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COVID-19 in the Setting of HIV and Severe Hemophilia A: A Case Report. COVID-19 在艾滋病和严重血友病 A 中的应用:病例报告。
HCA healthcare journal of medicine Pub Date : 2024-04-30 eCollection Date: 2024-01-01 DOI: 10.36518/2689-0216.1615
Ryan Wilson, Chae Ko, Rahul Kashyap
{"title":"COVID-19 in the Setting of HIV and Severe Hemophilia A: A Case Report.","authors":"Ryan Wilson, Chae Ko, Rahul Kashyap","doi":"10.36518/2689-0216.1615","DOIUrl":"10.36518/2689-0216.1615","url":null,"abstract":"<p><strong>Introduction: </strong>A hyperactive immune response is the driving force behind severe Coronavirus disease 2019 (COVID-19). Complications of severe COVID-19 include acute respiratory distress syndrome, acute respiratory failure, and increased risk of venous thromboembolism (VTE). The management of patients with COVID-19 includes respiratory support, decreasing immune response to the virus to prevent the progression of disease, and anticoagulation to prevent VTE.</p><p><strong>Case presentation: </strong>We present the case of a patient with a history of human immunodeficiency virus (HIV) and hemophilia A admitted with COVID-19. This case demonstrates the difficulties present when managing COVID-19 in patients with specific comorbidities. Anticoagulation is a recommended component of COVID-19 treatment but is contraindicated in patients with severe hemophilia due to increased risk for bleeding. Research has also shown that dexamethasone decreases mortality in patients with COVID-19, but doctors should use dexamethasone cautiously in patients with HIV since it is an immunosuppressant. Taking certain antiretroviral therapies, such as rilpivirine, also contraindicates the use of dexamethasone.</p><p><strong>Conclusion: </strong>In this case, it is important to monitor for the risk and presence of superimposed bacterial or opportunistic infections. Treating a patient with these comorbidities who is infected with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) highlights the importance of balancing the risks and benefits.</p>","PeriodicalId":73198,"journal":{"name":"HCA healthcare journal of medicine","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-04-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11229595/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141565240","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Actinic Granuloma Complicated by Secondary Syphilis: A Case Report. 继发性梅毒并发放线菌肉芽肿:病例报告。
HCA healthcare journal of medicine Pub Date : 2024-04-30 eCollection Date: 2024-01-01 DOI: 10.36518/2689-0216.1636
Kevin H Nguyen, Christopher M Wong, Ethan Q Nguyen
{"title":"Actinic Granuloma Complicated by Secondary Syphilis: A Case Report.","authors":"Kevin H Nguyen, Christopher M Wong, Ethan Q Nguyen","doi":"10.36518/2689-0216.1636","DOIUrl":"10.36518/2689-0216.1636","url":null,"abstract":"<p><strong>Introduction: </strong>Actinic granuloma (AG) is a rare skin eruption thought to result from a sun-induced inflammatory response attracting giant cells, which are large, multinucleated, and inflammatory, to form granulomas and degrade surrounding elastic material. Clinically, lesions begin on sun-exposed skin as pink papules and nodules that coalesce into demarcated annular plaques with a hypopigmented center. Histologically, actinic elastosis surrounds the outer annulus ring, with histiocytes and giant cells within the raised border, and the innermost central zone is filled with minimal to absent elastic fibers.</p><p><strong>Case presentation: </strong>We present a middle-aged female with a pruritic eruption of diffuse erythematous macules and papules coalescing into plaques with mild scale involving the scalp, face, neck, torso, and upper and lower extremities, including the palms and soles, but sparing the ears, bilateral axillae, elbows, and knees. Skin biopsies revealed solar elastosis and abundant multinucleated foreign body giant cells with ingested elastic fibers. The patient's clinical presentation and histopathology were consistent with a diagnosis of AG. Furthermore, spirochete immunostaining of the specimens revealed multiple <i>Treponema pallidum</i> spirochetes throughout the epidermis and dermis. Secondary syphilis with primary chancre was added to the diagnosis. Treatment included oral and topical steroids followed by intravenous penicillin G. After 1 month, all lesions had resolved with post-inflammatory erythema.</p><p><strong>Conclusion: </strong>Our patient differs from the typical presentation in describing intense pruritus with her eruption. This interesting collision reminds clinicians to retain a high index of suspicion for multiple diagnoses in a single patient.</p>","PeriodicalId":73198,"journal":{"name":"HCA healthcare journal of medicine","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-04-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11229604/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141565572","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A Case Series of Unusual IgA Vasculitis. 非同寻常的 IgA 血管炎病例系列。
