[2023-05-30]YAHOO新聞-打擊密護!立院三讀修正護理人員法 無照執業最重關3年-
高血壓 高尿酸 慢性腎病 胰島素 https://2019medicinenote.blogspot.com/2019/12/blog-post_57.html . 糖尿病相關筆記~目錄 https://2019medicinenote.blogspot.com/2020/01/blog-post_4.html
高血壓 高尿酸 慢性腎病 胰島素 https://2019medicinenote.blogspot.com/2019/12/blog-post_57.html . 糖尿病相關筆記~目錄 https://2019medicinenote.blogspot.com/2020/01/blog-post_4.html
2023年7月13日 星期四
護理人員法第三十七條修正案
[2023-05-30]YAHOO新聞-打擊密護!立院三讀修正護理人員法 無照執業最重關3年-
2023年7月12日 星期三
高齡友善健康照護機構認證-高齡定義
看診順序可參考台大的做法:
順號→順號→85歲以上高齡(敬老)→檢後再診號→過號→特殊狀況號,安排叫號順序
台北榮總則將看診與掛號的優先條件區隔開來. 且限制對象為榮民及警消空勤人員. 75歲以上就可優先掛號. 但 85 歲以上才能優先看診. 一般民眾不適用這個條件.
[112-03-17]衛生福利部國民健康署-112 年高齡友善健康照護機構認證-作業說明(衛生所版)
裡面並未對高齡做出定義
國泰醫院--- 高齡及特殊族群友善服務
臺大醫院
順號→順號→85歲以上高齡(敬老)→檢後再診號→過號→特殊狀況號,安排叫號順序
台北榮總
[2021-10-25]台北榮總-高齡長者綠色通道服務
[2011-10-27]由活躍老化觀點談國民健康新願景 陳姿伶 衛生署國民健康局成人及中老年保健組組長
2014-11-04
高齡友善健康照護機構,守護長者健康 -高齡友善健康照機構推動成果發表會
落實高齡友善政策,營造組織文化
節錄
新光醫院自88年起即開始推動長者照護之服務,102年宣誓為「高齡友善年」,全院同仁致力於高齡友善環境建置及服務品質的改善。從志工或為您服務人員陪同就醫,為長者提供無障礙的就醫環境,設立高齡友善整合門診,建立80歲以上長者無縫式就醫優先服務
2023年7月10日 星期一
衛教資料
新光醫院營養科-營養衛教內容非常多.
心臟衰竭飲食原則
口腔癌術前飲食原則
大腸直腸癌術後飲食原則
全流質飲食原則
血液透析飲食原則
低油飲食原則
低渣飲食原則
吞嚥困難飲食原則
肝癌飲食原則
肝臟疾病飲食原則
乳癌術後營養飲食原則
使用抗凝血劑飲食原則
放化療期間之飲食原則
肺癌術後飲食原則
胃術後飲食原則
胃癌術後飲食原則
限鈉飲食原則
食道癌術後飲食原則
高三酸甘油脂血症飲食原則
高脂血症飲食原則
鈣質補充飲食原則
溫和飲食原則
慢性阻塞性肺病飲食原則
慢性腎臟病飲食原則
管灌配方保存方式
燒燙傷飲食原則
糖尿病飲食原則
癌症治療飲食原則
簡易食物代換表
體重控制飲食原則
2023年7月4日 星期二
急性複雜性(較嚴重的)泌尿道感染抗生素選擇 Antibiotics choice of acute complicated UTI
Asymptomatic bacteriuria 無症狀菌尿症
2018-09-21 UPTODATE 建議
複雜性UTI診斷:
Diagnosis — The diagnosis of acute complicated UTI is made in the following clinical scenarios:
1. 發燒. 或其他全身性症狀. 畏寒. 神智改變.
2. 軀幹疼痛. 懷疑腎臟發炎. 通常伴隨發燒或其他膀胱炎症狀. CT可看到腎臟周圍發炎. 有時候伴隨膿瘍. 但CT正常無法排除輕微腎盂腎炎.
3. 發燒或敗血症. 排除其他感染源.. 如果沒有膿尿. 不太可能是複雜性 UTI.
●Symptoms of cystitis (dysuria, urinary urgency, and/or urinary frequency) along with fever (>99.9ºF/37.7ºC) or other signs or symptoms of systemic illness, such as chills, rigors 嚴格.嚴酷, or acute mental status changes. In such cases, pyuria and bacteriuria support the diagnosis.
●Flank pain and/or costovertebral angle tenderness in the setting of pyuria and bacteriuria. This is suggestive of pyelonephritis. Fever and typical symptoms of cystitis are usually present, but their absence does not rule out the diagnosis. CT findings that support the diagnosis include low attenuation extending to the renal capsule on contrast enhancement with or without swelling and complications such as renal abscesses. However, a normal CT does not rule out the possibility of mild pyelonephritis.
●Fever or sepsis without localizing symptoms in the setting of pyuria and bacteriuria may be attributed to UTI if other causes have been ruled out. Careful clinical assessment is necessary. The diagnosis of is unlikely if pyuria is absent.
因複雜性 UTI 住院病患. 依據病患是否可能有多重抗藥性細菌的危險因子, 決定使用的藥物種類. 依照流程圖, 先評估病患是否需要收 ICU. 是否敗血症. 是否尿道阻塞.
再來評估是否有抗藥性: 尿培養出MDR細菌. 曾經使用 FQ. BAKTAR. 廣效效 BETA-LACTAM. 三代以上的頭孢素抗生素. 曾經去高抗藥性地區旅行. (印度.以色列. 西班牙. 墨西哥). 如果以上皆否. 可選擇
CEFTRIAXONE 1gm QD.
tazocin 3.375g Q6H 或 TAZOCIN 4.5g Q6H
CIPROXIN 400 MG Q12H IV.
CIPROXIN 500 mg PO BID
CIPROXIN 1000 mg EXTENDED RELEASE QD.
CRAVIT 750 mg IV QD.
CRAVIT 750 mg PO QD.
如果懷疑是抗藥性的 Gram positive infection. 加入下列一種
VANCOMYCIN 15mg/kg. Q12H
DAPTOMYCIN,UVOM 6mg/kg QD
LINEZOLID 600 mg IV OR oral Q12H
●No risk factors for infection with a multidrug-resistant gram-negative organism (table 2) – For these patients, we favor ceftriaxone (1 gram IV once daily) or piperacillin-tazobactam (3.375 grams IV every six hours) for parenteral treatment because of their safety profile and narrow spectrum compared with other parenteral agents. Oral or parenteral fluoroquinolones (ciprofloxacin or levofloxacin) are also reasonable alternatives if the patient has not had a urinary isolate resistant to fluoroquinolones in the prior three months and the community prevalence of E. coli fluoroquinolone resistance is not known to be higher than 10 percent.
