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  1. Article ; Online: Snoring Survivors: the impact of obstructive sleep apnoea and continuous positive airway pressure use on in-hospital mortality, length of stay and costs among patients hospitalised with acute cardiovascular disease - A retrospective analysis of 2016-2019 National Inpatient Sample Data.

    Ogbu, Ikechukwu / Hakobyan, Bagrat / Sossou, Christoph / Levisman, Jeffrey / Obiagwu, Chukwudi / Danielian, Alfred

    BMJ open

    2024  Volume 14, Issue 2, Page(s) e073991

    Abstract: Background: The routine administration of supplemental oxygen to non-hypoxic patients with acute myocardial infarction (AMI) has been abandoned for lack of mortality benefit. However, the benefits of continuous positive airway pressure (CPAP) use in ... ...

    Abstract Background: The routine administration of supplemental oxygen to non-hypoxic patients with acute myocardial infarction (AMI) has been abandoned for lack of mortality benefit. However, the benefits of continuous positive airway pressure (CPAP) use in patients hospitalised with acute cardiovascular disease and concomitant obstructive sleep apnoea (OSA) remain to be elucidated.
    Methods: In this retrospective case-control analysis, using 10th International Classification of Diseases, Clinical Modification (ICD-10) codes, we searched the 2016-2019 Nationwide Inpatient Sample for patients diagnosed with unstable angina (UA), AMI, acute decompensated heart failure (ADHF) and atrial fibrillation with rapid ventricular response (AFRVR), who also carried a diagnosis of OSA. We identified in-hospital CPAP use with ICD-10-Procedure Coding System codes. In-hospital death, length of stay (LOS) and hospital charges were compared between patients with and without OSA, and between OSA patients with and without CPAP use.
    Results: Our sample included 2 959 991 patients, of which 1.5% were diagnosed with UA, 30.3% with AMI, 37.5% with ADHF and 45.8% with AFRVR. OSA was present in 12.3%. Patients with OSA were more likely to be younger, male, smokers, obese and have chronic obstructive pulmonary disease, renal failure and heart failure (p<0.001 for all). Patients with OSA had significantly lower in-hospital mortality (aOR 0.71, 95% CI (0.7 to 0.73)). Among patients with OSA, CPAP use significantly increased the odds of in-hospital death (aOR 1.51, 95% CI (1.44 to 1.60)), LOS (adjusted mean difference of 1.49 days, 95% CI (1.43 to 1.55)) and hospital charges (adjusted mean difference of US$1168, 95% CI (273 to 2062)).
    Conclusion: Our study showed that patients with recognised OSA hospitalised for AMI, ADHF and AFRVR had significantly lower mortality regardless of CPAP use, while CPAP treatment among these patients was associated with significantly higher in-hospital mortality and resource utilisation. The routine use of CPAP during acute cardiovascular encounters could neutralise the impact of chronic intermittent ischaemic preconditioning.
    MeSH term(s) Humans ; Male ; Cardiovascular Diseases/complications ; Retrospective Studies ; Length of Stay ; Hospital Mortality ; Inpatients ; Continuous Positive Airway Pressure/methods ; Snoring ; Acute Disease ; Myocardial Infarction/complications ; Heart Failure/complications ; Heart Failure/therapy ; Sleep Apnea, Obstructive/complications ; Sleep Apnea, Obstructive/therapy
    Language English
    Publishing date 2024-02-05
    Publishing country England
    Document type Journal Article
    ZDB-ID 2599832-8
    ISSN 2044-6055 ; 2044-6055
    ISSN (online) 2044-6055
    ISSN 2044-6055
    DOI 10.1136/bmjopen-2023-073991
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: A Rare Culprit of Infective Endocarditis in an IV Drug User:

    Nnaoma, Christopher / Chika-Nwosuh, Ogechukwu / Sossou, Christoph

    Case reports in medicine

    2019  Volume 2019, Page(s) 6403943

    Abstract: Infective endocarditis (IE) is an infection of the cardiac native or prosthetic valves typically caused ... ...