HCA healthcare journal of medicine Pub Date : 2024-04-30 eCollection Date: 2024-01-01 DOI: 10.36518/2689-0216.1627
Jared Bradley, Ian Whitaker, Brittany Lyons, Amy Mangla
{"title":"A Case Series of Unusual IgA Vasculitis.","authors":"Jared Bradley, Ian Whitaker, Brittany Lyons, Amy Mangla","doi":"10.36518/2689-0216.1627","DOIUrl":"10.36518/2689-0216.1627","url":null,"abstract":"<p><strong>Introduction: </strong>Immunoglobulin A vasculitis (IgA)is a rare condition characterized by palpable purpura, often involving the skin, gastrointestinal tract, joints, and kidneys. Presentation is usually acute and is more common in children and adolescents of Southeast Asian and European descent. In the adult population, it is less common and therapies are not as well-established.</p><p><strong>Case presentation: </strong>Disease prevalence of IgA vasculitis outside Southeast Asian and European populations is not well-documented. In this case series, we present 2 cases of IgA vasculitis in 2 older adult males, one of Native American descent and one of African American descent.</p><p><strong>Conclusion: </strong>IgA vasculitis must be considered within the adult population, and it is not limited to certain ethnic groups. Further research is needed to give clarity on the best treatment options for adults with IgA vasculitis. We believe that patients presenting with IgA vasculitis are best managed in a multidisciplinary approach, especially those patients with limited improvement despite the initiation of corticosteroids. Our 2 cases should raise awareness of IgA vasculitis in patients with skin rashes and elevated creatinine levels.</p>","PeriodicalId":73198,"journal":{"name":"HCA healthcare journal of medicine","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-04-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11229601/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141565236","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Mpox-Induced Proctitis. Mpox诱发的直肠炎。
HCA healthcare journal of medicine Pub Date : 2024-04-30 eCollection Date: 2024-01-01 DOI: 10.36518/2689-0216.1585
Saif Ghias, Niyati Joshi, Dzenana Cabaravdic, Ramesh Nathan, Jasprit Takher
{"title":"Mpox-Induced Proctitis.","authors":"Saif Ghias, Niyati Joshi, Dzenana Cabaravdic, Ramesh Nathan, Jasprit Takher","doi":"10.36518/2689-0216.1585","DOIUrl":"10.36518/2689-0216.1585","url":null,"abstract":"<p><strong>Introduction: </strong>Mpox, formerly known as monkeypox, is a zoonotic virus in the genus <i>Orthopoxvirus</i>, which has a variable incubation period and an extensive array of symptoms. While those infected with Mpox have displayed generalized viral prodromal symptoms, atypical symptoms such as proctitis have also been seen. Proctitis associated with Mpox is a relatively infrequent initial presenting symptom with a reported incidence of 14-32.9% that has seen an uptick in prevalence since the 2022 global endemic.</p><p><strong>Case presentation: </strong>We present a confirmed case of Mpox in a 27-year-old male who presented with 3 days of intermittent anorectal bleeding and various forms of cutaneous lesions at different stages of healing. He had engaged in unprotected sexual intercourse 8 days prior to the onset of his symptoms in New York, which at the time was the epicenter of the endemic. Computed tomography imaging showed thickening of the rectum with associated lymphadenopathy, consistent with findings of acute proctitis.</p><p><strong>Conclusion: </strong>The intent of this case report is to acknowledge the prevalence of the Mpox virus. Since the endemic, increased cases of Mpox have led to more complications that have been identified and studied by public health experts. The complication of proctitis due to Mpox in a certain subset of patients is important to fully understand that while this virus presents with a generalized prodrome like other viruses, these unique gastrointestinal presentations and findings may be the first step in identifying this infection and ensuring rapid treatment if future endemics arrive.</p>","PeriodicalId":73198,"journal":{"name":"HCA healthcare journal of medicine","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-04-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11229591/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141565246","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Colon Cancer Metastasis to Spermatic Cord Presenting as an Inguinal Hernia. 结肠癌转移至精索,表现为腹股沟疝。
