腹腔鏡作為外科手術(shù)的 “眼睛”，其精密程度堪比微縮版的光學(xué)儀器，一旦出現(xiàn)故障，維修過(guò)程就像給這臺(tái) “神器” 做 “微創(chuàng)手術(shù)”，每一個(gè)操作都需謹(jǐn)小慎微。從拆解到組裝，從清潔到調(diào)試，這些關(guān)鍵要點(diǎn)決定了維修的成敗與器械的安全性。

　　Laparoscopy, as the "eye" of surgical procedures, has a precision comparable to miniature optical instruments. Once a malfunction occurs, the repair process is like performing a "minimally invasive surgery" on this "artifact", requiring careful attention to every operation. From disassembly to assembly, from cleaning to debugging, these key points determine the success or failure of maintenance and the safety of equipment.

　　拆解：像 “拆鐘表” 一樣精準(zhǔn)定位故障

　　Disassembly: Accurately locate faults like dismantling a clock

　　維修的第一步是精準(zhǔn)判斷故障源，常見(jiàn)問(wèn)題如鏡頭模糊（可能因內(nèi)部鏡片污染或損壞）、光束不亮（光纖斷裂或接口接觸不良）、器械通道卡頓（異物堵塞或機(jī)械結(jié)構(gòu)磨損）。拆解時(shí)必須使用專(zhuān)用工具（如微型螺絲刀、鑷子），避免蠻力操作 —— 曾有案例顯示，非專(zhuān)業(yè)人員用普通鉗子拆卸鏡頭，導(dǎo)致螺紋滑絲，原本簡(jiǎn)單的清潔變成整體更換。對(duì)于集成度高的部件（如攝像頭接口），需先記錄接線(xiàn)順序和位置，必要時(shí)拍照存檔，防止組裝時(shí)出現(xiàn) “多余零件” 的尷尬。

　　The first step in maintenance is to accurately identify the source of the malfunction. Common problems include blurry lenses (possibly due to internal lens contamination or damage), dim light beams (fiber breakage or poor interface contact), and instrument channel jamming (foreign object blockage or mechanical structure wear). Special tools (such as micro screwdrivers and tweezers) must be used during disassembly to avoid brute force operation - there have been cases where non professionals used ordinary pliers to disassemble lenses, causing thread slippage and turning simple cleaning into complete replacement. For highly integrated components (such as camera interfaces), it is necessary to first record the wiring sequence and position, and if necessary, take photos for archiving to prevent the embarrassment of "extra parts" during assembly.

　　清潔：對(duì)抗 “微米級(jí)污染” 的持久戰(zhàn)

　　Cleanliness: a protracted battle against 'micron level pollution'

　　腹腔鏡的光學(xué)系統(tǒng)對(duì)污染極其敏感，0.1mm 的灰塵就可能導(dǎo)致視野模糊。清潔鏡頭時(shí)，禁用普通酒精或紙巾，需用無(wú)塵布蘸取專(zhuān)用光學(xué)清潔劑（成分多為異丙醇），沿鏡片同心圓方向輕拭，避免來(lái)回擦拭產(chǎn)生劃痕。光纖束的清潔更需耐心 —— 若發(fā)現(xiàn)端面發(fā)黑，需用光纖切割刀重新打磨，打磨后需通過(guò)顯微鏡檢查端面平整度（合格標(biāo)準(zhǔn)為平面度誤差＜5μm）。對(duì)于金屬鞘管內(nèi)的血漬或組織殘留，不能僅用清水沖洗，需配合酶洗液超聲震蕩（功率控制在 30-40kHz，時(shí)間不超過(guò) 5 分鐘），再用高壓氣槍吹干，防止水汽殘留導(dǎo)致內(nèi)部銹蝕。

