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1.
Appl Environ Microbiol ; 70(9): 5274-82, 2004 Sep.
Article in English | MEDLINE | ID: mdl-15345410

ABSTRACT

Enterohemorrhagic and enteropathogenic Escherichia coli (EHEC and EPEC, respectively) strains are closely related human pathogens that are responsible for food-borne epidemics in many countries. Integration host factor (IHF) and the locus of enterocyte effacement-encoded regulator (Ler) are needed for the expression of virulence genes in EHEC and EPEC, including the elicitation of actin rearrangements for attaching and effacing lesions. We applied a proteomic approach, using two-dimensional polyacrylamide gel electrophoresis in combination with matrix-assisted laser desorption ionization-time of flight mass spectrometry and a protein database search, to analyze the extracellular protein profiles of EHEC EDL933, EPEC E2348/69, and their ihf and ler mutants. Fifty-nine major protein spots from the extracellular proteomes were identified, including six proteins of unknown function. Twenty-six of them were conserved between EHEC EDL933 and EPEC E2348/69, while some of them were strain-specific proteins. Four common extracellular proteins (EspA, EspB, EspD, and Tir) were regulated by both IHF and Ler in EHEC EDL933 and EPEC E2348/69. TagA in EHEC EDL933 and EspC and EspF in EPEC E2348/69 were present in the wild-type strains but absent from their respective ler and ihf mutants, while FliC was overexpressed in the ihf mutant of EPEC E2348/69. Two dominant forms of EspB were found in EHEC EDL933 and EPEC E2348/69, but the significance of this is unknown. These results show that proteomics is a powerful platform technology for accelerating the understanding of EPEC and EHEC pathogenesis and identifying markers for laboratory diagnoses of these pathogens.


Subject(s)
Escherichia coli Proteins/genetics , Escherichia coli/genetics , Escherichia coli/pathogenicity , Proteome/genetics , Escherichia coli/classification , Escherichia coli/growth & development
2.
Cell Microbiol ; 3(12): 865-71, 2001 Dec.
Article in English | MEDLINE | ID: mdl-11736997

ABSTRACT

Enteropathogenic Escherichia coli (EPEC) uses a type III secretion system (TTSS) to inject effector proteins into the plasma membrane and cytosol of infected cells. To translocate proteins, EPEC, like Salmonella and Shigella, is believed to assemble a macromolecular complex (type III secreton) that spans both bacterial membranes and has a short needle-like projection. However, there is a special interest in studying the EPEC TTSS owing to the fact that one of the secreted proteins, EspA, is assembled into a unique filamentous structure also required for protein translocation. In this report we present electron micrographs of EspA filaments which reveal a regular segmented substructure. Recently we have shown that deletion of the putative structural needle protein, EscF, abolished protein secretion and formation of EspA filaments. Moreover, we demonstrated that EspA can bind directly to EscF, suggesting that EspA filaments are physically linked to the EPEC needle complex. In this paper we provide direct evidence for the association between an EPEC bacterial membrane needle complex and EspA filaments, defining a new class of filamentous TTSS.


Subject(s)
Bacterial Proteins/ultrastructure , Carrier Proteins/ultrastructure , Escherichia coli Proteins , Escherichia coli/ultrastructure , Cell Membrane/ultrastructure , Escherichia coli/metabolism
3.
J Bacteriol ; 183(13): 4004-11, 2001 Jul.
Article in English | MEDLINE | ID: mdl-11395465

