Al Haddabi Amjad, Al Jabri Musab, Al Balushi Abdulmajeed, Al Mamari Issa, Mohsin Hussain
Child Health Department, Sultan Qaboos University Hospital, Muscat, Oman.
Resident in Pediatric Surgery, Assistance Publique-Hôpitaux de Paris, Necker-Enfants Malades Hospital, Université Paris Cité, Paris, France.
Oman Med J. 2025 Mar 31;40(2):e737-e737e. doi: 10.5001/omj.2025.69. eCollection 2025 Mar.
Cystic fibrosis (CF) is a multisystemic genetic disease. Progressive decline in lung function is the major cause of morbidity and mortality in this population, primarily related to chronic airway infection and recurrent pulmonary exacerbations. We sought to assess the pattern of airway bacterial growth among patients with CF in Oman and identify possible risk factors for the hypothesized early acquisition among this population.
We conducted a retrospective single-center cross-sectional study that included all patients who attended the CF clinic at Royal Hospital, Oman between 2004 and 2020. Collected data included age, sex, geographic region, date of CF diagnosis, CF genotype, number of siblings with CF, and the date and results of all positive respiratory cultures. Early acquisition was defined by a positive respiratory culture for before the age of two years. Multi-drug resistant was defined as not susceptible to ≥ 1 agent in ≥ 3 classes of antimicrobials. The above factors were compared between the early and late acquisition groups.
A total of 114 patients were included, and 2393 positive bacterial cultures were analyzed. Eighty-four (73.7%) patients were identified to have a positive culture for , including 40 (47.6%) who acquired it before the age of two years. remained the most common organism across all age groups. Twenty-six (22.8%) patients were positive for on their first respiratory culture, while 56 (49.1%) patients had three or more positive respiratory cultures for Methicillin-resistant accounted for 7.2% of all positive cultures under the age of one year and peaked at 14.8% between the ages of four and five years. A significant association were found between early acquisition and male sex. No significant association was observed between CF genotype, geographic region, age at diagnosis, or the presence of a sibling with CF and early acquisition.
Our study demonstrated earlier acquisition of and its predominance among children with CF in Oman. Male sex was associated with a higher risk for early acquisition. Further prospective studies are needed to confirm this association and identify other possible risk factors. These findings will impact the clinical practice of CF physicians in Oman.
囊性纤维化(CF)是一种多系统遗传病。肺功能进行性下降是该人群发病和死亡的主要原因,主要与慢性气道感染和反复肺部加重有关。我们旨在评估阿曼CF患者气道细菌生长模式,并确定该人群中推测的早期感染的可能危险因素。
我们进行了一项回顾性单中心横断面研究,纳入了2004年至2020年间在阿曼皇家医院CF诊所就诊的所有患者。收集的数据包括年龄、性别、地理区域、CF诊断日期、CF基因型、患有CF的兄弟姐妹数量以及所有阳性呼吸道培养物的日期和结果。早期感染定义为两岁前呼吸道培养阳性。多重耐药菌定义为对≥3类抗菌药物中的≥1种药物不敏感。对早期和晚期感染组的上述因素进行比较。
共纳入114例患者,分析了2393份阳性细菌培养物。84例(73.7%)患者被确定为培养阳性,其中40例(47.6%)在两岁前感染。在所有年龄组中,仍是最常见的病原体。26例(22.8%)患者首次呼吸道培养阳性,而56例(49.1%)患者有三次或更多次呼吸道培养阳性。耐甲氧西林在一岁以下所有阳性培养物中占7.2%,在四岁至五岁之间达到峰值14.8%。发现早期感染与男性性别之间存在显著关联。未观察到CF基因型、地理区域、诊断年龄或患有CF的兄弟姐妹与早期感染之间存在显著关联。
我们的研究表明,阿曼CF儿童中感染较早且占主导地位。男性性别与早期感染风险较高相关。需要进一步的前瞻性研究来证实这种关联并确定其他可能的危险因素。这些发现将影响阿曼CF医生的临床实践。