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1.
J Med Vasc ; 46(2): 80-89, 2021 Apr.
Article in English | MEDLINE | ID: mdl-33752850

ABSTRACT

INTRODUCTION: May-Thurner syndrome has been recognized as a cause of chronic venous insufficiency and a trigger for venous thromboembolism. There is no consensus about the definition, diagnosis, and therapeutic approach. We are aiming to describe its characteristics and a scoping literature review. METHODS: A retrospective review of patients with May-Thurner syndrome from March 2010 to May 2018 and scoping literature review were made. RESULTS: Seven patients were identified. All patients were female with a median age of 36 (20-60) years. The median time from the first symptom to diagnosis was 3.41 (0.01-9) years. The primary clinical presentation was post-thrombotic syndrome (4 patients). Six patients had at least one risk factor for deep venous thrombosis. All patients underwent angioplasty with stent; patients with acute deep venous thrombosis, furthermore mechanic thrombectomy with or without catheter-directed thrombolysis were done. There were three complications (one patient, lymphedema, and two venous stent thrombosis). Scoping review results were descriptively summarized. CONCLUSION: May-Thurner syndrome has a varied spectrum of clinical presentation, and clinical awareness is paramount for diagnosis. Its principal complication is the post-thrombotic syndrome, which is associated with high morbidity. There is no consensus on the antithrombotic treatment approach.


Subject(s)
Angioplasty , May-Thurner Syndrome/therapy , Postthrombotic Syndrome/therapy , Thrombectomy , Thrombolytic Therapy , Venous Thrombosis/therapy , Adult , Angioplasty/adverse effects , Angioplasty/instrumentation , Female , Humans , Male , May-Thurner Syndrome/complications , May-Thurner Syndrome/diagnostic imaging , Middle Aged , Postthrombotic Syndrome/diagnosis , Postthrombotic Syndrome/etiology , Recurrence , Retrospective Studies , Stents , Thrombectomy/adverse effects , Thrombolytic Therapy/adverse effects , Treatment Outcome , Venous Thrombosis/diagnostic imaging , Venous Thrombosis/etiology , Young Adult
2.
Phys Rev Lett ; 113(23): 233901, 2014 Dec 05.
Article in English | MEDLINE | ID: mdl-25526129

ABSTRACT

Experimental evidence demonstrating that anomalous localization of waves can be induced in a controllable manner is reported. A microwave waveguide with dielectric slabs randomly placed is used to confirm the presence of anomalous localization. If the random spacing between slabs follows a distribution with a power-law tail (Lévy-type distribution), unconventional properties in the microwave-transmission fluctuations take place revealing the presence of anomalous localization. We study both theoretically and experimentally the complete distribution of the transmission through random waveguides characterized by α=1/2 ("Lévy waveguides") and α=3/4, α being the exponent of the power-law tail of the Lévy-type distribution. As we show, the transmission distributions are determined by only two parameters, both of them experimentally accessible. Effects of anomalous localization on the transmission are compared with those from the standard Anderson localization.

3.
Prenat Diagn ; 34(11): 1049-54, 2014 Nov.
Article in English | MEDLINE | ID: mdl-24861354

ABSTRACT

OBJECTIVES: To analyze trends in cytogenetic prenatal diagnosis in Cuba and to analyze possible causes leading to a low Down syndrome prevalence in a country where the triple test is not available. METHODS: An analysis of the Cuban program in prenatal cytogenetic diagnosis from 1984 to 2012 was conducted. Results are described, with particular emphasis on indications, abnormal results, types of invasive procedures, and terminations of pregnancy. RESULTS: Cytogenetic prenatal diagnostic analyses (n = 75,095) were conducted; maternal age was the indication for 77.9% of the amniocenteses and chorionic villus samplings. The detection rate of chromosomally abnormal pregnancies was 2.3% for maternal age and increased to 8-9% for other indications. When a chromosomal abnormality was identified, 88.5% terminated the pregnancy. In 2002, the live birth prevalence of Down syndrome was 8.4 per 10,000 live births, and in 2012, 7 per 10,000. CONCLUSION: Prenatal diagnosis in Cuba has contributed to a significant reduction in chromosomal aberrations. The impact increased because of the demographic trends of the population, the high index of terminations of pregnancy, and the establishment of a network of cytogenetic laboratories throughout Cuba.


