Showing posts with label Journal of Neonatology. Show all posts
Showing posts with label Journal of Neonatology. Show all posts

Friday, 15 September 2023

Lupine Publishers | Congenital Diaphragmatic Hernia: Case Report

 Lupine Publishers | Journal of Pediatrics and Neonatology


Abstract

Congenital diaphragmatic hernia is a malformation resulting from incomplete fusion of the pleuroperitoneal membrane, it occurs in around 1/5000 live newborns, it produces in the vast majority of cases severe symptoms of respiratory failure and pulmonary arterial hypertension in this age group. Treatment is based on maintaining the best respiratory conditions in the child through intensive neonatal therapy management and, once this objective is achieved, surgical correction of the anatomical defect should proceed. Unfortunately, despite the progress in respiratory management of the seriously ill newborn, mortality from this disease is reported above 75%. We present a case in which the left diaphragmatic hernia associated with pulmonary hypertension led to a fatal outcome in a newborn, despite timely and adequate interventions.

Keywords: Congenital Diaphragmatic Hernia; Pulmonary Hypertension; Respiratory Failure of The Newborn; Surgical Correction

Introduction

Congenital diaphragmatic hernia (CDH) is the most common developmental abnormality of the diaphragm and is one of the most common malformations in the newborn, occurring with a frequency of 1 in 2000 pregnancies and 1 in 2,200 to 5,000 live births. Its presentation is greater in males and is generally located on the left side of the diaphragm, at the site of the Boch dalek foramen, although it is occasionally right (Morgagni foramen) or, with less incidence, it can be bilateral or central [1,2]. The etiology is generally unknown, and most cases are likely to be multifactorial; It has also been associated with chromosomal abnormalities from 20% to 53% and an autosomal recessive form has been described. Despite intense research and aggressive therapeutic intervention in infants with CHD, morbidity and mortality continue to be elevated between 40% and 70% because the hypoplasia and persistent pulmonary hypertension that occur in these patients complicate efforts to maintain a gas exchange with conventional ventilation [3,4].

Case Presentation

From a nearby municipality, a 37-week-term male newborn was referred to us by Ballard, obtained on 04/16/21 by vaginal delivery without immediate complications. It is the product of the second pregnancy, the son of a 20-year-old mother with a controlled pregnancy twice without ultrasound control. He was born with an APGAR score of 8/10 at 1 minute and at 5 minutes, but at 14 hours of age he presented an episode of apnea with desaturations and generalized cyanosis, requiring positive pressure ventilation and fluid resuscitation with little improvement, due to the persistence of distress. respiratory system, a chest X-ray was performed where intestinal loops were observed in the left lung field, diagnosing diaphragmatic hernia, which is why they were referred to our institution. He was admitted to the neonatal intensive care unit in a fair general condition, cyanotic, hypotonic, desaturated and with a distant audible moan, requiring an orotracheal intubation protocol and invasive mechanical ventilation. The diagnosis was corroborated with a chest X-ray (Figure 1). Orogastric tube was placed to decompress abdominal content, water support and inotropics to maintain adequate mean arterial pressure. He was evaluated by pediatric surgery, who requested presurgical examinations, in which he found prolonged clotting times. Given the instability and the alteration in the coagulogram, surgery was postponed, management with vitamin K was started, and a pediatric hematologist was consulted, who indicated a transfusion of fresh plasma.

Once his hemodynamic part had stabilized and the clotting times normalized, the patient was taken to surgery on 04/24/21 where a left diaphragmatic defect of more or less 5 cm in diameter was observed and inside the thoracic cavity the presence of small intestine, descending colon, stomach and spleen, for which a reduction of the contents to the abdominal cavity was performed, hernial defect was corrected, diaphragmatic integrity was verified and a chest tube was left, ending the procedure without immediate complications. At 12 hours after surgery, a control X-ray was performed, showing a cardiac silhouette in good position and left lung expansion, and diffuse infiltrates predominantly in the middle lobe were seen in the right lung (Figure 2). An echocardiogram was performed that reported severe pulmonary hypertension with PSAP of 80 mmHg, requiring a phosphodiesterase-5 inhibitor (sildenafil), triple inotropic support and minimal manipulation protocol. Subsequently, a new chest X-ray was performed (Figure 3). Since the newborn presented clinical deterioration, increased work of breathing, generalized mucocutaneous paleness, peri-buccal and distal cyanosis; bradycardia, marked hypotension and desaturation despite established management and high ventilatory parameters. The patient presented cardiorespiratory arrest for which he began advanced cardiopulmonary resuscitation maneuvers for more than 20 minutes without obtaining a response, for which he was declared dead.

Figure 1: Chest X-ray before the surgical procedure.

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Figure 2: Chest x-ray after surgical procedure.

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Figure 3: Enlarged cardiac silhouette, with enlargement of the atrial cavities and veiling of the left pulmonary trunk, findings suggestive of pulmonary hypertension.

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Discussion

The first description of the anatomy and pathophysiology of congenital diaphragmatic hernia was made by Hunter and Mc Cauley in the year 1754; this was defined as the protrusion of the abdominal organs into the thorax, or the descent of the thoracic organs into the abdomen as a result of incomplete closure of the pleuroperitoneal canals. Its incidence is estimated at 1 in 2000 to 5000 births. The defect is more frequent on the left side for 80% and the rest for the right; bilateral ones are extremely rare. The incidence of associated malformations is 10–50% and mortality is high, reaching up to 70% of cases [5,6]. There are reports of high morbidity in patients who survive the initial management of congenital diaphragmatic hernia. Long-term use of mechanical ventilation is associated with bronchopulmonary dysplasia in a higher proportion of children with diaphragmatic hernia. Other types of problems are esophageal ectasia with gastroesophageal reflux in cases of very large defects; recurrence of the hernia or intestinal obstruction are serious complications, although not frequently reported. In a group of patients in which the extracorporeal oxygenation membrane was used, a higher incidence of neurocognitive problems is reported at school [7,8]. Even though there are innovative methods in intrauterine treatment and immediate postnatal therapy, the real solution to this problem will be, in the future, through the knowledge and prevention of the embryological cause and the creation of techniques that induce lung growth [9,10]. In conclusion, this case report brings us closer to knowing this pathology and thus being able to make an early diagnosis and timely management, taking into account its high morbidity and mortality and associated complications.

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Friday, 28 July 2023

Lupine Publishers | Resistance of Neisseria gonorrhoeae on oral and mucosa : A Review Article

 Lupine Publishers | Journal of Pediatrics and Neonatology


Abstract

Introduction: Gonorrhea is one of the four most common sexually transmitted diseases worldwide. Globally, the highest incidence of gonorrhea cases is in the African and Western Pacific regions (including China, Indonesia and Australia). Gonorrhea is a sexually transmitted disease caused by the bacteria Neisseria gonorrhoeae. These bacteria are gram-negative bacteria in the form of diplococci located intracellularly from PMN cells. Infection from Neisseria gonorrhoeae can be transmitted by sexual intercourse or vertical transmission at the time of delivery. In children, infection can occur as a result of sexual abuse by an individual infected with Gonorrhea or it can also occur from touching items contaminated with N. gonorrhoeae bacteria.

