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Green, Danielle

0009-0003-7723-3320

Mayo Clinic

Mayo Clinic

Citations 2

An Observational Analysis of a Large Cohort of Pneumocystis jirovecii Pneumonia
Pulsipher, Aaron M. , Vikram, Holenarasipur R. , Gotway, Michael B. , Cartin‐Ceba, Rodrigo , Henry, Kyle J, Johnson, Alec M, Gassner, Ryan R , Zhou, Kevin , Green, D., Thompson, Emily , Sen, Ayan , Lee, Augustine S. , Ham, Kealy R., Green, Danielle , Thompson, Emily R , Sen, Ayan , Lee, Augustine S , Ham, Kealy , Vikram, Holenarasipur R. , Gotway, Michael B , Pulsipher, Aaron M , Henry, Kyle J, Johnson, Alec M, Limper, Andrew H.

Open Forum Infectious Diseases | June 28, 2025 | Volume: 12 | Issue: 7 | Pages: No page available

10.1093/ofid/ofaf390 Get It

Abstract Background Pneumocystis jirovecii pneumonia (PCP) is increasingly seen in patients who are non-HIV immunocompromised hosts, yet modern risk factors and outcomes are poorly recognized and defined. Methods A retrospective review was conducted of adult patients who met criteria for proven or probable PCP from 2017 to 2024 across a large academic multicenter health system. The primary outcome was mortality among cohorts, defined by etiology of immunosuppression through univariate and age-adjusted logistic regression. Secondary analyses included trends in annual diagnoses and testing patterns. Results A total of 701 patients met criteria for inclusion, representing one of the largest clinically characterized cohorts of PCP to date. The median age was 65 years (IQR, 54–73) and 62% were male. The most common risk groups were hematologic malignancy (32.2%), solid tumor cancers receiving chemotherapy (22.4%), and autoimmune disease with immunosuppression (17.7%). Annual PCP diagnoses increased at a rate of 15.8% (95% CI, 8.9%–23.2%) in parallel with increased testing. Only 5.4% of patients were receiving prophylaxis at the time of diagnosis. Overall mortality was 20% (95% CI, 17%–23%) and highest in cirrhosis (adjusted odds ratio, 6.24; 95% CI, 2.84–13.69; P < .001). Conclusions PCP in the current era affects a broad range of patients who are immunocompromised, with high associated mortality and low rates of prophylaxis. Patients with solid tumors and those with cirrhosis are at particularly high risk of mortality. These findings highlight the need to reassess and redefine PCP prophylaxis guidelines in specific populations and our understanding of who is at risk.
Navigating Sarcopenia Risks in GLP-1RA Therapy for Advanced Heart Failure
Wang, Winston , Green, Danielle B., Ibrahim, Ramzi, Abdelnabi, Mahmoud , Pham, Hoang Nhat , Forst, Beani, Allam, Mohamed , Sarkis, Patrick , Bcharah, George , Farina, Juan M. , Sorajja, Dan , Arsanjani, Reza , Green, Danielle , Farina, Juan M , Sorajja, Dan , Arsanjani, Reza , Allam, Mohamed N , Nhat, Hoang , Ibrahim, Ramzi

Biomedicines | May 2, 2025 | Volume: 13 | Issue: 5 | Pages: 1108

10.3390/biomedicines13051108 Get It

Cardiac cachexia (CC) is a severe complication of advanced heart failure (HF), characterized by involuntary weight loss and muscle wasting, leading to poor outcomes and higher mortality. Despite its severity, CC remains under-recognized and undertreated, lacking targeted therapies specifically addressing its pathophysiology. Glucagon-like peptide-1 receptor agonists (GLP-1RAs), though beneficial in reducing cardiovascular risk in patients with HF, may exacerbate muscle wasting in cachectic patients, necessitating further investigation. Non-pharmacological strategies, including tailored nutritional support and exercise programs, have shown positive effects on body composition and quality of life in patients with CC. However, there remains a gap in recommendations tailored to preventive strategies and pharmacologic therapies for patients with CC and concomitant GLP-1RA use. This review highlights the multifactorial mechanisms underlying CC and current and emerging therapeutic approaches for mitigating HF-related sarcopenia while on GLP-1RAs.