Concern for particular pathogens should further inform the choice between these options. If Enterococcus or Staphylococcus species are suspected (eg, because of prior urinary isolates or gram-positive cocci on a current urine Gram stain), piperacillin-tazobactam is preferred because it has activity against these organisms (if the patient cannot use piperacillin-tazobactam because of allergies or otherwise, vancomycin plus one of the other gram-negative agents can be used). If drug-resistant gram-positive organisms are suspected because of previous urinary isolates or other risk factors, vancomycin (for MRSA) or linezolid or daptomycin (for vancomycin-resistant Enterococcus [VRE]) should be added. If there is a risk of P. aeruginosa (eg, because of prior urinary isolates or febrile neutropenia), piperacillin-tazobactam at a higher dose (4.5 grams IV every eight hours) or a fluoroquinolone should be chosen. Other antipseudomonal agents that can be used include cefepime (2 grams IV every eight hours) and ceftazidime (2 grams IV every eight hours).
●At least one risk factor for infection with a multidrug-resistant gram-negative organism (table 2) – For these patients, we favor empiric treatment with an antipseudomonal carbapenem (imipenem 500 mg IV every six hours, meropenem 1 gram IV every eight hours, or doripenem 500 mg IV every eight hours).
Concern for particular pathogens should further inform regimen selection. If Enterococcus species or MRSA are suspected (eg, because of prior urinary isolates or gram-positive cocci on a current urine Gram stain), we add vancomycin (for MRSA) or daptomycin or linezolid (for vancomycin-resistant Enterococcus [VRE]).
Advanced cephalosporin or carbapenem combinations with beta-lactamase inhibitors (such as ceftazidime-avibactam, ceftolozane-tazobactam, and meropenem-vaborbactam) also have activity against some ESBL-producing and multidrug-resistant P. aeruginosa isolates and are effective for acute complicated UTI [29-31], but because of cost and antimicrobial stewardship concerns, they should only be used in select cases of highly resistant infections. If carbapenem resistance is suspected based on prior susceptibility testing results, an infectious diseases consult should be obtained.
Results of urine culture and susceptibility testing should be followed to ensure that the chosen empiric antimicrobial regimen is appropriate and to guide selection of definitive therapy.
complicated cystitis UTI 抗生素選擇
泌尿道感染應該使用多少天的抗生素
哪些情況需考慮作尿液培養(eMedicine連結)
Urine Culture
Urine culture remains the criterion standard for the diagnosis of UTI. Collected urine should be sent for culture immediately; if not, it should be refrigerated at 4°C. Two culture techniques (dip slide, agar) are widely used and accurate.
The 2010 Infectious Disease Society of America (IDSA) consensus limits for cystitis and pyelonephritis in women are more than 1000 colony-forming units (CFU)/mL and more than 10,000 CFU/mL, respectively, for clean-catch midstream urine specimens. Historically, the definition of UTI was based on the finding at culture of 100,000 CFU/mL of a single organism. However, this misses up to 50% of symptomatic infections, so the lower colony rate of greater than 1000 CFU/mL is now accepted. [22]
The definition of asymptomatic bacteriuria still uses the historical threshold. Asymptomatic bacteruria in a female is defined as a urine culture (clean-catch or catheterized specimen) growing greater than 100,000 CFU/mL in an asymptomatic individual.
Note that any amount of uropathogen grown in culture from a suprapubic aspirate should be considered evidence of a UTI. Approximately 40% of patients with perinephric abscesses have sterile urine cultures.
An uncomplicated UTI (cystitis) does not require a urine culture unless the woman has experienced a failure of empiric therapy. Obtain a urine culture in patients suspected of having an upper UTI or a complicated UTI, as well in those in whom initial treatment fails.
If the patient has had a UTI within the last month, relapse is probably caused by the same organism. Relapse represents treatment failure. Reinfection occurs in 1-6 months and usually is due to a different organism (or serotype of the same organism). Obtain a urine culture for patients who are reinfected.
If a Gram stain of an uncentrifuged, clean-catch, midstream urine specimen reveals the presence of 1 bacterium per oil-immersion field, it represents 10,000 bacteria/mL of urine. A specimen (5 mL) that has been centrifuged for 5 minutes at 2000 rpm and examined under high power after Gram staining will identify lower numbers. In general, a Gram stain has a sensitivity of 90% and a specificity of 88%.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2875701/
Urine culture
The diagnosis of UTI from simple cystitis to complicated pyelonephritis with sepsis can be established with absolute certainty only by cultures of urine. The major indications for urine cultures are:
Patients with symptoms or signs of UTIs;
Follow-up of recently treated UTI;
Removal of indwelling urinary catheter;
Screening for asymptomatic bacteriuria during pregnancy; and
Patients with obstructive uropathy and stasis, before instrumentation.
Urine specimens must be cultured promptly within 2h or can be preserved by refrigeration or a suitable chemical additive (boric acid sodium formate). Acceptable methods of collection are:
Midstream urine after careful washing;
Urine obtained by single catheterization;
Urine obtained by supra pubic needle aspiration; and
Sterile needle aspiration of urine from the tube of a closed catheter drainage system.
Results of cultures depend on the clinical setting in which bacteriuria occurs. For example, E. coli are found in the urine of 80-90% of patients with acute uncomplicated cystitis and acute uncomplicated pyelonephritis. Many patients with staghorn calculi harbour urea-splitting proteus organisms in their urine. Klebsiella, Pseudomonas and Enterobacter infections are commonly acquired in the hospital. The presence of Staphylococcus aureus often is a clue to concomitant Staphylococcal bacteremia, unless an underlying risk factor exists.
Micro-organisms in young men are similar to the organisms that cause uncomplicated infections in women. Enterococci and coagulase-negative staphylococci are more common in elderly men; most likely representing recent instrumentation or catheterization. C. albicans is rarely encountered except in patients with indwelling catheters, nosocomial UTIs or relapsing infections after multiple courses of antibiotics. Although the likely organism and usual susceptible patterns are sufficient to guide initial empiric therapy of uncomplicated UTI, adequate treatment of acute bacterial pyelonephritis and complicated UTIs necessitates precise therapy based on isolation of the causative bacterium and its antimicrobial susceptibility.[13]
Significant bacteriuria
It is defined as the presence of 100 000 or more colony forming units (CFU) per ml of urine. This Kass[1] criteria has been questioned and bacterial counts of 102 or more organism per ml particularly when accompanied by pyuria (>10 wbc/mm3) provide impressive evidence of urinary tract infection in symptomatic young women.[2] The Infectious Disease Society of America (IDSA) gave a slightly more relaxed consensus definition requiring 103 organisms per ml to diagnose cystitis and 104 per ml for pyelonephritis.[3]
Clinical setting
Asymptomatic bacteriuria 無症狀菌尿症
This is especially common in women as evidenced by a minimum prevalence of 2-4% in young and 10% in elderly women. The cumulative prevalence of asymptomatic bacteriuria in women increases about 1% per decade throughout life regardless of ethnicity and geographic locations.
In contrast to women, the occurrence of asymptomatic bacteriuria in men is rare until after 55 years of age, at which time the prevalence increases per decade and approaches the rate in elderly women. Prostatic hypertrophy and increased likelihood of instrumentation account for the bacteriuria in older men.[11]
Differences between men and women in the rates of bacteriuria have been attributed to the shorter female urethra and its proximity to the vagina and rectal mucosa and their abundant microbial flora.
