AI Article Synopsis

  • The study aimed to assess the prevalence of sleep-related disturbances, specifically nocturnal hypoxaemia, in patients with Eisenmenger syndrome.
  • The research involved 25 patients with Eisenmenger syndrome and compared them to 12 control patients with similar congenital heart conditions, utilizing overnight polysomnogram studies for data collection.
  • Results indicated that both groups experienced significant nocturnal hypoxaemia without apnoea, with higher incidences of oxygen drops linked to elevated haemoglobin levels in Eisenmenger syndrome patients.

Article Abstract

Objectives: The objective of the study was to find the prevalence of sleep-related disturbances in patients of Eisenmenger syndrome.

Design: Prospective observational study.

Setting: Tertiary care referral centre in North India.

Participants: The study included 25 patients with Eisenmenger syndrome (mean age 25.2±9.6 years, 18 men) and 12 patients with cyanotic congenital heart disease with pulmonary stenosis physiology (mean age 20.5±8.5 years, 8 men) as controls.

Interventions: All the patients underwent an overnight comprehensive polysomnogram study and pulmonary function testing.

Main Outcome Measure: Oxygen desaturation index, which is the number of oxygen drops per hour.

Results: The patients and controls had significant nocturnal hypoxaemia in the absence of apnoea and hypopnoea. The mean oxygen drop index in Eisenmenger syndrome group was 9.0±6.2 and in the control group was 8.0±5.9 (p=0.63). The apnoea-hypopnoea index was 3.37±5.0 in the Eisenmenger syndrome group and was 2.1±3.6 in the control group. Patients with >10 oxygen drops per hour had significantly higher haemoglobin (17.2±1.3% vs 14.4±1.5%, p<0.001) than those with oxygen drops less than 10.

Conclusions: Eisenmenger syndrome patients have significant nocturnal hypoxaemia unrelated to hypopnoea and apnoea. Nocturnal desaturation occurred more frequently in patients with greater haemoglobin values.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3612812PMC
http://dx.doi.org/10.1136/bmjopen-2012-002039DOI Listing

Publication Analysis

Top Keywords

eisenmenger syndrome
16
patients eisenmenger
12
nocturnal hypoxaemia
8
years men
8
oxygen drops
8
syndrome group
8
control group
8
patients
7
eisenmenger
5
hypoxaemia patients
4

Similar Publications

Adult aortopulmonary window is a rare presentation of a rare disease; only a few cases are reported to have undergone successful surgical closure without development of Eisenmenger syndrome. We describe the second oldest patient, a 25-year-old woman, who underwent successful surgical repair of aortopulmonary window after favorable indirect measures on echocardiography without the "gold standard" preoperative cardiac catheterization study. At 2 months after the operation, the patient remains in New York Heart Association class II.

View Article and Find Full Text PDF

This case report presents a 37-year-old male with a complex medical history, including HIV, chronic methamphetamine and cocaine use, and an atrial septal defect, who developed severe pulmonary arterial hypertension (PAH), biventricular failure, and recurrent stroke. The patient was admitted with acute neurological deficits and respiratory failure, which rapidly progressed despite intensive management. Laboratory and imaging studies revealed severe cardiac dysfunction and elevated pulmonary vascular resistance.

View Article and Find Full Text PDF

The aim of this single-centre retrospective observational study was to evaluate the safety, tolerability, and efficacy of an in-class combination therapy switch from bosentan plus sildenafil to ambrisentan plus tadalafil in children with pulmonary arterial hypertension. Children aged over 5 years who were established on sildenafil plus bosentan were offered to undergo a therapy switch from May 2014 to May 2021 and, if remaining in the service, followed up to May 2024. Children with Eisenmenger syndrome, open intra or extra-cardiac shunt, or with pulmonary hypertension-associated lung disease were excluded.

View Article and Find Full Text PDF

Eisenmenger syndrome during pregnancy: A true anesthetic challenge.

Med J Armed Forces India

December 2024

Professor & Senior Advisor, (Anaesthesia & Critical Care), Command Hospital (Eastern Command), Kolkata, West Bengal, India.

Eisenmenger syndrome (ES) is a rare congenital heart disease (CHD) that occurs in persons with large intracardiac anatomical defects which may go undetected for many years, consequently results in reduced life expectancies and high mortality in the third and fourth decade of life. Pregnancy in patients with CHD and pulmonary arterial hypertension (PAH) is presaged with challenges, and perioperative management of such cases remains a topic of debate. Our case had both, atypical presentation, not diagnosed until her third trimester of third pregnancy and a quick progression to a severe stage with PAH and CorPulmonale.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!