access the de-identified individual participant data and supporting documents. Proposals should be directed to the principal investigator at pjm731@hotmail.com. To gain access, requestors will be required to sign a data access agreement, and data will be shared for the purpose of achieving the aims in the approved proposal.

IPD-delning som stöder informationstyp

  • STUDY_PROTOCOL
  • SAV
  • ICF
  • ANALYTIC_CODE
  • CSR

Läkemedels- och apparatinformation, studiedokument

Studerar en amerikansk FDA-reglerad läkemedelsprodukt

Nej

Studerar en amerikansk FDA-reglerad produktprodukt

Nej

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