Clinical Features
Acute urethral syndrome
The cardinal symptoms of frequency and dysuria occur in more than 90% of ambulatory patients with acute genitourinary tract infections. However, one-third to one- half of all these patients do not have significant bacteriuria, although most have pyuria. These patients have acute urethral syndrome which can mimic both bladder and renal infections. Vaginitis, urethritis and prostatitis are common causes of the acute urethral syndrome.[14]
Vaginitis
The presence of an abnormal vaginal discharge (leucorrhoea) and irritation makes vaginitis the likely cause of dysuria unless a concomitant UTI can be confirmed by culture. Candida albicans, the most common specific cause of vaginitis, can be demonstrated by culture or by finding yeast cells in a gram-stained smear of vaginal secretions or in a saline preparation with the addition of potassium hydroxide.
Trichomoniasis can be documented with a saline preparation that shows the motile protozoa of trichomonas vaginitis. Generally, nonspecific vaginitis is associated with gardenerella vaginitis. A clue of this diagnosis is the presence of many small Gram-negative bacilli that adhere to vaginal epithelial cells.
Urethritis
Acute urinary frequency, dysuria and pyuria in the absence of vaginal symptoms favor the diagnosis of urethritis or UTI. Chlamydia trachomatis is the common cause of the acute urethral syndrome in women and of nonspecific urethritis in men. Neisseria gonorrhoeae is an important cause of urethritis and dysuria. Herpes simplex virus, usually type 2, is another sexually transmitted agent that can cause severe dysuria through ulceration in close proximity to the urethral orifice. The diagnosis of Herpes progenitalis can be confirmed by finding giant multinucleated transformed cells in epidermal scrapings stained with Wright's stain (Tzanck Smear), by isolating the virus in tissue cultures or by direct fluorescent antibody test.
Prostatitis
Prostatitis is a common problem in men that causes dysuria and urinary frequency in middle-aged and younger men more frequently than urinary tract infection do. Prostate syndromes have classically been divided into four clinical entities
Acute bacterial prostatitis
Chronic bacterial prostatitis
Nonbacterial prostatitis
Prostatodynia
Recently, consensus classification of prostatitis syndromes has come up. This classification includes four categories and two subcategories.[15]
Acute bacterial prostatitis;
Chronic bacterial prostatitis;
Chronic prostatitis/chronic pelvic pain syndrome (CP/CPPS);
Asymptomatic inflammatory prostatitis.
CP/CPPS has been divided in to two sub-categories:
Inflammatory CP/CPPS; and
Non- inflammatory CP/CPPS
Acute bacterial prostatitis: The patient often appears acutely ill with the sudden onset of chills and fever, urinary frequency and urgency, dysuria, perineal and low back pain and constitutional symptoms. Rectal examination should be avoided because of the risk of precipitating sepsis, but may disclose a tender, hot and swollen prostate. Microscopic examination of the urine usually displays numerous white cells. Urine culture is usually positive for enteric Gram-negative bacteria and Gram-positive bacteria staphylococci and enterococci are less frequently isolated.
Chronic bacterial prostatitis: Relapsing UTIs is a hallmark of chronic bacterial prostatitis. Urinary frequency, dysuria, nocturia and low back and perineal pain are the usual symptoms, although patients may have a minimum of symptoms between UTIs. The patient is often afebrile, does not appear acutely ill, and may have an unremarkable prostate examination. Initially, there is a negative midstream urine examination and culture but after prostate massage, the urine is positive for white blood cells and culture grows a uropathogen.
Nonbacterial prostatitis: This is the most common form of chronic prostatitis. It mimics chronic bacterial prostatitis clinically and displays inflammatory cells on post-prostate massage specimens. However, a bacteriological culture of urine and prostatic secretions are sterile. The etiology is unknown, but some evidence exists for an infectious cause involving organisms that are difficult to culture.
Prostatodynia: This has also been referred to as chronic noninflammatory prostatitis. Clinically, it presents with symptoms similar to other forms of chronic prostatitis. It is distinguished by the absence of inflammatory cells or uropathogens from all specimens.
Chronic prostatitis/chronic pelvic pain syndrome: The traditional classification suggested that the prostate was the cause for some patients (nonbacterial prostatitis), whereas other problems were responsible in others (prostatodynia). The characteristic symptoms for either group were very poorly defined. CP/ CPPS acknowledges the central role of pain complaints in the syndrome. Also there is inherent recognition that the prostate gland may not be responsible for every patient's symptoms. Its two subcategories are as follows:
Inflammatory CP/CPPS: The consensus classification considers symptomatic patients without bacteriuria but who have inflammation in their expressed prostate secretions, their voided bladder 3 (VB3) or their semen fluid analysis (SFA), to have inflammatory CP/CPPS.
Noninflammatory CP/CPPS: Patients without inflammation in their expressed prostate secretions, their voided bladder 3 (VB3) or their semen fluid analysis (SFA) are considered to have noninflammatory CP/CPPS.
Asymptomatic inflammatory prostatitis: The consensus classification also includes a category for patients with objective evidence of prostatic inflammation noted during histological evaluation of prostatic tissue. This diagnosis commonly occurs in patients who have inflammation documented during evaluation of other urologic conditions, for example, prostatic evaluated for a raised prostate-specific antigen. Another example is seminal fluid inflammation noted during evaluation from an infertile couple. The long-term consequences of such asymptomatic inflammation are unknown. Further, only limited data are available on the relative merits of antimicrobial or other therapies for such asymptomatic patients.
Urinary tract infection: Despite the mimicking syndromes, a presumptive diagnosis of infections of urinary tract can be established economically by analyzing urine in patients with characteristic signs and symptoms. Acute uncomplicated UTIs mainly occur in women of child-bearing age. The presenting features are only suggestive of the site of infection. Patients with bacterial cystourethritis, as distinct from urethritis caused by sexually transmitted disease (STD) pathogens, will have prior episodes and experienced symptoms for less than one week and will experience suprapubic pain
女性單純UTI口服抗生素選擇
女性單純UTI口服抗生素選擇
2023-02-02 08:36AM 目前建議第一線用藥還是選 baktar. 而 cefa 可做為第二線用藥
如果局部地區的baktar抗藥性超過 20%, 就別選 baktar.
from uptodate
Trimethoprim-sulfamethoxazole – Dosed as one double-strength tablet (160/800 mg) orally twice daily for three days. Randomized trials suggest a 79 to 100 percent clinical cure rate with a three- to seven-day regimen [48,56-58]. Empiric trimethoprim-sulfamethoxazole should be avoided if the regional prevalence of resistance is known to exceed 20 percent [29,30]. In some regions, trimethoprim (100 mg twice daily for three days) is used in place of trimethoprim-sulfamethoxazole and is considered equivalent [59].
關於台灣的大腸桿菌對 baktar 抗藥性問題. 沒有搜尋到直接的研究. 在2018年台中榮總婦產科蔡青倍醫師的文章. 有提到抗藥性問題. cefa 和 baktar 都有抗藥性的憂慮 .
