Denise Nassisi, MD
- Department of Emergency Medicine
- Mount Sinai School of Medicine
- New York, New York
The presentation can vary classes and when operating snow blowers medicine rocks state park buy genuine combivent, power lawn mow from irritability to emesis symptoms hypoglycemia buy combivent 100mcg amex, change in mental status symptoms bipolar disorder discount combivent 100mcg visa, or ers medicine 751 best buy combivent, and power tools, or when using hammers and nails. Sports-related eye injuries can be prevented with protective Neuroimaging of the brain as well as a skeletal survey are eyewear. Sports goggles and visors of polycarbonate plastic tools used to diagnose shaken baby syndrome. Ophthalmic will prevent injuries in games using fast projectiles such as consultation and a dilated retinal examination are necessary tennis or racquet balls, or where opponents may swing to document retinal hemorrhages. Whereas retinal hemorrhages tend to resolve always wear polycarbonate eyeglasses and goggles for all fairly quickly, those in the vitreous do not. High-risk activities such as boxing and the martial over the macula, deprivation amblyopia may occur and may arts should be avoided by one-eyed children. Other ocular findings associated with nonaccidental trauma include American Academy of Pediatrics, Committee on Sports Medicine lid ecchymosis, subconjunctival hemorrhage, hyphema, reti and Fitness; American Academy of Ophthalmology, Eye Health nal folds, retinoschisis, and optic nerve edema. Acute-onset and Public Information Task Force: Protective eyewear for young athletes. Brophy M et al: Pediatric eye injury-related hospitalizations in the United States. Blepharitis is inflammation of the lid margin characterized by crusty debris at the base of the lashes; varying degrees of Treatment erythema at the lid margins; and in severe cases, secondary Management of any systemic injuries is required. Observa corneal changes such as punctate erosions, vascularization, tion by an ophthalmologist of retinal hemorrhages for reso and ulcers. When conjunctival injection accompanies bleph lution is the usual course of treatment. Treatment includes lid scrubs with a nonburning baby shampoo several times a week and application of a topical antibiotic ointment such as erythromycin or bacitracin at bedtime. Rosacea Rosacea can also occur in the pediatric age group and cause chronic blepharoconjunctivitis with corneal changes that decrease vision. Pediculosis Pediculosis of the lids (phthiriasis palpebrarum) is caused by A Phthirus pubis. Nits and adult lice can be seen on the eyelashes when viewed with appropriate magnification. Mechanical removal and application to the lid margins of phospholine iodide or 1% mercuric oxide ointment can be effective. Treatment modalities include cryotherapy, cautery, carbon dioxide laser, and surgery. A chalazion is an inflammation of the meibomian glands, Any coexisting blepharitis should be treated. If incision and curettage are needed because the lesion is slow to resolve, the child will require a general anesthetic. Clinical Findings Herpes simplex virus may involve the lids at the time of primary herpes simplex infection. Hordeolum and blepharitis, left upper ease in association with a skin eruption in the dermatome of lid. If near a synkinesis or simultaneous firing of either the external or the lid margin, the lesions may shed and cause conjunctivitis. Fluorescein dye should be administered topically to both eyes followed by examination with a cobalt blue light to Treatment determine if corneal or conjunctival involvement is present. Herpes simplex or herpes zoster can be diagnosed by rapid Mild cases less often require operative management. When either the con presents with signs of unequal pupils (anisocoria), eyelid junctiva or the cornea is involved, treatment should include ptosis, iris heterochromia, and anhidrosis. Treatment of ophthalmic herpes zoster with nucleoside Clinical Findings analogues within 5 days after onset may reduce the morbid Parents may notice unequal pupils or different colored eyes. When vesicles are present on the tip of the nose with Penlight examination of the eyes may reveal unequal pupils herpes zoster (Hutchinson sign), ocular involvement, includ (anisocoria), iris heterochromia, and eyelid ptosis of the ing iritis, may develop. The ptosis is usually mild with a well-defined upper lid Molluscum contagiosum lesions may be treated with crease. Anhidrosis can occur in con Eyelid ptosis results in a droopy eyelid that may be unilateral genital and acquired cases. If the pupil is obstructed, deprivation amblyopia must be present to make the diagnosis. The congenital variety is most commonly the result of birth Clinical Findings trauma. Other causes of ptosis are myas neuroblastoma of the sympathetic chain in the apical lung thenia gravis, lid injuries, third nerve palsy, and Horner region. An excellent screening test for this is the spot urine syndrome (see next section). Pharmacologic assessment of the pupils with topical An association sometimes seen with congenital ptosis is the cocaine and hydroxyamphetamine or epinephrine will help Marcus Gunn jaw-winking phenomenon. Intermittent reduc determine whether the Horner syndrome is due to a pregan tion of the