Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    Online Resource
    Online Resource
    Valley International ; 2022
    In:  Research and Analysis Journal Vol. 5, No. 8 ( 2022-08-04), p. 01-06
    In: Research and Analysis Journal, Valley International, Vol. 5, No. 8 ( 2022-08-04), p. 01-06
    Abstract: Interatrial communication is a common congenital heart disease in adulthood. It is subdivided into four distinct groups based on location. Coronary sinus type is the rarest one and represents less than 1% of interatrial septal defects. Its echocardiographic diagnosis can be difficult. We report the case of a 27-year-old female patient, admitted to the emergency department for management of a poorly tolerated supraventricular tachycardia, referred to cardiology after cardioversion. Clinical examination revealed a SaO2 of 95%, a B2 burst at the pulmonary site. The ECG in sinus rhythm showed right bundle branch block and right atrial hypertrophy. Echocardiography showed dilated right chambers, coronary sinus atrial septal defect with a left-to-right shunt, dysplastic mitral valve, and pulmonary pression was estimated at 85mmhg on tricuspid insufficiency flow; right ventricular function was normal. The patient was treated with B-blocker and VKA with a good clinical course. She is waiting a right catheterization to decide on surgical closure of the atrial septal defect. Through this case, we wanted to underline the importance of not omitting the echocardiographic search for a defect of the roof of the interatrial septum in front of a volumetric overload of the right cavities.
    Type of Medium: Online Resource
    ISSN: 2589-9228 , 2589-921X
    Language: Unknown
    Publisher: Valley International
    Publication Date: 2022
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    Online Resource
    Online Resource
    International Journal Of Advanced Research ; 2022
    In:  International Journal of Advanced Research Vol. 10, No. 02 ( 2022-02-28), p. 652-659
    In: International Journal of Advanced Research, International Journal Of Advanced Research, Vol. 10, No. 02 ( 2022-02-28), p. 652-659
    Abstract: Steinerts disease or myotonic dystrophy type 1 is a genetic neuromuscular disorder with autosomal dominant transmission. It leads to multisystemic damage, including a cardiac localization that is life-threatening.We report the case of a 55 year old patient, without cardiovascular risk factors, with a history of distal muscle damage since the age of 25 years, in his family history we find a brother followed for an unlabelled skeletal muscle damage.He consulted for exertional dyspnea and lipothymic discomfort. The clinical examination revealed a decrease in muscle strength in the lower limbs with amyotrophy. Walking is difficult with the help of crutches and the patient uses a wheelchair. The neurological investigation concluded in Steinerts myotonic dystrophy on the electromyogram.The patients ECG showed a bifascicular block consisting of a left anterior hemiblock and a complete right bundle branch block. The echocardiography did not show any structural abnormalities but found a disturbance of the LV relaxation on the mitral profile.The electrophysiological exploration carried out for the measurement of infrahisical conduction revealed a long HV at 100ms indicating the implantation of a double chamber stimulation.The interest of reporting this case was to underline the importance of screening for cardiac damage of rhythmic origin. But also to inform with the help of literature data the incidence of these forms and the place of cardiac stimulation in the prevention of sudden death in steinerts myotonia.
    Type of Medium: Online Resource
    ISSN: 2320-5407
    Language: Unknown
    Publisher: International Journal Of Advanced Research
    Publication Date: 2022
    detail.hit.zdb_id: 2733321-8
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 3
    In: International Journal of Advanced Research, International Journal Of Advanced Research, Vol. 10, No. 05 ( 2022-05-31), p. 1245-1250
    Abstract: Submit: Abnormal coronary artery birth from the pulmonary artery (PA) is a rare disease, characterized by age-dependent clinical forms. We will describe the clinical, electrical and echocardiography features and the management strategy of this disease in adults. Materials and methods: We enrolled 9 patients, 6 with the diagnosis of ALCAPA and 3 of ARCAPA. The mean age was 32 years with a sex ratio of 1.5/1. The presentations consisted of exertion symptoms and incidental findings. LVEF was reduced in 33% of patients with ALCAPA. Moderate mitral regurgitation (MR) was found in 44% of cases, particularly in cases of ALCAPA. Coronary CT scans confirmed that all our patients had coronary artery anomalies from the PA. The surgical treatment of coronary reimplantation was the therapeutic method of choice and was performed in 88% of our patients. Conclusion: Coronary birth defect from PA is a very rare congenital pathology. The clinical symptomatology that leads to the discovery of the disease is diverse. Doppler imaging and CT scann is a key tool in the positive diagnosis. Early re-implantation surgery can avoid complicated forms.