Subject(s)
Down Syndrome/diagnosis , Down Syndrome/epidemiology , Prenatal Diagnosis/statistics & numerical data , Adult , Amniocentesis/statistics & numerical data , Chorionic Villi Sampling/statistics & numerical data , Cross-Sectional Studies , Cuba/epidemiology , Cytogenetic Analysis/statistics & numerical data , Female , Humans , Maternal Age , Pregnancy , Prevalence , Registries , Young Adult
4.
Rheumatol Int ; 34(5): 723-5, 2014 May.
Article in English | MEDLINE | ID: mdl-23292188

ABSTRACT

We report an adult female patient with Takayasu arteritis (TA) receiving conventional medical treatment and anti-TNF therapy, which developed progressive thoracic and abdominal aortic aneurysms. She developed imminent rupture of the thoracic aneurysm and an endovascular stent-graft (EVSG) was emergency implanted and a year after this procedure the abdominal aneurysm increased in size requiring reoperation and placement of another EVSG. Both procedures had a very good outcome. This case shows the effectivity and security of multiple EVSG implantations in multiple aortic aneurisms in patients with TA.


Subject(s)
Aortic Aneurysm, Abdominal/surgery , Aortic Aneurysm, Thoracic/surgery , Blood Vessel Prosthesis Implantation/instrumentation , Blood Vessel Prosthesis , Endovascular Procedures/instrumentation , Stents , Takayasu Arteritis/complications , Takayasu Arteritis/drug therapy , Adult , Aortic Aneurysm, Abdominal/diagnosis , Aortic Aneurysm, Abdominal/etiology , Aortic Aneurysm, Thoracic/diagnosis , Aortic Aneurysm, Thoracic/etiology , Aortography/methods , Biological Products/therapeutic use , Female , Humans , Reoperation , Takayasu Arteritis/diagnosis , Takayasu Arteritis/immunology , Tomography, X-Ray Computed , Treatment Outcome , Tumor Necrosis Factor-alpha/antagonists & inhibitors
5.
Eur J Trauma Emerg Surg ; 38(3): 281-93, 2012 Jun.
Article in English | MEDLINE | ID: mdl-26815960

ABSTRACT

BACKGROUND: Popliteal arterial injuries carry a high risk of amputation. The currently available literature from both civilian and military experiences is characterized by a wide variation of recommendations for surgical management. We questioned how these recommendations have been applied in our practice. Therefore, we aimed to identify predictors of amputation after popliteal arterial injury. METHODS: We conducted an observational study of 175 patients with popliteal arterial injuries who underwent surgical treatment from 1992 to 2006 at a level I trauma center in Cali, Colombia. Information on demographic characteristics, clinical information, and surgical management was collected from clinical records. The outcome measure was amputation within 30 days following the first surgical intervention. RESULTS: The amputation rate was 17.1%. A multivariable logistic regression model indicates that blunt mechanism (odds ratio [OR] 4.79, 95% confidence interval [CI] 1.49-15.42), signs of ischemia (OR 5.29, 95% CI 1.48-18.91), ligation of the popliteal vein of the compromised limb during surgical exploration (OR 3.83, 95% CI 1.20-12.18), and the development of arterial thrombosis (OR 56.51, 95% CI 12.36-258) were found to be independent predictors of amputation. Fractures, popliteal venous injuries, prolonged time between injury and surgery, fasciotomies, and graft arterial repair were not statistically significant predictors of amputation. CONCLUSIONS: Emphasis on the early assessment and prompt identification of signs of ischemia after popliteal arterial injury continue to be the most important factor for reducing the risk of amputation, especially in blunt trauma. Vascular trauma teams must emphasize the need for the specialized management of popliteal veins. Clinical research is needed in order to identify means of decreasing arterial thrombosis after popliteal repair.