Discussion: Gonococcal infection occurs by invading the mucosa, so that gonococcal infection can occur in many places. Gonococcal infection can occur in male and female external genitalia, anorectal, pharynx and eyes. There can be a local infection in the genital area (most common), infection in the abdominal cavity (peritonitis), infection around the liver (perihepatitis), meningitis, endocarditis, dermatitis, arthritis and can spread to the bloodstream and cause a Disseminated Gonococcal Infection (DGI) which can spread systemically. The manifestations of gonococcal infection in the female external genitalia can be asymptomatic but may also include periurethral edema and urethritis. There may be a purulent discharge from the cervix but it does not represent vaginitis, dysuria or painful urination, dyspareunia or pain during sexual intercourse and lower abdominal pain. There can also be a vulvovaginitis, bartolin abscess, and in gonococcal infections that are not treated properly, a complication can occur in the form of pelvic inflammatory disease (PID), characterized by lower abdominal pain, increased body discharge from the vagina and urethra, dysuria and intermenstruals. bleeding accompanied by signs of peritonitis, endocervicitis, endosalfingitis and endometritis, causing a deep pelvic or lumbar pain. Currently, the resistance rate of Neisseria gonorrhoeae to antibiotics is increasing rapidly. This condition is not good for prognosis.

Conclusion: The administration of dual therapy with this drug regimen is expected to increase the cure rate so that it can prevent more serious complications and reduce the possibility of resistance to cephalosporins.

Keywords: Gonorrhoea; Resistance; Oral Management

Introduction

Gonorrhea is an infectious disease of the mucosa caused by gram-negative cocci bacteria Neisseria gonorrhoeae which can be transmitted through sexual or perinatal contact. This infection occurs co-infection with Chlamydia trachomatis [1,2]. Gonorrhea can occur in men or women, generally at productive age, but infection by bacteria in women is asymptomatic. This infection can also occur in newborns due to vertical media from the mother during labor. Most gonorrhea manifests as infection of the genital tract, but it can also cause pharyngitis, proctitis and conjunctivitis in certain groups. Clinical findings of conjunctivitis were found in infants with a history of perinatal infection[1-3]. Gonococcal infection is the most common cause of urethritis in men, who experience complaints of pus from the genitals. In women, gonococcal infection causes cervicitis, but this condition manifests asymptomatically so that patients present after a pelvic inflammatory disease (PID), infertility, ectopic pregnancy, or a chronic pelvic inflammation. Diagnosis of a gonococcal infection is done by taking pus from the genitalia, rectum, oropharynx or eye secretions in conjunctivitis gonorrhea and doing a gram examination, where an image of gramnegative diplococcal bacteria can be found in PMN cells, which is confirmed by culture on gonococcal selective media such as Martin. -Lewis medium and Thayer-Martin medium [1,4].

The management of gonorrhea is done by administering antibiotics with a recommended treatment regimen using Ceftriaxone 250 mg IM in a single dose, plus offering Azithromycin 1 gram orally in a single dose. In patients with cephalosporin allergy, an alternative therapeutic regimen can be used using a single dose of Gentamycin 240 mg IM and Azithromycin 1 g orally as a single dose [1,2,4,5]. Currently, the resistance rate of Neisseria gonorrhoeae to antibiotics is increasing rapidly. The high rate of Gonorrhea resistance to the penicillin, tetracycline and quinolone classes has made this drug class no longer accepted for use as a Gonorrhea therapy in most countries in the world. Even in some countries, it has been found that Gonorrhea resistance to cephalosporin therapy creates the 3rd that is given orally[6,7].

Discussion

Gonorrhea is one of the four most common sexually transmitted diseases worldwide. In 2015, the World Health Organization (WHO) estimated that around 357 million new infections from one of the four infectious diseases occurred each year [8]. In an epidemiological study based on data collected from 2005 to 2012, it was found that the global incidence of gonorrhea in women was 0.8%, while in men, it was found that the global incidence of gonorrhea was 0.6% of the worldwide population in 2012, so that if converted In total, there were 26,819,000 cases of gonorrhea worldwide in men and women aged 15-49 years, where there were 19 cases per 1000 women and 24 cases per 1000 men based on World Bank data in 2012 [9,10]. Globally, the highest incidence of gonorrhea cases is in the African and Western Pacific regions (including China, Indonesia and Australia). There are several potential causes for the increased incidence of Gonorrhea globally. One possible cause of this is the increasing prevalence of HIV infection in developing countries. Improvements in diagnostic capabilities and case reporting systems in several countries can also contribute to increasing the incidence of Gonorrhea globally [3].

Gonorrhea is a sexually transmitted disease caused by the bacteria Neisseria gonorrhoeae. These bacteria are gram-negative bacteria in the form of diplococci located intracellularly from PMN cells. Infection from Neisseria gonorrhoeae can be transmitted by sexual intercourse or vertical transmission at the time of delivery. These bacteria mainly attack the columnar epithelium of the host, so that all mucous membranes can be infected by these bacteria[1,2]. There are many factors that influence N. gonorrhoeae bacteria on their virulence and pathogenicity. Fili help the attachment of bacteria to the mucosal surface thereby contributing to the resistance that occurs by preventing ingestion and destruction of bacteria by neutrophils. Opacity-associated (Opa) protein increases the adhesion between gonococcal bacteria and phagocytes, thereby increasing the ability of bacteria to invade host cells and can cause a decreased immune response [4].

Clinical Manifestation

Manifestations of gonococcal infection in male external genitalia can be urethritis, which is the most common manifestation of Gonorrhea in male external genitalia, balanoposthitis, balanitis, prostatitis, epididymitis, vesiculitis or cystitis, often characterized by a purulent and thick body body, sometimes accompanied by complaints of pain when urinating or dysuria. The manifestations of gonococcal infection in the female external genitalia can be asymptomatic but may also include periurethral edema and urethritis. There may be a purulent discharge from the cervix but it does not represent vaginitis, dysuria or painful urination, dyspareunia or pain during sexual intercourse and lower abdominal pain. In gonococcal infection that is not treated properly, a complication can occur in the form of pelvic inflammatory disease (PID) [1,5]. Anorectal manifestations include proctitis accompanied by pain and a purulent fever. In some cases complaints of burning or pain during defecation, tenesmus, and blood in the stool may also be found. Gonorrhea diagnosis is done by taking anamnesis and physical examination that leads to a gonococcal infection and finding an intracellular gram-negative diplococcal image from the results of gram staining of the secretions or body fluids of a patient suspected of a gonococcal infection and the growth of N. gonorrhoeae from culture results. The differential diagnosis of a gonorrhea urethritis includes urethritis caused by genital herpes, urethritis due to C. trachomatis, urethritis due to Ureaplasma urealyticum, urethritis due to Trichomonas vaginalis, bacterial vaginosis, Reiter’s syndrome [11].

The manifestations of gonococcal infection in the male external genitalia can be in the form of urethritis which is the most common manifestation of Gonorrhea in male external genitalia, balanoposthitis, balanitis, prostatitis, epididymitis, vesiculitis or cystitis. This condition is often characterized by the presence of a body discharge that varies from clear and clear to purulent and thick, sometimes accompanied by complaints of pain during urination or dysuria. In some cases, edema may also be found in the external urethral meatus, prepuce or penis. Gonorrhea manifestations of the pharynx occur due to sexual exposure to oral-genital contact. It can also occur as a result of an inoculation after holding an infected limb or object and then putting the hand in the mouth. In this condition, there is erythema of the pharynx, mild sore throat, and often an infection of the genitalia is also found [1,2]. There is a hyperemic pharynx and swelling of the tonsils and there is a purulent white discharge on the wall of the pharynx. It is important to dig for the coitus suspectus with orogenital sexual intercourse and to do a throat swab to check with gram stain or for culture (Figure 1).

Figure 1: Gonorrhea of the pharynx (Pharyngitis Gonorrhea).

