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1.
Braz J Biol ; 83: e269317, 2023.
Article in English | MEDLINE | ID: mdl-36722663

ABSTRACT

Bacteria may be the initial cause of certain pathologies as well as a secondary agent responsible for the development of complications such as pressure ulcer infections. Pressure ulcers are a persistent health problem, especially in immunocompromised patients, and associated with infection by opportunistic microorganisms with antimicrobial resistance, such as Klebsiella pneumoniae, highlight the need for the development of new antimicrobial approaches. Thus, the aim of this study was to evaluate the antibacterial and anti-adherent activity of Origanum vulgare L. (oregano) essential oil against Klebsiella pneumoniae strains, as well as the effect of its association with synthetic antimicrobials. To this end, the Minimum Inhibitory Concentration (MIC) and Minimum Bactericidal Concentration (MBC) analyses were performed on microdilution plates. The assay of the Minimum Inhibitory Adherence Concentration (MIAC), with test tubes. As well as, the association study through the infusion disc method containing ampicillin (AMP), gentamicin (GEN), ciprofloxacin (CIP) and ceftriaxone (CEF). Therefore, it was possible to obtain that the essential oil of oregano presents antimicrobial and bactericidal activity, with MIC ranging between 128µg/mL and 256 µg/mL and MBC between 256 µg/mL and 512 µg/mL, on the tested K. pneumoniae strains. When used in association with ampicillin and gentamicin, oregano essential oil showed synergistic effect for some strains. Therefore, it is observed that the tested essential oil can act as a promising antibacterial in the treatment of diseases caused by K. pneumoniae.


Subject(s)
Oils, Volatile , Origanum , Humans , Klebsiella pneumoniae , Anti-Bacterial Agents/pharmacology , Ampicillin , Gentamicins , Oils, Volatile/pharmacology
2.
Braz J Biol ; 83: e269245, 2023.
Article in English | MEDLINE | ID: mdl-36629625

ABSTRACT

The present study sought to evaluate the antibacterial activity of trans-anethole against food-borne strains of Enterobacter cloacae and Enterococcus faecalis. The study was performed using Minimum Inhibitory Concentration (MIC), and Minimum Bactericidal Concentration (MBC) methods, in addition, disc diffusion technique was used to evaluate the association of trans-anethole with synthetic antimicrobials. Minimum Inhibitory Concentration for Adherence (MICA) testing was also performed. The results revealed that trans-anethole presents no antibacterial activity at any of the concentrations used against the E. cloacae strains tested. However, trans-anethole presented antibacterial effect against five of the six E. faecalis bacterial strains tested, with MIC values ranging from 500 µg/mL to 1000 µg/mL. Further, when analyzing the MBC results against E. faecalis, it was observed that the compound presented values ranging from 500 µg/mL to 1000 µg/mL. As for the associations, it was observed that trans-anethole when combined with the antimicrobials ampicillin, gentamicin, ciprofloxacin, and ceftriaxone presented synergistic effect against most strains of E. faecalis. However, both trans-anethole and the control chlorhexidine (0.12%) presented no antibiofilm effects against strains of E. faecalis. In short, trans-anethole presented potential antibacterial against E. faecalis strains of food origin, and may upon further study, it may be used alone or in association with synthetic antimicrobials to combat infections caused by this bacterium.


Subject(s)
Anti-Infective Agents , Enterococcus faecalis , Enterococcus , Anti-Bacterial Agents/pharmacology , Anisoles/pharmacology , Anti-Infective Agents/pharmacology , Microbial Sensitivity Tests
3.
Int J Oral Maxillofac Surg ; 46(12): 1615-1625, 2017 Dec.
Article in English | MEDLINE | ID: mdl-28610818

ABSTRACT

This study aimed to evaluate whether pre-emptive analgesia modifies the tissue expression of tumour necrosis factor alpha (TNF-α) and interleukin 1 beta (IL-1ß), and whether there is an association with postoperative surgical outcomes. A triple-blind, randomized, placebo-controlled study of patients undergoing mandibular third molar removal was performed. Volunteers were allocated randomly to receive etoricoxib 120 mg, ibuprofen 400 mg, or placebo 1h before surgery. Twenty-four surgical sites per group were required (95% confidence level and 80% statistical power). Pain scores differed significantly between groups (P<0.001). Etoricoxib and ibuprofen reduced pain scores compared to placebo (P<0.05). Pain scores peaked at 4h postoperative in the experimental groups, but at 2h postoperative in the placebo group (P<0.05). A significant reduction in TNF-α concentration from time 0' to time 30' was seen for ibuprofen (P=0.001) and etoricoxib (P=0.016). The ibuprofen group showed a significant reduction in IL-1ß levels from time 0' to time 30' (P=0.038). In conclusion, TNF-α and IL-1ß levels and the inflammatory events in third molar surgery were inversely associated with the degree of cyclooxygenase 2 selectivity of the non-steroidal anti-inflammatory drugs used pre-emptively. Patients given pre-emptive analgesia showed significant reductions in the clinical parameters pain, trismus, and oedema when compared to the placebo group.