6.
Rev. méd. Chile ; 131(7): 741-747, jul. 2003.
Article in Spanish | LILACS | ID: lil-356066

ABSTRACT

BACKGROUND: The incidence of abdominal aortic aneurysms has increased. Its predisposing factors are smoking, high blood pressure and dislipidemia. Progressive aneurysmal enlargement may lead to its rupture, which is associated to a mortality rate above 80 per cent. AIM: To assess the prevalence of abdominal aortic aneurysms in Chilean subjects with cardiovascular risk factors. SUBJECTS AND METHODS: Through announcements in open media we invited individuals aged over 60 years, who smoked, had hypertension and/or had occlusive arterial disease, to participate in a study that included medical history and physical examination. An aortic ultrasound was performed in all subjects in whom the aorta was not palpable or there was a suspicion of dilatation. Aortic diameter over 3 cm was considered aneurysmal. RESULTS: Three hundred fifty six subjects aged 67.1 +/- 6.7 years, (73.9 per cent males), were evaluated. The study group included 62 per cent hypertensives, 39 per cent with abnormal lipids and 46 per cent smokers. Known coronary heart disease or peripheral arterial diseases were present in 14 per cent and 10 per cent, respectively. Ultrasound was required in 159 subjects. Aneurysms were detected in 21 persons (5.9 per cent), 7.6 per cent in males and 1.1 per cent in females. The mean transverse diameter of the aneurysm was 4.1 cm (3-7.5). Aneurysm was found in 2.3 per cent of subjects younger than 65 years and 8.3 per cent of subjects aged over 65 years. CONCLUSIONS: In this sample the prevalence of abdominal aortic aneurysms was 5.9 per cent, affecting predominantly males, with a notorious increase with advanced age.


Subject(s)
Humans , Male , Female , Middle Aged , Aortic Aneurysm, Abdominal/epidemiology , Cardiovascular Diseases/epidemiology , Aortic Aneurysm, Abdominal , Aorta, Abdominal , Chile/epidemiology , Age Distribution , Cardiovascular Diseases , Age Factors , Sex Factors , Risk Factors , Prevalence
7.
Rev. cuba. obstet. ginecol ; 26(1): 28-35, ene.-abr. 2000. tab
Article in Spanish | LILACS | ID: lil-299648

ABSTRACT

Se trata de demostrar la efectividad y seguridad del misoprostol sin la necesidad del curetaje sistemático posexpulsión, en abortos del segundo trimestre temprano, es decir, en gestaciones entre 13 y 15 semanas. Un grupo de 151 mujeres con gestaciones desde 85 hasta 105 días, recibieron 800 µg de misoprostol vaginal cada 24 horas hasta un máximo de 3 dosis, sin la realización de curetaje sistemático preventivo. Las variables evaluadas incluyen aborto exitoso (aborto completo sin requerir curetaje sistemático preventivo, efectos secundarios, tiempos medios de expulsión y de sangramiento vaginal). El aborto completo ocurrió en 121/151 (80 porciento, 95 porciento IC 73, 87) mujeres. El decrecimiento de la hemoglobina fue estadísticamente significativo (p=0,0001) pero sin relevancia clínica: 11,8 mg/dL (DS 0,9) antes del tratamiento y 11,4 mg/dL (DS 1.0) después. No se encontró diferencias estadísticamente significativas entre las tasas de éxito para ninguna de las características de las mujeres. El sangrado vaginal duró 6 ñ 3 días, las manchas 6 ñ 3, y el sangrado total 12 ñ 5 días (mediana 11 días, rango 1-29 días). Se indica que el tiempo medio de expulsión en el 80 porciento de los casos, el hecho de que no se requirió curetaje sistemático posaborto, la pérdida clínicamente insignificante de hemoglobina y la tasa de éxito obtenida, muestran que el misoprostol vaginal puede ser una alternativa para interrumpir gestaciones entre 13 y 15 semanas