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Gonorrhea manifestations in the eye may include conjunctivitis, palpebral edema, chemosis and profuse and purulent discharge. In some cases, this gonococcal infection can even cause a corneal ulcer to perforate which can lead to permanent blindness. In neonates, ophthalmia neonatorum can occur, which is a bilateral conjunctivitis condition characterized by eye pain, conjunctival hyperemia, and the presence of purulent secretions[1]. Diagnosis of gonorrhea is carried out by taking anamnesis and physical examination that leads to a gonococcal infection and finding an intracellular gramnegative diplococcal image from the gram stain of the secretions or body fluids of a patient suspected of a gonococcal infection. However, because the sensitivity is low, a negative gram test result is not sufficient to rule out a diagnosis of gonorrhea, so it is necessary to have another gram-test or a culture examination done. Swab culture examination of the infected area is currently. The standard for diagnosis of Gonorrhea, which is very useful especially in cases with unclear clinical picture, when there is a condition of failure of therapy or when it is difficult to extract the history of the disease. However, empiric therapy can be done first considering the culture results take 24-48 hours [2,4].

Gonorrhea Resistance

Antibiotic resistance, especially in the case of Gonorrhea, is a threat in reducing the consequences of sexually transmitted diseases worldwide. Based on data from WHO, the incidence of gonorrhea infection that is resistant to antibiotics is increasing every year. This is of particular concern to public health observers, especially for the prevention of infertility in women [8]. Gonorrhea is currently still one of the four largest sexually transmitted diseases worldwide that can be cured. However, in recent years, Gonorrhea has become increasingly resistant to antibiotics that were previously sensitive, which has led to fears that Gonorrhea will not cure. Gonorrhea with multiple drug resistance (MDR) was reported by more than 36 countries in the world in 2015 [9-10]. Untreated gonorrhea can lead to more severe complications, such as female infertility, complications in pregnancy and blindness in newborns who are infected during pregnancy. the delivery process [12]. Resistance of Neisseria gonorrhoeae to penicillin and tetracyclines was first discovered in Asia in 1970. The high rate of resistance to quinolones (Ciprofloxacin) emerged since mid-2000. Recent data shows that there is an increase in resistance and failure of Neisseria gonorrhoeae treatment against third generation cephalosporins given orally. Several serotypes of N. gonorrhoeae that have been associated with failed cephalosporin therapy have also been shown to have resistance to other antibiotics and have been classified as multi-drug resistant gonococci [13].

Therapeutic Management

Initially, the therapeutic regimen given in cases of gonorrhea can be done by providing single therapy using cephalosporins. However, due to the resistance of these bacteria to oral cephalosporins as monotherapy, dual therapy using ceftriaxone and azithromycin is recommended as the standard therapy for gonorrhea cases worldwide, especially in the United States. Dual therapy with ceftriaxone and azithromycin should be given simultaneously on the same day and under direct supervision. Since most N. gonorrhoeae infections are co-infected with C. trachomatis, the principle of dual therapy is also considered quite effective because basically azithromycin is a class of antibiotics given to C. trachomatis infections [14]. In recent years, gonorrhea has become increasingly resistant to previously sensitive antibiotics, which has led to fears of incurable gonorrhea. Gonorrhea with multiple drug resistance (MDR) was reported by more than 36 countries in the world in 2015. Untreated gonorrhea can lead to more severe complications, such as female infertility, complications in pregnancy and blindness in newborns who are infected during pregnancy. childbirth process. Due to the resistance of these bacteria to oral cephalosporins as monotherapy, dual therapy using ceftriaxone 250 mg IM single dose and azithromycin 1 g PO single dose is recommended as the standard therapy in cases of gonorrhea worldwide. The administration of dual therapy with this drug regimen is expected to increase the cure rate so that it can prevent more serious complications and reduce the possibility of resistance to cephalosporins [15,16].

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Thursday, 15 June 2023

Lupine Publishers | Prevalence and Determinants of Low Birth Weight in Burundi: An Investigation from The National Demographic and Health Survey

 Lupine Publishers | Journal of Pediatrics and Neonatology


Abstract

Background: Birth weight is an important determinant of neonatal and child health outcome. For instance, evidence has shown that low birth weight (LBW) has a negative impact on the baby’s growth, cognitive development, and on neuro-motor development and immune function. Underweight babies are prone to increased risk of infections and stunting. LBW remains prevalent worldwide and is more pronounced in low- and middle-income countries. Several factors including mothers’ socio-economic characteristics, maternal health behaviors and maternal and pregnancy health conditions determine birth weight outcome. This study sought to determine the prevalence and investigate determinants of LBW among Burundian women of reproductive age.

Methods: This study used data extracted from the 2016-2017 National Demographic and Health Survey (DHS) conducted on 7047 women who reported a live birth history in the five years preceding the survey and whose birth weight was recorded at childbirth. The study used linear regression to explore socio-economic, maternal, and pregnancy related factors that determine birth weight and further employed a logistic model to unpack factors with higher likelihood of LBW.
Results: Of 7,047 babies born between 2012 and 2017, 660 (10%) were underweight. Findings suggested that birth weight decreases with older women’s age, multiple pregnancies (twin or triplet), and female babies. Conversely, birth weight increases with a diabetes condition, wealthier quintiles, and higher party orders. Results from the linear regression were supported by those implemented in the discrete model. In fact, higher parity orders and wealthier women were more likely to deliver normal weight babies. High blood pressure, smoking, multiple pregnancies, and female child’s sex were negative predictors of normal birth weight. For instance, twin babies were twice more likely to be underweight compared to single pregnancies.

Conclusion: This study unpacked high prevalence of LBW in Burundi and further highlighted areas of improvement to deliver on global neonatal and child health targets.

Results: From this work could be used to implement targeted interventions to reduce poverty, tackle chronic conditions in pregnancy, and reduce tobacco use among pregnant women as the above predicted LBW. Other interventions include modern contraception through health educational programs.

Keywords: Low birth weight; Determinants; Burundi

Introduction

Normal birth weight, defined as live-born neonates weighing from 2500 g to 4000 g at birth, is an important determinant of better neonatal and child health. Evidence has established the impact of low birth weight (LBW) on increased neonatal deaths and child stunting [1,2]. Furthermore, low-birth babies experience perinatal growth failure, reduced cognitive and neuro-motor functioning, and poor school performance [3, 4]. There exists a widening negative correlation between birth weight and children’s better health with extreme low-birth-weight babies experiencing major health conditions [4, 5]. Most importantly, underweight babies who survive tend to have impaired immune function and increased risk of disease; they are likely to remain undernourished, with reduced muscle strength, cognitive abilities, and intelligence quotient (IQ) throughout their lives [6]. Despite efforts to improve pregnancy experience and combat LBW, many countries still report high numbers of underweight babies until today. In 2012, the World Health Assembly (WHA) resolution set the goal to achieve 30% reduction in the number of LBW newborns by 2025 [7]. This target was further reemphasized by the Sustainable Development Goals (SDGs) agenda by setting an aim to “end all forms of malnutrition” including among pregnant women to “reduce neonatal mortality to at least as low as 12 per 1,000 live births and under-5 mortality to at least as low as 25 per 1,000 live births” [8]. Global efforts did not yield expected results as some countries continue to experience high rates of LBW.

