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1.
Egyptian Journal of Chest Diseases and Tuberculosis [The]. 2013; 62 (4): 687-695
in English | IMEMR | ID: emr-187196

ABSTRACT

Objectives: To assess the value of PCT as a rapid and sensitive marker for diagnosis, prognosis, and therapy of lower respiratory tract bacterial infections necessitating antimicrobial treatment and comparing this marker with other markers of infections including C-reactive protein [CRP] and total white-blood cell counts [WBCs]


Patients and methods: Sixty Patients were enrolled in the study, they were subjected to complete history taking, physical examination, laboratory investigations including complete blood count, blood gases, blood chemistry, bacteriological culture for sputum and blood, serology for atypicals, and PCR for respiratory viruses, serum C-reactive protein [CRP] and PCT levels were measured. The patients were divided into two groups, group 1 included 26 patients who were culture negative for bacterial infection and group 2 included 34 patients who were culture positive. Group 2 patients were given antibiotic therapy according to the culture sensitivity


Result: The results revealed that, there was no significant difference between group 1 and group 2 patients as regards age, sex, clinical manifestations, final diagnosis, white blood cell counts, blood gases, number of admitted patients, intensive care unit admission and length of hospital stay. A significant increase of PCT and CRP levels was detected in group 2 compared to group 1 at initial diagnosis. At cutoff value >0.5 ng/ml, PCT gave a sensitivity of 94.1%, specificity of 88.4%, positive predictive value [PPV] of 91.4%, negative predictive value [NPV] of 92% and diagnostic efficiency of 91.6% for diagnosis of respiratory tract bacterial infections. However, at a cutoff value >8 mg/L, CRP gave a sensitivity of 85.2%, specificity of 76.9%, PPV of 82.8%, NPV of 80% and diagnostic efficiency of 81.7%. After antibiotic therapy PCT and CRP levels dropped in group 2 patients as compared to their pre-treatment levels


Conclusion: Serum PCT level could be used as a novel marker of lower respiratory tract bacterial infections for diagnosis, prognosis and follow up of therapy. This reduces side-effects of an unnecessary antibiotic use, lowers costs, and in the long-term, leads to diminishing drug resistance


Subject(s)
Humans , Male , Female , Respiratory Tract Infections/therapy , Calcitonin/therapeutic use , Protein Precursors/therapeutic use , Prognosis , Respiratory Tract Infections/microbiology
2.
Scientific Medical Journal. 2006; 18 (1): 1-11
in English | IMEMR | ID: emr-81013

ABSTRACT

Recent studies of radiation toxicity in the treatment of breast cancer have shown that; the effects on normal tissues can constitute a significant health problem. One of these problems is skin toxicity. The aim of the current study is to compare the acute skin toxicity between two different fractionation schedules of adjuvant breast radiation: the conventional radiation [CFR] versus hypofractionated radiation [HFR]. This is a prospective randomized study done in breast cancer patients referred for adjuvant radiation therapy. Radiation therapy was given in either one of two ways: CFR [5000 cGy/ 25 fractions I 5 weeks; 200 cGy per fraction] or HFR [4005 cGy/15 fractions / 3 weeks; 267 cGy per fraction] Acute radiation reactions were graded according to the Radiation Therapy Oncology Group toxicity grading system [RTOG] [1]. A comparison was done between the incidence of these reactions and different variables as: total radiation dose, type of surgery, number of surgically dissected nodes.etc. Seventy eight patients were accrued to the study, of whom 57.7% had breast conservative surgery [BCS], while 42.3% had modified radical mastectomy [MRM]. Patients who had received HFR represented 53.8%, while those who received CFR represented 46.2% of all patients. The majority of patients [64.1%] had grade 0/II radiation reaction, and 35.9% had grade III/IV reaction. On univariate analysis, there was a statistically significant difference between the two radiation arms regarding the incidence of radiation reaction, with higher incidence [52.8%] in CFR as compared to 21.4% in HFR [p 0.004], while the other variables [type of surgery, number of surgically removed nodes, etc] were not statistically significant. On multivariate analysis; the only factor of statistical significance regarding the incidence of radiation reaction was the radiation therapy schedule, with a higher incidence in CFR [p value 0.03]. There is a statistically less incidence of acute radiation reactions in hypofractionated arm as compared to conventional fractionated arm in the adjuvant radiation of breast cancer.