Subject(s)
Humans , Female , Pregnancy , Abortion, Induced , Administration, Intravaginal , Misoprostol , Pregnancy Trimester, Second , Pregnancy Trimester, First
8.
Urol. colomb ; 9(1): 67-70, abr. 2000. tab
Article in Spanish | LILACS | ID: lil-337262

ABSTRACT

Objetivo: definir que el melanoma es una más de las histologías a tener en cuenta en la sospecha de neoplasias del pene, que aunque es poco frecuente, debe identificarse precozmente para poder ofrecer algún tipo de terapia. Materiales y métodos: un paciente captado en el Servicio de Urgencias de nuestra institución, remitido de un centro de salud periférico en 1997. Resultados: paciente con estadio clínico avanzado, con compromiso a distancia donde fue imposible ofrecer tratamiento alguno. Melanoma primario de pene con alto grado de penetración en estratos dérmicos profundos. Metástasis ganglionares de región inguinal, retroperitoneal y metástasis a bases pulmonares. Conclusiones: pocos son los casos reportados en la literatura mundial acerca de esta patología. Su evolución, terapéutica y pronóstico dependen del estadio clínico en el que se capte al paciente. Siempre debe sospecharse en pacientes con lesiones tipo nevus melanocítico en genitales externos, además de tener presente que la lesión puede ser primaria en uretra


Subject(s)
Humans , Male , Middle Aged , Penile Neoplasms , Melanoma
9.
Eur J Contracept Reprod Health Care ; 5(4): 227-33, 2000 Dec.
Article in English | MEDLINE | ID: mdl-11245549

ABSTRACT

The objectives of the present clinical study were to evaluate the safety and efficacy of misoprostol (Cytotec) self-administered into the vagina for medical abortion in adolescents under the age of 18 years. After obtaining written consent from the patients and parents or guardians, a group of 150 adolescents with gestations between 35 and 63 days received 800 microg of vaginal misoprostol every 24 h, up to a maximum of three main doses, for abortion. Outcomes assessed included successful abortion (complete abortion without surgery), side-effects, decrease in hemoglobin, mean time of vaginal bleeding, mean expulsion time and mean time for the return of menses. Complete abortion occurred in 133/150 (88.7%, 95% confidence interval 82-93) patients. The frequencies of nausea, vomiting and diarrhea were statistically significantly higher when compared to those obtained for adult females. Vaginal bleeding lasted for 12.7 +/- 5.7 days (median 12 days, range 1-23 days). The mean expulsion time was 6.8 +/- 2.4 h (median 6 h, range 3-14 h) for those who aborted after the first misoprostol dose. The mean time for the return of menses, for those who aborted with misoprostol, was 34.7 +/- 3.4 days. The mean decrease in hemoglobin was statistically significant (p = 0.001), but had no clinical relevance. Taking into account the high abortion rate obtained, we could conclude that misoprostol alone is a valid method for terminating unwanted pregnancies in adolescents under the age of 18 years.


Subject(s)
Abortifacient Agents, Nonsteroidal/administration & dosage , Abortion, Induced , Misoprostol/administration & dosage , Abortifacient Agents, Nonsteroidal/adverse effects , Administration, Intravaginal , Adolescent , Female , Humans , Misoprostol/adverse effects , Pregnancy , Pregnancy Trimester, First , Pregnancy in Adolescence , Self Administration , Treatment Outcome
10.
Eur J Contracept Reprod Health Care ; 4(1): 35-40, 1999 Mar.
Article in English | MEDLINE | ID: mdl-10367194

