แสดงบทความที่มีป้ายกำกับ surgery แสดงบทความทั้งหมด
แสดงบทความที่มีป้ายกำกับ surgery แสดงบทความทั้งหมด

วันพุธที่ 19 สิงหาคม พ.ศ. 2552

Peritonitis

Hx.
A teenage boy visit ER with evolve abdomimal pain 3hr before.He doesn' t have fever.
He deny underlying disease.
2 yrs ago he had appendectomy at surin Hospital .

PE
A teenage boy looked distress by pain
Lieing on bed
BP 120/80 PR 94 BT 37.5 RR 20
HEENT Normal
Heart and lung audible S1 S2 no murmur , normal breath sound
Abd : Boardlike rigidity
generalized tender , rebound positive
Resonance on percussion RUQ
PR : Normal

LAB : CBC Hct 37.0 wbc 12,000 PMN 78 Lymphocyte 20 Mono 2 plt 160,000
Film acute abdomen series : free air of Rt diaphram


Peritonitis
Peritonitis is defined as inflammation of peritoneum.it may be localised or generalized,generally has an acute course,and may depended on either infection(often due to rupture of hallow organ as may occur inabdominal trauma) or non infection process
Three type of peritonitis
1. Primary(spontaneous)
2. Secondary (anatomic)
3. tertiary (peritoneal dialysis related)

Mechanisms and manifestations
Abdominal pain and tenderness

The main manifestations of peritonitis are acute abdominal pain, abdominal tenderness, and abdominal guarding, which are exacerbated by moving the peritoneum, e.g. coughing, flexing the hips, or eliciting the Blumberg sign (a.k.a. rebound tenderness, as the peritoneum snaps back into place). The presence of these signs in a patient is sometimes referred to as peritonism.[1]

The localization of these manifestations depends on whether peritonitis is localized (e.g. appendicitis or diverticulitis before perforation), or generalized to the whole abdomen. In either case pain typically starts as a generalized abdominal pain (with involvement of poorly localizing innervation of the visceral peritoneal layer), and may become localized later (with the involvement of the somatically innervated parietal peritoneal layer). Peritonitis is an example of an acute abdomen.
Causes

Infected peritonitis
Perforation of a hollow viscus is the most common cause of peritonitis. Examples include perforation of the distal oesophagus (Boerhaave syndrome), of the stomach (peptic ulcer, gastric carcinoma), of the duodenum (peptic ulcer), of the remaining intestine (e.g. appendicitis, diverticulitis, Meckel diverticulum, inflammatory bowel disease (IBD), intestinal infarction, intestinal strangulation, colorectal carcinoma, meconium peritonitis), or of the gallbladder (cholecystitis).
Other possible reasons for perforation include abdominal trauma, ingestion of a sharp foreign body (such as a fish bone, toothpick or glass shard), perforation by an endoscope or catheter, and anastomotic leakage.
The latter occurrence is particularly difficult to diagnose early, as abdominal pain and ileus paralyticus are considered normal in patients who just underwent abdominal surgery.
In most cases of perforation of a hollow viscus, mixed bacteria are isolated; the most common agents include Gram-negative bacilli (e.g. Escherichia coli) and anaerobic bacteria (e.g. Bacteroides fragilis). Fecal peritonitis results from the presence of faeces in the peritoneal cavity. It can result from abdominal trauma and occurs if the large bowel is perforated during surgery.
Disruption of the peritoneum, even in the absence of perforation of a hollow viscus, may also cause infection simply by letting micro-organisms into the peritoneal cavity. Examples include trauma, surgical wound, continuous ambulatory peritoneal dialysis, intra-peritoneal chemotherapy. Again, in most cases mixed bacteria are isolated; the most common agents include cutaneous species such as Staphylococcus aureus, and coagulase-negative staphylococci, but many others are possible, including fungi such as Candida.

Spontaneous bacterial peritonitis (SBP) is a peculiar form of peritonitis occurring in the absence of an obvious source of contamination. It occurs either in children, or in patients with ascites. See the article on spontaneous bacterial peritonitis for more information.
Systemic infections (such as tuberculosis) may rarely have a peritoneal localisation.