HCA healthcare journal of medicine Pub Date : 2024-04-30 eCollection Date: 2024-01-01 DOI: 10.36518/2689-0216.1593
Jessica G Laenger, Eamon Ff Rooney, Patrick F Dial, Candie T Le, Sanda A Tan
{"title":"Colon Cancer Metastasis to Spermatic Cord Presenting as an Inguinal Hernia.","authors":"Jessica G Laenger, Eamon Ff Rooney, Patrick F Dial, Candie T Le, Sanda A Tan","doi":"10.36518/2689-0216.1593","DOIUrl":"10.36518/2689-0216.1593","url":null,"abstract":"<p><strong>Introduction: </strong>Inguinal hernias are very common. Their pathology and treatment are typically strait forward. Metastatic cancer can sometimes present as an inguinal hernia, but this presentation is often local metastasis.</p><p><strong>Case presentation: </strong>Herein we describe the case of a 68-year-old man who presented with a 2-month history of an inguinal hernia. Intraoperatively, the hernia sac was found to contain a mass attached to the spermatic cord, which was later determined to be a metastatic lesion from a locally advanced proximal transverse colon adenocarcinoma.</p><p><strong>Conclusion: </strong>A spermatic cord mass can be a rare presentation of colon cancer metastasis. Colon cancer should be considered a rare but possible primary lesion when evaluating tumors of the spermatic cord.</p>","PeriodicalId":73198,"journal":{"name":"HCA healthcare journal of medicine","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-04-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11229589/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141565238","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Presentations of Cutaneous Disease in Various Skin Pigmentations: Chronic Atopic Dermatitis. 各种皮肤色素沉着的皮肤病表现:慢性特应性皮炎
HCA healthcare journal of medicine Pub Date : 2024-04-30 eCollection Date: 2024-01-01 DOI: 10.36518/2689-0216.1644
Cecilia Nguyen, Jordan Thompson, Daniel A Nguyen, Christopher M Wong, Christian J Scheufele, Michael Carletti, Stephen E Weis
{"title":"Presentations of Cutaneous Disease in Various Skin Pigmentations: Chronic Atopic Dermatitis.","authors":"Cecilia Nguyen, Jordan Thompson, Daniel A Nguyen, Christopher M Wong, Christian J Scheufele, Michael Carletti, Stephen E Weis","doi":"10.36518/2689-0216.1644","DOIUrl":"10.36518/2689-0216.1644","url":null,"abstract":"<p><p>Description Atopic dermatitis is a chronic inflammatory skin disorder classically affecting flexural areas of the body. It is present in children and adults, including those with darker skin pigmentation. Chronic lesions are hyperpigmented plaques that are dry, cracked, and/or scaly often with lichenification. Differential diagnoses include psoriasis, seborrheic dermatitis, ichthyosis, and pityriasis rosea. This article will showcase clinical images with varying presentations of chronic atopic dermatitis in a range of age groups and skin colors according to the Fitzpatrick scale.</p>","PeriodicalId":73198,"journal":{"name":"HCA healthcare journal of medicine","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-04-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11229590/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141565290","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Presentations of Cutaneous Disease in Various Skin Pigmentations: Porokeratosis. 各种皮肤色素沉着中的皮肤病表现:角化病
HCA healthcare journal of medicine Pub Date : 2024-04-30 eCollection Date: 2024-01-01 DOI: 10.36518/2689-0216.1682
Henry Lim, Christopher M Wong, Christian J Scheufele, Daniel A Nguyen, Michael Carletti, Stephen E Weis