Subject(s)
Analgesia/methods , Anti-Inflammatory Agents, Non-Steroidal/therapeutic use , Cyclooxygenase 2 Inhibitors/therapeutic use , Ibuprofen/therapeutic use , Interleukin-1beta/metabolism , Molar, Third/surgery , Pain Management/methods , Pain, Postoperative/prevention & control , Pyridines/therapeutic use , Sulfones/therapeutic use , Tooth Extraction , Tumor Necrosis Factor-alpha/metabolism , Adolescent , Adult , Cross-Over Studies , Etoricoxib , Female , Humans , Male , Pain Measurement , Placebos , Treatment Outcome
4.
Eur J Pain ; 18(9): 1280-9, 2014 Oct.
Article in English | MEDLINE | ID: mdl-24715714

ABSTRACT

BACKGROUND: We investigated both the efficacy and the sub-chronic toxicity of Tephrosia toxicaria Pers. in the zymosan-induced temporomandibular joint (TMJ) inflammatory hypernociception in rats evaluating the possible role of heme oxygenase-1 (HO-1). METHODS: Rats were pretreated with T. toxicaria (0.2, 2.0 or 20 mg/kg) 60 min before the intra-articular injection of zymosan (2 mg, 40 µL) in the left TMJ. In another series of experiments, rats were treated with ZnPP-IX (3 mg/kg), a specific HO-1 inhibitor, before T. toxicaria (20 mg/kg). Von Frey test was used to evaluate inflammatory hypernociception (g) 4 h after zymosan injection. Six hours after zymosan injection, the synovial lavage was collected for total cell count and myeloperoxidase (MPO) activity, and joint tissue for histopathological analysis and immunohistochemistry for HO-1. To evaluate the sub-chronic toxicity, mice received T. toxicaria (20 mg/kg) or saline once a day for 14 days to analyse body mass, organ weight and biochemical parameters. RESULTS: T. toxicaria partially reversed the zymosan-induced head withdrawal threshold, the number of cells and the MPO activity. T. toxicaria reduced the inflammatory cell influx in the synovial membrane. TMJ immunohistochemical analyses treated with T. toxicaria showed increased HO-1 expression. These effects of T. toxicaria were not observed in the presence of ZnPP-IX. T. toxicaria treatment for 14 days did not show significant signs of toxicity when administrated to mice. CONCLUSIONS: T. toxicaria did not produce any signs of toxicity and effectively decreased zymosan-induced TMJ inflammatory hypernociception dependent, at least in part, upon the HO-1 pathway integrity.


Subject(s)
Heme Oxygenase-1/metabolism , Hyperalgesia/drug therapy , Phytotherapy , Plant Preparations/pharmacology , Temporomandibular Joint Disorders/drug therapy , Tephrosia , Animals , Disease Models, Animal , Enzyme Inhibitors/administration & dosage , Enzyme Inhibitors/pharmacology , Heme Oxygenase-1/antagonists & inhibitors , Hyperalgesia/chemically induced , Inflammation/chemically induced , Inflammation/drug therapy , Male , Metabolic Networks and Pathways , Mice , Plant Preparations/administration & dosage , Plant Preparations/adverse effects , Protoporphyrins/administration & dosage , Protoporphyrins/pharmacology , Rats , Rats, Wistar , Temporomandibular Joint Disorders/chemically induced , Temporomandibular Joint Disorders/physiopathology , Zymosan/pharmacology
5.
J Nat Med ; 67(1): 143-51, 2013 Jan.
Article in English | MEDLINE | ID: mdl-22450730