Subject(s)
Humans , Female , Radiotherapy Dosage , Radiotherapy, Adjuvant , Dose Fractionation, Radiation , Multivariate Analysis , Skin , Prospective Studies
3.
Medical Journal of Cairo University [The]. 2006; 74 (4): 725-731
in English | IMEMR | ID: emr-79299

ABSTRACT

The use of concomitant radiation and chemotherapy in the management of carcinoma of the cervix improved the overall and disease free rates for patients with carcinoma of the cervix and this combined modality is considered now the standard of care in many oncology centres. The aim of the current study was to assess the treatment results [mainly response rate and disease free survival] for patients with cancer cervix treated with concomitant chemoradiation therapy using high dose rate brachytherapy after external beam radiation therapy. This is a prospective phase II study done in patients with carcinoma of cervix referred for concomitant radiation and chemotherapy. Patients were treated with external beam radiation therapy [EBRT] given as 4500cGy/25 fractions/5 weeks [180cGy per fraction] using linear accelerator with 18M v photons, followed after one week with high dose rate brachytherapy using iridium 192 giving a dose of 600cGy to point A as once weekly outpatient session for four consecutive weeks [so the total dose of brachythrapy given was 2400cGy]. Meanwhile; a concomitant chemotherapy with cisplatinum was given as a radiosensetizer during EBRT at a weekly intravenous [IV] infusion of 40mg/m[2]. Assessment of response rate to treatment was done clinically as well as by magnetic resonance imaging [MRI] at 6 weeks after the end of treatment, and then a regular follow up at 3 monthly intervals was done. At the end of follow up; assessment of disease free survival [DFS] was done. A correlation between different prognostic variables [like histopatho-logical grade, stage, initial response to treatment] and DFS was done. Twenty four patients with carcinoma of the cervix were included in the study. Their mean age was 51.6 years [ +/- 15.5 years SD; standard deviation]. All patients had squamous cell carcinoma; 54.2% had grade [G] II, 33.3% had GIII, and the least was GI [12.5%]. Staging was done according to FIGO [Federation Internationale de Gynecologic et d'Obstetrique] system [appendix I]; and the results showed stage IA 12.5%, IB 4.2%, IIA 16.7%, IIB 25%, IIIA 8.3%, and stage IIIB as 20.8% stage IVA 12.5%. Sequelae of treatment were assessed by Radiation Therapy Oncology Group [RTOG] toxicity criteria [appendix 2], whereby diarrhea GII was seen in 12.5%, GII cystitis in 21% and GII neutropenia in 8.3%. Initial post treatment response showed 50% complete remission [CR], 25% partial response [PR], 8.3% stable disease [SD], and 16.7% disease progression [DP]. After a mean follow up period of 26 months [SD 9.7 months] [range 10-40 months], the mean DFS was 27.29 months [standard error SE 1.93], and [95% confidence interval 9CI]: 23.52-31.07]. The median DFS was 29 months [SE 3.06], [95% CI, 23-35 months]. The 2 year DFS for the whole group was 60% and the 3 year DFS was 27%. Correlation of different prognostic variables with response rate revealed that: The histopathological grade of the tumour had a borderline significance [p value 0.057] with better response in GI, and GII as compared to GIII. FIGO stage did not influence response to treatment [p value 0.59]. There was no correlation between DFS and histopathological grade [p value 0.53]; FIGO stage [p value 0.66]; although there was a difference in DFS between different stages [in stage I the 3 years DFS rate was 90% as compared to stage IVA where the 3 years DFS rate was only 10%] however it was statistically not significant. Also no correlation was found between DFS and response to treatment [p value 0.88]. On multivariate analysis none of the prognostic variables mentioned [histopathological grade, FIGO stage, initial response to treatment] influenced DFS. The use of external beam radiation therapy concomitant with systemic chemotherapy [cisplatinum], and followed by high dose rate brachytherapy is an acceptable treatment modality for carcinoma of the cervix with mild treatment related toxicity


Subject(s)
Humans , Female , Chemotherapy, Adjuvant , Brachytherapy , Carcinoma, Squamous Cell , Follow-Up Studies , Survival Rate , Treatment Outcome
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