Of about 21 million low birth babies – representing nearly 15% of all live-births worldwide – 19 million of too small babies are from Africa and Asia (excluding Japan). Altogether, more developed regions namely Northern America, Europe, Japan and Australia, and New Zealand account for less than 10% of low births [5]. According to available data, the whole sub-Saharan Africa excluding Rwanda suffers from LBW. Countries with higher LBW rates (15 to 20% of all live births) include Angola, Benin, Burundi, Botswana, Cote d’Ivoire, Guinea Equatorial, Madagascar, Namibia, Togo, and Western Sahara. Guinea Bissau exceeds 25% of LBW rate and is among the highest worldwide [5]. Despite Burundi having declined LBW from 17.4% [CI: 11.9–22.9] in the year 2000 to 15.1% [10.9– 19.4] in 2015; the country remains above the global average and is further top-ranked LBW rates [5, 9]. To better tackle LBW and deliver on maternal and children global targets, countries need to invest into evidence-based interventions that have been found to undermine childbearing and fraught with child growth among pregnant women.

An amounting evidence has established a causal link between a woman’s characteristics, maternal and pregnancy health conditions, and maternal health behaviors with birth weight outcome. For instance, WHO developed a framework that explains causal pathways for an increased risk of LBW. The framework comprises distal and proximal or immediate factors leading to small babies. Among distal determinants of LBW include

a) maternal characteristics such as extreme age, multiple parity, poor birth spacing, and wealth index.
b) maternal health conditions namely chronic diseases
which have been found to increase maternal risk (i.e. high blood pressure and diabetes).
c) maternal malnutrition characterized by anemia and extreme maternal weight.
d) and other risk behavioral factors such as increased alcohol and tobacco consumption [5]. During the course of the pregnancy, LBW can result from a premature birth (a birth occurring before 37 weeks of pregnancy) and/or the growth faltering in the mother’s womb [5]. Other researchers of whom Alfred Kwesi Manyeh in Ghana [10] and Getaneh Baye Mulu in Ethiopia [11] found similar evidence. They both established the effect of the mother’s age, wealth, parity, gestational hypertension, maternal height, antenatal care (ANC), mother’s education attainment and the child’s sex on birth weight [10, 11]. Furthermore, a study conducted on 10 developing countries incriminated the place of the woman’s age, ANC, literacy level, body max index, and wealth on babies weight at birth [12]. Despite the topic being of national focus today, little has been done to explore factors leading to LBW in Burundi. The aim of this study was to determine the prevalence and investigate determinants of LBW in Burundi. Results of this study inform the design of maternal and neonatal policies with an aim to deliver on global and national targets by 2030.

Methods

Source of data

This study is a secondary data analysis using the Burundi Demographic and Health Surveys (DHS) 2017 datasets. To better understand predictors of birth weight, the study used women’s individual recorde dataset. This study used a sample of 7,047 women who reported a birth history during five years prior to the survey and whose information on birth weight was included in the dataset.

Outcome and explanatory variables

This study used “birth weight” as the dependent variable which was considered as continuous first to allow a linear regression analysis and again as dichotomous to enable the discrete model. We based on WHO guidelines to define cut-offs of the dichotomous “birth weight” outcome [13]. A dummy variable was generated taking value 0 for babies weighing less than 2,500 g at birth and value 1, otherwise. Selection of independent variables was informed by the literature search and by the understating of local context. We included individual woman’s characteristics, behaviors and underlying health conditions as well as factors related to pregnancy health. With an aim to better grasp the effect of coefficients on birth weight, all explanatory variables were categorized as summarized in Table 1.

Table 1: Socio-economic and demographic characteristics.

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Key: X+SD: Mean + Standard deviation.

Data management and models specification

In the first instance, owing to DHS study design which used multiple sampling stages, the dataset was survey set before analysis. In the second stage, we constructed the linear and logistic models as specified below:

In the above linear estimation, Yi is the outcome variable (i.e. birth weight). The model includes an intercept and a random error term. Independent variables are represented by a vector of covariates Xi and B1 captures the magnitude of change in birth weight corresponding to a unit change in explanatory variables. Significance of linear coefficients was ascertained based on p-value at α = 0.05.

Equation 2 is the logistic specification model. In this model, the dependent variable is the log odds that a woman i delivers a normal weight baby (i.e. a baby weighing at least 2,500 g) relative to those giving birth to underweight babies (i.e. babies with less than 2,500 g). 0 β captures fixed effects and 1 β detects random effects on the probabilities of giving birth to normal weight babies. The vector of covariates Xi includes independent variables described in Table 1. For the logistic model, significance of explanatory factors was determined based on a corresponding 95% confidence interval that does not contain value 1.

Results

Results of this study are sectioned into three main subheadings. In the first instance, we describe socio-demographic characteristics of study participants. In the second time, we summarize findings from the linear model of socio-economic and maternal health factors on birth weight. In the final stage, we present results of the logistic model on the probability of low versus normal birth weight.

Socio-economic characteristics

Table 1 summarizes socio-economic characteristics of participants. Of 7047 women of reproductive age, half were aged between 25 and 34 years old. Overall, majority of women did not achieve university education. Further, the prevalence of tobacco and alcohol consumption as well as the prevalence of health conditions with evidence to complicate pregnancy or childbirth was considerably low. Results also showed that mothers delayed in attending ANC as only about 7% attended their first ANC in the first trimester and only about 16% achieved recommended four or more ANC visits during the course of the pregnancy. More than half of surveyed women were married, and majority had a parity of two to three. Surveyed women were evenly scattered across the wealth quintiles. Low birth weight babies represented the vast minority (less than 10%) and male babies constituted a slightly higher proportion.

Determinants of birth weight

As can be viewed in Table 2 below, birth weight significantly decreases with older women’s age and increases with a diabetes condition. Also, there was evidence of a sharp increase in birth weight with wealthier quintiles. For instance, women who belong to the richer and richest quantiles gave birth to babies with almost 130 grams and 200 grams more; respectively. Moreover, there was a significant increase of birth weight with party. Mothers who had four to five and six and more parity gave birth to babies with 253grams and 320 grams more respectively. Most importantly, diabetic women gave birth to babies with 750 grams more compared to women without diabetes condition. The effect of a woman’s age on birth weight is linearly negative with a 70 g decrease for women above the age of 35 years. In contrary to the above, multiple pregnancies and female babies are associated with low birth weights. The decrease in birth weight is more evident for triplet pregnancies; reaching nearly 1800 grams lower compared to single pregnancies. The decrease in birth weight halves from triplet to twin pregnancies (1800 versus 900 grams). In the same perspective, female births tended to yield lower birth weights up to 130 grams less compared to male babies.

Table 2: The effect of socio-economic determinants on birth weight.

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Determinants of low birth weight

On the one hand, women’s education attainment, parity, and wealth index were predictors of higher likelihood of normal birth weight. With reference to poorest women, the likelihood that a woman gives birth to a normal weight baby increases with wealth quintiles to nearly double for women belonging to richer quantiles. Similarly, higher education level predicted higher likelihood of normal birth weight. For instance, women who attained tertiary education were about twice more likely to deliver normal weight babies compared to their counterparts who did not attend schooling. Furthermore, compare to women with one parity, the likelihood that a woman gives birth to a normal weight baby increases with high parity to become two times more and nearly three times for women with four to five and six and more parity respectively. On the other hand, high blood pressure, multiple pregnancies, smoking cigarette, and bearing a female child were negative predictors of normal birth weight. In other words, chances of low birth weight among women who reported smoking cigarette and those with high blood pressure were more than twice likely compared to women without the above conditions. Furthermore, the likelihood that women give birth to underweight babies was nearly double among women bearing female children or multiple pregnancies. Results of the logistic model are summarized in Table 3.

Table 3: The effect of socio-economic determinants on low birth weight.