    Type of Medium: Online Resource
    ISSN: 2320-5407
    Language: Unknown
    Publisher: International Journal Of Advanced Research
    Publication Date: 2022
    detail.hit.zdb_id: 2733321-8
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 4
    Online Resource
    Online Resource
    International Journal Of Advanced Research ; 2022
    In:  International Journal of Advanced Research Vol. 10, No. 02 ( 2022-02-28), p. 646-651
    In: International Journal of Advanced Research, International Journal Of Advanced Research, Vol. 10, No. 02 ( 2022-02-28), p. 646-651
    Abstract: Implantable cardiac devices (pacemaker, ICD, resynchronisation) are increasingly indicated in recent years. Complications secondary to these implants are encountered more frequently.We report the case of a 60 year old patient with a double chamber pacing device, implanted 6 months before her consultation date for a complete AVB.She was referred by her attending physician for exertional dyspnea and lipothymic discomfort following the implantation of the device.Clinical examination revealed no abnormalities. The ECG showed a spontaneous sinus rhythm at 60cpm.The interrogation of the device showed a DDDR pacing mode with the most frequent pacing mode in ASVS found at 80%.The EGMs listed were not consistent with the programmed dual chamber mode. The atrial endocavitary signals are labelled VS and the ventricular ones AP. The change of mode to VVI which should generate a ventricular drive showed us a spontaneous atrial signal coded VS. The AAI mode produces ventricular pacing with AP coded ventriculograms.A reversal of the lead connection at the box level was evoked.The patient has undergone a correct reconnection of the leads to the box with a rhythm at the end of the procedure in DDD.Follow-up telemetry 1 month after reconnection showed atrial and ventricular EGM signals appropriate to the paced and detected chamber.
    Type of Medium: Online Resource
    ISSN: 2320-5407
    Language: Unknown
    Publisher: International Journal Of Advanced Research
    Publication Date: 2022
    detail.hit.zdb_id: 2733321-8
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 5
    Online Resource
    Online Resource
    International Journal Of Advanced Research ; 2022
    In:  International Journal of Advanced Research Vol. 10, No. 05 ( 2022-05-31), p. 1251-1254
    In: International Journal of Advanced Research, International Journal Of Advanced Research, Vol. 10, No. 05 ( 2022-05-31), p. 1251-1254
    Abstract: Introduction: ischemic left bundle branch block (LBBB) is left coronary occlusion. We report an atypical case of de novo ischemic LBBB in relation to a tight right coronary lesion. Material and methods: Mr H, 53 years old with no modifiable risk factors, consulted for a typical angina pain evolving since 4 hours. The per-critical ECG showed a complete de novo LBBB with criteria of acute coronary ischemia. Coronary angiography showed a tight lesion of the right coronary artery that was stented with a good evolution marked by the regression of symptoms and signs of LBBB ischemia. Discussion: Ischemic LBBB is a coronary emergency requiring urgent coronary reperfusion. The diagnosis is facilitated by the commonly used Sgarbossa and Smith criteria. An occlusion of the anterior interventricular artery is most often incriminated. There is no evidence of a relationship with a right coronary lesion. The literature is poor in the description of the culprit lesions in ischemic LBBB.
    Type of Medium: Online Resource
    ISSN: 2320-5407
    Language: Unknown
    Publisher: International Journal Of Advanced Research
    Publication Date: 2022
    detail.hit.zdb_id: 2733321-8
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 6
    Online Resource
    Online Resource
    Valley International ; 2022
    In:  Research and Analysis Journal Vol. 5, No. 8 ( 2022-08-04), p. 07-11
    In: Research and Analysis Journal, Valley International, Vol. 5, No. 8 ( 2022-08-04), p. 07-11
    Abstract: Improving quality of life in AF is a clinical issue in the management of this disease. The choice of therapeutic strategy; rhythm or rate control would influence the parameters of quality of life assessment. The aim of our study was to describe the impact of maintaining sinus rhythm after cardioversion on the quality of life of patients followed for AF.To do this we conducted a prospective descriptive study including 24 patients followed for paroxysmal, persistent and prolonged persistent AF. Quality of life was assessed by two scores (AFEQT, SF-36) validated for atrial fibrillation. The average age of our population was 53.3 years. Half of our sample had no underlying heart disease. We observed an improvement in quality of life in patients who maintained sinus rhythm. A contradictory result was observed in patients who had a recurrence of the arrhythmia. We also found that age, treatments and comorbidities influenced the quality of life of patients followed for AF. The results found in our study are consistent with the literature; the differences found are probably related to the size of our random sample and the number of scales used to assess quality of life. The use of quality of life scores could be a key issue for the follow-up of these patients in order to integrate a global management approach.
    Type of Medium: Online Resource
    ISSN: 2589-9228 , 2589-921X
    Language: Unknown
    Publisher: Valley International
    Publication Date: 2022
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. Further information can be found on the KOBV privacy pages