{"title":"Presentations of Cutaneous Disease in Various Skin Pigmentations: Porokeratosis.","authors":"Henry Lim, Christopher M Wong, Christian J Scheufele, Daniel A Nguyen, Michael Carletti, Stephen E Weis","doi":"10.36518/2689-0216.1682","DOIUrl":"10.36518/2689-0216.1682","url":null,"abstract":"<p><p>Description Porokeratosis was first described in 1893. It is a relatively rare disorder with over 9 subtypes. Lesions are clinically characterized as well-demarcated, erythematous papules (raised, <1 cm) or plaques (raised, >1 cm), with an atrophic center, and raised scaly border. Porokeratosis is an important diagnosis to identify because it may undergo malignant transformation and mimics many commonly encountered diagnoses. These commonly mimicked diagnoses include squamous cell carcinoma, tinea corporis, nummular dermatitis, and psoriasis vulgaris, to name a few. The clinical images in this review focus on identifying porokeratosis along the full spectrum of skin tones.</p>","PeriodicalId":73198,"journal":{"name":"HCA healthcare journal of medicine","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-04-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11229592/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141565291","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Dercum's Disease: The Clinical Presentation, Diagnosis, Radiological Findings, and Treatment of a Rare, Debilitating Inflammatory Disorder. 德库姆氏病:一种罕见的、使人衰弱的炎症性疾病的临床表现、诊断、放射学发现和治疗。
HCA healthcare journal of medicine Pub Date : 2024-04-30 eCollection Date: 2024-01-01 DOI: 10.36518/2689-0216.1642
Obyda Al-Housni, Constantinos Boufeas, Valori Slane
{"title":"Dercum's Disease: The Clinical Presentation, Diagnosis, Radiological Findings, and Treatment of a Rare, Debilitating Inflammatory Disorder.","authors":"Obyda Al-Housni, Constantinos Boufeas, Valori Slane","doi":"10.36518/2689-0216.1642","DOIUrl":"10.36518/2689-0216.1642","url":null,"abstract":"<p><strong>Introduction: </strong>Dercum's disease, also known as adiposis dolorosa, is a rare syndrome characterized by the growth of multiple, and painful, subcutaneous adipose tissues that commonly present in the abdomen and extremities. The scientific community hypothesizes that Dercum's disease is a combination of neurologic and endocrine disorders. Patients commonly describe it as chronic adipose pain, which manifests as sporadic painful flares throughout their history with the disease.</p><p><strong>Case presentation: </strong>We share the case of a 32-year-old woman who presented to the emergency department for an acute episode of left lower extremity pain and swelling associated with a previously diagnosed history of Dercum's disease. The patient had similar events in the past, with her last episode being 3 months earlier. A diagnosis is based on clinical presentation, findings on imaging, and the exclusion of other diseases that are associated with lipomas. While there is no standard approach to treatment, healthcare professionals focus on pain management.</p><p><strong>Conclusion: </strong>Dercum's disease is a chronic debilitating disorder, with multiple types that are diagnosed through imaging. The treatment of Dercum's disease is predicated on the patient's symptoms and the effectiveness of medications that vary based on the patient's needs.</p>","PeriodicalId":73198,"journal":{"name":"HCA healthcare journal of medicine","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-04-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11229597/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141565241","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Acute Bilateral Pyelonephritis in the Setting of Newly Diagnosed Diabetes Mellitus: A Case Report. 新诊断糖尿病患者的急性双侧肾盂肾炎:病例报告。
HCA healthcare journal of medicine Pub Date : 2024-04-30 eCollection Date: 2024-01-01 DOI: 10.36518/2689-0216.1626
Jessenia Ariana Contreras, Satwinder Singh, Ramesh Alwarappan
{"title":"Acute Bilateral Pyelonephritis in the Setting of Newly Diagnosed Diabetes Mellitus: A Case Report.","authors":"Jessenia Ariana Contreras, Satwinder Singh, Ramesh Alwarappan","doi":"10.36518/2689-0216.1626","DOIUrl":"10.36518/2689-0216.1626","url":null,"abstract":"<p><strong>Introduction: </strong>Acute pyelonephritis is a bacterial infection that starts in the bladder and ascends to the kidneys, causing inflammation of the renal parenchyma. Women are more likely to get infected compared to men, with diabetics being at higher risk. The pathophysiology of how diabetics are more prone to getting urinary tract infections/pyelonephritis has been studied, particularly the difference between bilateral pyelonephritis and unilateral pyelonephritis.