ABSTRACT

Chresta martii (Asteraceae) is a plant found in the Xingó region (semi-arid area) in Northeastearn Brazil, and is recognized by the local population as a traditional herb used to treat gastric diseases. This is the first report of the chemical composition, acute toxicity, and gastroprotective effect in mice of the hydroalcoholic extract (HAE) from the aerial parts (leaves and flowers) of Chresta martii. Animals received HAE doses from 10 to 2000 mg/kg, i.p. or 50 to 3000 mg/kg, p.o.) and were observed over 48 h for toxicity signs and mortality; sub-chronic toxicity was evaluated through 14 days treatment with once-daily HAE doses (400 mg/kg, p.o.). The gastroprotective effect of HAE was demonstrated on the indomethacin-induced gastric ulcer model after the administration of extracts. Data comparison of ulcer index averages between saline and HAE (100 or 400 mg/kg, p.o.) groups showed significant (P < 0.01) inhibition (71.73 and 76.72 %, respectively) of indomethacin-induced gastric lesions. Histological analyses showed significant (P < 0.05) inhibition of leukocyte migration in HAE-treated groups. A fingerprint of the HAE obtained by HPLC/UV/MS analysis showed major peaks characteristic of sesquiterpene lactones. Compound 1 was isolated and elucidated as a new natural product. Its capacity to prevent leukocyte chemotaxis was demonstrated in vitro, corroborating the pharmacological effects observed for C. martii HAE.


Subject(s)
Asteraceae/chemistry , Indomethacin/toxicity , Plant Extracts/therapeutic use , Stomach Ulcer/chemically induced , Stomach Ulcer/drug therapy , Animals , Anti-Ulcer Agents/chemistry , Anti-Ulcer Agents/therapeutic use , Flowers/chemistry , Male , Mice , Plant Extracts/chemistry , Plant Leaves/chemistry , Stomach Diseases/drug therapy
6.
Braz J Med Biol Res ; 39(9): 1241-7, 2006 Sep.
Article in English | MEDLINE | ID: mdl-16981050

ABSTRACT

Third molar extraction is a common procedure frequently accompanied by moderate or severe pain, and involves sufficient numbers of patients to make studies relatively easy to perform. The aim of the present study was to determine the efficacy and safety of the therapeutic combination of 10 mg piroxicam, 1 mg dexamethasone, 35 mg orphenadrine citrate, and 2.5 mg cyanocobalamin (Rheumazin) when compared with 20 mg piroxicam alone (Feldene) in mandibular third molar surgery. Eighty patients scheduled for removal of the third molar were included in this randomized and double-blind study. They received (vo) Rheumazin or Feldene 30 min after tooth extraction and once daily for 4 consecutive days. Pain was determined by a visual analogue scale and by the need for escape analgesia (paracetamol). Facial swelling was evaluated with a measuring tape and adverse effects and patient satisfaction were recorded. There was no statistically significant difference in facial swelling between Rheumazin and Feldene (control group). Both drugs were equally effective in the control of pain, with Rheumazin displaying less adverse effects than Feldene. Therefore, Rheumazin appears to provide a better risk/benefit ratio in the mandibular molar surgery. Since the side effects resulting from nonsteroidal anti-inflammatory drug administration are a severe limitation to the routine use of these drugs in clinical practice, our results suggest that Rheumazin can be a good choice for third molar removal treatment.


Subject(s)
Anti-Inflammatory Agents/administration & dosage , Molar, Third/surgery , Muscle Relaxants, Central/administration & dosage , Tooth Extraction , Vitamin B Complex/administration & dosage , Adolescent , Adult , Anti-Inflammatory Agents/adverse effects , Dexamethasone/administration & dosage , Dexamethasone/adverse effects , Double-Blind Method , Drug Therapy, Combination , Edema/prevention & control , Female , Humans , Male , Middle Aged , Muscle Relaxants, Central/adverse effects , Orphenadrine/administration & dosage , Orphenadrine/adverse effects , Pain Measurement , Pain, Postoperative/drug therapy , Piroxicam/administration & dosage , Piroxicam/adverse effects , Prospective Studies , Severity of Illness Index , Vitamin B 12/administration & dosage , Vitamin B 12/adverse effects , Vitamin B Complex/adverse effects
7.
Braz. j. med. biol. res ; 39(9): 1241-1247, Sept. 2006. ilus, graf
Article in English | LILACS | ID: lil-435419