    Abstract Infective endocarditis (IE) is an infection of the cardiac native or prosthetic valves typically caused by
    Language English
    Publishing date 2019-04-10
    Publishing country United States
    Document type Case Reports
    ZDB-ID 2502642-2
    ISSN 1687-9635 ; 1687-9627
    ISSN (online) 1687-9635
    ISSN 1687-9627
    DOI 10.1155/2019/6403943
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: A Rare Culprit of Spontaneous Abortion, Latent Tuberculosis Complicated by Disseminated Peritoneal TB.

    Sossou, Christoph / Pal, Chaitanya / Bustillo, Jose R

    Case reports in infectious diseases

    2018  Volume 2018, Page(s) 2318539

    Abstract: This is a case of a 38-year-old female with latent TB complicated by disseminated peritoneal TB with associated spontaneous abortion, who was initially thought to have an ovarian neoplasm, prompting extensive workup. Laparoscopy with biopsy later ... ...

    Abstract This is a case of a 38-year-old female with latent TB complicated by disseminated peritoneal TB with associated spontaneous abortion, who was initially thought to have an ovarian neoplasm, prompting extensive workup. Laparoscopy with biopsy later confirmed the patient's condition; she was initiated on the appropriate therapy and had a full recovery.
    Language English
    Publishing date 2018-10-28
    Publishing country Egypt
    Document type Case Reports
    ZDB-ID 2627642-2
    ISSN 2090-6633 ; 2090-6625
    ISSN (online) 2090-6633
    ISSN 2090-6625
    DOI 10.1155/2018/2318539
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Atypical Presentation of Small Lymphocytic Lymphoma with Pericardial Effusion.

    Nnaoma, Christopher / Chika-Nwosuh, Ogechukwu / Mbonu, Ikechukwu / Sossou, Christoph W / Okonkwo, Christian C / Isedeh, Anthony

    The American journal of case reports

    2019  Volume 20, Page(s) 1128–1131

    Abstract: BACKGROUND Small lymphocytic lymphoma (SLL) is a low-grade B-cell non-Hodgkin lymphoma and is the solid tumor equivalent of chronic lymphocytic leukemia (CLL) that is found in the peripheral blood. SLL typically presents with lymphadenopathy and is ... ...

    Abstract BACKGROUND Small lymphocytic lymphoma (SLL) is a low-grade B-cell non-Hodgkin lymphoma and is the solid tumor equivalent of chronic lymphocytic leukemia (CLL) that is found in the peripheral blood. SLL typically presents with lymphadenopathy and is rarely associated with cardiac involvement. This report is of a case of lymphomatous pericardial effusion in a 61-year-old woman who presented with dyspnea. CASE REPORT A 61-year-old woman presented to the emergency department with a three-month history of worsening shortness of breath on exertion. Her symptoms progressed to shortness of breath at rest, with night sweats and chills. She had no weight loss. She was found to have a pericardial effusion, and an urgent pericardiocentesis was performed to prevent cardiac tamponade. Analysis of the pericardial fluid was consistent with a diagnosis of SLL. A bone marrow biopsy and a biopsy of a renal mass were consistent with a diagnosis of SLL. She was treated with rituximab and bendamustine with granulocyte-colony stimulating factor (G-CSF) support and was discharged home. CONCLUSIONS A case is presented of a rare association between SLL and pericardial effusion with a favorable outcome following urgent pericardiocentesis to prevent cardiac tamponade followed by chemotherapy.
    MeSH term(s) Computed Tomography Angiography ; Dyspnea/etiology ; Female ; Humans ; Leukemia, Lymphocytic, Chronic, B-Cell/diagnosis ; Middle Aged ; Pericardial Effusion/diagnostic imaging ; Pericardial Effusion/etiology ; Tomography, X-Ray Computed
    Language English
    Publishing date 2019-07-31
    Publishing country United States
    Document type Case Reports ; Journal Article
    ZDB-ID 2517183-5
    ISSN 1941-5923 ; 1941-5923
    ISSN (online) 1941-5923
    ISSN 1941-5923
    DOI 10.12659/AJCR.915576
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: A Case of Systemic Lupus Erythematosus Presenting as Autoimmune Myelofibrosis.

    Mbonu, Ikechukwu / Sossou, Christoph / Nnaoma, Christopher B / Sun, Xinlai / Schleicher, Lori / Xiong, Wen

    The American journal of case reports

    2019  Volume 20, Page(s) 937–940

    Abstract: BACKGROUND Systemic lupus erythematosus (SLE) is characterized by multiorgan involvement and presence of autoantibodies. SLE has a broad range of presentations and manifestations, and as such, its course and organ involvement are unpredictable. The ... ...