　　The optical system of laparoscopy is extremely sensitive to contamination, and 0.1mm dust may cause blurred vision. When cleaning the lens, do not use regular alcohol or paper towels. Instead, use a dust-free cloth dipped in specialized optical cleaning agents (mostly isopropanol) and gently wipe along the concentric circles of the lens to avoid scratches caused by back and forth wiping. The cleaning of fiber bundles requires more patience - if the end face is found to be blackened, it needs to be re polished with a fiber optic cutting knife. After polishing, the flatness of the end face needs to be checked under a microscope (the qualified standard is flatness error<5 μ m). For blood stains or tissue residues inside the metal sheath tube, it is not enough to rinse with clean water alone. It is necessary to use enzyme wash solution and ultrasonic oscillation (power controlled at 30-40kHz, time not exceeding 5 minutes), and then dry it with a high-pressure air gun to prevent internal corrosion caused by water vapor residue.

　　零件檢修：從 “發(fā)絲裂痕” 中發(fā)現(xiàn)隱患

　　Parts maintenance: hidden dangers discovered from "hair cracks"

　　鏡頭鏡片組的檢修需借助體視顯微鏡（放大倍數(shù)≥10 倍），重點(diǎn)觀(guān)察鏡片是否有脫膜、裂紋或氣泡 —— 曾有維修案例中，表面看似完好的鏡片在強(qiáng)光照射下，發(fā)現(xiàn)細(xì)微的徑向裂紋，這種隱患在手術(shù)中可能因溫度變化導(dǎo)致鏡片崩裂。金屬部件（如穿刺錐、操作鉗）的檢修需關(guān)注關(guān)節(jié)軸的磨損程度，可用塞尺測(cè)量軸孔間隙（正常應(yīng)＜0.1mm），超過(guò)則需更換軸套或銷(xiāo)釘。光纖束的斷點(diǎn)檢測(cè)需使用光源檢測(cè)儀，將光纖一端對(duì)準(zhǔn)光源，另一端觀(guān)察光斑均勻性，若出現(xiàn)暗斑或亮度衰減超過(guò) 30%，則需更換整束光纖。

　　The maintenance of the lens assembly requires the use of a stereo microscope (magnification ≥ 10x), with a focus on observing whether the lens has detachment, cracks, or bubbles - in previous maintenance cases, seemingly intact lenses were found to have subtle radial cracks under strong light, which may cause lens breakage due to temperature changes during surgery. The maintenance of metal components (such as puncture cones and operating pliers) should pay attention to the degree of wear of the joint shaft. The clearance between the shaft holes can be measured with a feeler gauge (normally<0.1mm). If it exceeds this limit, the shaft sleeve or pin needs to be replaced. The breakpoint detection of fiber optic bundles requires the use of a light source detector. Align one end of the fiber optic cable with the light source and observe the uniformity of the light spot at the other end. If dark spots or brightness attenuation exceeds 30%, the entire fiber optic bundle needs to be replaced.

　　組裝：“納米級(jí)精度” 的復(fù)位藝術(shù)

　　Assembly: The art of resetting with "nanoscale precision"

　　組裝鏡頭時(shí)，鏡片組的軸向間距需嚴(yán)格按原廠(chǎng)參數(shù)（通常精確到 0.01mm），可用千分尺配合墊片調(diào)整，間距過(guò)大或過(guò)小都會(huì)導(dǎo)致焦距偏移。攝像頭與鏡體的連接需注意螺紋咬合度，正確的手感是 “輕微阻力但能順暢旋入”，若過(guò)緊可能是螺紋錯(cuò)位，過(guò)松則會(huì)影響圖像穩(wěn)定性。器械通道的密封件安裝是防漏關(guān)鍵，O 型圈需涂抹專(zhuān)用硅基潤(rùn)滑劑（禁用石油基油脂，以防老化），并檢查唇邊是否外翻，安裝后需進(jìn)行水壓測(cè)試（0.2MPa 壓力下保持 3 分鐘無(wú)泄漏）。

　　When assembling the lens, the axial spacing of the lens group must strictly follow the original factory parameters (usually accurate to 0.01mm), which can be adjusted with a micrometer and shims. If the spacing is too large or too small, it will cause focal length deviation. The connection between the camera and the mirror body should pay attention to the degree of thread engagement. The correct hand feel is "slight resistance but smooth screwing in". If it is too tight, it may be due to thread misalignment, and if it is too loose, it will affect image stability. The installation of sealing components in the instrument channel is crucial for leak prevention. The O-ring needs to be coated with a special silicon-based lubricant (petroleum based grease is prohibited to prevent aging), and the lip edge should be checked for outward rotation. After installation, a water pressure test should be conducted (maintain a pressure of 0.2MPa for 3 minutes without leakage).