ptosis occurs during mastication or sucking, due to glionic or postganglionic lesion of the sympathetic chain. There are preliminary studies that suggest that topical apra clonidine may also be useful in the diagnosis of Horner syndrome. Other surgical procedures, Nasolacrimal obstruction occurs in up to 6% of infants. Much less often, dacryocystorhinostomy is from incomplete canalization of the duct or membranous required. Light sensitivity and blepharospasm sug Congenital dacryocystocele is thought to result from gest possible congenital glaucoma and warrant an urgent obstructions proximal and distal to the nasolacrimal sac. At birth, the nasolacrimal sac is distended and has a bluish hue that often leads to an the differential diagnosis of tearing includes nasolacrimal erroneous diagnosis of hemangioma. Repeated probing and endoscopic marsupialization of the intranasal Treatment cyst under general anesthesia may be required. Dacryocysti Massage over the nasolacrimal sac may empty debris from this and sepsis can result from dacryocystocele. Topical antibiotic administration is adjunctive and is also used with recurrent chronic infections. If it cannot be drained via the intranasal portion of the nasolacrimal duct, external drainage may be necessary. Trauma, irritation of the conjunctiva, and Dacryocystitis is an infection of the nasolacrimal sac and intraocular inflammation also can cause injection of conjuncti results in erythema and edema over the nasolacrimal sac. In devel Acute dacryocystitis presents with inflammation, swelling, oped countries, Chlamydia is the most common cause. A purulent cause of neonatal conjunctivitis, since it may indicate sys discharge and tearing can be expected, because the cause of temic herpes simplex infection. Signs of chronic dacryocystitis are mucopurulent debris Clinical Findings on the lids and lashes, tearing, injection of the palpebral Ophthalmia neonatorum is characterized by redness and conjunctiva, and reflux of pus at the puncta when pressure is swelling of the lids and conjunctiva and by discharge Figure applied over the sac. Gram staining, Giemsa staining for elementary bod episodes of low-grade dacryocystitis are caused by nasolacri ies, polymerase chain reaction amplification for Chlamydia mal obstruction. Treatment Treatment of severe acute dacryocystitis is with intravenous Prevention & Treatment antibiotics after attempts at identifying the offending organism Although no single prophylactic medication can eliminate all by culture and staining. Oral antibiotics can be tried in milder cases of neonatal conjunctivitis, povidone-iodine may provide broader coverage against the organisms causing this disease than silver nitrate or erythromycin ointment.

Likewise symptoms ear infection generic combivent 100 mcg without a prescription, women with gestational diabetes may Tetany with facial and extremity numbness treatment 1 degree av block discount combivent online visa, tingling medicine of the future 100 mcg combivent with amex, have relative hyperparathyroidism in the third trimester and cramps treatment 001 order 100mcg combivent free shipping, spontaneous muscle contractures, carpopedal their infants may experience transient hypoparathyroidism. Phosphate binds calcium and pro In hypoparathyroidism or pseudohypoparathyroidism: duces functional hypocalcemia. Hypocalcemia may also occur in Rickets is a term describing the characteristic clinical and intestinal malabsorption of calcium, chronic renal disease, bony radiologic features associated with vitamin D defi tumor lysis syndrome, or rhabdomyolysis, or as the result of ciency (see Chapter 10). Table 32-6 Hypocalcemia associated with disorders of parathyroid hormone secretion or action. Occult vitamin D deficiency is proba minemia, the total serum calcium may be low and yet the bly more common than is presently recognized. Ionized calcium cern forms the basis for the recommendation by the is the test of choice for hypocalcemia in patients with low American Association of Pediatrics that breast-fed infants serum albumin. Cardiac monitoring should be per this condition is abnormal renal phosphate loss. Maintenance Management of Hypoparathyroidism or Chronic Hypocalcemia Clinical Findings the objective of treatment is to maintain the serum calcium A. Symptoms and Signs and phosphate at near normal levels without excess urinary Prolonged hypocalcemia from any cause is associated with calcium excretion. Some patients with hypocalcemia exhibit bizarre behavior, irritability, loss of consciousness, and con of serum level and urinary calcium excretion. Headache, vomiting, increased intracranial pres tal calcium can often be discontinued in patients with rickets after vitamin D therapy has stabilized. Selection are reduced in many hypocalcemic conditions, but may be and dosage of vitamin D supplements varies with the under elevated in pseudohypoparathyroidism or severe vitamin D lying condition and the response to therapy. Measurement of urinary excretion of calcium as therapy is essential to avoid toxicity. Imaging month intervals is necessary to ensure adequate therapy and Soft tissue and basal ganglia calcification may occur in to prevent hypercalcemia and nephrocalcinosis. Various skeletal changes are associated with