    Abstract BACKGROUND Systemic lupus erythematosus (SLE) is characterized by multiorgan involvement and presence of autoantibodies. SLE has a broad range of presentations and manifestations, and as such, its course and organ involvement are unpredictable. The disease results from the interaction of genes, environment, and random effects combining to lead to a loss of tolerance to self-antigens and active autoimmunity. Autoimmune myelofibrosis is a type of non-malignant bone marrow fibrosis that occurs in the presence of systemic autoimmune disease. Cytopenias such as anemia, leukopenia, and thrombocyotopenia are common manifestations of SLE; however, myelofibrosis is a less common and far less recognized complication of SLE. CASE REPORT We report a case of a young African American female who presented with severe anemia and leukopenia, subsequently diagnosed with myelofibrosis and then eventually SLE. The identification of myelofibrosis in SLE is critical as it can be a devastating condition when untreated. Fortunately, autoimmune myelofibrosis in SLE is reversible with treatment of the underlying condition. CONCLUSIONS Autoimmune myelofibrosis is a rare complication of SLE. Autoimmune myelofibrosis could be the first and only presenting feature of SLE. It is sensible to recognize this relationship, as prompt diagnosis and treatment is crucial. Corticosteroids have been shown to be useful in treating both SLE and the associated autoimmune myelofibrosis.
    MeSH term(s) Anemia/etiology ; Autoimmunity ; Diagnosis, Differential ; Female ; Humans ; Leukopenia/etiology ; Lupus Erythematosus, Systemic/complications ; Lupus Erythematosus, Systemic/diagnosis ; Primary Myelofibrosis/etiology ; Thrombocytopenia/etiology ; Young Adult
    Language English
    Publishing date 2019-07-01
    Publishing country United States
    Document type Case Reports
    ZDB-ID 2517183-5
    ISSN 1941-5923 ; 1941-5923
    ISSN (online) 1941-5923
    ISSN 1941-5923
    DOI 10.12659/AJCR.916001
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article: A Band That Causes Leaky Valves: Severe Mitral Regurgitation due to Left Atrial Fibrous Band-A Case Report and Literature Review.

    Nnaoma, Christopher / Sandhu, Gurdarshan / Sossou, Christoph / Vavilin, Ilan / Bustillo, Jose / Garg, Anshu

    Case reports in cardiology

    2019  Volume 2019, Page(s) 2458569

    Abstract: Left atrial fibrous band is a rare clinical and echocardiographic finding characterized by the presence of a fibrous band attached to the mitral valve. Diagnosis is accomplished with transesophageal echocardiography (TEE), live 3D imaging, or cardiac MRI. ...

    Abstract Left atrial fibrous band is a rare clinical and echocardiographic finding characterized by the presence of a fibrous band attached to the mitral valve. Diagnosis is accomplished with transesophageal echocardiography (TEE), live 3D imaging, or cardiac MRI. Most patients are asymptomatic and incidental findings. However, in rare cases, an atrial fibrous band can produce symptoms such as dyspnea on exertion, fatigue, and lightheadedness secondary to mitral regurgitation (MR) which can lead to heart failure if unattended to. More serious complications such as cardioembolic phenomenon can occur. We herein report a case of a 55-year-old male with hypertension who presented with dyspnea on exertion and chest pain. Transthoracic echocardiography (TTE) showed mitral valve prolapse with moderate to severe mitral regurgitation. TEE showed an atrial fibrous band. Given the patient's poor exercise tolerance, he was taken to surgery for a mitral annuloplasty.
    Language English
    Publishing date 2019-03-19
    Publishing country United States
    Document type Case Reports
    ZDB-ID 2627627-6
    ISSN 2090-6412 ; 2090-6404
    ISSN (online) 2090-6412
    ISSN 2090-6404
    DOI 10.1155/2019/2458569
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Diversity in U.S. Cardiovascular Trainees and Leadership Where we are and What the Future Holds.