女性單純膀胱炎 (cystitis/UTI) 通常開
BAKTAR 400mg BID * 3 days or
CEFA 500mg Q6H * 3-7 days
[參考資料]反反覆覆的婦女泌尿道感染 [更新日期 2018/10/8 11:30:44]
Trimethoprim-Sulfamethzazole(TMP-SMX)160/800mg. ㄧ天兩次服用三天廣效性。然而目前研究顯示對TMP-SMX有抗藥性的大腸桿菌越來越多(>17%),但由於此藥便宜,且濫用Fluoroquinolone會衍生出更多抗藥性的問題,故目前此藥還是泌尿道感染的首選藥物。
Cefalexin 250mg 一天四次服用7-10天.抗菌效果較廣泛,但其抗藥性也是與日俱增,且因其廣效性,所以可能破壞人體的正常菌叢,造成不必要的念珠菌感染,但其可以當成孕婦泌尿道感染的第二線用藥
2023-02-02 09:02AM
美國感染症學會的單純泌尿道感染指引(連結在此), 最近更新日期是 2011年3月. 已經11年沒有改版了. 
JOURNAL ARTICLE GUIDELINES-International Clinical Practice Guidelines for the Treatment of Acute Uncomplicated Cystitis and Pyelonephritis in Women: A 2010 Update by the Infectious Diseases Society of America and the European Society for Microbiology and Infectious Diseases .
Clinical Infectious Diseases, Volume 52, Issue 5, 1 March 2011, Pages e103–e120, https://doi.org/10.1093/cid/ciq257
Published: 01 March 2011
上面這篇指引放在 Oxford Academic(牛津學術?不知道有沒有比較統一正式的翻譯). 這個平台收錄牛津大學出版社 (Oxford Univerity Press, OUP) 發行的圖書與電子期刊,
2023-01-02 19:12
另一篇相關文章建議看看. 無症狀之菌尿症評估處置. from uptodate
下面這段是很久很久以前的筆記. 放在另一篇文章.
2021-07-30 參考資料 uptodate acute simple cystitis in women
第一線藥物可選下列之一
BAKTAR 比較容易遇到抗藥性. (近期曾感染. 或反覆膀胱炎/尿路感染. 需考慮抗藥性問題)
pivmecillinam 效果較差三個月內若曾服用其中一種抗生素, 再次感染可選擇另一類(避免遇到抗藥性)
First-line antimicrobial options —
The preferred agents for empiric therapy of acute simple cystitis are nitrofurantoin monohydrate/macrocrystals, trimethoprim-sulfamethoxazole, fosfomycin, and, if available, pivmecillinam because of the favorable balance between efficacy and adverse effects (including the risk of selecting for resistant organisms) [1]. None of the first-line agents clearly outweighs the others in terms of the efficacy/adverse effects balance, with the exception that resistance is more likely with trimethoprim-sulfamethoxazole and that pivmecillinam (and possibly fosfomycin) is somewhat less effective; the optimal antimicrobial in one region may be different from that in another depending on resistance prevalence (see 'Resistance trends in E. coli' above). Thus, the choice among them should be individualized based on patient circumstances (allergy, tolerability, expected adherence), local community resistance prevalence, availability, cost, and patient and provider threshold for failure. If the patient has taken one of the agents in the preceding three months, a different one should be selected.
2011-07-18
2010 update. Acute Uncomplicated Cystitis and Pyelonephritis in Women: A 2010 Update by the Infectious Diseases Society of America and the European Society for Microbiology and Infectious Diseases
不建議用FQ作為一線用藥.
FQ可用於單純的APN. 或者複雜性CYSTITIS.
https://jamanetwork.com/journals/jama/fullarticle/1832532
Empiric antimicrobial selection for women with acute uncomplicated cystitis
uncomplicated UTI in women.
如果沒有抗藥性細菌的危險, 不需要做尿液細菌培養, 抗藥性細菌風險包括過去三個月內
1. 尿曾分離出抗藥菌
2. 住養護中心/住院病患/住長照中心 (但肺炎抗藥性細菌與此無關, 與宿主本身因素有關)
3. 曾使用廣效抗生素(FQ/TMP-SMX/ 3rd cefa)
4. 曾在高抗藥細菌盛行區旅行(印度,以色列,西班牙,墨西哥)
如果以上幾種一線藥物都不適合給(沒進貨?). 可以考慮下面處方
如果不適合給 BETA-LACTAM 可以考慮給 FQ.
UTI一般給CEFA 500mg Q6H OR BAKTAR 400mg BID
慢性腎病/腎衰竭病患 CKD病患 UTI 可以給ZINNAT(CEFUROXIME) 250mg BID OR CIPROXIN 250mg BID
UPTODATE 裡面提到: 如果抗藥性細菌的機率不高, 可給一線口服抗生素. (nitrofurantoin monohydrate/macrocrystals, trimethoprim-sulfamethoxazole, fosfomycin, or pivmecillinam
Low risk for resistance — For patients who do not have risk factors for an MDR infection (table 1), we typically choose one of the first-line antimicrobial regimens (nitrofurantoin monohydrate/macrocrystals, trimethoprim-sulfamethoxazole, fosfomycin, or pivmecillinam) (algorithm 1).
For patients who have reasons to avoid all these options (either because of allergies or intolerances or a history of a urinary isolate resistant to these agents within the prior three months), we choose an alternative option.
First-line antimicrobial options — The preferred agents for empiric therapy of acute uncomplicated cystitis are nitrofurantoin monohydrate/macrocrystals, trimethoprim-sulfamethoxazole, fosfomycin, and, if available, pivmecillinam because of the favorable balance between efficacy and adverse effects (including the risk of selecting for resistant organisms) [1]. None of the first-line agents clearly outweighs the others in terms of the efficacy/adverse effects balance; the optimal antimicrobial in one region may be different from that in another depending on resistance prevalence (see 'Resistance trends in E. coli' above). Thus, the choice among them should be individualized based on patient circumstances (allergy, tolerability, expected adherence), local community resistance prevalence, availability, cost, and patient and provider threshold for failure. If the patient has taken one of the agents in the preceding three months, a different one should be selected.
If all these are appropriate options based on patient circumstances and prior urinary isolates, we suggest nitrofurantoin or trimethoprim-sulfamethoxazole rather than fosfomycin or pivmecillinam. Fosfomycin retains activity against many MDR isolates, but overuse may result in increasing rates of resistance; thus, we reserve its use for suspected MDR infections when there are no other oral options. Pivmecillinam is somewhat less effective but is commonly used in Europe because of a low risk of selection for resistance.