rickets, nance of serum calcium and phosphorus concentrations including cupped and irregular long bone metaphyses. Tor within normal ranges, (2) normalization of alkaline phos sional deformities can result in genu varum (bowleg). Accen phatase activity for age, (3) regression of skeletal changes, tuation of the costochondral junction gives the rachitic and (4) maintenance of an age-appropriate urine calcium rosary appearance seen on the chest wall. Chronic renal disease with eratively and is continued until serum calcium concentrations impaired phosphate excretion is the most common second are normal and stable. Long-term therapy for hypercalcemia of malig nancy is the treatment of the underlying disorder. The prognosis following subtotal parathyroidectomy behavior; nausea, vomiting, abdominal pain, constipation, for diffuse hyperplasia or removal of multiple adenomas is and weight loss; hyperextensibility of joints; and hyperten usually good and depends on correction of the underlying sion, cardiac irregularities, bradycardia, and shortening of the defect. Familial hypocalciuric hypercalcemia is distinguished by low to normal urinary calcium excretion as a result of high renal 3. There is a there is generalized demineralization with high risk of sub low rate of new mutations. A severe form of symptomatic neonatal hyperparathyroidism may occur in infants homo B. Vitamin D intoxication is almost always the result of inges tion of excessive amounts of vitamin D. Severe hypercalcemia Initial management is vigorous hydration with normal saline requires hospitalization and aggressive intervention. Due to and forced calcium diuresis with a loop diuretic such as the storage of vitamin D in the adipose tissue, several months furosemide (1 mg/kg given every 6 hours). Chronic Hypercalcemia characterized by elfin-appearing facies and hypercalcemia in Treatment options vary with the underlying cause. Abrupt immobilization, particularly in a rapidly growing ado lescent, may cause hypercalcemia and hypercalciuria. Hypophosphatasia is a rare autosomal recessive condition When an infant is born with ambiguity, immediate consulta characterized by deficiency of alkaline phosphatase activity in tion with pediatric endocrinology, urology, and if possible serum, bone, and tissues. Disorders of sexual differentiation skeletal mineralization with clinical and radiographic features stem from alterations in three main processes: gonadal similar to rickets. Disorders of Gonadal Differentiation failure to thrive, hypotonia, and craniosynostosis. They have phoethanolamine associated with low serum alkaline phospha completely normal female external genitalia and present as tase. Calci characterized by masculine or ambiguous genital develop tonin may be of value for the acute treatment of hypercalcemia. In Lifshitz must have both ovarian and testicular tissue and typically has F (editor): Pediatric Endocrinology, 5th ed. Dysge Zajickova K et al: Identification and functional characterization of netic gonads have an increased risk for neoplastic transfor a novel mutation in the calcium-sensing receptor gene in mation. Because of decreased testosterone production in familial hypocalciuric hypercalcemia. The genital ridge contains gonadal tissue, and and produces antimullerian hormone. Thus, females with congenital adrenal hyperplasia who are virilized as the result of circulating androgens do not have wolffian duct development. Normal male development is also dependent on regression of mullerian duct derivatives through the local action of mullerian inhibiting factor elaborated by the Sertoli cells of the adjacent testis. Elevated concentrations of other (adrenal) androgens, as occurs in females with congenital adrenal hyperplasia, can virilize the genital tubercle, and cause genital swelling and genital/urethral folds, resulting in varying degrees of ambiguity. Maternal plete, the external genitalia may masculinize at puberty when exposure to androgens or androgen antagonists is a rare testosterone production increases. Disorders of Androgen Action Precocious puberty is defined as pubertal development occur Defects in testosterone action result from absent or defective ring below the age limit set for normal onset of puberty. Depending on Puberty is considered precocious in girls if the onset of second the degree of abnormality in androgen binding, the genital ary sexual characteristics occurs before age 8 years. Precocious phenotype can range from relatively mild male ambiguity to puberty is more common in girls than in boys. The age tracheoesophageal fistula with esophageal atresia, and radial of pubertal onset may be advanced by obesity. The pathways illustrated are present in differing amounts in the steroid-producing tissues: adrenal glands, ovaries, and testes. In the adrenal glands, mineralocorticoids from the zona glomerulosa, glucocorticoids from the zona fasciculata, and androgens (and estrogens) from the zona reticularis are produced. The major adrenal androgen is androstenedione, because the activity of 17-ketoreductase is relatively low. The pathways leading to the synthesis of mineralocorticoids and glucocorticoids are not present to any significant degree in the gonads; however, the testes and ovaries each produce both androgens and estrogens.