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Discussion

This study used secondary data from the national Demographic and Health Survey 2017 to determine LBW prevalence and explore socioeconomic and demographic factors that predict LBW among Burundian women. LBW in Burundi was found to be close to other low- and middle-income countries namely Ethiopia and Iran. In Burundi, LBW is nearly 10% against 10% and 9.4% in Ethiopia [14] and Iran [15]; respectively. Conversely, LBW was found to be much higher in other countries such as India with one fifth of live births weighing less than 2,5 kilograms [16]. In our study, significant determinants of birth weights included wealth, parity, chronic health condition, pregnancy type (single versus multiple), woman’s age, and child’s sex. On the one hand, birth weight consistently increases with higher wealth quintiles, higher parity levels, and having diabetes. Compared to poorest women, birth weight increases of 50 grams for women belonging to poorer families. This increase doubles (100 grams) for women from middle class and again doubles for richest women who gave birth to babies weighing 200 grams more. Similarly, second and third order newborns weighed 220 grams more compared to first order babies. The increase in birth weight was consistent with higher birth orders and reached more than 300 grams for babies born to multiparous women from sixth pregnancy going forward. Diabetes was associated with an increase of more than 700 grams. On the other hand, multiple pregnancies, older age, and female babies were significant predictors of decreased birth weight. The most appealing evidence concerns multiple pregnancies which cause birth weight to decrease of about 1900 grams for triplet babies and about 920 grams for twin babies. Women older than 35 years gave birth to babies lower of 70 grams weigh and female newborns weighed 130 grams less compared to their male counterparts. Results from the linear model corroborate with those implemented using the logistic regression. Wealth index and higher parity determined the likelihood of giving normal weight babies while smoking, multiple pregnancies, child’s sex, and a woman’s chronic condition were significant predictors of the likelihood of LBW. Higher birth orders were associated with more than twice likelihood of bearing a normweight baby compared to first pregnancies.

In the same perspective, wealthier mothers and those highly educated were nearly two times more likely to give birth to normal weight babies. However, similar to the linear model results, twin pregnancies and female babies were nearly twice more likely to be underweight. Additionally, there was a double chance of giving birth to underweight babies among women who smoke cigarettes during the course of pregnancy were and those who had high blood pressure. Determinants of birth weight in Burundi corroborate with evidence from other settings. In Sri Lanka for instance, wealthier women and higher educated women were more likely to give birth to normal weight babies [17]. In this study, other significant determinants of birth weight were mother’s age at childbirth, newborn’s sex, and parity level. Contrary to the context of Burundi where antenatal care did not predict birth weight, Indian women who completed at least four recommended ANC visits were more likely to deliver normal weight babies [17]. Similar evidence has also been found in India [18]. Furthermore, similar to our findings, a wealth evidence has established the correlation between women with chronic health conditions such as diabetes with macrosomia [19, 20]. Multiple pregnancies were significant predictors of LBW in Burundi and in other similar settings. The example is the study by Taywade et. Al [21] in India where women bearing multiple pregnancies were 21 more likely to give birth to underweight babies [21]. Additionally, male sex was found to be a protective predictor of LBW in India and Ghana [18, 22]. Smoking was also a negative predictor as women who reported having smoked cigarette during pregnancy were at high risk of LBW in Ethiopia [23] and in India [21].

Conclusion

This study which used a nationally representative sample of Burundian women of reproductive age yielded evidence on LBW prevalence and factors affecting it. The prevalence of LBW was considerable when compared to many countries around the world (10%). Among important predictors affecting birth weight included a women’s age, wealth, education, parity, chronic health condition, smoking, pregnancy type (single versus multiple) and child’s sex. Markedly, LBW was highly associated with multiple pregnancies, female babies, the history of smoking over the course of the pregnancy, and high blood pressure. Despite considerable efforts put in place by the government to improve maternal and child health, LBW remains a public health concern. This study suggests the need for the implementation of targeted innovative interventions to tackle identified LBW risk factors among women of reproductive age. For instance, socio-economic interventions targeting poor household may help to improve economic status of women with an aim to reduce LBW prevalence among poorer women. Our study used secondary data analysis which has limit in establishing causal inference between predictors and the study outcome. This shortcoming could be addressed by cohort studies of pregnant women which have the possibility to unpack factors determining LBW with a much stronger evidence than cross-sectional surveys. Therefore, this study provides important evidence and a threshold for further research works in the field.

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Saturday, 8 April 2023

Lupine Publishers | Aquatic Exercise Intervention Is Effective for Spasticity Inhibition in Children with Cerebral Palsy: A Clinical Controlled Study

 Lupine Publishers | Journal of Pediatrics and Neonatology


Abstract

Introduction: Spasticity has been implicated as a major hindrance to motor development and overall functional performance in children with cerebral palsy (CP). Recent evidence have suggested aquatic therapy as an alternative means for inhibiting spasticity in children with CP. However, these previous studies have provided contrasting results, thereby creating some dearth of evidence in the use of aquatic therapy to manage spasticity in children with CP.

Objective: To investigate the effectiveness of aquatic exercise intervention in inhibiting spasticity in children with CP.

Materials and methods: Thirty children aged 1-12 years participated in this study. They were randomised into 2 groups (experimental and control). The experimental groups received manual passive stretching on affected muscles of both upper and lower extremities followed by weight bearing exercises in water (temperature 28-32ºC) while the control group received same exercises on land for 10 weeks. Degree of spasticity on treated group of muscles was assessed using Modified Ashworth Scale (MAS). Mann-Whitney-U test was used to compare the change in degree of spasticity between both groups. The level of significance was set at p<0.05.

Results: The experimental group showed significant reduction in spasticity of all the tested muscle groups while the control group showed no significant improvement in spasticity of wrist flexors and knee flexors. No significant difference was observed for change in spasticity between both groups.

Conclusion: Aquatic exercise intervention is effective for inhibiting muscle spasticity in children with cerebral palsy.

Keywords: Aquatic Exercise; Intervention; Spasticity; Cerebral Palsy.

Introduction

Spasticity is a widespread problem among children with cerebral palsy (CP) as it affects function and can lead to musculoskeletal complications [1]. It occurs as a result of pathologically increase in muscle tone and hyperactive reflexes mediated by a loss of upper motor neuron inhibitory control [2]. Spasticity is considered an important neural contributor to muscle hypertonia in children with cerebral palsy [3].It adversely affects muscles and joints of the extremities, causing abnormal movements, and it is especially harmful in growing children[4]. Reduction of spasticity and improvement of motor control is a prerequisite for functional performance in children with cerebral palsy [5,6]. With reduction in spasticity, improvement in gross motor function and independent performance of ADLs are expedited which in turn reduces the burden cerebral palsy poses on the children and their caregivers [5,6,7] .The management of spasticity in children with CP is often complex and poses a great challenge to healthcare professionals. Effective treatment requires a multidisciplinary approach involving pediatricians, physiotherapists, occupational therapists, orthotists and surgeons. Previous studies have suggested various treatment approaches and modalities to manage spasticity associated with spastic CP. These include the use of oral neuropharmacological agents, injectable materials such as botulinum – a toxin or surgical treatment, use of orthotic devices, massage techniques, strengthening exercises to the antagonist musculature, use of electrical stimulation and the application of cryotherapy or ice therapy [8,9]. Aquatic intervention is one of the most popular supplementary treatments for children with neuromotor impairments, particularly CP [10]. Several studies have reported aquatic intervention as a veritable tool in the rehabilitation of children with CP [11-13]. The intervention may provide safe and beneficial alternative low-impact exercise for children with disabilities [14]. This study was aimed at investigating the effectiveness of aquatic exercise intervention in inhibiting spasticity in children with spastic cerebral palsy.