ABSTRACT

OBJECTIVE: The effectiveness and safety of misoprostol have been reported for abortion up to 22 weeks' gestation. The objective of this study was to demonstrate the effectiveness and safety of self-administration of misoprostol every 12 h, without the need of postexpulsion systematic curettage, in late first-trimester abortions (10-13 weeks' gestation). METHODS: A group of 180 women with gestations from 64 to 91 days, self-administered 800 micrograms of vaginal misoprostol every 12 h for a maximum of three doses without performing postexpulsion systematic preventive curettage. Outcome measures included successful abortion (complete and incomplete abortion without requiring a surgical procedure), side-effects, mean expulsion time and vaginal bleeding. RESULTS: Successful abortion occurred in 153/180 (85%) subjects (95% confidence interval (CI) 79-90). The decrease of hemoglobin was statistically significant (p = 0.0001) but clinically unimportant: 12.1 mg/dl (SD 1.1) before treatment and 11.7 mg/dl (SD 1.1) afterwards. The mean expulsion time for patients who aborted after the first dose was 8.3 +/- 3.6 h (median 8 h, range 2-12 h). Vaginal bleeding lasted 6 +/- 3 days, spotting 7 +/- 3 days and total bleeding 13 +/- 4 days. The median dose of misoprostol administered was 1780 micrograms (range 1400-3000 micrograms). CONCLUSIONS: The high degree of acceptability, its efficacy and the fact that postabortion systematic curettage was not needed make misoprostol a suitable alternative to the currently available methods for termination of pregnancy at 10-13 weeks' gestation.


Subject(s)
Abortifacient Agents, Nonsteroidal/administration & dosage , Abortion, Induced , Misoprostol/administration & dosage , Administration, Intravaginal , Adolescent , Adult , Cuba , Dose-Response Relationship, Drug , Educational Status , Ethnicity , Female , Hospitalization , Humans , Parity , Patient Satisfaction , Pregnancy , Pregnancy Trimester, First , Self Administration
12.
Article in English | MEDLINE | ID: mdl-9710713

ABSTRACT

OBJECTIVES: To demonstrate the effectiveness and safety of misoprostol without the need of postexpulsion systematic curettage in early second-trimester abortions, i.e. at 13-15 weeks' gestation. METHODS: A group of 151 women, with gestations from 85 to 105 days, received 800 micrograms of vaginal misoprostol every 25 h for a maximum of three doses, without having postexpulsion systematic preventive curettage performed. Outcome measures included successful abortion (complete abortion without requiring a surgical procedure), side-effects, mean expulsion time and mean time of vaginal bleeding. RESULTS: Complete abortion occurred in 121/151 subjects (80%; 95% confidence interval, 78-87%). The decrease in hemoglobin was statistically significant (p = 0.0001), but without clinical relevance (11.8 mg/dl (SD, 0.9) before treatment and 11.4 mg/dl (SD, 1.0) afterwards. No statistically significant differences were found between the success rate and any of the women's characteristics. Vaginal bleeding lasted 6 +/- 3 days, spotting 6 +/- 3 days, and total bleeding 12 +/- 5 days (median, 11 days; range, 1-29). CONCLUSIONS: The acceptable expulsion time in 80% of the cases, the fact that postabortion systematic curettage was not needed, the clinically insignificant hemoglobin loss and the abortion rate obtained, show that misoprostol by vaginal administration may be an alternative for interrupting gestation in the early second trimester of pregnancy.