ABSTRACT

Lrp (leucine-responsive regulatory protein) plays a global regulatory role in Escherichia coli, affecting expression of dozens of operons. Numerous lrp-related genes have been identified in different bacteria and archaea, including asnC, an E. coli gene that was the first reported member of this family. Pairwise comparisons of amino acid sequences of the corresponding proteins shows an average sequence identity of only 29% for the vast majority of comparisons. By contrast, Lrp-related proteins from enteric bacteria show more than 97% amino acid identity. Is the global regulatory role associated with E. coli Lrp limited to enteric bacteria? To probe this question we investigated LrfB, an Lrp-related protein from Haemophilus influenzae that shares 75% sequence identity with E. coli Lrp (highest sequence identity among 42 sequences compared). A strain of H. influenzae having an lrfB null allele grew at the wild-type growth rate but with a filamentous morphology. A comparison of two-dimensional (2D) electrophoretic patterns of proteins from parent and mutant strains showed only two differences (comparable studies with lrp(+) and lrp E. coli strains by others showed 20 differences). The abundance of LrfB in H. influenzae, estimated by Western blotting experiments, was about 130 dimers per cell (compared to 3,000 dimers per E. coli cell). LrfB expressed in E. coli replaced Lrp as a repressor of the lrp gene but acted only to a limited extent as an activator of the ilvIH operon. Thus, although LrfB resembles Lrp sufficiently to perform some of its functions, its low abundance is consonant with a more local role in regulating but a few genes, a view consistent with the results of the 2D electrophoretic analysis. We speculate that an Lrp having a global regulatory role evolved to help enteric bacteria adapt to their ecological niches and that it is unlikely that Lrp-related proteins in other organisms have a broad regulatory function.


Subject(s)
Acetolactate Synthase , DNA-Binding Proteins/genetics , Escherichia coli Proteins , Haemophilus influenzae/genetics , Transcription Factors , Amino Acid Sequence , Bacterial Proteins/genetics , Bacterial Proteins/isolation & purification , Gene Expression Profiling , Gene Expression Regulation, Bacterial , Genes, Bacterial , Haemophilus influenzae/cytology , Leucine-Responsive Regulatory Protein , Molecular Sequence Data , Mutation , Phenotype , Protein Binding , Sequence Homology, Amino Acid
4.
Circulation ; 102(19 Suppl 3): III130-5, 2000 Nov 07.
Article in English | MEDLINE | ID: mdl-11082375

ABSTRACT

BACKGROUND: Few studies have explored the long-term function of cryopreserved homograft valves used for reconstruction of the right ventricular tract (RVOT) in patients with congenital heart disease. METHODS AND RESULTS: Among 205 patients receiving cryopreserved homografts for reconstruction of the RVOT between November 1985 and April 1999, the outcome of 220 homografts in 183 operative survivors was analyzed. There were 150 pulmonary and 70 aortic homografts used. Median age at implantation was 4.4 years (mean 6.9+/-7.6 years, range 3 days to 48 years). End points included (1) patient survival, (2) homograft failure (valve explant or late death), and (3) homograft dysfunction (homograft insufficiency or homograft stenosis). Survival was 88% at 10 years. Freedom from homograft failure was 74+/-4% at 5 years and 54+/-7% at 10 years. Univariable analysis identified younger age, longer donor warm ischemic time, valve Z: value <2, and previous procedure as risk factors for homograft failure and dysfunction. Aortic homograft type and extracardiac operative technique predicted homograft failure but not dysfunction. For patients

Subject(s)
Aortic Valve/transplantation , Graft Survival , Heart Defects, Congenital/surgery , Pulmonary Valve/transplantation , Ventricular Outflow Obstruction/surgery , Adolescent , Adult , Age Distribution , Cardiac Surgical Procedures/mortality , Child , Child, Preschool , Cryopreservation , Disease-Free Survival , Follow-Up Studies , Heart Defects, Congenital/complications , Humans , Infant , Infant, Newborn , Middle Aged , Multivariate Analysis , Proportional Hazards Models , Risk Factors , Survival Rate , Transplantation, Homologous/statistics & numerical data , Ventricular Outflow Obstruction/etiology
6.
Mol Microbiol ; 34(5): 941-52, 1999 Dec.
Article in English | MEDLINE | ID: mdl-10594820