2023年7月3日 星期一
泌尿道感染患者- 何時須做尿液培養
如果沒有抗藥性細菌的危險, 不需要做尿液細菌培養, 抗藥性細菌風險包括過去三個月內
1. 尿曾分離出抗藥菌
2. 住養護中心/住院病患/住長照中心 (但肺炎抗藥性細菌與此無關, 與宿主本身因素有關)
3. 曾使用廣效抗生素(FQ/TMP-SMX/ 3rd cefa)
4. 曾在高抗藥細菌盛行區旅行(印度,以色列,西班牙,墨西哥)
泌尿道感染患者. 何時須做尿液培養
尿培養仍然是診斷UTI的標準。收集的尿液應立即送培養;如果沒有,應冷藏在 4°C。兩種培養技術(浸玻片、瓊脂)被廣泛使用且準確。
2010 年美國傳染病學會 (IDSA) 對女性膀胱炎和腎盂腎炎的共識限制是,對於乾淨捕獲的中流尿液樣本,菌落形成單位 (CFU)/mL 和 10,000 CFU/mL 以上。歷史上,UTI 的定義是基於單個微生物培養物濃度為 100,000 CFU/mL 時的發現。然而,這會漏掉高達 50% 的有症狀感染,因此現在可接受大於 1000 CFU/mL 的較低菌落率。 [ 22 ]
無症狀菌尿的定義仍沿用歷史閾值。女性無症狀菌尿被定義為無症狀個體的尿液培養物(乾淨捕獲或導管插入的標本)生長超過 100,000 CFU/mL。
請注意,恥骨上抽吸培養物中培養的任何數量的尿路病原體均應被視為尿路感染的證據。大約 40% 的腎週膿腫患者進行了無菌尿培養。
單純性尿路感染(膀胱炎)不需要進行尿培養,除非女性經歷過經驗性治療失敗。對懷疑患有上尿路感染或複雜性尿路感染的患者以及初始治療失敗的患者進行尿培養。
如果患者在過去一個月內曾患過尿路感染,那麼復發可能是由同一種微生物引起的。復發代表治療失敗。再感染髮生在 1-6 個月內,通常是由不同的微生物(或同一微生物的血清型)引起的。對再次感染的患者進行尿培養。
如果對未離心的干淨捕獲的中流尿液樣本進行革蘭氏染色顯示每個油浸區域存在 1 個細菌,則代表每毫升尿液中有 10,000 個細菌。革蘭氏染色後以 2000 rpm 離心 5 分鐘並在高倍鏡下檢查的樣本 (5 mL) 將識別出較低的數字。一般來說,革蘭氏染色的敏感性為 90%,特異性為 88%。
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2875701/
尿液培養
從單純性膀胱炎到並發膿毒症的複雜性腎盂腎炎,只有通過尿液培養才能絕對準確地診斷尿路感染。尿培養的主要適應症是:
有尿路感染症狀或體徵的患者;
最近治療的尿路感染的隨訪;
拔除留置導尿管;
妊娠期間篩查無症狀菌尿;患有梗阻性尿路病變和瘀血的患者,在使用儀器之前。
尿液標本必須在2小時內立即培養,或者可以通過冷藏或合適的化學添加劑(硼酸鈉)保存。可接受的收集方法有:
仔細清洗後的中流尿液;
通過單次導尿獲得的尿液;
通過恥骨上針抽吸獲得尿液;從封閉式導管引流系統的管子中無菌針吸出尿液。
培養結果取決於發生菌尿的臨床環境。例如,80-90%的急性單純性膀胱炎和急性單純性腎盂腎炎患者的尿液中發現了大腸桿菌。許多鹿角結石患者的尿液中含有分解尿素的變形桿菌。醫院內常見克雷伯氏菌、假單胞菌和腸桿菌感染。除非存在潛在的危險因素,否則金黃色葡萄球菌的存在通常是並發葡萄球菌菌血症的線索。
年輕男性體內的微生物與導致女性單純感染的微生物相似。腸球菌和凝固酶陰性葡萄球菌在老年男性中更為常見;最有可能代表最近的儀器或導管插入術。除了留置導尿管、院內尿路感染或多個抗生素療程後復發感染的患者外,白色念珠菌很少見。儘管可能的微生物和通常的易感模式足以指導單純性尿路感染的初始經驗性治療,但急性細菌性腎盂腎炎和復雜性尿路感染的充分治療需要基於致病細菌及其抗菌敏感性的分離的精確治療。 [13]
Urine Culture
Urine culture remains the criterion standard for the diagnosis of UTI. Collected urine should be sent for culture immediately; if not, it should be refrigerated at 4°C. Two culture techniques (dip slide, agar) are widely used and accurate.
The 2010 Infectious Disease Society of America (IDSA) consensus limits for cystitis and pyelonephritis in women are more than 1000 colony-forming units (CFU)/mL and more than 10,000 CFU/mL, respectively, for clean-catch midstream urine specimens. Historically, the definition of UTI was based on the finding at culture of 100,000 CFU/mL of a single organism. However, this misses up to 50% of symptomatic infections, so the lower colony rate of greater than 1000 CFU/mL is now accepted. [22]
The definition of asymptomatic bacteriuria still uses the historical threshold. Asymptomatic bacteruria in a female is defined as a urine culture (clean-catch or catheterized specimen) growing greater than 100,000 CFU/mL in an asymptomatic individual.
Note that any amount of uropathogen grown in culture from a suprapubic aspirate should be considered evidence of a UTI. Approximately 40% of patients with perinephric abscesses have sterile urine cultures.
An uncomplicated UTI (cystitis) does not require a urine culture unless the woman has experienced a failure of empiric therapy. Obtain a urine culture in patients suspected of having an upper UTI or a complicated UTI, as well in those in whom initial treatment fails.
If the patient has had a UTI within the last month, relapse is probably caused by the same organism. Relapse represents treatment failure. Reinfection occurs in 1-6 months and usually is due to a different organism (or serotype of the same organism). Obtain a urine culture for patients who are reinfected.
If a Gram stain of an uncentrifuged, clean-catch, midstream urine specimen reveals the presence of 1 bacterium per oil-immersion field, it represents 10,000 bacteria/mL of urine. A specimen (5 mL) that has been centrifuged for 5 minutes at 2000 rpm and examined under high power after Gram staining will identify lower numbers. In general, a Gram stain has a sensitivity of 90% and a specificity of 88%.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2875701/
Urine culture
The diagnosis of UTI from simple cystitis to complicated pyelonephritis with sepsis can be established with absolute certainty only by cultures of urine. The major indications for urine cultures are:
Patients with symptoms or signs of UTIs;
Follow-up of recently treated UTI;
Removal of indwelling urinary catheter;
Screening for asymptomatic bacteriuria during pregnancy; and
Patients with obstructive uropathy and stasis, before instrumentation.
Urine specimens must be cultured promptly within 2h or can be preserved by refrigeration or a suitable chemical additive (boric acid sodium formate). Acceptable methods of collection are:
Midstream urine after careful washing;
Urine obtained by single catheterization;
Urine obtained by supra pubic needle aspiration; and
Sterile needle aspiration of urine from the tube of a closed catheter drainage system.
Results of cultures depend on the clinical setting in which bacteriuria occurs. For example, E. coli are found in the urine of 80-90% of patients with acute uncomplicated cystitis and acute uncomplicated pyelonephritis. Many patients with staghorn calculi harbour urea-splitting proteus organisms in their urine. Klebsiella, Pseudomonas and Enterobacter infections are commonly acquired in the hospital. The presence of Staphylococcus aureus often is a clue to concomitant Staphylococcal bacteremia, unless an underlying risk factor exists.