Subject(s)
Abortifacient Agents, Nonsteroidal/administration & dosage , Abortion, Induced/methods , Misoprostol/administration & dosage , Administration, Intravaginal , Adult , Female , Humans , Pregnancy , Pregnancy Trimester, Second , Treatment Outcome
13.
Contraception ; 57(2): 83-8, 1998 Feb.
Article in English | MEDLINE | ID: mdl-9589833

ABSTRACT

A prospective trial including 300 pregnant women seeking elective abortion was conducted to evaluate the safety and efficacy of methotrexate and misoprostol for abortion at < or = 63 days' gestation. Subjects received methotrexate 50 mg orally and were randomly allocated to receive 800 micrograms of misoprostol vaginally 3, 4, or 5 days after administration of the methotrexate. The misoprostol dose was repeated 48 and 96 h later if abortion did not occur. Outcome measures included successful abortion (complete abortion without requiring a surgical procedure) and side effects. Complete abortion occurred in 273 of 300 patients (91%, 95%, CI 87, 94%) patients. No significant statistical differences were found in the success rates when misoprostol was given days 3, 4, or 5 after the administration of methotrexate (p = 0.69). Vaginal bleeding lasted 7.1 +/- 3.8 days, spotting 4.1 +/- 2.5 days, and total bleeding 11.2 +/- 4.1 days. Side effects for methotrexate were minimal, whereas, for misoprostol they were mild and transient except for pain. The use of methotrexate and misoprostol together could be an alternative to the intramuscular use of methotrexate or the use of antiprogestins and prostaglandin for medical abortion.


PIP: The safety and effectiveness of oral methotrexate and vaginal misoprostol for early abortion were evaluated in a prospective study of 300 women who presented to the Cuidad de la Habana (Havana, Cuba) for termination of a pregnancy of a gestational age of 63 days or less. All women were given 50 mg of methotrexate at study entry and then were randomly allocated to receive 800 mcg of misoprostol either 3, 4, or 5 days later. If abortion did not occur, misoprostol was readministered 48 and 96 hours later. Complete abortion occurred in 273 women (91%); the success rate was 72% (216 cases) after just one dose of misoprostol. There were no significant differences in abortion rates based on the day on which misoprostol was administered. Vaginal bleeding lasted an average of 7.1 +or- 3.8 days, spotting continued for 4.1 +or- 2.5 days, and total bleeding persisted for 11.2 +or- 4.1 days. Side effects for methotrexate included nausea (9.7%), vomiting (6.7%), dizziness (10.3%), fatigue (6.3%), headache (5.3%), and chills (5.3%). For misoprostol, side effects included nausea (23.0%), vomiting (25.3%), diarrhea (51.7%), dizziness (18.3%), headache (18.0%), chills (60.0%), and pelvic pain (97.3%). All signs and symptoms were of low intensity and short duration, however. These results suggest that combined use of methotrexate and misoprostol represents a feasible alternative to the intramuscular use of methotrexate or of antiprogestins and prostaglandin for medical abortion. The efficacy and safety of this new regimen are very close to those of RU-486, but the cost is considerably less.


Subject(s)
Abortifacient Agents, Nonsteroidal , Abortion, Induced , Methotrexate/administration & dosage , Misoprostol/administration & dosage , Administration, Intravaginal , Administration, Oral , Female , Gestational Age , Humans , Methotrexate/adverse effects , Misoprostol/adverse effects , Pregnancy , Prospective Studies , Treatment Outcome
14.
Eur J Contracept Reprod Health Care ; 2(3): 181-5, 1997 Sep.
Article in English | MEDLINE | ID: mdl-9678090