ABSTRACT

Enteropathogenic Escherichia coli (EPEC) elicit changes in host cell morphology and cause actin rearrangement, a phenotype that has commonly been referred to as attaching/effacing (AE) lesions. The ability of EPEC to induce AE lesions is dependent upon a type III protein secretion/translocation system that is encoded by genes clustered in a 35.6 kb DNA segment, named the locus of enterocyte effacement (LEE). We used transcriptional fusions between the green fluorescent protein (gfp) reporter gene and LEE genes rorf2, orf3, orf5, escJ, escV and eae, together with immunoblot analysis with antibodies against Tir, intimin, EspB and EspF, to analyse the genetic regulation of the LEE. The expression of all these LEE genes was strictly dependent upon the presence of a functional integration host factor (IHF). IHF binds specifically upstream from the ler (orf1) promoter and appears to activate expression of ler, orf3, orf5 and rorf2 directly. The ler-encoded Ler protein was involved in activating the expression of escJ, escV, tir, eae, espB and espF. Expression of both IHF and Ler was needed to elicit actin rearrangement associated with AE lesions. In conclusion, IHF directly activates the expression of the ler and rorf2 transcriptional units, and Ler in turn mediates the expression of the other LEE genes.


Subject(s)
Bacterial Proteins/metabolism , Escherichia coli/genetics , Escherichia coli/pathogenicity , Gene Expression Regulation, Bacterial , Actins/metabolism , Bacterial Outer Membrane Proteins/genetics , Bacterial Outer Membrane Proteins/metabolism , Bacterial Proteins/genetics , DNA Footprinting , Enterocytes/microbiology , Escherichia coli/metabolism , Green Fluorescent Proteins , HeLa Cells , Humans , Immunoblotting , Integration Host Factors , Luminescent Proteins/genetics , Luminescent Proteins/metabolism , Mutation , Open Reading Frames/genetics , Promoter Regions, Genetic , Transcription, Genetic , Virulence/genetics
7.
Am J Ophthalmol ; 128(5): 647-8, 1999 Nov.
Article in English | MEDLINE | ID: mdl-10577541

ABSTRACT

PURPOSE: To describe three women with narrow-angle glaucoma who had transient blurred vision during sexual arousal. METHOD: Case reports. RESULTS: Three women, aged 37, 45, and 55 years, were seen with bilateral narrow-angle glaucoma and were treated with bilateral laser iridotomy. In each patient, additional surgery was required to control the glaucoma. After establishing a rapport with her physician, each patient described transient blurred vision, from a few minutes to several hours in duration, which began during sexual arousal. This symptom resolved after peripheral iridotomy and, in one patient, after laser iridoplasty. CONCLUSION: The association of transient blurred vision with sexual activity may delay presentation of patients with symptomatic narrow-angle glaucoma.


Subject(s)
Glaucoma/complications , Glaucoma/physiopathology , Sexual Behavior/physiology , Vision Disorders/etiology , Adult , Female , Humans , Iris/surgery , Middle Aged
8.
Pediatr Clin North Am ; 46(2): 221-34, 1999 Apr.
Article in English | MEDLINE | ID: mdl-10218071

ABSTRACT

Although SCD is relatively uncommon, its psychosocial impact is devastating. This article has reviewed the potential causes of SCD in infants, children, and adolescents. Many patients who die from SCD have identifiable cardiac disease and are known to have been at risk; however, the existence of other cardiac abnormalities, such as hypertrophic cardiomyopathy or long QT syndrome, may not be known, and SCD may be the first symptom. The authors' contention is that many of the patients in this latter group (e.g., patients who have hypertrophic cardiomyopathy or LQLTS but who have no symptoms) can be screened with a careful, accurate, and detailed history, including family history and review of systems, and physical examination. Any patient with a positive family history, positive review of systems, or positive physical examination should receive further in-depth evaluation, such as an ECG and echocardiogram. These studies permit the detection of most, if not all, of the entities potentially associated with SCD in the pediatric population.