ABSTRACT

Third molar extraction is a common procedure frequently accompanied by moderate or severe pain, and involves sufficient numbers of patients to make studies relatively easy to perform. The aim of the present study was to determine the efficacy and safety of the therapeutic combination of 10 mg piroxicam, 1 mg dexamethasone, 35 mg orphenadrine citrate, and 2.5 mg cyanocobalamin (Rheumazin®) when compared with 20 mg piroxicam alone (Feldene®) in mandibular third molar surgery. Eighty patients scheduled for removal of the third molar were included in this randomized and double-blind study. They received (vo) Rheumazin or Feldene 30 min after tooth extraction and once daily for 4 consecutive days. Pain was determined by a visual analogue scale and by the need for escape analgesia (paracetamol). Facial swelling was evaluated with a measuring tape and adverse effects and patient satisfaction were recorded. There was no statistically significant difference in facial swelling between Rheumazin and Feldene (control group). Both drugs were equally effective in the control of pain, with Rheumazin displaying less adverse effects than Feldene. Therefore, Rheumazin appears to provide a better risk/benefit ratio in the mandibular molar surgery. Since the side effects resulting from nonsteroidal anti-inflammatory drug administration are a severe limitation to the routine use of these drugs in clinical practice, our results suggest that Rheumazin can be a good choice for third molar removal treatment.


Subject(s)
Humans , Male , Female , Adolescent , Adult , Middle Aged , Dexamethasone/administration & dosage , Molar, Third/surgery , Orphenadrine/administration & dosage , Piroxicam/administration & dosage , Tooth Extraction , /administration & dosage , Anti-Inflammatory Agents/administration & dosage , Anti-Inflammatory Agents/adverse effects , Double-Blind Method , Drug Combinations , Dexamethasone/adverse effects , Edema/prevention & control , Muscle Relaxants, Central/administration & dosage , Muscle Relaxants, Central/adverse effects , Orphenadrine/adverse effects , Pain Measurement , Prospective Studies , Pain, Postoperative/drug therapy , Piroxicam/adverse effects , Severity of Illness Index , /adverse effects , Vitamin B Complex/administration & dosage , Vitamin B Complex/adverse effects
8.
Braz J Med Biol Res ; 35(5): 613-6, 2002 May.
Article in English | MEDLINE | ID: mdl-12011948

ABSTRACT

Matrix metalloproteinases (MMP) are considered to be key initiators of collagen degradation, thus contributing to bone resorption in inflammatory diseases. We determined whether subantimicrobial doses of doxycycline (DX) (< or =10 mg kg-1 day-1), a known MMP inhibitor, could inhibit bone resorption in an experimental periodontitis model. Thirty male Wistar rats (180-200 g) were subjected to placement of a nylon thread ligature around the maxillary molars and sacrificed after 7 days. Alveolar bone loss (ABL) was measured macroscopically in one hemiarcade and the contralateral hemiarcade was processed for histopathologic analysis. Groups of six animals each were treated with DX (2.5, 5 or 10 mg kg-1 day-1, sc, 7 days) and compared to nontreated (NT) rats. NT rats displayed significant ABL, severe mononuclear cell influx and increase in osteoclast numbers, which were significantly reduced by 5 or 10 mg kg-1 day-1 DX. These data show that DX inhibits inflammatory bone resorption in a manner that is independent of its antimicrobial properties.


Subject(s)
Alveolar Bone Loss/prevention & control , Anti-Bacterial Agents/therapeutic use , Doxycycline/therapeutic use , Periodontitis/drug therapy , Animals , Anti-Bacterial Agents/administration & dosage , Doxycycline/administration & dosage , Jaw , Male , Matrix Metalloproteinase Inhibitors , Periodontitis/physiopathology , Rats , Rats, Wistar
9.
Braz. j. med. biol. res ; 35(5): 613-616, May 2002. ilus, tab
Article in English | LILACS | ID: lil-308277

ABSTRACT

Matrix metalloproteinases (MMP) are considered to be key initiators of collagen degradation, thus contributing to bone resorption in inflammatory diseases. We determined whether subantimicrobial doses of doxycycline (DX) (<=10 mg kg-1 day-1), a known MMP inhibitor, could inhibit bone resorption in an experimental periodontitis model. Thirty male Wistar rats (180-200 g) were subjected to placement of a nylon thread ligature around the maxillary molars and sacrificed after 7 days. Alveolar bone loss (ABL) was measured macroscopically in one hemiarcade and the contralateral hemiarcade was processed for histopathologic analysis. Groups of six animals each were treated with DX (2.5, 5 or 10 mg kg-1 day-1, sc, 7 days) and compared to nontreated (NT) rats. NT rats displayed significant ABL, severe mononuclear cell influx and increase in osteoclast numbers, which were significantly reduced by 5 or 10 mg kg-1 day-1 DX. These data show that DX inhibits inflammatory bone resorption in a manner that is independent of its antimicrobial properties