    Sossou, Christoph W / Fakhra, Sadaf / Batra, Kavita / Nouthe, Brice / Okoh, Alexis / Phillips-Wilson, Tasha / Kuria, Carolyne N / Hawwass, Dalia / Ogunniyi, Modele O / Singh, Aditi / Cohen, Marc / Dawn, Buddhadeb / Ahsan, Chowdhury H

    Current problems in cardiology

    2022  Volume 48, Issue 3, Page(s) 101518

    Abstract: Cardiovascular (CV) outcomes can be improved with commonality between provider and patient regarding gender and race/ethnicity. Slow growth in CV care provider diversity is an obstacle for women and underrepresented groups. The hope for more equitable ... ...

    Abstract Cardiovascular (CV) outcomes can be improved with commonality between provider and patient regarding gender and race/ethnicity. Slow growth in CV care provider diversity is an obstacle for women and underrepresented groups. The hope for more equitable outcomes is unlikely to be realized unless trends change in selection of CV fellows and program directors (PDs). We investigate longitudinal trends of gender and racial/ethnic composition of CV FITs. De-identified demographic data were compiled in a descriptive cross-sectional study from AAMC of internal medicine (IM) residents and CV FITs from 2011 through 2021 to evaluate gender and race/ethnicity trends among CV trainees. Trends of CV fellows who later became program directors were analyzed. In the US between 2011 and 2021, 53% of IM residents were male while 40% female (7% unreported). Among CV FITs, 78% were male and 21% female. Races/ethnicities among CV FITs consisted of 36% non-Hispanic white, 28% non-Hispanic Asian, 5% Hispanic, 4%Black, and 25% were classified within other race/ethnicity categories. The proportion who became CV program directors followed similarly: 79% of PDs were male and 21% female. Demographic profiles for CV FITs have not significantly changed over the past decade despite increased diversity among IM residents. Efforts to improve diversity of CV FITs and PDs need to be analyzed. Slow growth of diversity in CV FITs is outpaced by rising patient diversity, leading to disparities in care and poorer CV outcomes for women and underrepresented minorities. Recruiting, training, and retaining diverse CV FITs is necessary.
    MeSH term(s) Humans ; Male ; Female ; United States/epidemiology ; Cross-Sectional Studies ; Leadership ; Ethnicity ; Hispanic or Latino ; Minority Groups
    Language English
    Publishing date 2022-12-01
    Publishing country United States
    Document type Journal Article ; Review
    ZDB-ID 441230-8
    ISSN 1535-6280 ; 0146-2806
    ISSN (online) 1535-6280
    ISSN 0146-2806
    DOI 10.1016/j.cpcardiol.2022.101518
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Left Ventricular Function Recovery After Transapical TAVR in Patients With Previous Coronary Artery Bypass Graft Surgery.

    Okoh, Alexis K / Sossou, Christoph / Kang, Nathan / Decker, Jonathan / Dave, Devangi / Haik, Bruce / Chen, Chunguang / Cohen, Marc / Russo, Mark

    Innovations (Philadelphia, Pa.)

    2019  Volume 14, Issue 5, Page(s) 405–411

    Abstract: Objective: The transapical (TA) approach is an alternative access technique for transcatheter aortic valve replacement (TAVR) in patients with symptomatic aortic valve stenosis. The impact of prior coronary artery bypass graft (CABG) surgery and how it ... ...