Subject(s)
Death, Sudden, Cardiac/etiology , Death, Sudden, Cardiac/prevention & control , Adolescent , Cardiomyopathy, Hypertrophic/complications , Cardiomyopathy, Hypertrophic/diagnosis , Cardiomyopathy, Hypertrophic/therapy , Child , Child, Preschool , Death, Sudden, Cardiac/epidemiology , Electrocardiography , Family Practice , Humans , Incidence , Infant , Infant, Newborn , Long QT Syndrome/complications , Long QT Syndrome/diagnosis , Long QT Syndrome/therapy , Medical History Taking , Pediatrics , Physical Examination , Risk Factors
9.
Am J Ophthalmol ; 127(3): 329-39, 1999 Mar.
Article in English | MEDLINE | ID: mdl-10088745

ABSTRACT

PURPOSE: To describe the risks, benefits, and recommended use of the ganciclovir implant for the treatment of human immunodeficiency virus-related cytomegalovirus (CMV) retinitis in the era of potent antiretroviral therapy. METHODS: A panel of physicians with expertise in the use of the ganciclovir implant and in the management of CMV retinitis was convened by the International AIDS Society-USA. The panel reviewed and discussed available data, and developed recommendations for the use of the ganciclovir implant, the surgical technique, and related management issues. Recommendations were rated according to the strength and quality of the supporting evidence. RESULTS: The effect of potent antiretroviral therapy on the immunologic status of patients with human immunodeficiency virus disease has changed the manifestation and course of CMV retinitis in many patients. The clinical management of CMV retinitis and the role of the ganciclovir implant are thus changing. Factors in the decision to choose the ganciclovir implant include the patient's potential for immunologic improvement, location and severity of CMV retinitis, and the risks and costs associated with implantation and concomitant oral ganciclovir therapy. CONCLUSIONS: The ganciclovir implant is safe and effective for the treatment of CMV retinitis. The indications for its use should be modified to account for increased patient survival and the potential for CMV retinitis to be controlled by effective antiretroviral therapy. Optimal use of the ganciclovir implant and discontinuation of therapy in selected patients with improvement in immunity may result in better long-term visual outcomes.


Subject(s)
AIDS-Related Opportunistic Infections/drug therapy , Antiviral Agents/therapeutic use , Cytomegalovirus Retinitis/drug therapy , Ganciclovir/therapeutic use , AIDS-Related Opportunistic Infections/diagnosis , Antiviral Agents/economics , Contraindications , Cytomegalovirus Retinitis/diagnosis , Drug Implants , Ganciclovir/economics , Humans , Ophthalmologic Surgical Procedures , Safety , United States
10.
J Am Soc Echocardiogr ; 12(3): 221-4, 1999 Mar.
Article in English | MEDLINE | ID: mdl-10070188

ABSTRACT

Anomalous origin of the right coronary artery from the left sinus of Valsalva is a rare congenital defect that can be difficult to diagnose by echocardiography. We describe an infant with a ventricular septal defect that was diagnosed prospectively by transthoracic echocardiography as an anomalous origin of the right coronary artery from the left sinus of Valsalva. Subcostal imaging and Doppler color flow mapping were instrumental in the echocardiographic diagnosis of this unusual coronary abnormality.


Subject(s)
Coronary Vessel Anomalies/diagnostic imaging , Sinus of Valsalva/abnormalities , Heart Septal Defects, Ventricular/diagnostic imaging , Heart Septal Defects, Ventricular/surgery , Humans , Infant , Sinus of Valsalva/diagnostic imaging , Ultrasonography
11.
WMJ ; 97(8): 47-50, 1998 Sep.
Article in English | MEDLINE | ID: mdl-9775754

ABSTRACT

As we enter the next millennium, we are encouraged by the progress that has been made in the care of neonates, infants, and children with heart disease. Surgical repair can be offered at an earlier age with excellent results. Diseases that were uniformly fatal in the past have improved outcomes. Research continues in the area of interventional devices such that surgical repair might be eliminated or delayed. We continue to look forward to advances in the next several years that will allow for future improvement in outcome, better quality-of-life and better long-term results.