Subject(s)
Animals , Male , Rats , Alveolar Bone Loss , Doxycycline , Periodontitis , Tetracyclines , Doxycycline , Jaw , Matrix Metalloproteinases , Periodontitis , Rats, Wistar , Tetracyclines
10.
J Periodontol ; 71(6): 1009-14, 2000 Jun.
Article in English | MEDLINE | ID: mdl-10914805

ABSTRACT

BACKGROUND: Prostaglandins are implicated in periodontal bone destruction. We investigated the effect of a non-selective cyclooxygenase (COX) inhibitor (indomethacin-IND) or a type 2 COX inhibitor (meloxicam-MLX) in an experimental periodontal disease (EPD) model. METHODS: Wistar rats were subjected to placement of a nylon thread ligature around the maxillary molars and sacrificed after 7 days. Alveolar bone loss (ABL) was measured in one quadrant as the distance between the cemento-enamel junction and the alveolar bone. The other quadrant was processed for histopathologic analysis. Daily weight and white blood cell count were recorded. Groups were treated subcutaneously for 7 days with either IND (0.5, 1, or 2 mg/kg) or MLX (0.75, 1.5, or 3 mg/kg). Controls received no treatment. Macroscopic analysis of the gastric mucosa was done. The control group did not receive any manipulation, and a non-treated group consisted of rats subjected to periodontitis that received no pharmacological treatment. RESULTS: In the non-treated (NT) group, there was significant ABL, severe mononuclear influx, and an increase in osteoclast numbers. Significant neutrophilia and lymphomonocytosis occurred at 6 hours and at 7 days, respectively, as compared to controls. Significant weight loss persisted until the seventh day in the NT group. Both IND and MLX reduced ABL and histopathologic changes. Neutrophilia and lymphomonocytosis were also significantly reversed. Both IND and MLX induced earlier weight recovery. The stomachs of the IND (1 and 2 mg/kg) groups presented hemorrhage and ulcers, whereas in the MLX-treated groups, there were mild petechiae just in the 3 mg/kg group. CONCLUSIONS: COX inhibition prevented ABL in this experimental periodontal disease model. MLX displays similar efficacy and less gastric damage than IND. MLX may provide a better risk/benefit ratio in the treatment of human periodontitis than non-selective COX inhibitors.


Subject(s)
Alveolar Bone Loss/prevention & control , Cyclooxygenase Inhibitors/therapeutic use , Isoenzymes/antagonists & inhibitors , Periodontitis/prevention & control , Peroxidases/antagonists & inhibitors , Alveolar Process/pathology , Animals , Anti-Inflammatory Agents, Non-Steroidal/administration & dosage , Anti-Inflammatory Agents, Non-Steroidal/adverse effects , Anti-Inflammatory Agents, Non-Steroidal/therapeutic use , Body Weight , Cell Count , Cyclooxygenase 2 , Cyclooxygenase 2 Inhibitors , Cyclooxygenase Inhibitors/administration & dosage , Cyclooxygenase Inhibitors/adverse effects , Disease Models, Animal , Indomethacin/administration & dosage , Indomethacin/adverse effects , Indomethacin/therapeutic use , Injections, Subcutaneous , Leukocyte Count , Leukocytes, Mononuclear/drug effects , Leukocytes, Mononuclear/pathology , Leukocytosis/pathology , Leukocytosis/prevention & control , Male , Meloxicam , Molar , Neutrophils/drug effects , Neutrophils/pathology , Osteoclasts/pathology , Prostaglandin-Endoperoxide Synthases , Rats , Rats, Wistar , Stomach/drug effects , Thiazines/administration & dosage , Thiazines/adverse effects , Thiazines/therapeutic use , Thiazoles/administration & dosage , Thiazoles/adverse effects , Thiazoles/therapeutic use , Tooth Cervix/pathology
11.
Eur J Oral Sci ; 108(2): 123-9, 2000 Apr.
Article in English | MEDLINE | ID: mdl-10768725