They also represent an early ing of object permanence to good use by placing a picture of form of imitative behavior medicine jobs buy combivent 100mcg mastercard, which is important in later social the mother (or father) near the child or by leaving an object and cognitive development symptoms xanax addiction generic 100 mcg combivent mastercard. Chil he or she has now taken a major step toward indepen dren must be given some control over when elimination dence symptoms rectal cancer generic combivent 100 mcg with visa. If parents impose severe restrictions medicine used for anxiety order combivent online pills, the achieve ment and an emerging sense of self. Freud termed this period the anal attempt to develop a better idea of what is or might be stage because the developmental issue of bowel control is under his or her control. Ego development during this time generalized theme of socialized behavior and overall body should be fostered but with appropriate limits. As children cleanliness, which is usually taught or imposed on the child develop a sense of self, they begin to understand the at this age. They begin to understand how another child feels when he or she is harmed, and this realization Piaget characterized the 2 to 6-year-old stage as preopera helps them to inhibit their own aggressive behavior. This stage begins when language has facilitated the dren also begin to understand right and wrong and parental creation of mental images in the symbolic sense. Cause-effect relationships are con An area of child behavior that has often been over fused with temporal ones or interpreted egocentrically. Illness and the need skills, and relationships; a means of revisiting the past; a for medical care are also commonly misinterpreted at this means of actively mastering a range of experiences; and a age. The child may experience tification and roles), cognitive development (nonverbal significant guilt unless the parents are aware of these misper and verbal function and executive functioning and creativ ceptions and take time to deal with them. However, they do begin to ment of role playing, sexual identity, and emotional engage in symbolic play such as by drinking from a toy cup growth. Children test new experiences in fantasy, both in and then by giving a doll a drink from a toy cup. In their play, children often 3 years children begin to engage in parallel play (engaging create magical stories and novel situations that reflect in behaviors that are imitative). This form of play gradually issues with which they are dealing, such as aggression, evolves into more interactive or collaborative play by age relationships, fears, and control. There are of imaginary friends at this time, and nightmares or fears of course wide variations in the development of play, reflect monsters are common. At this stage, other children ing cultural, educational, and socioeconomic variables. Play gradually becomes more cooperative; sequence that can be assessed and can be very informative shared fantasy leads to game playing. The pediatrician must evaluate potential learning usually resolved and attachment is redirected to the parent disabilities in any child who is not developing adequately at of the same sex. The child is ready to relate to peers in a task can make a dramatic difference in success at school. The brain has reached 90% of its the clinician must consider all of these aspects in the adult weight. Sensorimotor coordination abilities are matur differential diagnosis of learning disabilities and behavioral ing and facilitating pencil-and-paper tasks and sports, both disorders. National Center for Education in Maternal and Child Health environment and because these activities are stressed in early Georgetown University, 2002. Magical thinking diminishes greatly at this time, and the reality of cause-effect relationships is better under stood. Practitioners will be familiar with most of the prob aggressive or sexual drives but instead devote most of their lems discussed in this chapter; however, with increasing energies to school and peer group interactions. In reality, knowledge of the factors controlling normal neurologic and throughout this period there is a gradual increase in sex behavioral development in childhood, new perspectives on drive, manifested by increasingly aggressive play and interac these disorders and novel approaches to their diagnosis and tions with the opposite sex. Organized sports, clubs, and intrinsic biologic characteristics and the environments with other activities are other modalities that permit preadoles which the children interact. The next section focuses on cent children to display socially acceptable forms of aggres some of the more common complaints about behavior sion and sexual interest. These behav For the 7-year-old child, the major developmental tasks ioral complaints are by and large normal variations in are achievement in school and acceptance by peers. There centrate on, attend to , and process increasingly complex are no cures for these behaviors, but