Publications by authors named "H Cajigas"

Objective: To determine the prevalence of portopulmonary hypertension in patients referred for liver transplant evaluation.

Methods: Medical records were reviewed for 986 consecutive patients referred for liver transplant evaluation who were screened for pulmonary hypertension with echocardiography from February 1, 2021, to January 31, 2022, across 3 liver transplant centers.

Results: Of 934 patients eligible for analysis, mean (SD) age was 57 (11) years, 558 (59.

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Article Synopsis
  • Pulmonary embolism (PE) is a significant health issue, being the third leading cause of illness and death globally, with submassive PE making up 40% of this burden.
  • A study reviewed 22 patients with submassive PE who underwent mechanical thrombectomy (MT), showing a successful thrombus removal rate of 82% and no major bleeding complications.
  • Results indicated that MT led to shorter hospital stays and lower in-hospital mortality rates compared to standard anticoagulation therapy alone, despite the small sample size.
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Background: Patients with COPD frequently demonstrate pulmonary hypertension (PH). Severe PH in patients with COPD, identified by pulmonary vascular resistance (PVR) of > 5 Wood units (WU), is closely linked to impaired transplant-free survival. The impact of PH-targeting pharmacotherapy in this context remains unclear.

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Article Synopsis
  • - Pulmonary hypertension (PH) is a serious and varied disease, necessitating accurate assessments for effective treatment, and its existing risk models require further investigation, especially outside of group 1 (PAH).
  • - This study analyzed 8,565 patients with different types of PH (groups 1 to 4) to determine if risk scores developed for pulmonary arterial hypertension (PAH) could predict outcomes in all groups.
  • - Results showed that all risk scores were effective in predicting patient outcomes across PH groups, with the REVEAL scores proving to be the most statistically powerful and detailed.
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Chronic lung disease (CLD) is the second leading cause of pulmonary hypertension (PH) and is associated with significant morbidity and mortality. Although PH associated with CLD (PH-CLD) leads to impaired health-related quality of life (HRQOL), there are no validated tools to assess HRQOL in PH-CLD. The Pulmonary Arterial Hypertension-Symptoms and Impact Questionnaire (PAH-SYMPACT) is an HRQOL instrument aimed at assessing the symptoms and impact of PH on overall function and well-being.

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