ABSTRACT

OBJECTIVE: To verify the efficacy and safety of misoprostol for abortion at < or = 63 days' gestation. METHOD: A total of 175 women seeking elective abortion at < or = 63 days' gestation received 800 micrograms of misoprostol vaginally. This dose was repeated at 48 and 96 h if abortion did not occur. Afterwards, up to three additional 600- or 400-micrograms doses of misoprostol were administered if the uterus was not empty, as judged by ultrasound. Outcome measures included successful abortion (complete abortion without requiring a surgical procedure), side-effects and vaginal bleeding. RESULTS: Complete abortion occurred in 161/175 (92.0%; 95% CI 87-96%) subjects and 14/175 (8.0%; 95% CI 4-13%) cases failed. The immediate success rate was 77.7% with the first dose, 13.7% with the second dose and 0.6% with the third dose. The decrease in hemoglobin was statistically significant (p = 0.009) but without clinical relevance; before treatment: 11.94 mg/dl (SD 1.60) and after treatment: 11.64 mg/dl (SD 1.08). No significant differences were obtained between success rates and failures in relation to age, gravidity, parity, previous abortions, race, gestational age and side-effects. The third main dose of misoprostol showed very little efficacy. Vaginal bleeding lasted 5.5 +/- 2.8 days, spotting 5.7 +/- 3.1 days and total bleeding 11.2 +/- 3.0 days. CONCLUSIONS: The success percentage attained shows that 800 micrograms of misoprostol administered vaginally effectively causes abortion at < or = 63 days' gestation.


Subject(s)
Abortifacient Agents, Nonsteroidal , Abortion, Induced/methods , Misoprostol , Abortifacient Agents, Nonsteroidal/administration & dosage , Abortifacient Agents, Nonsteroidal/adverse effects , Administration, Intravaginal , Adult , Female , Gestational Age , Humans , Misoprostol/administration & dosage , Misoprostol/adverse effects , Pregnancy , Pregnancy Trimester, First , Self Administration , Time Factors , Ultrasonography , Uterine Hemorrhage/chemically induced , Uterus/diagnostic imaging
17.
Arch Inst Cardiol Mex ; 61(6): 539-47, 1991.
Article in Spanish | MEDLINE | ID: mdl-1793306

ABSTRACT

At the Hospital de Ginecobstetricia del Centro Médico "La Raza", were taken EKG to 30 healthy premature newborn during a six month period. The first EKG was recorded 3 hours after birth, the second in 8 hours, the third in 24 h, the fourth in 48 h, the fifth in 72 hours, the sixth at the end of the first week, the seventh at the fifteen days and the eighth at 30 days after birth. The mean heart rate was 135 +/- 10 beats/min in the first week. There were heart rate elevation for the first three days after birth. The QRS mean axis were + 130 +/- 25 degrees, without changes during the study time. The QTc interval in all cases was higher than 0.42 sec. The voltage of waves R and S at right and left precordial leads were similar. At this gestational age the ventricular masses are equals. The T waves changes reflected hemodynamic changes. It is concluded what the healthy premature newborn had a typical EKG as a reflex to the cardiocirculatory adaptations.


Subject(s)
Electrocardiography , Infant, Premature/physiology , Adaptation, Physiological , Age Factors , Female , Gestational Age , Heart Rate , Hemodynamics , Humans , Infant, Newborn , Male
18.
J Burn Care Rehabil ; 10(3): 209-12, 1989.
Article in English | MEDLINE | ID: mdl-2501310

ABSTRACT

We present a new laboratory method to test the sensibility of clinically isolated strains to topical agents. It is a method of dilution of the whole cream in a solid medium. The cream is weighted, suspended in sterile water, and maintained at 45 degrees C. Then a volume of that suspension is added to the agar, maintained at 45 degrees C also. The mixture is agitated and plated. Afterwards 25 strains are inoculated by a Multinoculator (Cetin, Bs. As., Argentina). After incubation (18 hours at 37 degrees C), the results are obtained by observing the presence or absence of bacterial development. The minimal inhibitory concentration is calculated as the lowest concentration that inhibited growth. It is a simple, economical, and reproducible method.


Subject(s)
Anti-Infective Agents, Local/pharmacology , Microbial Sensitivity Tests/methods , Enterococcus faecalis/drug effects , Escherichia coli/drug effects , Humans , Mafenide/pharmacology , Ointments , Pseudomonas aeruginosa/drug effects , Silver Sulfadiazine/pharmacology , Staphylococcus aureus/drug effects
19.
Rev Soc Venez Hist Med ; 23(37): 129-33, 1975.
Article in Spanish | MEDLINE | ID: mdl-11628616
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