Methods

Thirty children undergoing rehabilitation were recruited for this study from a center for developmental challenges in Lagos, Nigeria. Their age range was from 1 to 12 years and were diagnosed with the spastic form of cerebral palsy. Those with other neurodevelopmental conditions were excluded from the study.

Ethical Approval and Informed Consent

Ethical approval for this study was obtained from the Health Research and Ethics Committee of the Lagos University Teaching Hospital, Idi-Araba, Lagos, Nigeria (Ref. No: ADM/DCST/HREC/ APP/1525). Parents of the participating children gave their informed consent.

Procedure

A detailed history and thorough physical examination was initially carried out on each participant. Those who met the criteria for the study were then randomly assigned into experimental and control groups. The flow chart of the study is presented in Figure 1.

Assessment Protocol

Functional Level Assessment: This was assessed using the Gross Motor Function Classification System- Expanded and Revised according to standard [15].

Degree of Spasticity Assessment: This was done using the Modified Ashworth Scale (MAS). Both upper limbs (shoulder adductors, elbow flexors and wrist flexors) and lower limbs (hip adductors, knee flexors and ankle plantar flexors) were assessed for spasticity bilaterally (left and right) according to the pattern presented by the participants. Each participant was placed in a relaxed supine position and the starting position of testing each muscle group was a maximal placement of the joint in a position of their primary function and then maximally moved to a lenghtened position opposite to their primary movement. Participants were then scored based on the amount of resistance to passive movement as described in MAS. To accommodate the score of “1+” modification for numeric analysis, grade ‘‘1+’’ was recorded as 1.5[16].

Figure 1: Flow chart of the study. Key: R: Randomization. ITT: Intention –to-treat.

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Intervention

The participants in both experimental and control groups had a total of 20 treatment sessions consecutively for 10 weeks at the rate of two sessions per week. It was ensured that participants in both groups were not on any form of anti-spastic medication throughout the study.

Those in the experimental group received exercise training in water of temperature ranging between 28-32 ºC for 10 weeks with the exercised parts fully immersed in water. The exercise protocol consisted of 3 categories of exercises:

Exercise 1 (Manual passive stretching): Each joint involving the spastic group of muscles was passively stretched and held in this in fully lengthened position of the muscle groups for up to 60 seconds follow by relaxation of 30 seconds. This procedure was repeated five times for each part

Exercise 2: Weight bearing one or both upper extremities in sitting with or without support for 60 seconds and repeated 5 times.

Exercise 3: Weight bearing on both lower extremities in standing with or without support for 60 seconds and repeated 5 times.

Control group

Participants in the control group received same exercise intervention as those in the experimental group except that the intervention was carried out on land.

Post-intervention Assessments

Participants in both groups were re-assessed after 4 weeks, after 8 weeks and after 10 weeks of intervention for changes in spasticity using the Modified Ashworth Scale (MAS). All assessments were carried out by blinded assessors.

Data Analysis

Data was analyzed using the Statistical Package for Social Sciences version 21.0 version. Participants in both groups were compared for age using the Independent t-test. Friedman test was used to compare post intervention changes in degree of spasticity within each group across the duration of treatment while Mann- Whitney U test was used to compare the change in spasticity between both groups. All statistical tests were performed at the 0.05 level of significance (p<0.05).

Results

Physical Characteristics

The mean age of all participants was 5.20+2.43 years and no significant difference in age was found between both groups of participants at baseline Table 1,2. Most of the participants were in level IV of the GMFCS. Quadriplegic spastic type of CP predominated among all the participants as shown in Figure 2.

Figure 1: Distribution of Type of Spastic Cerebral Palsy among Participants.

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Table 1: Comparison of Age and Mobility Level between both Groups at Baseline.

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Key: X+SD: Mean + Standard deviation.

Table 2: Mean Rank Comparison of Spasticity between both Groups at Baseline.

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Aquatic Intervention and Spasticity

Significant change in spasticity was observed on all tested group of muscles of participants in the experimental group following aquatic exercise intervention Table 3.

Land-based Exercises and Spasticity

Significant change in spasticity was also observed on tested group of muscles among participants in the control group following land-based exercise intervention, except for right and left wrist flexors; and right and left knee flexors as shown in Table 4.

Table 3: Comparison of Mean Rank Changes in Spasticity in Experimental group of Participants across the duration of Intervention.

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*Significant at p<0.05

Table 4: Comparison of Mean Rank Changes in Spasticity in Control group of Participants across the duration of Intervention.

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*Significant at p<0.05.

Comparison of Spasticity Change between Experimental and Control Groups

Despite the gross improvement in spasticity of participants in experimental group compared to the control group which showed no improvement for few groups of muscles, no significant difference was found in the spasticity change between both groups as represented in Table 5.

Table 5: Mean Rank Comparison of Spasticity between both Groups after 10 weeks of Intervention.

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Discussion

Quadriplegic type of spastic CP was more predominant in this study. This is consistent with reports from earlier studies in Nigeria [17-19]. However, reports from studies in other parts of the world showed that there were more diplegic type of spastic CP [11,20][21- 23]. Geographical differences may be considered for this variation.

In this present study, statistically significant improvement was observed in both intervention groups for spasticity of shoulder adductors, elbow flexors, hip adductors and ankle plantar flexors. This finding shows that therapeutic exercises such as manual passive stretching and weight bearing exercises which are used by physiotherapists in the management of spasticity in children with cerebral palsy are effective as documented in previous studies [21,24,25,26]. The report of statistically significant improvement in spasticity of hip adductors and knee flexors following 10 weeks of aquatic intervention in this study has been supported by a study by Chrysagis et al in 2009 where there was further significant improvement in the passive range of motion of the hip and knee joints [11]. However, the aquatic training adopted for their own study was different from the one used in this present study. This improvement in spasticity is attributable to the therapeutic benefit of buoyancy property of water which can help to relax spastic muscles by providing antigravity positioning. This study revealed that landbased exercise intervention improved the spasticity of shoulder adductors, elbow flexors, hip adductors and ankle plantar-flexors as observed among participants in the control group. This finding was corroborated by a systematic review on the effectiveness of passive stretching on spasticity in children with cerebral palsy [24]. They found out that 4 of the 6 reviewed studies reported significant reduction in spasticity including that of shoulder adductors, elbow flexors, hip adductors and ankle plantar flexors following passive stretching while the remaining 2 studies did not consider spasticity in their outcome variables. This improvement in spasticity may be attributed to fatigability of stretch receptors as a result of stretch on the muscle spindles which induces inhibition on the gamma-motor neurons and allowed more lengthening of muscle fibres thereby counteracting the effect of spasticity.

There was no significant improvement observed for spasticity of the wrist flexors and knee flexors in this present study after 10 weeks of land-based exercises. These findings are contrary to the findings of Akinbo et al. (2007) and Akinbo et al. (2007) who in their separate studies found out that manual passive stretching alone significantly improved spasticity of wrist flexors, passive range of motion of the wrist as well as hand function in children with spastic cerebral palsy with and without the use of cryotherapy. They however both concluded that a combination of passive stretching, and cryotherapy produced better improvement in the spasticity of wrist flexors in children with spastic cerebral palsy [25,26]. The reason for lack of significant improvement in spasticity of wrist flexors and knee flexors following 10 weeks of land-based exercises in this present study could not be ascertained but there may be needed to go further beyond 10 weeks to get a significant improvement. Comparison between the experimental and control groups revealed no significant difference in the change in spasticity of all tested muscle groups. This implies that either of the two forms of intervention can be adopted in the management of spasticity in children with cerebral palsy. However, considering the result of this study which had earlier shown that aquatic intervention significantly improved the spasticity of all the tested muscle groups including those of wrist flexors and knee flexors which were not significantly improved by land-based exercises after 10 weeks, the beneficial pendulum might as well be tilted towards the aquatic exercise intervention when there is need for clinical decision making in the management of a patient presenting with spasticity of all the tested muscle groups in this study.