</p><p><strong>Case presentation: </strong>This case presentation follows a 51-year-old Spanish-speaking woman with a past medical history of prediabetes, bilateral tubal ligation, and perimenopause. She presented to the hospital for abdominal and back pain, fevers, and weakness that she had for a week. An intake of her history and a physical examination led to the initial diagnosis of cystitis, but the imaging drove the authors to the correct diagnosis of acute bilateral pyelonephritis with <i>Escherichia coli</i> growing in the urine. She was then treated with the appropriate antibiotics. During her hospital stay, she was also diagnosed with type 2 diabetes mellitus. Imaging is not usually used to diagnose pyelonephritis, but it is necessary in some cases and can help identify complications. There are multiple case reports about acute pyelonephritis, but there are few that touch on acute bilateral pyelonephritis.</p><p><strong>Conclusion: </strong>We are highlighting this case presentation since it shows how a patient with newly diagnosed diabetes is at more of a risk of developing acute bilateral pyelonephritis. This information is important not only to add to medical knowledge but also to allow physicians to emphasize diabetic control in order to minimize the chance of developing pyelonephritis.</p>","PeriodicalId":73198,"journal":{"name":"HCA healthcare journal of medicine","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-04-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11229605/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141565237","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Evaluation of the Efficacy of Remdesivir for the Treatment of Coronavirus Disease 2019. Remdesivir 治疗冠状病毒疾病的疗效评估 2019。
HCA healthcare journal of medicine Pub Date : 2024-04-30 eCollection Date: 2024-01-01 DOI: 10.36518/2689-0216.1406
Alexandra Flannery, Anastasia Knecht, Koravangala Sundaresh
{"title":"Evaluation of the Efficacy of Remdesivir for the Treatment of Coronavirus Disease 2019.","authors":"Alexandra Flannery, Anastasia Knecht, Koravangala Sundaresh","doi":"10.36518/2689-0216.1406","DOIUrl":"10.36518/2689-0216.1406","url":null,"abstract":"<p><strong>Background: </strong>Coronavirus disease 2019 (COVID-19), caused by a novel coronavirus, SARS-CoV-2, has accounted for more than 1 000 000 deaths in the United States alone. In May 2020, the Food and Drug Administration issued an Emergency Use Authorization to allow the investigational use of intravenous remdesivir for the treatment of suspected or confirmed COVID-19 in hospitalized children and adults. Several other agents, such as hydroxychloroquine, dexamethasone, and tocilizumab have been investigated as potential treatment options; however, dexamethasone is currently the only agent that has been proven to reduce mortality in patients who require supplemental oxygen. The purpose of this study was to determine if initiation of remdesivir treatment in patients who presented with early symptoms of COVID-19 (defined as symptom onset < 7 days) had a significant impact on in-patient all-cause mortality compared to initiation of remdesivir treatment in patients who presented with symptom onset of at least 7 days.</p><p><strong>Methods: </strong>This ethics-committee-approved, retrospective, multicenter, double-arm study was conducted across 10 facilities in the HCA Healthcare West Florida Division. Adult inpatients age 18 and older with confirmed COVID-19 and administered intravenous remdesivir from May 1, 2020, to July 31, 2020, were included. Exclusion criteria included patients less than 18 years of age, the concomitant use of hydroxychloroquine or tocilizumab for any indication, or an estimated glomerular filtration rate less than 30 milliliters per minute. The primary outcome of this study was in-patient all-cause mortality. Secondary outcomes included total length of stay, time to discharge, oxygen requirements, and number of ventilator days.</p><p><strong>Results: </strong>A total of 217 patients from facilities in the HCA Healthcare West Florida Division were evaluated for inclusion. The primary outcome of all-cause mortality occurred in 34.9% of patients with symptom onset of fewer than 7 days versus 31.0% of patients with symptom onset of at least 7 days (<i>P</i> = .57). There were no statistical differences found among the secondary outcomes.</p><p><strong>Conclusion: </strong>Time since symptom onset did not result in a statistically significant difference in all-cause mortality in patients who received intravenous remdesivir for the treatment of COVID-19.</p>","PeriodicalId":73198,"journal":{"name":"HCA healthcare journal of medicine","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-04-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11229600/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141565243","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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