Subject(s)
Heart Diseases/diagnosis , Heart Diseases/surgery , Child , Heart Diseases/physiopathology , Humans , Hypoplastic Left Heart Syndrome/surgery , Transposition of Great Vessels/surgery
12.
Arch Intern Med ; 158(9): 957-69, 1998 May 11.
Article in English | MEDLINE | ID: mdl-9588429

ABSTRACT

OBJECTIVE: To provide recommendations for the treatment of acquired immunodeficiency syndrome-related cytomegalovirus (CMV) end-organ diseases, including retinitis, colitis, pneumonitis, and neurologic diseases. PARTICIPANTS: A 17-member panel of physicians with expertise in clinical and virological research and inpatient care in the field of CMV diseases. EVIDENCE: Available clinical and virological study results. Recommendations are rated according to the quality and strength of available evidence. Recommendations were limited to the treatment of CMV diseases; prophylaxis recommendations are not included. PROCESS: The panel was convened in February 1997 and met regularly through November 1997. Subgroups of the panel summarized and presented available information on specific topics to the full panel; recommendations and ratings were determined by group consensus. CONCLUSIONS: Although the epidemiological features of CMV diseases are changing in the setting of potent, combination antiretroviral therapy, continued attention must be paid to CMV diseases in patients infected with the human immunodeficiency virus to prevent irreversible endorgan dysfunction. The initial and maintenance treatment of CMV retinitis must be individualized based on the characteristics of the lesions, including location and extent, specific patient factors, and characteristics of available therapies among others. Management of relapse or refractory retinitis must be likewise individualized. Ophthalmologic screening for patients at high risk for retinitis or who have a prior diagnosis of extraretinal disease is recommended. Recommendations for gastrointestinal, pulmonary, and neurologic manifestations are included.


Subject(s)
AIDS-Related Opportunistic Infections/drug therapy , Antiviral Agents/therapeutic use , Cytomegalovirus Infections/drug therapy , Organophosphonates , Anti-HIV Agents/therapeutic use , Cidofovir , Cytosine/analogs & derivatives , Cytosine/therapeutic use , Foscarnet/therapeutic use , Ganciclovir/therapeutic use , Humans , Lung Diseases/drug therapy , Lung Diseases/virology , Nervous System Diseases/drug therapy , Nervous System Diseases/virology , Organophosphorus Compounds/therapeutic use , Retinitis/drug therapy , Retinitis/virology
13.
Am J Ophthalmol ; 125(3): 301-5, 1998 Mar.
Article in English | MEDLINE | ID: mdl-9512146

ABSTRACT

PURPOSE: To report uveitis associated with human immunodeficiency virus (HIV) infection and to suggest guidelines for treatment. METHODS: Six HIV-seropositive patients (10 eyes) with anterior or posterior uveitis or both were evaluated. After ineffective prolonged treatment with systemic and topical corticosteroids, specific systemic antiretroviral therapy with zidovudine was initiated in all patients. Aqueous humor was cultured in three eyes of three patients, and vitreous humor was cultured in one eye of one patient. RESULTS: In all 10 eyes of six patients, there was resolution of inflammation in 10 to 42 days after commencement of treatment with zidovudine (600 to 800 mg/day), despite no or minimal response to corticosteroids. Cultures of aqueous humor from three eyes of three patients and culture of vitreous humor from one eye of one patient were positive for HIV; no other organism was isolated. Systemic evaluation disclosed no other identifiable cause for the uveitis in any patient. CONCLUSIONS: Infection with HIV appears to be a cause of uveitis. A trial of zidovudine may be warranted in HIV-seropositive patients with uveitis that is poorly responsive to corticosteroid treatment when no other cause is identified. The efficacy of other retroviral agents was not determined.


Subject(s)
Eye Infections, Viral , HIV Infections/complications , HIV-1 , Uveitis, Anterior/virology , Uveitis, Posterior/virology , Adult , Anti-HIV Agents/therapeutic use , Aqueous Humor/virology , CD4 Lymphocyte Count , CD4-Positive T-Lymphocytes/immunology , HIV Infections/drug therapy , HIV Infections/immunology , HIV Seropositivity/complications , HIV-1/isolation & purification , Humans , Male , Middle Aged , Practice Guidelines as Topic , Uveitis, Anterior/drug therapy , Uveitis, Posterior/drug therapy , Vitreous Body/virology , Zidovudine/therapeutic use
14.
Am J Ophthalmol ; 125(3): 312-24, 1998 Mar.
Article in English | MEDLINE | ID: mdl-9512148