management strategies auditory and visual information. The health care pro Thomas and Temperament is an independent psychologic vider can play a major role in diagnosis, in coordinating the Chess attribute, biologically determined, which is expressed as a response to an external stimulus. An appreciation of this phenomenon is important function rarely has doubts about what is abnormal. Varia because the physician may be able to enhance the parentstions in temperament and behavior are not as straightfor understanding of the child and influence their responses to ward. When of a continuum of responses by the child to a variety of goodness of fit is not present, tension and stress can result in internal and external experiences. Variations in tempera parental anger, disappointment, frustration, and conflict ment have been of interest to philosophers and writers since with the child. The Greeks believed there were four tempera Other models of temperament include those of Roth ment types: choleric, sanguine, melancholic, and phlegmatic. All models seek to identify intrinsic behavioral char as a genetically influenced behavioral disposition that is acteristics that lead the child to respond to the world in stable over time. One child may be highly emotional and ment have been proposed, the one usually used by pediatri another less so (ie, calmer) in response to a variety of cians in clinical practice is that of Thomas and Chess, who experiences, stressful or pleasant. Temperament is an independent psychological are neither good nor bad, right nor wrong, normal nor attribute that is expressed as a response to an external abnormal; they are simply part of the child.

Janice Raymond medications known to cause weight gain discount combivent 100mcg overnight delivery, The Transsexual Empire: The Making of the She-Male (Boston: Beacon symptoms gallbladder purchase 100 mcg combivent, 1979) medicine kit for babies buy on line combivent. Julia Epstein and Kristina Straub medicine ubrania discount combivent online, Body Guards: The Cultural Politics of Gender Ambiguity (New York: Routledge, 1991). David Halperin, Saint Foucault: Toward a Gay Hagiography (New York: Oxford, 1996). On third terms and the disruption of binaries, see Marjorie Garber, Vested Interests: Cross-Dressing and Cultural Anxiety (New York: Routledge, 1992. Donna Haraway, Simians, Cyborgs and Women: The Reinvention of Nature (New York: Routledge, 1991); Judith Hal berstam and Ira Livingston, eds. Fredric Jameson, Postmodernism, or The Cultural Logic of Late Capitalism (Chapel Hill: Duke University Press, 1992). On intersex issues, see Alice Domurat Dreger, Hermaphrodites and the Medical Invention of Sex (Cambridge: Harvard University Press, 1998); Anne Fausto-Sterling, Sexing the Body: Gender Politics and the Construction of Sexuality (New York: Basic Books, 2000); and Suzanne J. For a range of feminist poststructuralist, antifoundationalist critiques of the sex/gender relationship, with particular reference to the question of postmodernity, see Judith Butler and Joan Scott, eds. Jean-Francois Lyotard, The Postmodern Condition: A Report on Knowledge (Manchester: Manchester University Press, 1984), p. Don Kulick, Travesti: Sex, Gender, and Culture among Brazilian Transgendered Prostitutes. His landmark study, Psychopathia Sexualis, has been in print in various revised editions ever since its frst publication in 1877. The text undertakes a vast taxonomic project, attempting to distinguish and clas sify specifc features of the various case studies Kraf-Ebing ofers for consideration. Unlike today, when homosexuality is most ofen considered to be an erotic or romantic attraction between two otherwise typical women, or between two otherwise typical men, Kraf-Ebbing considered homosexuality to be a form of gender variance. Tat is, he considered a man who loved a man to be more like a woman; conversely, he considered a woman who loved a woman to be more like a man. Tese deviations from standard gender could be relatively minor and inconsequential, or relatively major and signifcant. Kraf-Ebing thought such individuals were profoundly disturbed, and considered their desire for self-afrming transformation to be psychotic. The cases Kraf-Ebing presents are doubly interesting, in that they document the extensive discursive and historical interconnections between transgender and homosexual phenomena, but also demon strate the remarkable persistence of highly specifc forms of subjectivity that are readily identifable in current terminology. This anthropological form of the cerebral anomaly apparently represents a very high degree of degeneration; but that this variation is based on an entirely diferent ground than the teratological manifestation of hermaphroditism, in an anatomical sense, is clearly shown by the fact that thus far, in the domain of contrary sexuality, no transitions to hermaphroditic malformation of the genitals have been observed. The genitals of these persons always prove to be fully diferentiated sexually, though not