Authors

  • Akmalova Nasiba Alisherovna
  • Aliyev A.L

Author Biographies

  • Akmalova Nasiba Alisherovna

    Tashkent Pediatric Medical Institute

  • Aliyev A.L

    Scientific supervisor: Associate Professor of Medical Sciences

DOI:

https://doi.org/10.71337/inlibrary.uz.mead.87356

Keywords:

pneumonia congenital anomalies of cleft lip and palate young children clinic X- ray studies.

Abstract

In this study, clinical and anamnestic features of the course of severe pneumonia in early age children with congenital anomalies of the cleft lip and palate were observed with analysing of life history and current condition of the children. Research methods are analysis, clinical observations, x-ray studies. Clinical and anamnestic features of the course of severe pneumonia in early age children with congenital anomalies of the cleft lip and palate were determined. It was revealed that the severity of the condition of examined children was due to a burdened maternal history, premorbid background, artificial feeding and prematurity factor itself and such conditions of the microflora of the gastrointestinal tract.


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CLINICAL AND ANAMNESTIC FEATURES OF THE COURSE OF

SEVERE PNEUMONIA IN EARLY AGE CHILDREN WITH CONGENITAL

ANOMALIES OF CLEFT LIP AND PALATE

Akmalova Nasiba Alisherovna

Tashkent Pediatric Medical Institute

Scientific supervisor: Associate Professor of Medical Sciences

Aliyev A.L.

Annotation:

In this study, clinical and anamnestic features of the course of

severe pneumonia in early age children with congenital anomalies of the cleft lip and

palate were observed with analysing of life history and current condition of the

children. Research methods are analysis, clinical observations, x-ray studies. Clinical

and anamnestic features of the course of severe pneumonia in early age children with

congenital anomalies of the cleft lip and palate were determined. It was revealed that

the severity of the condition of examined children was due to a burdened maternal

history, premorbid background, artificial feeding and prematurity factor itself and

such conditions of the microflora of the gastrointestinal tract.

Key words:

pneumonia, congenital anomalies of cleft lip and palate, young

children, clinic, X- ray studies.

Relevance:

Acute pneumonia in young children remains a significant cause

of morbidity and mortality, despite the introduction of potent broad-spectrum

antimicrobial agents, comprehensive supportive treatment regimens, and preventive

measures (4). An unfavorable background for pneumonic dysbiosis is a cause of

recurrent pneumonia in children, prolonged disease duration, and a tendency toward

exacerbations, relapses, and complications (2).

Patients with congenital anomalies of the maxillofacial tissues and organs

occupy a special place. Of particular interest is the assessment of the clinical course

of acute pneumonia in these premature infants. However, despite this, there are few

studies or literature data with theoretical or practical significance regarding the

treatment of this group of patients. Treatment is associated with particular difficulties


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and requires the involvement of highly qualified specialists, consistency, and a

comprehensive approach.

Since ancient times, external factors have been thought to play a certain role

in the origin of congenital anomalies such as cleft lip and palate (CLP), as well as

maternal illnesses during pregnancy (infectious diseases, uterine pathology,

spontaneous or induced miscarriages), psychological trauma, malnutrition, and other

factors (1).

CLP represents a severe developmental defect that leads to serious

consequences. From birth, there are pronounced dysfunctions of the lip and palate.

Sucking and swallowing are impaired, and later on, chewing functions are also

affected, which in turn leads to developmental delays in the child and, in some cases,

death within the first weeks of life. In CLP, nutrition, swallowing, and breathing are

severely disrupted. This can lead to aspiration of oral cavity contents and various

complications involving the respiratory tract and lungs (1;3).

The above facts highlight the need to study the clinical and anamnestic

features of acute pneumonia in the context of CLP in young children.

Research Objective:

To analyze the clinical and anamnestic features of the

course of acute pneumonia in young children with congenital cleft lip and palate

anomalies.

Materials and Methods:

A total of 45 archived medical records of children

with severe acute pneumonia and congenital cleft lip and palate anomalies (CLP) were

analyzed, along with 18 premature infants weighing between 1500g and 1800g and

aged from 3 to 11 days.

Results and Discussion:

The age of the mothers ranged from 19 to 49 years:

5% were under 20, 23% were 20–25 years old, 51% were 26–30, and 17% were 30–

35. About 28% of the children were born from a first pregnancy. The outcome of

previous pregnancies was unfavorable (miscarriage, stillbirth, or premature birth) in

3% of cases. Fetal protein-energy deficiency was noted in 17%. Gynecological

diseases were present in 11% of the mothers.


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Chronic infections and conditions such as pyelonephritis, glomerulonephritis,

rheumatism, diabetes mellitus, obesity, and acute/chronic bronchitis were observed in

24.6% of women. Acute respiratory viral infections (ARVI) with high fever in the

first half of pregnancy were reported by 16.2% of women, and 6% in the second half.

The pregnancies were often complicated: early toxicosis occurred in 32.6% of cases;

gestosis of varying severity in 27%; the threat of miscarriage in 18%; chronic

intrauterine hypoxia in 8%; and infectious diseases in 20%. Labor was timely in

67.1% and premature or delayed in 33%. The most frequent complications were

premature rupture of membranes (12%) and anhydrous intervals of 6 to 12 hours

(11%). Abnormal labor activity was observed in 4% of women, requiring labor

stimulation in 2% of cases. At birth, 7% of newborns had an Apgar score of 7–8, 25%

had 4–5, and 5% had 3–4 points.

The study of the clinical course showed that the majority of children (12) had

a normal div temperature throughout the illness, 4 had subfebrile temperatures, and

only 4 cases were accompanied by high fever (up to 39°C). All premature infants with

CLP showed clinical signs of pneumonia accompanied by respiratory distress

syndrome, cyanosis (2 cases), acrocyanosis (6 cases), weakened breathing in the

lungs, and abdominal distention (13 cases) either at admission or within 2–3 days.

Intestinal syndrome developed at the onset of the illness or within 2–3 days after

admission and remained a leading feature during the entire acute phase. The diagnosis

of pneumonia was radiologically confirmed: in 14 children, focal shadows were found

on chest X-rays, and in three children, even confluent lesions were observed.

Conclusion:

The findings indicate that the severity of the children's condition

was due to a complicated maternal history, premorbid background, artificial feeding,

and the very fact of prematurity. Children with low birth weight and various forms of

immunodeficiency have intestinal flora that becomes pathogenic, triggering

inflammatory processes in both the intestines and lungs. The effectiveness of therapy

depends on an individualized approach, considering the etiology of the disease, the

course and stage of the pathological process, the child’s age, and the severity of

extrapulmonary organ involvement.


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References:

1. Bazhanov N.N. Dentistry. Moscow: Medicina, 1978. pp. 410–414.

2. Geppe N.A. Respiratory infections: problems and prospects. Proceedings of the

VIII Congress of Pediatricians of Uzbekistan, Tashkent, 2019.

3. Murtazaev S.M. "Condition of intestinal digestion and absorption in children with

congenital cleft lip and palate", Conference materials “Ibn Sino - Avicenna”, No. 1-

2, 2005, p. 37, Tashkent.

4. XXV National Congress on Respiratory Diseases, October 13–16, 2015, Moscow.

Proceedings edited by Acad. A.G. Chuchalin. Moscow, 2015, pp. 10–15.