ABSTRACT

Chlorpromazine (CPZ), a phenothiazine derivative, possesses anti-inflammatory properties, inhibition of tumor neurosis factor-alpha (TNF-alpha) synthesis and bone resorption. TNF-alpha promotes inflammatory changes and bone resorption in periodontitis. We have studied the effect of CPZ in experimental periodontitis. Wistar rats were subjected to a ligature placement around the cervix of the right second upper molars. Alveolar bone loss was evaluated by the sum of the distances between the cusp tip and the alveolar bone along the axis of each molar root, which was subtracted from the contralateral side. Histopathological analysis of the periodontium was based on cell influx, osteoclast number, and alveolar bone and cementum integrity. Animals were weighed daily and total and differential peripheral white blood cell counts were performed 6 h and 1, 7 and 11 d after periodontitis induction. Groups were treated with CPZ 1 h before and daily up to the 11th d of periodontitis. Alveolar bone loss was inhibited 46%, 55.4%, and 76.5% by CPZ at 1, 3 and 9 mg/kg, respectively. Histological analysis showed a significant reduction of cell influx and osteoclast number, as well as preservation of the alveolar process and cementum. CPZ reversed leukocytosis but not weight loss. In conclusion, CPZ reduces bone loss in experimental periodontitis, probably via TNF-alpha blockade.


Subject(s)
Alveolar Bone Loss/drug therapy , Anti-Inflammatory Agents/therapeutic use , Chlorpromazine/therapeutic use , Dopamine Antagonists/therapeutic use , Periodontitis/drug therapy , Alveolar Bone Loss/pathology , Alveolar Bone Loss/prevention & control , Alveolar Process/drug effects , Analysis of Variance , Animals , Bone Resorption/prevention & control , Cell Count/drug effects , Dental Cementum/drug effects , Leukocyte Count/drug effects , Leukocytosis/drug therapy , Male , Molar/pathology , Osteoclasts/drug effects , Periodontitis/pathology , Periodontitis/prevention & control , Rats , Rats, Wistar , Tooth Cervix/pathology , Tooth Root/pathology , Tumor Necrosis Factor-alpha/antagonists & inhibitors , Weight Loss
12.
Rev Bras Enferm ; 51(1): 77-92, 1998.
Article in Portuguese | MEDLINE | ID: mdl-10776272

ABSTRACT

Qualification for nursing professionals is important for they deal with lives that need qualified care. This study aims at analysing health professionals opinions about nursing attendants. It was accomplished between March and July, 1997. Nurses, physicians, nursing aids and technicians at public and philanthropic hospitals in Fortaleza--CE were interviewed. The outcomes show that nursing attendants, most times, perform the same procedures as the nursing aids and may interfere with the provided service quality and cause iatrogenics; others consider them as important at institutions for their practice; some others express themselves completely against the non-qualified professionalization process; anothers express themselves for this process, but disagree on how it is accomplished for they do not perceive any change in their professional profile after being qualified. We do understand that this question is deserving of immediate attitudes for it is related to nursing principal subject: Caring.


Subject(s)
Attitude of Health Personnel , Job Description , Nursing Assistants/education , Nursing Assistants/organization & administration , Personnel, Hospital/psychology , Brazil , Certification , Clinical Competence/standards , Hospitals, Private , Hospitals, Public , Humans , Quality of Health Care , Surveys and Questionnaires
13.
Arch. latinoam. nutr ; 42(4): 437-42, dic. 1992. tab, graf
Article in English | LILACS | ID: lil-134596

ABSTRACT

The effectiveness of the Quality Control System (QCS) implemented by the Fundaçäo de Assistência ao Escolar (FAE) for quality control of food products from different types and origins purchased by the National School-Feeding Programme (NSFP) in Pernambuco, Northeast Brazil, was evaluated. Physicochemical, microbiological, microscopical and organopetical analyses were performed in 4,860 food samples and the main causes of alterations were detected. Perishability was the characteristic used for distribution of food items into 3 main groups: A, B, and C. In accordance with 972 Quality Certificates between 1985 and 1988, 31.89 of the samples were rejected. The main reasons for rejection were innacuracies of net weight and drained weight and high moisture contents. Group B presented the smallest number of altered samples (27%); for Groups A and C these values were 33% and 44%, respectively. Our data lead to the conclusion that the QCS implemented by FAE is of paramount importance for an adequate quality control of foods provided to beneficiaries and for a good cost effectiveness of the school-feeding programme


Subject(s)
Humans , Food Analysis , National Health Programs , Brazil , Child , Child Nutrition , Food Microbiology , Nutritional Requirements , Program Evaluation , Quality Control
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