infrequently there are present anatomical signs of degeneration (epispadiasis, etc. A sister of the maternal grandmother was hysterical, a somnam bulist, and lay seventeen years in bed, on account of fancied paralysis. A second great-aunt spent seven years in bed, on account of a fancied fatal illness, and at the same time gave balls. Afer the death of this lady, there were found in this chamber a number of shawls, ornaments, bank-notes, etc. A fourth great-aunt, during two years, did not leave her room, and neither washed herself nor combed her hair; then she again made her appearance. The majority of her male relatives are unusually talented; the females are decidedly narrow and domestic. Among many foolish things that her father encouraged in her was the fact that he brought her up as a boy, called her Sandor, allowed her to ride, drive, and hunt, admiring her muscular energy. On the other hand, this foolish father allowed his second son to go about in female attire, and had him brought up as a girl. Sarolta returned to her mother, who, however, could do nothing, and was compelled to allow her daughter to again become Sandor, wear male clothes, and, at least once a year, to fall in love with persons of her own sex. She early became independent, and visited cafes, even those of doubtful character, and, indeed, boasted one day that in a brothel she had had a girl sitting on each knee. She felt herself drawn particularly toward actresses, or others of similar position, and, if possible, toward those who were not very young. She asserts that she never had any inclination for a young man, and that she has felt, from year to year, an increasing dislike for young men. If I noticed that any of the men awakened the sympathies of the ladies, I felt jeal ous. I preferred ladies who were bright and pretty; I could not endure them if they were fat or much inclined toward men. At the same time, she carried on literary work, and was a valued collaborator on two noted journals of the Capital. Her passion for ladies was very changeable; constancy in love was entirely wanting. She fell in love with her, made a marriage-contract with her, and they lived together, as man and wife, for three years at the Capital. The pair lived happily, and, without the interference of the step-father, this false marriage, probably, would have lasted much longer. It is remarkable that, during the comparatively long existence of the relation, S. The father-in-law also, on one occasion, noticed something like an erected member on his future son-in-law (probably a priapus).

Standardization of sonographic lung-to-head ratio measurements in isolated congenital diaphragmatic hernia: Impact on the reproducibility and efficacy to predict outcomes symptoms kidney pain buy combivent 100mcg. Influence of congenital heart disease on survival in children with congenital diaphragmatic hernia medications j tube combivent 100 mcg otc. Stomach position in prediction of survival in left-sided congenital diaphragmatic hernia with or without fetoscopic endoluminal tracheal occlusion medications not to take with grapefruit purchase combivent 100 mcg on-line. Prediction of postnatal outcomes in fetuses with isolated congenital diaphragmatic hernias using different lung-to-head ratio measurements symptoms 0f parkinson disease purchase combivent 100mcg visa. Longitudinal assessment of lung area measurements by two dimensional ultrasound in fetuses with isolated left-sided congenital diaphragmatic hernia. The lung-to-thorax transverse area ratio at term and near term correlates with survival in isolated congenital diaphragmatic hernia. Pediatric pulmonary hypertension: Guidelines from the American Heart Association and American Thoracic Society. Expert consensus statement on the diagnosis and treatment of pediatric pulmonary hypertension. Pulmonary hypertension associated with acute or chronic lung diseases in preterm or term neonate and infant. Clinical utility of echocardiography for the diagnosis and management of pulmonary vascular disease in young children with chronic lung disease. Cardiac anomalies in patients with congenital diaphragmatic hernia and their prognosis: A report from the Congenital Diaphragmatic Hernia Study Group. Clinical characteristics and outcomes of patients with cardiac defects and congenital diaphragmatic hernia. Congenital heart anomaly in newborns with congenital diaphragmatic hernia: A single-center experience. Prediction of survival in infants with congenital diaphragmatic hernia based on stomach position, surgical timing, and oxygenation index. Best oxygenation index on day 1: A reliable marker for outcome and survival in infants with congenital diaphragmatic hernia. Using serial oxygenation index as an objective predictor of survival for antenatally diagnosed congenital diaphragmatic hernia. A clinical prediction rule for the severity of congenital diaphragmatic hernias in newborns. Surfactant does not improve survival rate in preterm infants with congenital diaphragmatic hernia. Is surfactant therapy