Micro-organisms in young men are similar to the organisms that cause uncomplicated infections in women. Enterococci and coagulase-negative staphylococci are more common in elderly men; most likely representing recent instrumentation or catheterization. C. albicans is rarely encountered except in patients with indwelling catheters, nosocomial UTIs or relapsing infections after multiple courses of antibiotics. Although the likely organism and usual susceptible patterns are sufficient to guide initial empiric therapy of uncomplicated UTI, adequate treatment of acute bacterial pyelonephritis and complicated UTIs necessitates precise therapy based on isolation of the causative bacterium and its antimicrobial susceptibility.[13]
急性憩室炎 acute diverticulitis - StatPearls - NCBI Bookshelf
資料來源. Acute Diverticulitis - StatPearls - NCBI Bookshelf
下面中文部分是直接用 google 翻譯的. 所以有些慣用的字詞與台灣醫界使用的不同.
例如腸梗阻
介紹
急性憩室炎是由憩室微穿孔引起的炎症。憩室是結腸壁的囊狀突起。約 10% 至 25% 的憩室病患者可出現憩室炎。憩室炎可以是簡單的,也可以是簡單的和復雜的。無並發症併發症的憩室炎沒有任何相關的並發症併發症。複雜性憩室炎與膿腫、瘻管、腸梗阻或直接穿孔的形成有關。憩室炎傳統上被認為是一種主要的外科疾病並被治療,但即使在最急性的階段,它也已轉變為一種醫療管理的實體內科治療的疾病。[1] [2] [3]
病因學
增加患憩室炎機會的危險因素與憩室病相關的危險因素相同。飲食似乎發揮著重要作用。低纖維、高脂肪和紅肉飲食可能會增加患憩室病和可能的憩室炎的風險。已知肥胖和吸煙會增加憩室炎和憩室出血的可能性。最後,接觸一些藥物,包括非甾體抗炎藥 (NSAID)、類固醇和阿片類藥物,與憩室炎有關。相反,接觸他汀類藥物可能會降低症狀性憩室炎的發生率。儘管人們普遍認為堅果、種子和爆米花與憩室病、憩室炎或憩室出血的風險增加無關。[4] [5]
流行病學
大約 60% 的 60 歲以上人群患有憩室病。約 10% 至 25% 的憩室病患者會發生憩室炎。根據美國最大的全付費住院護理數據庫全國住院患者樣本 (NIS) 的數據顯示,從 1998 年到 2005 年,急性憩室炎住院人數增加了 26%,擇期手術增加了 38%。顯示年輕患者(18 至 44 歲)比老年患者(45 至 74 歲)更有可能入院。這一趨勢可能是由於診斷測試方式的及時診斷和改進。西方國家絕大多數人可能患有左側憩室病,而亞洲人後裔則可能患有右側憩室病。世界各地的,急性憩室炎入院的平均年齡為 63 歲。儘管最初發現這種疾病在男性中更為普遍,但最近的數據顯示,憩室炎在男性和女性中的分佈是相等的。憩室炎更常見於50歲以下的男性和50至70歲的女性。70歲以上患者發生憩室炎的女性較多。[6]
病理生理學
憩室炎是憩室壁微觀和宏觀穿孔的結果。此前,醫生認為糞便堵塞結腸憩室會導致憩室內壓力增加,進而導致穿孔。他們現在推測,腔內壓力增加是由於食物顆粒導致憩室壁侵蝕。這會導致該區域的局灶性炎症和壞死,從而導致穿孔。周圍的腸系膜脂肪很容易含有微穿孔。這可能導致局部膿腫形成、鄰近器官瘻管或腸梗阻。最終,如果不進行快速診斷和治療,直接的腸壁穿孔可能會導致腹膜炎和死亡。[7]
歷史和身體
急性憩室炎的臨床表現根據疾病的嚴重程度而有所不同。患有單純性憩室炎的患者通常會出現左下腹疼痛,這反映了西方國家左側疾病的傾向。然而,亞裔患者主要表現為右側腹痛。疼痛可以是持續性的,也可以是間歇性的。排便習慣的改變,無論是腹瀉(35%)還是便秘(50%),都可能與腹痛有關。患者還可能出現噁心和嘔吐,可能繼發於腸梗阻。膿腫和穿孔患者發燒並不少見。當腸道發炎部分直接接觸膀胱壁時,患者可能會出現排尿困難、尿頻和尿急,這被稱為交感性膀胱炎。
在體檢時,由於腹膜刺激,炎症區域幾乎總是存在觸診壓痛。如果存在膿腫,大約 20% 的患者可能會感覺到腫塊。腸鳴音通常不活躍,但也可以正常。患者可出現腹膜體徵(僵硬、衛衛、反跳痛)並伴有腸壁穿孔。另一方面,發燒幾乎總是存在,但低血壓和休克並不常見。
評估
僅根據病史和體格檢查即可在臨床上診斷急性憩室炎。然而,24% 至 68% 的病例臨床診斷可能不准確。因此,實驗室和放射學檢查在急性憩室炎的準確診斷中起著重要作用。實驗室檢查可能顯示白細胞增多和急性期反應物升高,例如紅細胞沉降率 (ESR) 和 C 反應蛋白 (CRP)。急性憩室炎的首選放射學檢查是腹部和骨盆 CT,最好使用水溶性口服或直腸(如果有明顯噁心和嘔吐)造影劑和靜脈注射造影劑,前提是沒有禁忌症。據報導,CT 掃描的敏感性、特異性和陰性預測值大於 97%。[8]
腹部超聲可準確診斷急性憩室炎,與 CT 相比具有相對敏感性(84% 至 94%)和特異性(80% 至 93%)。然而,超聲(US)結果高度依賴於操作者,儘管數據令人鼓舞、成本較低且易於獲得,但其使用仍受到限制。MRI 是另一種可能的診斷方式。由於成本以及無法直接比較敏感性或特異性,通常首選 CT。腹部 X 光片可能只會顯示非特異性異常,例如腸脹氣;然而,如果患者患有腸梗阻,則可能會出現氣液平面。
由於穿孔風險增加,疑似急性憩室炎應避免進行內窺鏡檢查。建議在症狀消失後大約六到八週進行結腸鏡檢查,以排除惡性腫瘤、炎症性腸病或可能的結腸炎(如果患者最近沒有接受過結腸鏡檢查)。
治療/管理
根據臨床表現,急性憩室炎可以通過門診或住院治療進行治療。根據美國結腸和直腸外科醫生協會的說法,不能耐受口服攝入、過度嘔吐、出現腹膜炎跡象、免疫功能低下或高齡的患者應住院治療。如果不存在這些情況,並且如果可以進行適當的及時隨訪,則可以在門診治療急性憩室炎。據悉,門診管理成功率約為94%至97%。門診護理的標準包括腸道休息、增加液體攝入量和口服抗生素治療(單一或多種藥物療法),涵蓋革蘭氏陰性桿菌和厭氧菌。[8] [3] [9]
憩室炎的住院治療需要靜脈注射抗生素、靜脈輸液和疼痛治療。同樣,抗生素應覆蓋革蘭氏陰性桿菌和厭氧菌,並服用 3 至 5 天,然後改用口服抗生素,療程為 10 至 14 天。對於需要住院的患者,優先選擇腸道休息。通常,應在住院兩到四天內觀察退熱和白細胞增多的改善,否則應懷疑其他診斷或併發症。應考慮立即進行手術評估。
大約 15% 的急性憩室炎患者會出現膿腫,特別是結腸周圍和腸系膜內膿腫。臨床上,如果儘管靜脈注射足夠的抗生素,發燒和白細胞增多仍未消退,則應懷疑膿腫形成。體檢時,腹部壓痛和腫塊壓痛提示可能形成膿腫。小於2厘米至3厘米的膿腫可以用靜脈注射抗生素保守治療。大膿腫應在CT引導下經皮引流。
瘻管形成是急性憩室炎的另一個並發症。據報導,只有不到5%的人會出現瘻管;然而,大約 20% 接受憩室炎手術的患者中發現了這種情況。最常見的瘻管是膀胱瘻管,約佔 65% 的病例。糞尿是結腸膀胱瘺的特有症狀。手術修復瘻管並進行一期吻合術是首選治療方法。結腸陰道瘺、結腸腸瘺、結腸瘺、結腸瘺和結腸皮膚瘺是急性複雜性憩室炎中其他可能出現的瘻管。
結腸腸梗阻引起的部分腸梗阻或假性梗阻也可能發生,可以保守治療。急性憩室炎中完全性腸梗阻很少見。如果發生游離穿孔,應進行手術治療。
預後
憩室炎患者的預後取決於就診年齡、合併症的存在和疾病的嚴重程度。一般來說,年輕人的發病率往往較高,因為他們從不懷疑自己患有這種疾病,而且往往較晚就診。此外,免疫功能低下的患者往往具有較高的發病率和死亡率。[10]
現行療法及其他議題
如前所述,大約 15% 的急性憩室炎患者會出現並發症。百分之二十到百分之五十的患者會出現憩室炎反復發作。多次發作似乎不會直接增加並發症的風險。它可能會增加纖維化的風險,導致狹窄形成和隨後的阻塞。一些患者(約 20%)會因腸易激綜合徵或慢性低度憩室炎而出現慢性腹痛。這些患者可能會被轉診進行選擇性結腸切除術以控制症狀。自 1998 年以來,憩室炎的選擇性手術增加了約 30%。
通過適當的保守治療,無並發症的憩室炎的死亡率可以忽略不計。需要手術的複雜性憩室炎可能導致大約 5% 的患者死亡。腸穿孔引起的腹膜炎會使死亡風險增加至 20%。
Continuing Education Activity
Acute diverticulitis is inflammation of a diverticulum, a sac-like protrusion from the colon wall, due to micro-perforation. Diverticulitis presents in 10% to 25% of patients with diverticulosis. In the past, diverticulitis was treated surgically, however it is now a medically-managed entity, even in its most acute phase. This activity reviews the evaluation and management of diverticulitis and highlights the importance of a well-coordinated interprofessional team in caring for patients with this condition
Objectives:
- Identify risk factors for diverticulitis.
- Explain the clinical evaluation of a patient with diverticulitis.
- Explain how to manage a patient with diverticulitis.
- Outline the role of a collaborative interprofessional team in caring for patients with diverticulitis.
Introduction