Conclusion

Aquatic exercise intervention is effective in inhibiting spasticity in children with Cerebral Palsy and should be an intervention of choice when considering affectation of all muscles of both upper and lower extremities.

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Friday, 30 September 2022

Lupine Publishers | Common Types of Neurogenetic Disorders, A Brief Review

 Lupine Publishers | Journal of Pediatrics and Neonatology


Mini Review

There are various genetic disorders which can involve the nervous system or confined to the nervous system alone. This is a brief review on some neurogenetic disorders. Gene mutations disorders are the most common types of neurogenetic disorders. Myotonic syndromes, muscular dystrophies and motor neuron disease are some examples of these disorders. Genetic imprinting in some disorders like Prader–Willi syndrome and Angelman’s syndrome can be seen. In both of these syndromes there is a disruption on a part of chromosome 15 which the autosomal genes differential expression depends on their parental origin (maternal genes disruption in Prader–Willi syndrome and father’s genes disruption in Angelman’s syndrome). Duplication of part of chromosome 17 which includes the peripheral myelin protein 22 gene coding, can cause some types of hereditary motor and sensory neuropathy. The patients with such disorder would develop sensory loss, distal weakness and wasting. Hereditary neuropathy with a liability to pressure palsies is an example of neurogenetic disorders with gene deletions. In this disorder there is a deletion on chromosome 17. This large deletion includes the peripheral myelin protein 22 gene coding. The affected patients can develop recurrent focal entrapment neuropathies. Mitochondrial disorders are other disorders which may result from mitochondria genome defects and nuclear-coded genes defects [1-2].
Disorders related to Trinucleotide repeat are other neurogenetic disorders. Expanded and abnormal triplet repeat in the genome can cause some disorders to appear. Friedreich’s ataxia and Huntington’s disease are two examples of Trinucleotide repeat disorders [3-4]. As the new genetic studying methods have been developed and is now under development, finding the genetic basis of some neurological disorders can be possible due to such developments and this causes to know the certain neurogenetic pathologies better.

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Thursday, 25 August 2022

Lupine Publishers| Chrono-Nutrition for Pregnant Women: Metabolic and Pediatric Insights

 Lupine Publishers | Journal of Pediatrics and Neonatology


Abstract

Pregnant women undergo metabolic adaptations and challenges that predispose them to a variety of complications. The objective of this article was to highlight the importance of eating timing and especially limited evening eating on optimizing pregnancy status and pediatric health and welfare. Because of limited evening and nocturnal metabolic capacity to handle nutrients (e.g., glucose), pregnant women are recommended to take smaller and earlier evening meals and instead distribute their main food meals over the course of morning and day hours. Such a food intake regimen would considerably reduce diabetes and obesity risks and improve upcoming lactation performance and pediatric health and welfare.

Keywords: Eating Timing; Pregnant Woman; Chrono-Nutrition; Pediatric Health

Philosophy

Chrono-nutrition is emerging as a new research area with growing interest (1). Chrono-nutrition deals with optimizing eating timing. The goal of chrono-nutrition is to synchronize eating patterns with circadian physiological rhythms of human metabolism (2,3). This synchrony aims to reduce risks from a multitude of metabolic disorders (e.g., diabetes, obesity, cancer) and improve human health and welfare. Basically, human glucose tolerance is known to decline during evening hours and overnight. This means that cells are not as much capable to assimilate and metabolize nutrients in the evening as are they in the morning (3). In other words, if large evening meals are taken, because of incomplete and inefficient nutrient utilization by different cells, nutrient overload will occur that will in turn predispose the body to a variety of metabolic complications, such as diabetes, obesity, and metabolic syndrome.
Pregnant women undergo physiological adaptations and are already prone to metabolic challenges (e.g., diabetes and obesity) (2,3). The above complications are, thus, very likely to happen in pregnant women. As such, making the evening meal smaller and taking it earlier (not later overnight) would help the pregnant body better cope with the metabolic challenges. As another complementary strategy, pregnant women are recommended to take several small evening meals made of mainly fruits and vegetables instead of starch and fats. This practice would be predicted to improve insulin action and prevent obesity. Improving evening nutrient and hormonal metabolism by evening exercise has also been advised (4). The goal has been to optimize circadian timing of eating and exercise towards optimal lifestyle. Optimizing meal properties is a new research area with many unanswered questions. Future research is required to address different aspects of this promising field of study.

Conclusion

Smaller and earlier evening meals made of mainly fruits and vegetables instead of starch and fat are recommended for pregnant women to help improve intermediary metabolism and reduce metabolic complications. These effects will result in improved lactation physiology and pediatric health and welfare.

Acknowledgments

Thanks to Ferdows Pars Agricultural and Livestock Holding Co., (Tehran, Iran) for supporting the author’s programs of optimizing science education in the third millennium.

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Friday, 1 October 2021

Lupine Publishers | A Profile of Microbial Isolates and Antibiotic Susceptibility Patterns in Neonatal Sepsis at a Tertiary Care Centre in South India - A Post HOC Analysis

 Lupine Publishers | Journal of Pediatrics and Neonatology



Abstract

Background: Neonatal sepsis is a common problem in Neonatal intensive care units. Neonatal sepsis is classified as early onset and late onset based on the time of occurrence of clinical symptoms in the neonate. Organisms causing sepsis in neonates vary from unit to unit and from time to time within the same unit. Study of microbial pattern and their antibiotic sensitivity pattern is essential part of managing septic neonates.

Methods: The study was carried out in Govt Kilpauk medical college hospital between October 2010 to October 2012

Results: A total of 207 newborns with clinical sepsis were admitted. Blood culture was positive in 88 out of the 207 cases (42.51%) Klebsiella is the commonest organism causing sepsis (45%) in our Neonatal Intensive Care Unit. Other gram-negative isolates included Escherichia Coli (31%), Pseudomonas (6%), Enterobacter (1%) and Acinetobacter (2%). The Gram-positive organisms grown were Coagulase Positive and Coagulase negative Staphylococci (8%), Group B Beta Hemolytic Streptococcus (5%) and Enterococcus (2%). Late-onset sepsis cases were found to be 1.5 times higher than early-onset sepsis. Out of 88 cases, 34(38.64%) had early-onset sepsis and 54(61.36%) had late-onset sepsis.

Conclusion: A insight knowledge of the microbial isolate and their sensitivity pattern in Neonatal intensive care unit is essential in preventing mortality. The commonly pathogens isolated in the study are found to be resistant to the commonly used antibiotics.

Keywords: Neonatal Sepsis; Antibiotic Sensitivity; Gram Positive Organism; Multi Drug Resistant Organisms; Antibiotic Stewardship

Introduction

Neonatal sepsis is a clinical syndrome of bacteremia with systemic signs and symptoms of infection in the neonatal period [1,2]. Neonatal sepsis is broadly classified into two types namely early onset sepsis and late onset sepsis. Early onset sepsis is caused by organisms prevalent in the maternal genital tract, labour room or operating theatre, while late onset sepsis usually results from nosocomial or community-acquired infection. Sepsis is one of the major causes of mortality in neonates. According to World Health Organization (WHO) estimates, there are about 5 million neonatal deaths a year, with 98% occurring in developing countries [3]. The incidence of neonatal sepsis according to the data from National Neonatal Perinatal Database (NNPD, 2002-03) is 30 per 1000 live births and contributes to 19% of all neonatal deaths [4]. Neonatal sepsis is caused by a variety of Gram +ve as well as Gram -ve bacteria and rarely by fungus and yeast [5]. Diagnosis of neonatal sepsis clinically is difficult as the symptoms and signs are non-specific.