Non-infected peritonitis

Treatment
Depending on the severity of the patient's state, the management of peritonitis may include:
General supportive measures such as vigorous intravenous rehydration and correction of electrolyte disturbances.
Antibiotics are usually administered intravenously, but they may also be infused directly into the peritoneum. The empiric choice of broad-spectrum antibiotics often consist of multiple drugs, and should be targeted against the most likely agents, depending on the cause of peritonitis (see above); once one or more agents are actually isolated, therapy will of course be targeted on them.
Surgery (laparotomy) is needed to perform a full exploration and lavage of the peritoneum, as well as to correct any gross anatomical damage which may have caused peritonitis.[2] The exception is spontaneous bacterial peritonitis, which does not benefit from surgery. http://en.wikipedia.org/wiki/Peritonitis

วันเสาร์ที่ 15 สิงหาคม พ.ศ. 2552

Necrotizing fasciitis



Necrotizing fasciitis at a possible site of insulin injection in the left upper part of the thigh in a 50-year-old obese woman with diabetes.



Necrotizing fasciitis can occur after trauma or around foreign bodies in surgical wounds, or it can be idiopathic, as in scrotal or penile necrotizing fasciitis.
Necrotizing fasciitis has also been referred to as hemolytic streptococcal gangrene, Meleney ulcer, acute dermal gangrene, hospital gangrene, suppurative fascitis, and synergistic necrotizing cellulitis. Fournier gangrene is a form of necrotizing fasciitis that is localized to the scrotum and perineal area.
Necrotizing fasciitis is a progressive, rapidly spreading, inflammatory infection located in the deep fascia, with secondary necrosis of the subcutaneous tissues. Because of the presence of gas-forming organisms, subcutaneous air is classically described in necrotizing fasciitis. This may be seen only on radiographs or not at all. The speed of spread is directly proportional to the thickness of the subcutaneous layer. Necrotizing fasciitis moves along the deep fascial plane.
These infections can be difficult to recognize in their early stages, but they rapidly progress.
They require aggressive treatment to combat the associated high morbidity and mortality.






The causative bacteria may be aerobic, anaerobic, or mixed flora, and the expected clinical course varies from patient to patient.




Penicillin G (Pfizerpen)
Interferes with synthesis of cell wall mucopeptide during active multiplication, resulting in bactericidal activity against susceptible microorganisms.
Adult
8-10 million U/d IV divided q4-6h
Pediatric
500,000-800,000 U/kg/d IV divided q4-6h
Clindamycin (Cleocin)
Lincosamide for treatment of serious skin and soft tissue staphylococcal infections. Also effective against aerobic and anaerobic streptococci (except enterococci). Inhibits bacterial growth, possibly by blocking dissociation of peptidyl t-RNA from ribosomes causing RNA-dependent protein synthesis to arrest. To be used as an alternative to penicillin G.

Adult
600 mg IV q6h
Pediatric
5 mg/kg IV q6h

Metronidazole (Flagyl)

imidazole ring-based antibiotic active against various anaerobic bacteria and protozoa. Used in combination with other antimicrobial agents (except for C difficile enterocolitis). Appears to be absorbed into cells of microorganisms containing nitroreductase. Unstable intermediate compounds that bind DNA and inhibit synthesis are formed, causing cell death.

Adult
Loading dose: 15 mg/kg or 1 g for 70-kg adult IV over 1 hMaintenance dose: 6 h following loading dose; infuse 7.5 mg/kg or 500 mg IV for 70-kg adult over 1 h q6-8h; not to exceed 4 g/d
Pediatric
15-30 mg/kg/d IV divided bid/tid; not to exceed 2 g/d

Ceftriaxone (Rocephin)

DOC in initial treatment. Third-generation cephalosporin with broad-spectrum, gram-negative activity. Lower efficacy against gram-positive organisms and higher efficacy against resistant organisms. Arrests bacterial growth by binding to one or more penicillin-binding proteins.

