Purpose: Multi-series CT examination is common in the clinic, but no metric is agreed upon to report the overall dose from such an examination. This work proposes a relevant metric for tracking patient dose from multi-series examinations and illustrates the evaluation method through explanatory examples. Materials and methods: In each acquisition series, a previously reported method was used to evaluate the cross-sectional average dose along the z-axis of a water phantom, with inputs of CTDI vol , scan length, tube current, and patient water-equivalent diameter. With a multi-series examination, the dose at each z-location was accumulated over all acquisition series. This method was applied to four clinical CT examinations. In three abdominal/pelvic examinations (patient weight, 107, 79, 79 kg), tube current modulation was applied in five acquisition series with scan lengths of 30-41.8 cm, while tube current was fixed in other series with short scan lengths (1.0, 7.9 cm). In another CT-guided liver ablation procedure (patient weight, 114 kg), 22 series were acquired with constant mA and scan lengths of 1-30 cm. The maximum value of the overall dose profile of each examination was compared to five dose quantities, including CTDI vol,sum and SSDE sum by the ACR CT Dose Index Registry, scan length-weighted CTDI vol and SSDE by a CT dose monitoring platform, and "max z location CTDI vol " by a CT manufacturer. Results: A simple graphic display of dose as a function of the z-axis location was presented for each acquisition series and for the whole examination. Differences up to 43.4% and 42.8%, or down to À93.5%, À93.5%, and À49.0%, were observed between the maximum value of the overall dose profile and five dose quantities (in the above order), respectively. Conclusion: The overall dose profile gives a complete description of z-axis dose distribution for the studied CT examinations under a wide range of patient variables and acquisition conditions, including multiple acquisition series. Simple visualization of the doses across and beyond the scan ranges may provide a new tool for CT dose optimization.