    Abstract Objective: The transapical (TA) approach is an alternative access technique for transcatheter aortic valve replacement (TAVR) in patients with symptomatic aortic valve stenosis. The impact of prior coronary artery bypass graft (CABG) surgery and how it affects left ventricular function recovery is not well defined.
    Methods: Patients who had TAVR at a single center between June 2012 and December 2016 were reviewed. High-risk patients who underwent the procedure via a TA approach were divided into 2 groups based on their history of CABG surgery. Postoperative outcomes were compared between groups. CABG/TA-TAVR patients were subdivided into 2 per baseline left ventricular ejection fraction (LVEF) <50%. The changes in LVEF and valve function at follow-up (1 to 12 months) were analyzed using paired
    Results: Of 923 cases in total, 183 (19.8%) were performed via a TA approach. The mean ± SD Society of Thoracic Surgeons risk score of TA patients was 10.2 ± 4.6. Forty-nine (27%) had a surgical history of CABG. Overall all-cause mortality rates at 30 days, 1 year, and 2 years were similar for both groups (
    Conclusions: TA-TAVR can be safely performed with acceptable postoperative outcomes in patients with a history of CABG surgery. In those with reduced EF, significant improvements in LV and valve functions are seen at 1-year follow-up.
    MeSH term(s) Aged, 80 and over ; Aortic Valve Stenosis/complications ; Aortic Valve Stenosis/physiopathology ; Aortic Valve Stenosis/surgery ; Coronary Artery Bypass/adverse effects ; Coronary Artery Bypass/mortality ; Coronary Disease/complications ; Coronary Disease/physiopathology ; Coronary Disease/surgery ; Female ; Humans ; Kaplan-Meier Estimate ; Male ; Retrospective Studies ; Transcatheter Aortic Valve Replacement/methods ; Transcatheter Aortic Valve Replacement/mortality ; Treatment Outcome ; Ventricular Function, Left
    Language English
    Publishing date 2019-07-29
    Publishing country United States
    Document type Journal Article
    ISSN 1559-0879
    ISSN (online) 1559-0879
    DOI 10.1177/1556984519864080
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article: Misdiagnosis: Acute Chest Syndrome That Evolved into Acute Respiratory Distress Syndrome in a Patient without a Documented History of Hemoglobinopathy.

    Sossou, Christoph / Chika-Nwosuh, Ogechukwu / Nnaoma, Christopher / Bustillo, Jose / Chohan, Asad / Okundaye, Etinosasere / Patel, Pratik

    Case reports in medicine

    2019  Volume 2019, Page(s) 2893056

    Abstract: Acute chest syndrome (ACS) is a feared complication of sickle cell disease. Here is a case of a patient who presented with symptoms suggestive of acute chest syndrome yet had a delayed diagnosis presumably due to the lack of documented history of sickle ... ...

    Abstract Acute chest syndrome (ACS) is a feared complication of sickle cell disease. Here is a case of a patient who presented with symptoms suggestive of acute chest syndrome yet had a delayed diagnosis presumably due to the lack of documented history of sickle cell disease of the patient, consequently evolving into acute respiratory distress syndrome (ARDS). He was subsequently diagnosed with heterozygous sickle cell SC disease on hemoglobin electrophoresis. After appropriate management with mechanical ventilator, broad-spectrum empiric intravenous antibiotics, exchange transfusion, and intravenous fluid resuscitation, the patient was medically optimized and safely discharged home, with significant improvement noted on successive follow-up visits.
    Language English
    Publishing date 2019-02-03
    Publishing country United States
    Document type Case Reports
    ZDB-ID 2502642-2
    ISSN 1687-9635 ; 1687-9627
    ISSN (online) 1687-9635
    ISSN 1687-9627
    DOI 10.1155/2019/2893056
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article: A Rare Culprit of Simultaneous Arteriovenous Thromboembolism: Acute Viral Perimyocarditis.

    Sossou, Christoph / Ogundare, Tobi / Chika-Nwosuh, Ogechukwu / Sodha, Amee / Nnaoma, Christopher / McKinney, Cynthia / Bustillo, Jose

    Case reports in cardiology

    2019  Volume 2019, Page(s) 5361529

    Abstract: Simultaneous arteriovenous embolism is extremely rare. Herein, we present a rare case of systemic arteriovenous emboli in a healthy 33-year-old male after an episode of acute viral perimyocarditis. The culprits are postulated to be viral-induced ... ...

    Abstract Simultaneous arteriovenous embolism is extremely rare. Herein, we present a rare case of systemic arteriovenous emboli in a healthy 33-year-old male after an episode of acute viral perimyocarditis. The culprits are postulated to be viral-induced myocardial necrosis and resulting proinflammatory state in the setting of negative malignant, autoimmune, genetics, and chronic infectious conditions. The patient was successfully managed with guideline-directed medical therapy and safely discharged to a subacute rehabilitation facility.
    Language English
    Publishing date 2019-01-08
    Publishing country United States
    Document type Case Reports
    ZDB-ID 2627627-6
    ISSN 2090-6412 ; 2090-6404
    ISSN (online) 2090-6412
    ISSN 2090-6404
    DOI 10.1155/2019/5361529
    Database MEDical Literature Analysis and Retrieval System OnLINE

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