beneficial in the treatment of the term newborn infant with congenital diaphragmatic hernia Surfactant replacement therapy for preterm and term neonates with respiratory distress. Temporary tracheal occlusion in fetal sheep with lung hypoplasia does not improve postnatal lung function. Tracheal ligation: the dark side of in utero congenital diaphragmatic hernia treatment. Increasing mean arterial blood pressure and heart rate with catecholaminergic drugs does not improve the microcirculation in children with congenital diaphragmatic hernia: A prospective cohort study. A meta-analysis of dopamine use in hypotensive preterm infants: Blood pressure and cerebral hemodynamics. Early repair of congenital diaphragmatic hernia on extracorporeal membrane oxygenation. A risk-stratified analysis of delayed congenital diaphragmatic hernia repair: Does timing of operation matter Improved survival in left liver-up congenital diaphragmatic hernia by early repair before extracorporeal membrane oxygenation: Optimization of patient selection by multivariate risk modeling. Factors influencing survival in newborns with congenital diaphragmatic hernia: the relative role of timing of surgery. Congenital diaphragmatic hernia requiring extracorporeal membrane oxygenation: Does timing of repair matter Patch repair is an independent predictor of morbidity and mortality in congenital diaphragmatic hernia. Thoracoscopic repair in congenital diaphragmatic hernia: Patching is safe and reduces the recurrence rate. Hypercapnia and acidosis during open and thoracoscopic repair of congenital diaphragmatic hernia and esophageal atresia: Results of a pilot randomized controlled trial. Congenital diaphragmatic hernia: An evaluation of risk factors for failure of thoracoscopic primary repair in neonates. Neonatal endosurgical congenital diaphragmatic hernia repair: A systematic review and meta-analysis. Impact of a current treatment protocol on outcome of high-risk congenital diaphragmatic hernia. Congenital diaphragmatic hernia in 120 infants treated consecutively with permissive hypercapnia /spontaneous respirations / elective repair. Experience in the management of eighty-two newborns with congenital diaphragmatic hernia treated with high-frequency oscillatory ventilation and delayed surgery without the use of extracorporeal membrane oxygenation. Permissive hypercapnia in the management of congenital diaphragmatic hernia: Our institutional experience. Detrimental effects of standard medical therapy in congenital diaphragmatic hernia. Improvement in the outcome of patients with antenatally diagnosed congenital diaphragmatic hernia using gentle ventilation and circulatory stabilization. Reduction in ventilator-induced lung injury improves outcome in congenital diaphragmatic hernia Conventional mechanical ventilation versus high-frequency oscillatory ventilation for congenital diaphragmatic hernia: A randomized clinical trial. Congenital diaphragmatic hernia: Survival treated with very delayed surgery, spontaneous respirations, and no chest tube. Tidal volume in infants with congenital diaphragmatic hernia supported with conventional mechanical ventilation. Ventilation and spontaneous breathing at birth of infants with congenital diaphragmatic hernia. Umbilical venous catheter malposition and errors in interpretation in newborns with Bochdalek hernia. Congenital diaphragmatic hernia in neonates: Variations in umbilical catheter and enteric tube position. Inhaled nitric oxide improves systemic microcirculation in infants with hypoxemic respiratory failure. Factors affecting the response to inhaled nitric oxide therapy in persistent pulmonary hypertension o the newborn infants. Initial oxygenation response to inhaled nitric oxide predicts improved outcome in congenital diaphragmatic hernia. Implementation of an inhaled nitric oxide protocol decreases direct cost associated with its use. Hydrocortisone administration for the treatment of refractory hypotension in critically ill newborns. Hydrocortisone for hypotension and vasopressor dependence in preterm neonates: A meta-analysis. Estimating disease severity of congenital diaphragmatic hernia in the first five minutes of life. Persistent hypercarbia after resuscitation is associated with increased mortality in congenital diaphragmatic hernia patients. Role of admission gas exchange measurement in predicting congenital diaphragmatic hernia survival in the era of gentle ventilation. A simplified formula using early blood gas analysis can predict survival outcomes and the requirements for extracorporeal membrane oxygenation in congenital diaphragmatic hernia. Does a highest pre-ductal O2 saturation < 85% predict non-survival for congenital diaphragmatic hernia Efficacy of the circulatory management of an antenatally diagnosed congenital diaphragmatic hernia: Outcomes of the proposed strategy. Management of pulmonary hypertension in congenital diaphragmatic hernia: Nitric oxide with prostaglandin-E1 versus nitric oxide alone.
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