ABSTRACT

PURPOSE: To describe the clinical features of a disorder characterized by chronic multifocal retinal infiltrates and uveitis in individuals with human immunodeficiency virus (HIV) disease. METHODS: We reviewed the medical records of HIV-infected patients with multifocal retinal infiltrates of unknown cause seen by investigators at four institutions. The following data were collected: demographic characteristics, presenting signs and symptoms, laboratory test results, and course of disease. RESULTS: We identified 26 HIV-infected patients (50 involved eyes) with this syndrome. Median CD4+ T-lymphocyte count at presentation was 272 per microl (range, 7 to 2,118 per microl). The most common presenting symptom was floaters. Median visual acuity of involved eyes at presentation was 20/20 (range, 20/15 to 20/100) and remained stable (median, 20/20; range, 20/15 to 20/70) after a median follow-up period of 9 months (range, 0 to 110 months). Typical retinal lesions were gray-white or yellow, irregular in shape, and less than 200 microm in greatest dimension. All were located in the midperiphery or anterior retina and enlarged slowly or remained static in size. Mild to moderate anterior chamber or vitreous humor inflammatory cells were present in 47 of 50 eyes (26 of 26 patients). Retinal lesions possibly responded to zidovudine but not to acyclovir or ganciclovir. Anterior chamber and vitreous humor inflammatory reactions responded to topical or periocular injections of corticosteroid. CONCLUSIONS: Uveitis with chronic multifocal retinal infiltrates is a distinct clinical entity of unknown cause that occurs in HIV-infected patients. Retinal lesions may respond to antiretroviral therapy. Visual prognosis is good.


Subject(s)
HIV Infections/complications , Retinal Diseases/complications , Uveitis/complications , Acyclovir/therapeutic use , Adult , Anti-HIV Agents/therapeutic use , CD4 Lymphocyte Count , CD4-Positive T-Lymphocytes/immunology , Chronic Disease , Fundus Oculi , Ganciclovir/therapeutic use , HIV Infections/drug therapy , HIV Infections/pathology , Humans , Male , Middle Aged , Retinal Diseases/drug therapy , Retinal Diseases/pathology , Syndrome , Uveitis/drug therapy , Uveitis/pathology , Visual Acuity , Zidovudine/therapeutic use
16.
Am Heart J ; 133(5): 558-69, 1997 May.
Article in English | MEDLINE | ID: mdl-9141378

ABSTRACT

Aortic outflow tract obstruction can complicate the clinical course and surgical management of patients with heterotaxy syndromes, but its anatomic basis has not been described in detail. In 20 postmortem cases with asplenia (n = 4) or polysplenia (n = 16), the anatomic causes of aortic outflow tract obstruction were absence of the subaortic conus in association with (1) narrowing of the subaortic outflow tract between the conal septum anteriorly and the common atrioventricular (AV) valve posteriorly in six (30%) patients; (2) aortic valvar atresia in four (25%), three with asplenia and one with polysplenia; (3) redundant AV valve leaflets in four (20%); (4) excessive AV valve fibrous tissue in four (20%); (5) marked hypoplasia of the mitral valve and left ventricle in two (10%); and (6) aneurysm of membranous septum in one (5%). One patient belonged to group (1) and (4). Aortic outflow tract obstruction was much more common with polysplenia (28%) than with asplenia (4%) (p < 0.001).