Hence a high index of suspicion is a must while managing a neonate with suspected sepsis. Antibiotics are the mainstay in the treatment of neonatal sepsis and must be stated at the earliest in case of late onset sepsis after obtaining the blood culture, while in case of early onset sepsis the decision to start antibiotics is governed by the presence of risk factors and the clinical signs and results of the Septic screen. Adjuvant therapy used in neonatal sepsis include GM-CSF, G-CSF, blood products and exchange transfusion on rare occasions. The organisms responsible for neonatal sepsis vary from place to place and with time even in a particular unit. Because of this changing pattern of organisms it is imperative to periodically audit the microbial pattern in the unit and change the management protocol periodically over time [6].

Aim of the study

This study was done to determine the microbial pattern and antibiotic sensitivity patterns of microbial isolates from blood cultures of neonates with sepsis, in Govt Kilpauk Medical College Hospital, a tertiary care center.

Methodology

An analysis was conducted on all blood culture reports obtained between 1st of October 2010 to the 1st of October 2012 from newborns admitted to the Department of Pediatrics and the Neonatal Intensive Care Unit (NICU) at Govt Kilpauk Medical College Hospital. Institutional Ethics committee approval and informed consent from the parents were obtained. The newborns were included in the study group if they satisfy any one of the following criteria.

Neonatal Criteria: Neonates showing the under-mentioned signs and symptoms, Respiratory distress or apnea or gasping respiration, Temperature instability - Hypothermia or Fever, Lethargy, poor cry, refusal of feeds, vomiting, ileus, abdominal distension, Poor peripheral perfusion, Bradycardia or Tachycardia, more than 10 pustules in the body or purulent umbilical discharge along with periumbilical erythema, Neonatal convulsions, irritability, hypotonia, altered sensorium.

Maternal Criteria: Maternal fever with evidence of bacterial infection within 2 weeks prior to delivery, Rupture of membranes more than 18 hours, Foul smelling liquor, Evidence of chorioamnionitis, More than 3 vaginal examinations or one unclean vaginal examination during labor, Prolonged labor (sum of first and second stage of labor more than 24 hours).

Blood Collection: Blood culture was done for all neonates suspected to have septicemia. Blood culture sample included a single sample collected from a peripheral vein under aseptic conditions. The local site was cleansed with 70% alcohol and povidone iodine (1%), followed by 70% alcohol again. Blood cultures were incubated at 37˚C and analysed at Microbiology department of Govt Kilpauk Medical College Hospital. Isolates were identified by the characteristic appearance on their respective media, Gram staining and confirmed by the pattern of biochemical reactions using the standard method and antibiotic sensitivity was also tested. C-reactive protein estimation and platelet count was also done as per unit policy before administration of empirical antibiotic

Results

Figure 1: Blood culture positive.

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During the study period, a total of 207 newborns with clinical sepsis were admitted. Of the 207 neonates admitted with suspected sepsis 112 were males and 97 were female. Male:female ratio was 54.1%:45.9%. On categorizing the newborns based on birth weight, 11 babies were of very low birth weight, 107 newborns were of low birth weight, 88 babies were in normal birth weight and one baby weighed more than 4,000 grams. Blood culture was positive in 88 out of the 207 cases (42.51%). Klebsiella is the commonest organism causing sepsis (45%) in our Neonatal Intensive Care Unit. Other gram-negative isolates included Escherichia Coli (31%), Pseudomonas (6%), Enterobacter (1%) and Acinetobacter (2%). The Gram-positive organisms grown were Coagulase Positive and Coagulase negative Staphylococci (8%), Group B Beta Hemolytic Streptococcus (5%) and Enterococcus (2%). Late-onset sepsis cases were found to be 1.5 times higher than early-onset sepsis. Out of 88 cases, 34 (38.64%) had early-onset sepsis and 54(61.36%) had late-onset sepsis. Best overall sensitivity among Gram-negative isolates was to Imipinem (92%) followed by Amikacin (82.66%) and best sensitivity among Gram-positive isolates was to Vancomycin (84.61%), followed by Cloxacillin and Ampicillin (61.53%). Out of 88 positive cultures 6 were multi-drug resistant (6.8%) (Figures 1-5).

Figure 2: Common causative organisms (Total=88).

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Figure 3: Antibiotic sensitivity pattern of Klebsiella (Total=39).

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Figure 4: Antibiotic sensitivity pattern of Staphylococcus Aureus (Total=7).

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Figure 5: Antibiotic sensitivity pattern of other organisms (E.Coli, Streptococci, Pseudomonas, Acinetobacter) (Total=42).

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Discussion

The organisms implicated in neonatal sepsis in developing countries differ from those seen in developed countries [3]. In our study, out of 88 positive cultures, majority of causative organisms were Gram negative (85.22%), and specifically, the most common organisms were Klebsiella (45%) and E.coli (31%). Among the Grampositive organisms Staphylococcus aureus (8%) predominated. It is consistent with the data from NNPD 2000, that the most common organisms responsible for neonatal sepsis in India are Klebsiella [1]. Gram-negative and Gram-positive septicemia was encountered in 85.22% and 14.78% of the culture-positive cases in our study which is in contradiction to results of study by Agnihotri et al. [7] where a predominace of gram negative organism was encountered but gram positive isolates contributed to nearly 42% of sepsis cases .This could be possibly explained by the fact that most of our cases were late onset sepsis cases and even among early onset sepsis cases there was a predominance of gram negative organisms.

The analysis of drug resistance pattern showed that, among Gram-negative isolates nearly 60% were resistant to cefotaxime and 66% resistant to ciprofloxacin which are commonly used a first line drugs. Six out of 88 isolates were multidrug resistant and this was more common among the common pathogen isolated (Klebsiella and E.Coli). Prevalence rate of Group B streptococci is comparable to the results of Donal Waters et al. [8].

Conclusion

There cannot be a single recommendation for the antibiotic regimen for neonatal sepsis in all settings. The choice of antibiotics depends on the prevailing flora responsible for sepsis in the given unit and their antibiotic sensitivity. Microbial Isolates seem to be resistant to commonly used antibiotic for neonatal sepsis, cefotaxime and ciprofloxacin. There is an increase in the multidrug resistant (ESBL) Gram Negative which needs vigilant surveillance.

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Thursday, 21 March 2019

Journal of Pediatrics-Lupine Publishers

Apnea in Neonates - Concepts and Controversies by Edwin Dias in Progressing Aspects in Pediatrics and Neonatology in Lupine Publishers

Apnoea of prematurity (AOP) is a common problem affecting premature infants. Apnoea is defined as cessation of breathing for more than 20 seconds or for lesser duration when associated with bradycardia and desaturation. The most likely and accepted pathogenesis is the “physiologic” immaturity of respiratory control in the neonates. The physiological immaturities include altered ventilatory responses to hypoxia, hypercapnia, and altered sleep states. Other hypotheses include gastroesophageal reflux and anaemia which are still controversial. Three types have been identified namely obstructive, central and mixed types of apnoea. Management options include the use of supplemental oxygen, position chages and drug therapy with methyxanthines. Other supportive therapies include kangaroo care, packed cell transfusions. The long term neurodevelopmental consequences of AOP and its treatment still needs to be studied further.

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