Adult
1-2 g IV qd or divided bid
Pediatric
75 mg/kg/d IV divided bid

Gentamicin (Garamycin)

Aminoglycoside antibiotic for gram-negative coverage. Used in combination with both an agent against gram-positive organisms and one that covers anaerobes. Not the DOC. Consider if penicillins or other less toxic drugs are contraindicated, when clinically indicated, and in mixed infections caused by susceptible staphylococci and gram-negative organisms.Adjust dose based on CrCl and changes in volume of distribution. Follow each regimen by at least a trough level drawn on the third or fourth dose (0.5 h before dosing). Peak level may be drawn 0.5 h after 30-min infusion.

ที่ รพ.สังขะ อาจพิจารณาใช้
regimen PGS+ Genta+ metro

Cloxa + clinda

Cloxa+cef-3 + Metro

Cloxa+clinda+metro

clinda+cef-3



บทคัดย่อและคำสำคัญ (Abstract and Keyword)
เอกสารลำดับที่ :
2139
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บทคัดย่อไทย :

ได้ศึกษาจากรายงานผู้ป่วยจำนวน 8 ราย ที่ได้รับการวินิจฉัยเป็น cervicofacial necrotizing fasciitis ในโรงพยาบาลนครพิงค์ จังหวัดเชียงใหม่ ตั้งแต่ปี พ.ศ. 2545 ถึงปี พ.ศ. 2550 พบว่าผู้ป่วย 4 ราย (50%) มีสาเหตุจากฟันผุและผู้ป่วย 2 ราย (25%) มีสาเหตุจากฝีที่ต่อมน้ำลายหน้าหู ผู้ป่วยส่วนมากมีปัญหาด้านสุขภาพ คือ โรคเบาหวานและภาวะขาดสารอาหารร่วมด้วย อาการแสดงทางคลินิก ผู้ป่วยจะมีไข้สูง ก้อนที่คอกดเจ็บ และตรวจพบ soft tissue crepitation ได้ในผู้ป่วย 5 ราย (63%) ผู้ป่วย 4 รายมีอาการแสดงของภาวะ sepsis เชื้อแบคทีเรียที่เป็นสาเหตุที่พบมากที่สุด คือ Streptococcus sp. เช่นเดียวกับรายงานอื่น แนวทางการรักษาประกอบด้วยการให้ยาปฏิชีวนะทางหลอดเลือดดำหลายชนิดที่ครอบคลุมเชื้อต่างๆ การผ่าตัดเพื่อระบายหนองและตัดเนื้อเยื่อที่อักเสบและเน่าตาย การเฝ้าระวังและรักษาโรคแทรกซ้อนรวมทั้งการผ่าตัดซ้ำหลายครั้งเพื่อตัดเนื้อเยื่อที่อักเสบและเน่าตายออกมีความสำคัญในการช่วยลดอัตราการเสียชีวิต ผู้ป่วยได้รับการผ่าตัดซ้ำโดยเฉลี่ย 3 ครั้ง มีผู้ป่วย 1 ราย เกิดโรคแทรกซ้อนที่รุนแรง คือ mediastinitis อัตราเสียชีวิตร้อยละ 13
คำสำคัญไทย :
cervicofacial necrotizing fasciitis, อาการแสดงทางคลินิก, แนวทางการรักษา
English Abstract :

A retrospective study of 8 cervicofacial necrotizing fasciitis patients presented at Nakornping Hospital between 2002 to 2007 was carried out and showed dental origin in 4 cases (50%) and parotid abscess in 2 cases (25%). Ascociated diseases were diabetes mellitus and hypoalbuminemia. Clinical manifestations were neck mass and inflammation skin. Five patients (63%) of cases were positive for soft tissue crepitation. Four patients had sepsis at first presentation. All of pus cultures were positive and the most common bacteria was Streptococcus sp. Treatment included administration of broad spectrums intravenous antibiotics and surgical debridement. Frequent neck debridement was necessary to decrease mortality. One case severe complication with a of mediastinitis was reported. This study show 13% mortality rate.
English Keyword:
cervicofacial necrotizing fasciitis, clinical manifestations clinical, management

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