Subject(s)
Abnormalities, Multiple/pathology , Aortic Valve/abnormalities , Heart Defects, Congenital/pathology , Spleen/abnormalities , Viscera/abnormalities , Child , Child, Preschool , Female , Humans , Infant , Infant, Newborn , Male , Syndrome
18.
Article in English | MEDLINE | ID: mdl-9058611

ABSTRACT

Cytomegalovirus (CMV) retinitis is a disease of advanced immunosuppression that occurs almost exclusively in patients with CD4+ counts of < or =50 cells/mm3. Therefore, this disease usually presents in patients who have already been diagnosed with acquired immunodeficiency syndrome (AIDS). The rate of progression of untreated CMV retinitis is variable. Typical initial complaints of patients with CMV retinitis may include blurred or decreased vision, loss of peripheral or central vision, and multiple "floaters." The diagnosis of CMV retinitis requires ruling out a number of other ocular disorders that may be confused with CMV retinitis. This review discusses the different appearances of CMV retinitis at presentation and the possible retinal responses to therapy for CMV retinitis. An overview of intravenous (i.v.) ganciclovir or i.v. foscarnet as systemic therapy for treatment of CMV retinitis and their use in combination is also presented. Results indicate that combination therapy with both ganciclovir and foscarnet is more effective in controlling progression of CMV retinitis in relapsed patients than is monotherapy with either drug. However, combination systemic therapy is time-consuming, and this regimen has the greatest negative impact on quality of life. Treatment should involve a cooperative effort between the patient's ophthalmologist and the primary AIDS-treating physician. Both must be aware of the location and activity of the retinitis and of other medical conditions and concomitant medications.


Subject(s)
AIDS-Related Opportunistic Infections/diagnosis , AIDS-Related Opportunistic Infections/drug therapy , Cytomegalovirus Retinitis/diagnosis , Cytomegalovirus Retinitis/drug therapy , Antiviral Agents/therapeutic use , Diagnosis, Differential , Drug Therapy, Combination , Foscarnet/therapeutic use , Ganciclovir/therapeutic use , Humans , Ophthalmoscopy
20.
Ann Thorac Surg ; 62(2): 419-24, 1996 Aug.
Article in English | MEDLINE | ID: mdl-8694600

ABSTRACT

BACKGROUND: To determine factors predicting mortality and morbidity after repair of complete atrioventricular septal defect, we retrospectively analyzed preoperative, operative, and postrepair factors on the outcome of 115 consecutive complete atrioventricular septal defect repairs at The Children's Hospital of Wisconsin between January 1974 and December 1993. METHODS: For the entire experience the operative mortality was 13.9% (16 patients). During the most recent era, January 1988 to December 1993, operative mortality was 3.6% (2 of 55 patients). This was significantly improved from the two previous eras, January 1974 to December 1980, 28% (7 of 25) and January 1981 to December 1987, 20% (7 of 35 patients) (p = 0.02). There were seven late deaths; 10-year actuarial survival, including operative mortality was 81%. Age at complete repair decreased; before 1982 all patients were more than 12 months of age, whereas after 1982 64% (56 of 88 patients) were 12 months of age or less. RESULTS: Moderate or severe preoperative left atrioventricular valve regurgitation was not a risk factor for operative mortality. For operative survivors with moderate to severe preoperative left atrioventricular valve regurgitation (n = 17), late postoperative left atrioventricular valve regurgitation (follow-up data available on 15 patients) was significantly reduced (severe = 1, moderate = 5, mild = 9; p = 0.007). CONCLUSIONS: Early mortality was predicted by the era of surgical repair. Conversion to routine repair during infancy was achieved with a simultaneous decrease in operative mortality. For patients with moderate to severe preoperative left atrioventricular valve regurgitation, significant improvement in the degree of left atrioventricular valve regurgitation can be expected without an increase in operative or late mortality or morbidity.


Subject(s)
Endocardial Cushion Defects/surgery , Actuarial Analysis , Adolescent , Age Factors , Blood Pressure , Cause of Death , Child , Child, Preschool , Down Syndrome/complications , Endocardial Cushion Defects/complications , Endocardial Cushion Defects/mortality , Endocardial Cushion Defects/physiopathology , Follow-Up Studies , Forecasting , Heart Defects, Congenital/complications , Humans , Infant , Mitral Valve Insufficiency/physiopathology , Mitral Valve Insufficiency/prevention & control , Pulmonary Artery , Respiration, Artificial , Retrospective Studies , Survival Rate , Treatment Outcome , Wisconsin/epidemiology
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