　　性能測(cè)試：比 “術(shù)前檢查” 更嚴(yán)格的驗(yàn)收

　　Performance testing: stricter acceptance than preoperative examination

　　維修后的腹腔鏡需通過(guò)多層級(jí)測(cè)試：光學(xué)性能測(cè)試中，需在分辨率測(cè)試板（如 USAF 1951）下，確認(rèn)能清晰分辨 5-6 組線(xiàn)對(duì)（對(duì)應(yīng)分辨率≥100lp/mm）；機(jī)械性能測(cè)試需模擬手術(shù)動(dòng)作，操作鉗開(kāi)合 50 次無(wú)卡頓，穿刺錐穿刺力≤20N；電氣安全測(cè)試要檢測(cè)絕緣電阻（≥20MΩ）和接地連續(xù)性（接地阻抗＜0.1Ω）。最關(guān)鍵的是密封性測(cè)試，將鏡體浸入水中，從器械通道注入 0.1MPa 空氣，觀(guān)察氣泡量（每分鐘氣泡數(shù)≤5 個(gè)為合格），任何細(xì)微漏氣都可能在手術(shù)中導(dǎo)致霧氣干擾視野。

　　The repaired laparoscope needs to pass multi-level testing: in optical performance testing, it is necessary to confirm that 5-6 sets of line pairs can be clearly distinguished under a resolution testing board (such as USAF 1951) (corresponding to a resolution ≥ 100lp/mm); Mechanical performance testing requires simulating surgical actions, operating the forceps open and close 50 times without jamming, and the puncture force of the puncture cone is ≤ 20N; electrical safety testing requires detecting insulation resistance (≥ 20M Ω) and grounding continuity (grounding impedance<0.1 Ω). The most crucial step is the sealing test. Immerse the mirror body in water, inject 0.1MPa air from the instrument channel, and observe the amount of bubbles (≤ 5 bubbles per minute is qualified). Any slight air leakage may cause fog to interfere with the field of view during surgery.

　　滅菌與追溯：給 “神器” 上雙保險(xiǎn)

　　Sterilization and traceability: double insurance for "artifacts"

　　維修后的腹腔鏡必須經(jīng)過(guò)低溫滅菌（如環(huán)氧乙烷或過(guò)氧化氫等離子），滅菌前需拆除不耐高溫部件（如電子元件），并用專(zhuān)用滅菌袋封裝（袋上注明維修日期和部件信息）。建立維修檔案是行業(yè)規(guī)范 —— 記錄故障現(xiàn)象、更換零件、測(cè)試數(shù)據(jù)等，這些信息不僅用于追溯，還能為后續(xù)維修提供參考。曾有醫(yī)院因缺失維修記錄，在器械出現(xiàn)重復(fù)故障時(shí)，無(wú)法判斷是舊傷復(fù)發(fā)還是新問(wèn)題，導(dǎo)致手術(shù)延誤，可見(jiàn)規(guī)范記錄的重要性。

　　After repair, the laparoscope must undergo low-temperature sterilization (such as ethylene oxide or hydrogen peroxide plasma). Before sterilization, non high temperature resistant components (such as electronic components) must be removed and sealed in a dedicated sterilization bag (with the repair date and component information indicated on the bag). Establishing maintenance records is an industry standard - recording fault phenomena, replacing parts, testing data, etc. This information is not only used for traceability, but also provides reference for subsequent repairs. There have been hospitals where, due to a lack of maintenance records, it was difficult to determine whether repeated equipment failures were caused by old injuries or new problems, resulting in surgical delays. This highlights the importance of standardized records.

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