Acute diverticulitis is inflammation due to micro-perforation of a diverticulum. The diverticulum is a sac-like protrusion of the colon wall. Diverticulitis can present in about 10% to 25% of patients with diverticulosis. Diverticulitis can be simple or uncomplicated and complicated. Uncomplicated diverticulitis is without any associated complications. Complicated diverticulitis is associated with the formation of abscess, fistula, bowel obstruction, or frank perforation. Diverticulitis has conventionally been known and treated as a primarily surgical illness, but this has transitioned to be a medically managed entity even in its most acute phase.[1][2][3]
Etiology
Risk factors that increase the chances of developing diverticulitis are the same as those related to diverticulosis. Diet appears to play a significant role. Low fiber, high fat, and red meat diets may increase the risk for development of diverticulosis and possible diverticulitis. Obesity and smoking are known to increase the potential for both diverticulitis and diverticular bleeding. Finally, exposure to some drugs including nonsteroidal anti-inflammatory drugs (NSAIDs), steroids, and opiates are associated with diverticulitis. Conversely, exposure to statin drugs may decrease the incidence of symptomatic diverticulitis. Despite a common popular belief, nuts, seeds, and popcorn are not associated with increased risk of diverticulosis, diverticulitis, or diverticular bleeding.[4][5]
Epidemiology
Diverticulosis is present in approximately 60% of people older than 60 years. Diverticulitis occurs in about 10% to 25% of patients with diverticulosis. According to the Nationwide Inpatient Sample (NIS), the largest, all-payer inpatient care database in the United States revealed that there was 26% increase in hospitalizations for acute diverticulitis and a 38% increase in elective operations from 1998 through 2005. It further shows that young patients (18 to 44 years) are more likely to be admitted to the hospital than older patients (45 to 74 years). This trend is likely due to prompt diagnosis and improvement in diagnostic testing modalities. Western nations are overwhelmingly likely to have left-sided diverticulosis, whereas those of Asian descent are likely to have the right-sided disease. Across the world, the mean age for admission for acute diverticulitis is 63 years old. Though the disease was initially noted to be more prevalent in males, more recent data shows that the distribution of diverticulitis is equal in both males and females. Diverticulitis more commonly occurs in men younger than the age of 50 and women 50 to 70 years old. Diverticulitis occurring in patients over the age of 70 are more likely to be female.[6]
Pathophysiology
Diverticulitis is the result of microscopic and macroscopic perforations of the diverticular wall. Previously, practitioners thought that obstruction of colonic diverticulum with fecaliths led to increased pressure within the diverticulum and subsequent perforation. They now theorized that increased luminal pressure is due to food particles that lead to erosion of the diverticular wall. This causes focal inflammation and necrosis of the region, causing perforation. Surrounding mesenteric fat may easily contain micro-perforations. This can result in local abscess formation, fistulization of adjacent organs, or intestinal obstruction. Ultimately, frank bowel wall perforations can lead to peritonitis and death without rapid diagnosis and treatment.[7]
History and Physical
Clinical manifestation of acute diverticulitis varies depending on the severity of the disease. Patients with uncomplicated diverticulitis typically present with left lower quadrant abdominal pain, reflecting that propensity of left-sided disease in Western nations. However, patients of Asian descent present with predominantly right-sided abdominal pain. The pain can be constant or intermittent. Change in bowel habits, either diarrhea (35%) or constipation (50%), can be associated with abdominal pain. Patients may also experience nausea and vomiting, possibly secondary to bowel obstruction. Fever is not uncommon in patients with abscesses and perforation. Dysuria, frequency, and urgency can occur in patients when the inflamed portion of the bowel comes into direct contact with the bladder wall, which is called as sympathetic cystitis.
On physical examination, tenderness to palpation over the area of inflammation is almost always present due to irritation of the peritoneum. A mass may be felt in approximately 20% of patients if an abscess is present. Bowel sounds are usually hypoactive but can be normoactive. Patients can present with peritoneal signs (rigidity, guarding, rebound tenderness) with bowel wall perforation. On the other hand, fever is almost always present, but hypotension and shock are uncommon.
Evaluation
Diagnosis of acute diverticulitis can be made clinically based on history and physical examination alone. However, clinical diagnosis can be inaccurate in 24% to 68% of cases. Hence, laboratory and radiological tests play an important role in the accurate diagnosis of acute diverticulitis. Laboratory tests may show leukocytosis and elevation of acute phase reactants such as erythrocyte sedimentation rate (ESR) and C-reactive protein (CRP). The radiological test of choice for acute diverticulitis is CT of the abdomen and pelvis, preferably with water-soluble oral or rectal (if significant nausea and vomiting) contrast and intravenous contrast provided there be no contraindications. The sensitivity, specificity, and negative predictive value of a CT scan have been reported as greater than 97%. Typical findings of acute diverticulitis in CT scans include bowel wall thickening, pericolic fat stranding, pericolic fluid, and small abscesses confined to the colonic wall as well as contrast extravasation, indicating intramural sinus and fistula formation.[8]
Abdominal ultrasound can accurately diagnose acute diverticulitis, with comparative sensitivity (84% to 94%) and specificity (80% to 93%) as of CT. However, ultrasound (US) results are highly operator dependent, and use is limited despite encouraging data, lower cost, and easy availability. MRI is another possible diagnostic modality. Due to cost and no direct comparison of sensitivity or specificity, CT is usually preferred. Radiographs of the abdomen will probably only show nonspecific abnormalities such as bowel gas; however, if the patient has an intestinal obstruction, air-fluid levels can be present.
Endoscopy should be avoided in suspected acute diverticulitis due to an increased risk of perforation. It is recommended that a colonoscopy is performed approximately six to eight weeks after symptoms have resolved to rule out malignancy, inflammatory bowel disease, or possibly colitis if the patient has not had a recent colonoscopy.
Treatment / Management
Upon clinical presentation, acute diverticulitis can be managed with either outpatient or inpatient care. According to American Society of Colon and Rectal Surgeons, a patient who cannot tolerate oral intake, is excessively vomiting, shows signs of peritonitis, is immunocompromised, or at an advanced age should be hospitalized. In the absence of these conditions, and if appropriate prompt follow-up can be established, acute diverticulitis can be managed on an outpatient basis. It is reported that success rate of outpatient management is about 94% to 97%. The standard of outpatient care includes bowel rest, increase fluid intake, and oral antibiotic therapy (single or multiple drug regimen) that covers gram-negative rods and anaerobic bacteria. The most common regimen used in the United States consists of quinolones (ciprofloxacin) or sulfa drugs (trimethoprim/sulfamethoxazole) in combination with metronidazole (or clindamycin, if the patient is intolerant to metronidazole) or single agent amoxicillin-clavulanate for 7 to 10 days.[8][3][9]
Inpatient management of diverticulitis requires intravenous antibiotics, intravenous fluids, and pain management. Again, antibiotics should cover gram-negative rods and anaerobes and be given for three to 5 days before switching to oral antibiotics for a ten to 14-day course. Bowel rest is preferred in patients requiring inpatient admission. Typically, defervescence and improvement in leukocytosis should be observed for two to four days of hospitalization, if not an alternative diagnosis or complications should be suspected. Prompt surgical evaluation should be considered.
About 15% patients with acute diverticulitis develop an abscess, specifically pericolonic and intra-mesenteric. Clinically, abscess formation should be suspected if fever and leukocytosis do not subside despite adequate intravenous (IV) antibiotics. On physical exam, a tender abdomen and tender mass suggest possible abscess formation. Abscesses that are less than 2 cm to 3 cm can be treated conservatively with IV antibiotics. Large abscesses should be drained percutaneously with CT guidance.
Fistula formation is another complication of acute diverticulitis. It is reported that less than 5% develops fistula; however, it has been found in about 20% of patients who undergo surgery for diverticulitis. The most common fistula is colovesicular fistula which occurs in about 65% of cases. Fecaluria is pathognomonic for colovesicular fistula. Surgical repair of the fistula with primary anastomosis is the treatment of choice. Colovaginal, coloenteric, colouterine, colourethral, and colocutaneous are other possible fistulae seen in acute complicated diverticulitis.
Partial bowel obstruction or pseudo-obstruction due to colonic ileus can occur as well, which can be managed conservatively. Complete bowel obstruction is rare in acute diverticulitis. Free perforation, if it occurs, should be managed surgically.
Differential Diagnosis
- Cholangitis
- Cholecystitis
- Chronic mesenteric ischemia
- Constipation
- Enterovesical fistula
- Gynecological pain
- Inflammatory bowel disease
- Intestinal perforation
- Irritable bowel syndrome (IBS)
- Large-bowel obstruction
Prognosis
The prognosis of patients with diverticulitis depends on age at presentation, the presence of comorbidity and severity of the disease. In general, younger people tend to have a higher morbidity as they never suspect they have the disorder and often present late. In addition, patients who are immunocompromised tend to have high morbidity and mortality.[10]
Complications
- Pelvic abscess
- Intestinal perforation
- Bowel fistula
- Peritonitis
- Bowel obstruction
- Sepsis
- Bleeding per rectum
Postoperative and Rehabilitation Care
After recovering from diverticulitis, the patient must be examined to rule out a malignancy. Options for investigation of the colon include colonoscopy, CT scan or a barium enema.
The patient should start a high-fiber diet, drink ample water, maintain a healthy weight and exercise.
Pearls and Other Issues
As previously stated, approximately 15% of patients with acute diverticulitis develop complications. Twenty percent to 50% of patients develop recurrent episodes of diverticulitis. Having multiple episodes does not appear to increase the risk for complications directly. It may increase the risk of fibrosis, leading to stricture formation and subsequent obstruction. Some patients, approximately 20%, will experience chronic abdominal pain due to either irritable bowel syndrome or chronic low-grade diverticulitis. These patients may be referred for elective colectomy for symptom control. Elective operations for diverticulitis have increased by approximately 30% since 1998.
The mortality rate in uncomplicated diverticulitis is negligible with appropriate conservative therapy. Complicated diverticulitis requiring surgery may lead to death in approximately 5% of patients. Perforation of the bowel with resulting peritonitis increases the risk of death to 20%.
Enhancing Healthcare Team Outcomes
Acute diverticulitis has enormous morbidity and while there are no universal guidelines, expert opinion recommends an interprofessional approach for diagnosis and management. The disorder needs to be staged radiologically. In addition, the patient needs a dietary consult regarding a high-fiber diet. Nurses need to assist in educating the patient on following dietary restrictions. An infectious disease consultant and a gastroenterologist need to determine the duration of antibiotic therapy and a general surgeon is necessary to develop a protocol for management of any pelvic abscess. Finally, a general or colorectal surgery should determine the proximal levels of colon resection but the amount of clear proximal margin needed remains unknown. Because the risk of colon cancer in patients with acute diverticulitis is slightly increased, a screening program has to be established.[11][12] [13] (Level III)
Outcomes
Many cases studies reveal that the majority of patients treated for acute diverticulitis do not have a recurrence after initial medical treatment. However, in patients with recurrence, surgical excision of the diseased bowel is recommended, especially in patients over the age of 50. (Level V) Finally, the decision to perform laparoscopic or open surgery for managing acute diverticulitis remains debatable. One study showed no difference in postoperative morbidity between the two. [2][14](Level III) Randomized clinical studies are needed to determine which surgery and what type of surgery is ideal for patients with acute diverticulitis.
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